Cited by 404Memory and Neural MechanismsNeural and Behavioral Psychology StudiesFunctional Brain Connectivity Studies

The DOI matches its Crossref record; 85 of the 86 references it cites were found in a registry or an index.

The connections of the amygdala and of the anterior temporal cortex in the human brain.

Klingler, J., Gloor, P.·1960·Journal of Comparative Neurology

DOI 10.1002/cne.901150305

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1002/cne.901150305

Cites

85 of 85 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

HIPPOCAMPAL PROJECTIONS AND RELATED NEURAL PATHWAYS TO THE MID-BRAIN IN THE CAT
Nauta, W. J. H. (1958) · Brain · doi:10.1093/brain/81.3.319 · Cited by 990
Further contributions to the study of the evolution of the forebrain
Johnston, J. B. (1923) · Journal of Comparative Neurology · doi:10.1002/cne.900350502 · Cited by 575
Subcortical projections from the temporal neocortex in Macaca mulatta
Whitlock, D., & Nauta, W. J. H. (1956) · The Journal of Comparative Neurology · doi:10.1002/cne.901060107 · Cited by 503
COMPARATIVE ANATOMY OF THE NERVOUS SYSTEM OF VERTEBRATES INCLUDING MAN
Kappers, C. V. A., Huber, J. C., & Crosby, E. C. (1937) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-193711000-00043 · Cited by 451
The diencephalon of the albino rat: studies on the brain of the rat. No. 2
Gurdjian, E. S. (1927) · Journal of Comparative Neurology · doi:10.1002/cne.900430102 · Cited by 439
Histological Studies on the Localization of Cerebral Function
Coriat, I. H., & Campbell, A. W. (1906) · The American Journal of Psychology · doi:10.2307/1412355 · Cited by 406
The Amygdaloid Complex
Marburg, O. (2007) · Stereotactic and Functional Neurosurgery · doi:10.1159/000105833 · Cited by 387
Anatomie Des Centres Nerveux
Meyer, A. (1895) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-189502000-00030 · Cited by 379
The nuclei and fiber paths of the avian diencephalon, with consideration of telencephalic and certain mesencephalic centers and connections
Huber, G. C., & Crosby, E. C. (1929) · The Journal of Comparative Neurology · doi:10.1002/cne.900480102 · Cited by 286
Corticifugal fiber connections of the cortex of Macaca Mullatta. The frontal region
Mettler, F. A. (1935) · The Journal of Comparative Neurology · doi:10.1002/cne.900610306 · Cited by 278

Flagged first, then by citations

Show all 86 references

1 of the 86 references couldn’t be matched to a known paper.

Research works printed but not linked: 42

Auer J., 1953, Some afferent connections of the hypothalamus in the cat, Anat. Rec., 115, 277
Bechterew W., 1885, Zur Frage über secondäre Degenerationen des Hirnschenkels. (Abstract), Neur. Zentralbl., 4, 398
von Brero G. C. J., 1897, La terminaison corticale du faisceau latéral pédonuclaire (Faisceau de Türck), (Abstract), Neur. Centralbl., 16, 949
Broca P., 1879, Recherches sur les centres olfactifs, Rev. d'anthrop., 2, 385
Brockhaus H., 1938, Zur normalen und pathologischen Anatomic des Mandelkerngebietes (Subzona semicorticalis amygdalea und Subzona claustralis praeamygdalea), J. Psychol. Neur., 49, 1
Cajal S. R., 1911, Histologie du Système Nerveux de l'Homme et des Vertébrés, 993
Déjerine J., 1897, Sur les dégénérescences secondaires consécutives aux lésions de la circonvolution de 1′hippocampe, de la corne d'Ammon, de la circonvolution godronnée et duxpli rétrolimbique (trigone cérébral, commissure antérieure, faisceau inférieur du forceps calleux, tapétum et faisceau occipito‐frontal), C. R. Soc. Biol., 49, 587
Déjerine J., 1904, Un cas de cécité verbale avec a graphie suivi d'autopsie, Rev. Neur., 12, 655
Dell P., 1952, Corrélations entre le système végétatif et le système de la vie de relation. Méséncephale, diencéphale et cortex cérébral, J. Physiol. (Paris), 44, 471
Dell P., 1951, Projections “secondaires” mésencéphaliques, diencéphaliques et amygdaliennes des afférences viscérales vagales, C. R. Soc. Biol., 145, 1088
Edinger L., 1904, Bau der nervösen Zentralorgane, 398
Edinger L., 1903, Untersuchungen über die vergleichende Anatomie des Gehirns 5. Das Vorderhirn der Vögel, Abhandl. der Senckenbergischen Naturf. Gesellsch., 20, 343
Fox C. A., 1949, Amygdalo‐thalamic connections. In Macaca mulatta, Anat. Rec., 103, 537
Gardner L. D., 1948, Degeneration of the cingulum in the monkey, Anat. Rec., 100, 663
Groebbels F., 1924, Untersuchungen über den Thalamus und das Mittelhirn der Vögel, Anat. Anz., 57, 385
Hall E.1959Ph. D. Thesis. University of Ottawa in preparation.
Hilpert P., 1928, Der Mandelkern des Menschen. I. Cytoarchitektonik und Faserverbindungen, J. Psychol. Neur., 36, 44
Hirasawa K., 1938, Beitrag zur Kenntnis über die corticalen extrapyiamidalen Fasern aus der Area temporalis superior (area 22) beim Affen, Ztschr, Mikr.‐ Anat. Forsch., 44, 74
Klingler J., 1935, Erleichterung der makroskopischen Präparation des Gehirns durch den Gefrierprozess, Schweiz. Arch. Neur. Psychiat., 36, 247
Klingler J., 1941, Ein zerlegbares Modell der Vorder‐ und Mittelhirnkerne des Menschen mit Einschluss der angrenzenden Rindenpartien, Ztschr. Anat., 111, 1
Klingler J., 1948, Die makroskopische Anatomieder Ammonsformation, Denkschr. Schweiz. Naturf. Ges., 78, 1
Klingler J., 1949, Makroskopische Darstellung des Faserverlaufes im Rhinencephalon, Schweiz Med. Wchnschr., 79, 460
Klingler J., 1953, Die Hirnschenkelschlinge auf Grund makroskopischer Präparation, Acta Anat., 19, 383
Klingler J., 1954, La commissure blanche antérieure, l'anse pédonculaire, et le genou temporal de la radiation optique vus sur des préparations macroscopiques, 1
Koelliker A., 1896, Handbuch der Gewebelehre des Menscheri, 874
Ludwig E., 1938, Noyaux et faisceaux du cerveau humain. Table VI
Ludwig E., 1956, Atlas Cerebri Humani
Macchi G., 1955, Richerche sulle connessioni talamo‐corticali. II Sulle proiezioni dei nuclei dell a linea mediana ed intralaminari: II. problema delle connessioni talamo‐rinencefaliche. (Studio sperimentale nel gatto.), Arch. Ital. Anat. Embryol., 60, 413
Nauta W. J. H., 1958, Some projections of the amygdaloid complex in the monkey, Anat. Rec., 130, 346
Neuburger M., 1910, Ludwig Türck's gesammelte neurclogische Schriften, Jahrb. Psychiat. Neurol., 31, 23
Obenchain J. B., 1925, The brains of the South American Marsupials Caenolestes and Orolestes. Field Museum of Natural History, Publ. 224, Zool. Series, 14, 175
Papez J. W., 1945, Fiber tracts of the amygdaloid region in the human brain, from a graphic reconstruction of fiber connections and nuclear masses, Anat. Rec., 91, 294
Popoff N., 1886, Zur Frage der Urspungsgebiete der vorderen Commissur in der Hirnrinde des Menschen, Neur. Zentralbl., 5, 521
Probst M.1901Zur Kenntnis des Faserverlaufes des Temporallappens des Bulbus olfactorius der vorderen Commissur und des Fornix nach entsprechenden Extirpations und Durchsclneidungsversuchen.Arch. Anat. Physiol. Anat. Abth. pp.338–356.
Probst M., 1903, Über die Leitungsbahnen des Grosshirns mit besonderer Berücksichtigung der Anatomie und Physiologic des Sheügels, Jahrb. Psychiat. Neur., 23, 18
Probst M.1903bÜber die Rinden‐Sheügelfasern über die Schweifkernfaserung und über die Vertheilung der Pyramidenfasern im Pyramidenareal.Arch. Anat. Physiol. Anat. Abth. pp.138–152.
Robinson F., 1951, Sensory mechanisms in hippocampus, cingulate gyrus and cerebellum of the cat, Fed. Proc., 10, 110
Schlesinger B., 1928, Die Vorder‐ und Mittelhirnganglien des Menschen als plastische Gebilde. Ein Beitrag zur Anatomie und Präparationstechnik des Zentralnervensystems, 55
Villiger E., 1922, Gehirn und Rückenmark
Vogt C., 1908, La myéloarchitecture du thalamus du cercopithèque, J. Psychol. Neurol., 12, 285
Walker A. E., 1938, The Primate Thalamus, 321
Zingerle N., 1912, Über einseitigen Schläfenlappendefekt beim Menschen, J. Psychol. Neur., 18, 205

Sorted by citations

Items 201–300 of 404

Anatomical pathways related to the clinical findings in aneurysms of the anterior communicating artery
Taren, J. A. (1965) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.28.3.228 · Cited by 20
Clinical and Chronotopographic Psychomotor Seizure Pattems (SEEG Study with Reference to Postoperative Results)
Wieser, H. G., Meles, H. P., Bernoulli, C., & Siegfried, J. (1980) · Acta neurochirurgica. Supplementum · doi:10.1007/978-3-7091-8592-6_12 · Cited by 20
Microsurgical anatomy of the amygdaloid body and its connections
Weiss, A., Carlo, D. T. D., di Russo, P., Weiss, F., Castagna, M., Cosottini, M., & Perrini, P. (2021) · Brain Structure and Function · doi:10.1007/s00429-020-02214-3 · Cited by 20
Space-Occupying Lesions of the Sensori-Motor Region
Ebeling, U., & Reulen, H.-J. (1995) · Advances and technical standards in neurosurgery · doi:10.1007/978-3-7091-6898-1_3 · Cited by 19
Cognition and Emotion
LeDoux, J. E. (1984) · Handbook of Cognitive Neuroscience · doi:10.1007/978-1-4899-2177-2_17 · Cited by 18
Number processing in temporal lobe epilepsy
Delazer, M. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.023614 · Cited by 18
Preserved Crossmodal Association Following Bilateral Amygdalotomy in Man
Lee, G. P., Meador, K. J., Smith, J. R., Loring, D. W., & Flanigin, H. F. (1988) · International Journal of Neuroscience · doi:10.3109/00207458808985727 · Cited by 18
Neocortico-limbic relations in the cat
Niemer, W. T., Goodfellow, E. F., & Speaker, J. (1963) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(63)90173-1 · Cited by 18
Ictal Central Apnea Is Predictive of Mesial Temporal Seizure Onset: An Intracranial Investigation
Lacuey, N., Talavera, B., Magana‐Tellez, O., Páez, O. M., Hupp, N. J., Luo, X., Hampson, J. P., Hampson, J. S., Rani, M. R. S., Ochoa‐Urrea, M., et al. (2024) · Annals of Neurology · doi:10.1002/ana.26888 · Cited by 17
“42 The posterior frontal operculum carries primary motor representation of the larynx, 43 – 45 and is involved in a variety of orofacial, 46 pharyngeal, and laryngeal movements, 47 some of which may contribute to volitional control of respiration.”
Background
The ansa peduncularis in the human brain: A tractography and fiber dissection study
Li, M., Ribas, E. C., Wei, P., Li, M., Zhang, H., & Guo, Q. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146978 · Cited by 17
Small petrosal approach to the middle portion of the mediobasal temporal region: technical case report
Türe, U., & Pamir, M. N. (2003) · Surgical Neurology · doi:10.1016/s0090-3019(03)00382-3 · Cited by 17
Limbic and Other Neural Pathways That Regulate Endocrine Function
de GROOT, J. (1966) · Elsevier eBooks · doi:10.1016/b978-1-4832-3228-7.50010-4 · Cited by 17
Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey
Mohedano‐Moriano, A., Muñoz, M., Sanz‐Arigita, E., Pró-Sistiaga, P., Martı́nez-Marcos, A., Legidos‐Garcia, M. E., Serrano, A. M. I., Sánchez, S. C., Jiménez, M. D. M. A., Marcos, P., et al. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23805 · Cited by 15
“The anatomical connection of the ATL and prefrontal cortex via the uncinate fasciculus has been known since the beginning of the last century (Curran, 1909; Kl€uver and Bucy, 1939; Nauta and Whitlock, 1956; Kaada, 1960; Klingler and Gloor, 1960).”
Background
Neuronal Migration and Axonal Pathways Linked to Human Fetal Insular Development Revealed by Diffusion MR Tractography
Das, A., & Takahashi, E. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx224 · Cited by 15
“…studies have been conducted examining connectivity of the insula in adults and adolescents (Angevine et al. 1962; Le Gros Clarkamd Russell 1939; Klinger and Gloor 1960; Yakovlev et al. 1960; Augustine 1996; Kalani et al. 2009; Cerliani et al. 2011; Cloutman et al. 2012; Dennis et al. 2014),…”
Background
A critical review of connectome validation studies
Sarwar, T., Ramamohanarao, K., & Zalesky, A. (2021) · NMR in Biomedicine · doi:10.1002/nbm.4605 · Cited by 20
Superior Longitudinal Fasciculus and Arcuate Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0013 · Cited by 19
Limbic and paralimbic respiratory modulation: From inhibition to enhancement
Chaitanya, G., Hampson, J. P., Tóth, E., Hupp, N. J., Hampson, J. S., Mosher, J. C., Pati, S. B. B., Lhatoo, S. D., & Lacuey, N. (2022) · Epilepsia · doi:10.1111/epi.17244 · Cited by 17
Neural Reorganization Due to Neonatal Amygdala Lesions in the Rhesus Monkey: Changes in Morphology and Network Structure
Grayson, D. S., Bliss‐Moreau, E., Bennett, J., Lavenex, P., & Amaral, D. G. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx080 · Cited by 14
“The amygdala also projects to the contralateral temporal cortex via the anterior commissure (Klingler and Gloor 1960; Demeter et al. 1990).”
Background
A novel male Japanese quail structural connectivity atlas using ultra-high field diffusion MRI at 11.7 T
Hot, R. Y., Siwiaszczyk, M., Love, S., Andersson, F., Calandreau, L., Poupon, F., Beaujoin, J., Herlin, B., Boumezbeur, F., Mulot, B., et al. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02457-2 · Cited by 14
“Supervised methods were the first to be introduced, as they adopt an approach similar to that adopted by neuroanatomists during the last century to dissect long white mater bundles (Cajal 1911; Klingler 1935; Klingler and Gloor 1960).”
Method
Moral conduct and social behavior
de Oliveira‐Souza, R., & Moll, J. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00016-1 · Cited by 14
Principles of Organization
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0005 · Cited by 14
The Human Amygdala: Electrophysiological Studies
Brazier, M. A. B. (1972) · Advances in behavioral biology · doi:10.1007/978-1-4615-8987-7_14 · Cited by 14
Fiber Microdissection Technique for Demonstrating the Deep Cerebellar Nuclei and Cerebellar Peduncles
Pruthi, N., Kadri, P. A. S., & Türe, U. (2020) · Operative Neurosurgery · doi:10.1093/ons/opaa318 · Cited by 13
Image-guided dissection of human white matter tracts as a new method of modern neuroanatomical training.
Skadorwa, T., Kunicki, J., Nauman, P., & Ciszek, B. (2009) · PubMed · Cited by 13
Anatomical Study of Intrahemispheric Association Fibers in the Brains of Capuchin Monkeys (Sapajussp.)
Borges, K. C. M., Nishijo, H., Aversi‐Ferreira, T. A., Ferreira, J. R., & Caixeta, L. F. (2015) · BioMed Research International · doi:10.1155/2015/648128 · Cited by 13
Striatal and septo-hypothalamic responses to anticipation and outcome of affiliative rewards
Bortolini, T., Melo, B. R. P., Basílio, R., Fischer, R. D., Zahn, R., de Oliveira‐Souza, R., Knutson, B. D., & Moll, J. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118474 · Cited by 26
“Both of these input pathways ensely project to a continuum of basal forebrain structures including he ventromedial and orbitofrontal prefrontal cortices, septal nuclei, reoptic area, and anterior hypothalamus ( Klingler and Gloor, 1960 ).”
Background
Certain Afferent Cortical Connections of the Rhinencephalon
Schneider, R. C., Ec, C., & Kahn, E. A. (1963) · Progress in brain research · doi:10.1016/s0079-6123(08)60574-9 · Cited by 13
Neocortical influence on the amygdala.
Niemer, W. T., & Goodfellow, E. (1966) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(66)90191-x · Cited by 12
Revisiting the microsurgical anatomy of the sagittal stratum and surgical implications: fiber microdissection and tractography study
Gülsuna, B., Güngör, A., Yazgan, P., Erol, G., Middlebrooks, E. H., Börcek, A. Ö., Weninger, W. J., & Türe, U. (2024) · Journal of neurosurgery · doi:10.3171/2024.2.jns232671 · Cited by 12
The effects of stimulation of substantia innominata and sensory receiving areas of the forebrain upon the activity of neurons within the amygdala of the anesthetized cat
Femano, P. A., Edinger, H. M., & Siegel, A. (1983) · Brain Research · doi:10.1016/0006-8993(83)90968-x · Cited by 12
Evolution of Telencephalic Commissures: Conservation and Change of Developmental Systems in the Origin of Brain Wiring Novelties
Suárez, R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00042-7 · Cited by 12
Tractography of the ansa lenticularis in the human brain
Li, M., Ribas, E. C., Zhang, Z., Wu, X., Wang, X., Liu, X.-H., Liang, J., Chen, G., & Li, M. (2021) · Clinical Anatomy · doi:10.1002/ca.23788 · Cited by 11
“…running alongside it for a short distance directly posterior to its amygdalothalamic pathway and dissociating from it after sweeping around the cerebral peduncle, finally turning posteriorly and entering the red nucleus, substantia nigra, subthalamic nucleus, and thalamus (Klingler & Gloor, 1960).”
BackgroundResult
Cerebral changes and disrupted gray matter cortical networks in asymptomatic older adults at risk for Alzheimer's disease
Cantero, J. L., Atienza, M., Sánchez‐Juan, P., Rodríguez‐Rodríguez, E., Vázquez‐Higuera, J. L., Pozueta, A., González‐Suárez, A., Vilaplana, E., Pegueroles, J., Montal, V., et al. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.12.010 · Cited by 11
Corpus Callosum
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0022 · Cited by 11
Stimulation‐induced respiratory enhancement in corticothalamic regions
Talavera, B., Chaitanya, G., Hupp, N. J., Pati, S. B. B., Hampson, J. P., Luo, X., Hampson, J. S., Vakilna, Y. S., Rani, M. R. S., Noor, R., et al. (2023) · Epilepsia · doi:10.1111/epi.17635 · Cited by 10
White Matter
Naidich, T. P., Krayenbühl, N., Kollias, S., Bou-Haidar, P., Bluestone, A. Y., & Carpenter, D. M. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4160-5009-4.50020-0 · Cited by 10
Cross-modal matching by amnesic subjects
Shaw, C., Kentridge, R. W., & Aggleton, J. P. (1990) · Neuropsychologia · doi:10.1016/0028-3932(90)90121-4 · Cited by 10
Track‐Weighted Dynamic Functional Connectivity Profiles and Topographic Organization of the Human Pulvinar
Basile, G. A., Quartarone, A., Cerasa, A., Ielo, A., Bonanno, L., Bertino, S., Rizzo, G., Milardi, D., Anastasi, G., Saranathan, M., et al. (2024) · Human Brain Mapping · doi:10.1002/hbm.70062 · Cited by 8
Impact of White Matter Dissection in Microneurosurgical Procedures
Güngör, A., Gurses, M. E., Demirtaş, O. K., Rahmanov, S., & Türe, U. (2023) · Springer eBooks · doi:10.1007/978-981-99-3412-6_3 · Cited by 9
Cingulate sulcus morphology and paracingulate sulcus variations: Anatomical and radiological studies
Selahi, Ö., Bektaşoğlu, P. K., Hakan, T., Fırat, Z., Güngör, A., & Çelikoğlu, E. (2022) · Clinical Anatomy · doi:10.1002/ca.23981 · Cited by 9
“One human cadaveric brain was fixated for 2 months in a 10% formalin solution in accordance with the Klingler method (Klingler & Gloor, 1960).”
Method
Visuotactile interactions in the congenitally acallosal brain: Evidence for early cerebral plasticity
Wolf, C. C., Ball, A., Ocklenburg, S., Otto, T., Heed, T., Röder, B., & Güntürkün, O. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.10.008 · Cited by 9
“…familiar information in AgCC patients is due to an early onset of compensatory mechanisms in cross-cortical pathways that remain intact, e.g. the anterior commissure, a small band of axons that connects the temporal lobes (Di Virgilio, Clarke, Pizzolato, & Schaffner, 1999; Klinger & Gloor, 1960).”
Background
Neurosurgical relevance of the dissection of the diencephalic white matter tracts using the Klingler technique
Silva, S. M., Cunha-Cabral, D., & Andrade, J. P. (2017) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2017.03.001 · Cited by 9
Beyond Commissurotomy: Clues to Consciousness
LeDoux, J. E., Wilson, D. H., & Gazzaniga, M. S. (1979) · Handbook of behavioral neurobiology · doi:10.1007/978-1-4613-3944-1_17 · Cited by 9
Thalamo-amygdalar relationships. An evoked potential study
Niemer, W. T., Goodfellow, E. F., Bertuccini, T. V., & Schneider, G. T. (1970) · Brain Research · doi:10.1016/0006-8993(70)90100-9 · Cited by 9
Microsurgical anatomy of the auditory radiations: revealing the enigmatic acoustic pathway from a surgical viewpoint
Aydın, A. E., Aydın, S., Bilgin, B., Mirkhasilova, M., Bayramli, N., & Tanrıöver, N. (2022) · Journal of neurosurgery · doi:10.3171/2022.7.jns22247 · Cited by 8
How fiber bundle alterations differ in presumed LATE and amnestic Alzheimer's disease
Lebrun, A., Leprince, Y., Lagarde, J., Olivieri, P., Moussion, M., Noiray, C., Bottlaender, M., & Sarazin, M. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.14156 · Cited by 8
The Three-Dimensional Architecture of the Internal Capsule of the Human Brain Demonstrated by Fiber Dissection Technique
Goga, C., Brînzaniuc, K., Florian, I. S., & Rodriguez Mena, R. (2015) · Ars medica tomitana · doi:10.2478/arsm-2014-0021 · Cited by 8
“The special freezing and dissection technique developed by Joseph Klingler, allowed for a new level of anatomical accuracy in the white matter investigations [4, 5, 24].”
Method
The Neural Bases of Normal and Deviant Moral Cognition and Behavior
de Oliveira‐Souza, R., & Moll, J. (2009) · Topics in Magnetic Resonance Imaging · doi:10.1097/rmr.0b013e3181f22f69 · Cited by 8
Morphologic Variations of the Collateral Sulcus on the Mediobasal Region of the Temporal Lobe: An Anatomical Study
Özdemir, A., Ovalıoğlu, T. C., Canaz, G., & Emel, E. (2018) · World Neurosurgery · doi:10.1016/j.wneu.2018.06.156 · Cited by 8
Extreme Capsule
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0014 · Cited by 11
New Possibilities of Stereotactic Treatment of Temporal Lobe Epilepsy (TLE)
Ganglberger, J. A. (1976) · Springer eBooks · doi:10.1007/978-3-7091-8444-8_33 · Cited by 8
Reponses associees incrementales corticales et oculaires d'origine amygdalienne
Gary-Bobo, E., & Bonvallet, M. (1970) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(70)90064-7 · Cited by 8
TractEM: Fast Protocols for Whole Brain Deterministic Tractography-Based White Matter AtlasPreprint
Bayrak, R. G., Wang, X., Schilling, K. G., Greer, J. M., Hansen, C. B., Blaber, J. A., Williams, O. A., Beason‐Held, L. L., Resnick, S. M., Rogers, B. P., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/651935 · Cited by 8
“The template image was generated by applying an affine transformation of Lancaster et al. (2007) to the probabilistic ICBM152space FA template image from the FSL atlas distribution (Mori et al.”
BackgroundMethod
Assessing the connectional anatomy of superior and lateral surgical approaches for medial temporal lobe epilepsy
Baran, O., Balak, N., Baydın, S. Ş., Aydin, I., Kayhan, A., Evran, Ş., Kemerdere, R., & Tanrıöver, N. (2020) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2020.10.016 · Cited by 7
Supramarginal Gyrus and Angular Gyrus Subcortical Connections: A Microanatomical and Tractographic Study for Neurosurgeons
Şahin, M. H., Akyüz, M. E., Karadağ, M. K., & Yalçın, A. (2023) · Brain Sciences · doi:10.3390/brainsci13030430 · Cited by 6
Tractography of the stria terminalis in the human brain
Li, M., Zhang, Z., Wu, X., Wang, X., Liu, X., Liang, J., Ge, C., Feng, Y., & Li, M. (2022) · Clinical Anatomy · doi:10.1002/ca.23843 · Cited by 7
“The ST tracked in our study, which connected the amygdala to the BNST, was consistent with previous fiber dissection studies (Baydin et al., 2016; Gungor et al., 2018; Klingler & Gloor, 1960; Serra et al., 2017; Yagmurlu et al., 2015).”
BackgroundResult
Multimodal anatomy of the human forniceal commissure
Akeret, K., Forkel, S. J., Buzzi, R. M., Vasella, F., Amrein, I., Colacicco, G., Serra, C., & Krayenbühl, N. (2022) · Communications Biology · doi:10.1038/s42003-022-03692-3 · Cited by 6
“After thawing, the brains were dissected 40,61,77,79 .”
Investigating form and content of emotional and non-emotional laughing
Lombardi, G., Gerbella, M., Marchi, M., Sciutti, A., Rizzolatti, G., & Cesare, G. D. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac334 · Cited by 6
“Interestingly, both these pathways interact one to the other and have also a common target: the amygdala (Klingler and Gloor 1960; Amaral et al. 2003; Rafal et al. 2015), a structure that we described above to be selectively activated during the perception of emotional laughing.”
Background
Deep temporal lobe projections to the nucleus of the diagonal band of Broca
Yoshihara, H., & France, J. M. (1976) · Cellular and Molecular Life Sciences · doi:10.1007/bf01932620 · Cited by 6
Microanatomy of Thalamic Radiations
KAKOU, M., Kouakou, F., Oka, D. N., Mbende, A. S., Peltier, J., & Velut, S. (2017) · International Journal of Human Anatomy · doi:10.14302/issn.2577-2279.ijha-17-1719 · Cited by 6
Direct evidence of the relationship between brain metastatic adenocarcinoma and white matter fibers: A fiber dissection and diffusion tensor imaging tractography study
Liu, X., Kinoshita, M., Shinohara, H., Hori, O., Ozaki, N., Hatta, T., Honma, S., & Nakada, M. (2020) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2020.05.043 · Cited by 6
Additional New Approach in Treatment of Temporal Lobe Epilepsy
Ganglberger, J. A. (1984) · Springer eBooks · doi:10.1007/978-3-7091-8726-5_23 · Cited by 6
Historical Roots of Modern Neurosurgical Cadaveric Research Practices: Dissection, Preservation, and Vascular Injection Techniques
On, T. J., Xu, Y., Meybodi, A. T., Alcantar-Garibay, O., Castillo, A. L., Özak, A., Abramov, I. T., Dagi, T. F., & Preul, M. C. (2024) · World Neurosurgery · doi:10.1016/j.wneu.2024.08.120 · Cited by 5
KLINGLER’S FIBER DISSECTION METHOD- AN ASSISTING APPROACH TOWARDS TEACHING NEUROANATOMY
Patil, S., Sethi, M., & Mishra, S. (2018) · International Journal of Anatomy and Research · doi:10.16965/ijar.2018.107 · Cited by 5
“It was used to isolate complete fibre pathways by removing parts of the cortex and underlying white matter of formalin-fixed brains [2-4].”
Method
3D microsurgical anatomy of the cortico-spinal tract and lemniscal pathway based on fibre microdissection and demonstration with tractography
Rodríguez-Mena, R., Piquer-Belloch, J., Llácer, J. L., Riesgo-Suárez, P., & Rovira-Lillo, V. (2018) · Neurocirugía (English Edition) · doi:10.1016/j.neucie.2018.09.001 · Cited by 5
The anterior perforated substance (APS) revisited: Commented anatomical and imagenological views
Fontana, H., Mazzucco, J., & Lescano, S. (2023) · Brain and Behavior · doi:10.1002/brb3.3029 · Cited by 4
“Their fibers show a characteristic curling “as a rope” (Klingler & Gloor, 1960) in this part of its course (Figure 11b).”
BackgroundMethodInfluential
Topographical anatomy of the septum verum and its white matter connections
Bárány, L., Meszaros, C., Alpár, A., Ganslandt, O., Hore, N., Delev, D., Schnell, O., & Kurucz, P. (2024) · Scientific Reports · doi:10.1038/s41598-024-68464-x · Cited by 4
Chapter 5.2 Using hippocampal amnesia to understand the neural basis of diencephalic amnesia
Aggleton, J. P., Saunders, R. C., & Vann, S. D. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00227-0 · Cited by 4
Three dimensional anatomical microdissection of rat brain using fiber dissection technique
Akakın, A., Yılmaz, B., Akakın, D., Dagbasi, N., & Kılıç, T. (2014) · Journal of Anatomical Society of India · doi:10.1016/j.jasi.2014.11.011 · Cited by 4
Transient hypoxemia induced by cortical electrical stimulation
Loizon, M., Ryvlin, P., Chatard, B., Jung, J., Bouet, R., Guénot, M., Mazzola, L., Bezin, L., & Rheims, S. (2020) · Neurology · doi:10.1212/wnl.0000000000009497 · Cited by 4
Remission of lifelong episodic dyscontrol after bilateral dorsolateral temporal lobe damage
Coutinho, G., Miele, F., Moll, J., Mattos, P., & de Oliveira‐Souza, R. (2016) · Neurocase · doi:10.1080/13554794.2016.1194999 · Cited by 4
“This system constitutes a functional unity with multiple behavioral functions which is anatomically defined by neural structures directly integrated by the uncinate fasciculus (UF), namely, the orbitofrontal, temporopolar, and anterior insular cortices (Klingler & Gloor, 1960).”
Background
Gross anatomy of the longitudinal fascicle of Sapajus sp.
Aversi‐Ferreira, T. A., Borges, K. C. M., Gonçalves-Mendes, M. T., & Caixeta, L. F. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252178 · Cited by 4
“Klingler’s preservation method, with minor adjustments, was used to put intrahemispheric fibers on evidence for the 24 hemispheres [45,46] and two full brains, including keeping them in formaldehyde subsequent to cutting to highlight white fibers.”
Method
Notes on Techniques
ten Donkelaar, H. J. (2011) · Springer eBooks · doi:10.1007/978-3-642-19134-3_3 · Cited by 4
Superior Temporal Region
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0007 · Cited by 4
Introduction
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0001 · Cited by 4
Afferent and efferent fiber systems of the human amygdala: anatomical, pathophysiological, and clinical significance
Bektaşoğlu, P. K., Ghare, A., Elias, C., Fırat, Z., & Güngör, A. (2025) · Journal of neurosurgery · doi:10.3171/2025.3.jns241544 · Cited by 3
Cognitive and behavioral abnormalities of vascular cognitive impairment
Jeong, J. H., Kim, E., Seo, S. W., & Na, D. L. (2016) · Cambridge University Press eBooks · doi:10.1017/9781139924771.020 · Cited by 3
Ventral amygdalofugal pathway as an integrated surgically important network: microsurgical anatomy and segmentation based on fiber dissection
Erkan, B., Hergünsel, Ö. B., Barut, O., Saygı, T., Koçak, B., Güngör, A., Yağmurlu, K., & Tanrıöver, N. (2024) · Journal of neurosurgery · doi:10.3171/2024.1.jns231541 · Cited by 3
Surgery of temporal lobe epilepsy: cortico-amygdalohippocampectomy
Olivier, A., Boling, W., & Tanrıverdi, T. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9781139021951.010 · Cited by 3
Fiber Dissection Technique for Demonstrating the Lateral Lemniscus of the Human Brain
Shinohara, H., YASUTAKA, S., Taniguchi, Y., Kominami, R., & Kawamata, S. (2004) · Okajimas Folia Anatomica Japonica · doi:10.2535/ofaj.80.115 · Cited by 3
“In the latter half of the 20th century, however, fiber dissection came to be regarded as a technique for demonstrating the structure and location of neuronal bundles to medical students (Curran, 1909; Klingler and Gloor, 1960).”
Background
Bases anatómicas de la hemisferotomía periinsular
Martínez, F., Soria, V., Sgarbi, N., Laza, S., & Prinzo, H. (2004) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 3
Abolition of lifelong specific phobia: a novel therapeutic consequence of left mesial temporal lobectomy
Binks, S. N. M., Chan, D., & Medford, N. (2014) · Neurocase · doi:10.1080/13554794.2013.873056 · Cited by 3
“As well as onward connections to the centromedial group, it has a ventral output system comprising amygdalohypothalamic and amygdaloseptal tracts (Klingler & Gloor, 1960; Le Doux, 2000).”
Background
Inferior Longitudinal Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0018 · Cited by 4
Anatomía microquirúrgica en 3 D del tracto corticoespinal y de la vía del lemnisco basada en microdisección de fibras y demostración a través de tractografía
Rodríguez-Mena, R., Piquer-Belloch, J., Llácer, J. L., Riesgo-Suárez, P., & Rovira-Lillo, V. (2018) · Neurocirugía · doi:10.1016/j.neucir.2018.06.005 · Cited by 3
Cingulum Bundle
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0017 · Cited by 3
Uncinate Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0016 · Cited by 4
Deep brain stimulation and psychosis: A case series and two candidate causal brain circuitsPreprint
Meyer, G. M., Pines, A. R., Roldán, A., Aracil‐Bolaños, I., Settle, E. G., Sahin, I. A., Schaper, F. L. W. V. J., Neudorfer, C., Järvenpää, S., Kamo, H., et al. (2025) · medRxiv · doi:10.1101/2025.11.18.25340443 · Cited by 3
“The second candidate circuit is centered on the medio-dorsal nucleus of the thalamus, including projections from the SNr and amygdala, which constitute two of its main subcortical afferents 55,64–66 .”
Neuroimaging signatures of mesial temporal lobe epilepsy: A coordinate-based meta-analysis of structural and resting-state functional imaging literature
Towne, J. M., Eslami, V., Barron, D. S., Cavazos, J. E., & Fox, P. T. (2025) · NeuroImage Clinical · doi:10.1016/j.nicl.2025.103908 · Cited by 5
“…and Gloor in their 1960 cadaveric study and others, subsequently extends to connect with anterior portions of the temporal lobe/temporal pole (Klingler and Gloor, 1960; Serra et al., 2017), also identified by our study; additional dissection/tracto-graphic research revealed further…”
“Hands‐On” white matter anatomy: Using Air Anatomy gestures and tractography on simple brain sections to enhance teaching of white matter directions
Yohannan, D. G., Punja, R., Iype, T., Kesavadas, C., Thomas, B., Govindapillai, U. K., Oommen, A. M., & Bhargavi, U. D. K. (2026) · Anatomical Sciences Education · doi:10.1002/ase.70200 · Cited by 2
The Limbic System
Buccilli, B., Paternò, G., Cortés-Contreras, A. P., Pineda, M. F. T., Monroy-Sosa, A., & Ascenzi, B. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-822404-5.00019-x · Cited by 2
Estandarización del método Klingler y su visualización tridimensional
Cruz, J. C. P., Serrano, S. P. G., Prevost, P. G., Soto, G. R., Gutiérrez, M. R. V., Vázquez, I. H., Martínez, S. M. A., Leu, P. H. S., & Delgado-Reyes, L. (2008) · Revista del Hospital Juárez de México · Cited by 2
Impaired biophysical integrity of macromolecular protein pools in the uncinate circuit in late-life depression
Yang, S., Wu, M., Ajilore, O., Lamar, M., & Kumar, A. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0085-6 · Cited by 3
“The OFC is connected to the amygdala and hippocampus through the uncinate fasciculus [11, 31].”
Cognitive and behavioral abnormalities of vascular dementia
Jeong, J. H., Kim, E., Seo, S. W., & Na, D. L. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511581410.021 · Cited by 2
Fronto-Occipital Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0019 · Cited by 2
White Matter Pathways in Early Neuroscience
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0002 · Cited by 2
Exploring Deep Space - Uncovering the Anatomy of Periventricular Structures to Reveal the Lateral Ventricles of the Human Brain
Colibaba, A. S., Calma, A. D., Webb, A. L., & Valter, K. (2017) · Journal of Visualized Experiments · doi:10.3791/56246 · Cited by 2
Development of a Neurosurgical Cadaver Laboratory despite Limited Resources.
del Valle, M. M., Jesús, O. D., Vicenty‐Padilla, J. C., Matos, A., & Inserni, J. A. (2022) · PubMed · Cited by 2
Role of the anterior commissure in the contralateral propagation of the after-discharge from amygdala and temporal cortex in the monkey
Philippon, J. H., & Baldwin, M. (1971) · Acta Neurochirurgica · doi:10.1007/bf01401861 · Cited by 2
Somatomotor activity and avoidance conditioned reflex performance following forebrain lesions
Korányi, L., Endröczi, E., & Lissák, K. (1963) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(63)90027-8 · Cited by 2
Update on Temporal Lobe Epilepsy
Mirsattari, S. M., & Blume, W. T. (2013) · Epilepsy Research and Treatment · doi:10.1155/2013/579487 · Cited by 2

Authors: Klingler, J., & Gloor, P.
Affiliations: Montreal Neurological Institute and Hospital (CA)
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1960-12
Volume: 115
Issue: 3
Pages: 333-369
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.901150305
OpenAlex: W2117029315
Cited by: 404
References: 86
Citations by year: 2026: 4 · 2025: 13 · 2024: 13 · 2023: 16 · 2022: 13 · 2021: 11 · 2020: 15 · 2019: 12 · 2018: 8 · 2017: 12 · 2016: 11 · 2015: 11 · 2014: 11 · 2013: 14 · 2012: 15
FWCI: 3.96
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 16017 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Keywords: amygdala, anterior temporal cortex, human brain, neural connections, white matter tracts, limbic system
MeSH terms: Amygdala, Basal Ganglia, Cerebral Cortex, Ganglia, Humans, Temporal Lobe

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The connections of the amygdala and of the anterior temporal cortex in the human brain.

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks