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

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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

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COMPARATIVE ANATOMY OF THE NERVOUS SYSTEM OF VERTEBRATES INCLUDING MAN
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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

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“However, in humans, the study of fiber pathways is limited by quantity and quality of available postmortem materials (Von Monakow, 1905), and can only be grossly identified using the Klingler’s method that is based on fiber dissection of the brain (Ludwig and Klingler, 1956; Klingler and Gloor, 1960; Zemmoura et al.,…”
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“Post mortem gross dissection in humans reveals a variety of connections between the insula and the rest of cerebral cortex, as well as numerous subcortical structures [Angevine et al., 1962; Le Gros Clark et al., 1939; Klinger and Gloor, 1960; Yakovlev et al., 1960].”
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“Longer distance connections can only be investigated by series of histological sections (Axer et al., 2002), blunt dissection, freeze-thaw dissection (Klingler and Gloor, 1960), or indirect evidence from anterograde degeneration due to brain lesions (Di Virgilio and Clarke, 1997).”
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BackgroundInfluential
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Background
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“Differences between various amygdaloid nuclei in the pattern of connectivity (Klinger and Gloor 1960; Nauta 1961; Jacobson and Trojanowski 1975; Herzog and Van Hoesen 1976; Krettek and Price 1977 a, b; Hopkins and Holstege 1978; Aggleton et al. 1980; Mehler 1980; Turner et al. 1980; Amaral and Cowan 1980; Mufson et al…”
Background
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“10, 11 by Klingler and Gloor, 1960) suggests that fibers arising from the temporal cortex in humans indeed course close to the amygdala.”
Background
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Thalamus
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Amygdala
Olucha-Bordonau, F. E., Fortes-Marco, L., Otero‐García, M., Lanuza, E., & Martínez‐Garciá, F. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00018-8 · Cited by 52
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Kucukboyaci, N. E., Girard, H. M., Hagler, D. J., Kuperman, J. M., Tecoma, E. S., Iragui, V. J., Halgren, E., & McDonald, C. R. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711001391 · Cited by 42
“It first runs backward, enters the external capsule, and then arches around the limen insulae as a compact tract, entering the temporal pole to project to the uncus, amygdala, and hippocampus (Klingler & Gloor, 1960).”
Background
Anatomic dissection tractography: a new method for precise MR localization of white matter tracts.
Kier, E. L., Staib, L. H., Davis, L. M., & Bronen, R. A. (2004) · PubMed Central · Cited by 42
Comparative neuroanatomical parcellation of the human and nonhuman primate temporal pole
Insausti, R. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23431 · Cited by 50
“…by the connections that the temporal pole has with various corti- cal and subcortical centers such as strong connections with the orbitofrontal cortex (via uncinate fasciculus), amygdaloid complex, and the pulvinar (temporoamygdaloid and temporopulvinar bundle (of Arnold) Klingler and Gloor, 1960).”
BackgroundInfluential
The Accumbofrontal Fasciculus in the Human Brain: A Microsurgical Anatomical Study
Rigoard, P., Buffenoir, K., Jaafari, N., Giot, J., Houeto, J. L., Mertens, P., Velut, S., & Bataille, B. (2011) · Neurosurgery · doi:10.1227/neu.0b013e3182098e48 · Cited by 42
“To better identify the neural connections between the frontal cortex and the NAcc in the human brain, we used a modified fiber-dissection technique previously described by Klingler.(11,12) This technique appears to be less time-consuming for an equivalent dissection quality.”
Method
Cerebral Lateralization and Specialization in Human Central Nervous System
Nass, R. D., & Gazzaniga, M. S. (1987) · Comprehensive physiology · doi:10.1002/cphy.cp010518 · Cited by 41
Hippocampal functions in learning.
Meissner, W. (1966) · Journal of Psychiatric Research · doi:10.1016/0022-3956(66)90018-5 · Cited by 35
A QUALITATIVE LIMITATION ON VISUAL TRANSFER VIA THE ANTERIOR COMMISSURE ; EVIDENCE FROM A CASE OF CALLOSAL AGENESIS
Martin, A. D. (1985) · Brain · doi:10.1093/brain/108.1.43 · Cited by 40
Unseen Fearful Faces Influence Face Encoding: Evidence from ERPs in Hemianopic Patients
Cecere, R., Bertini, C., Maier, M., & Làdavas, E. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00671 · Cited by 36
“…speculate that this was likely achieved through reciprocal anatomical connections between the left and right hemispheres, possibly via the anterior commissure, as suggested by previous studies (Brown, Jeeves, Dietrich, & Burnison, 1999; Demeter, Rosene, & Van Hoesen, 1990; Klingler & Gloor, 1960).”
Result
NEURAL CONNECTION BETWEEN BILATERAL BASAL TEMPORAL REGIONS
Umeoka, S. C., Terada, K., Baba, K., Usui, K., Matsuda, K., Tottori, T., Usui, N., Nakamura, F., Inoue, Y., Fujiwara, T., et al. (2009) · Neurosurgery · doi:10.1227/01.neu.0000344001.26669.92 · Cited by 36
“Furthermore, the anterior commissure has been documented to be an interhemi spheric connection be tween bilateral BTRs, especially the anterior third, in the human brain (6, 7, 11, 22, 30).”
Background
A match-mismatch theory of limbic system function
Cormier, S. M. (1981) · Physiological Psychology · doi:10.3758/bf03326955 · Cited by 36
“28 CORMIER Klinger & Gloor, 1960).”
Depth Recordings in Man in Temporal Lobe Epilepsy
Buser, P., Bancaud, J., & Talairach, J. (1973) · UCLA forum in medical sciences · doi:10.1016/b978-0-12-128650-7.50010-x · Cited by 36
Thalamus
Percheron, G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547626-3/50021-1 · Cited by 34
The ventromedial hypothalamus and the control of avoidance behavior and aggression: Fear hypothesis versus response-suppression theory of limbic system function
Colpaert, F. C. (1975) · Behavioral Biology · doi:10.1016/s0091-6773(75)92053-2 · Cited by 35
Long-Term Neuroanatomical Consequences of Childhood Maltreatment: Reduced Amygdala Inhibition by Medial Prefrontal Cortex
Kessler, R., Schmitt, S., Sauder, T., Stein, F., Yüksel, D., Grotegerd, D., Dannlowski, U., Hahn, T., Dempfle, A., Sommer, J. B., et al. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.00028 · Cited by 36
Microsurgical Anatomy of the Anterior Commissure
Peltier, J., Verclytte, S., Delmaire, C., Pruvo, J., Havet, É., & Gars, D. L. (2011) · Operative Neurosurgery · doi:10.1227/neu.0b013e31821bc822 · Cited by 34
“The anterior limb of the AC is believed to convex axons to and from the anterior perforated space and possibly the orbitofrontal cortex.(17) Few fibers of the AC have been followed into the occipital lobe, but the largest contingent of commissural axons originate in the inferior part of the temporal lobe and seem to r…”
Background
Visual Memory Deficits After Damage to the Anterior Commissure and Right Fornix
Botez-Marquard, T., & Botez, M. I. (1992) · Archives of Neurology · doi:10.1001/archneur.1992.00530270141032 · Cited by 34
Selective amygdalohippocampectomy via the transsylvian approach
Adada, B. (2008) · Neurosurgical FOCUS · doi:10.3171/foc/2008/25/9/e5 · Cited by 33
“19 The posteromedial surface of the uncus is divided horizontally by the uncal sulcus, above which are 3 gyri—the uncinate gyrus, the band of Giacomini, and the intralimbic gyrus—and below which is the entorhinal area.”
Background
Estimating Brain Connectivity With Diffusion-Weighted Magnetic Resonance Imaging: Promise and Peril
Grier, M. D., Zimmermann, J., & Heilbronner, S. R. (2020) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2020.04.009 · Cited by 32
“These can provide a visual framework from which to validate the results from dMRI studies of where large white matter bundles are located, and what their major orientations are(42,43).”
Background
Central core of the cerebrum
Choi, C., Han, S.-R., Yee, G.-T., & Lee, C. H. (2010) · Journal of neurosurgery · doi:10.3171/2010.9.jns10530 · Cited by 32
Microsurgical Anatomy of the White Matter Tracts in Hemispherotomy
Küçükyürük, B., Yağmurlu, K., Tanrıöver, N., Uzan, M., & Rhoton, A. L. (2014) · Operative Neurosurgery · doi:10.1227/neu.0000000000000288 · Cited by 31
“Twelve hemispheres were frozen at 216 C for 6 to 8 weeks to cause expansion of water crystals to facilitate the separation of the fiber tracts.(19,20) The dissection was carried out under a surgical microscope with surgical dissectors of different tip widths.”
Background
Visual learning and retention examined with reversible cold lesions of the anterior temporal lobe
Voytko, M. L. (1986) · Behavioural Brain Research · doi:10.1016/0166-4328(86)90078-1 · Cited by 31
Studies on the forebrain of the mouse. Golgi observations.
Valverde, F. (1963) · Europe PMC (PubMed Central) · Cited by 31
The Fiber Connections of the Temporal Lobe with Emphasis on the Rhesus Monkey
Streitfeld, B. (1980) · International Journal of Neuroscience · doi:10.3109/00207458009147579 · Cited by 30
Extended‐amygdala intrinsic functional connectivity networks: A population study
Berry, S. C., Wise, R. G., Lawrence, A. D., & Lancaster, T. M. (2020) · Human Brain Mapping · doi:10.1002/hbm.25314 · Cited by 29
“Whist amygdala structural connections to lateral temporal regions are well characterised (Folloni et al., 2019; Janak & Tye, 2015; Klingler & Gloor, 1960), this is not the case for the BST and it has been suggested that BST-temporal pole connectivity may even be unique to humans (Avery et al.,…”
Background
Interactions of Deep Structures during Seizures in Man
Brazier, M. A. B. (1972) · Springer eBooks · doi:10.1007/978-3-7091-8306-9_25 · Cited by 29
Electrophysiological studies of amygdalo-hypothalamic connections
Gloor, P., Murphy, J. T., & Dreifuss, J. J. (1969) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1969.tb12911.x · Cited by 28
Self-citation
Diencephalic amnesia: a reorientation towards tracts?
Markowitsch, H. J. (1988) · Brain Research · doi:10.1016/0006-8993(88)91226-7 · Cited by 28
Internal structure of the cerebral hemispheres: an introduction of fiber dissection technique
de Castro, I., Christoph, D. D. H., dos Santos, D. P., & Landeiro, J. A. (2005) · Arquivos de Neuro-Psiquiatria · doi:10.1590/s0004-282x2005000200011 · Cited by 28
Basic science and clinical aspects of procaine HCl as a limbic system excitant
Adamec, R. E., Stark-Adamec, C. I., Saint-Hilaire, J. M., & Livingston, K. E. (1985) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(85)90073-9 · Cited by 28
The Role of the Amygdala in Controlling Hypothalamic Output
Murphy, J. T. (1972) · Advances in behavioral biology · doi:10.1007/978-1-4615-8987-7_13 · Cited by 28
Insular‐diencephalic connections in the Macaque
Wirth, F. P. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901500402 · Cited by 27
Forebrain influences on an amygdaloid acute focus in the cat
Fariello, R. G. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90177-1 · Cited by 27
Emotion specific neural activation for the production and perception of facial expressions
Krautheim, J. T., Steines, M., Dannlowski, U., Neziroğlu, G., Acosta, H., Sommer, J. B., Straube, B., & Kircher, T. T. J. (2020) · Cortex · doi:10.1016/j.cortex.2020.01.026 · Cited by 26
White Matter Dissection of the Fetal Brain
Horgos, B., Mecea, M., Boer, A., Szabo, B. A., Buruiană, A., Stamatian, F. V., Mihu, C.-M., Florian, I. Ş., Șușman, S., & Paşcalău, R. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.584266 · Cited by 24
“It has been already used to describe connections in the human adult brain (Klingler and Gloor, 1960).”
Method
Ex vivo, in situ perfusion protocol for human brain fixation compatible with microscopy, MRI techniques, and anatomical studies
Insausti, R., Serrano, A. M. I., Muñoz, M., Lorenzo, I. M., Jiménez, M. D. M. A., Rabal, M. D. P. M., de la Rosa‐Prieto, C., Delgado‐González, J., Echeverría, J. M., Sánchez, S. C., et al. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1149674 · Cited by 30
“Different studies of human brain morphology—from gross anatomy and fiber bundle dissection (Klingler and Gloor, 1960) to electron microscopy—involve different methodological problems, which makes it difficult to apply a variety of anatomical methods in the same brain tissue (for review, see Grinberg et al.”
Background
A Understanding of the Temporal Stem
Choi, C., Han, S.-R., Yee, G.-T., & Lee, C. H. (2010) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2010.47.5.365 · Cited by 26
Task- and resting-state functional connectivity of brain regions related to affection and susceptible to concurrent cognitive demand
Kellermann, T. S., Caspers, S., Fox, P. T., Zilles, K., Roski, C., Laird, A. R., Turetsky, B. I., & Eickhoff, S. B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.01.046 · Cited by 25
Limbic Nuclei of Thalamus and Connections of Limbic Cortex
Angevine, J. B. (1964) · Archives of Neurology · doi:10.1001/archneur.1964.00460140051008 · Cited by 25
The temporoinsular projection system: an anatomical study
Nachtergaele, P., Radwan, A., Swinnen, S., Decramer, T., Uytterhoeven, M., Sunaert, S. G., Loon, J. V., & Theys, T. (2019) · Journal of neurosurgery · doi:10.3171/2018.11.jns18679 · Cited by 24
Structural connectivity of the ANT region based on human ex-vivo and HCP data. Relevance for DBS in ANT for epilepsy
Majtanik, M., Gielen, F. L. H., Coenen, V. A., Lehtimäki, K. A., & Mai, J. K. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119551 · Cited by 24
“Ithp is a composite bundle (Klingler and Gloor, 1960; Riley, 1960) that recruits its afferents mainly from the amygdala”
Background
Trait Aggressiveness Is Not Related to Structural Connectivity between Orbitofrontal Cortex and Amygdala
Beyer, F., Münte, T. F., Wiechert, J., Heldmann, M., & Krämer, U. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101105 · Cited by 24
“Reciprocal connections between prefrontal cortex and amygdala exist anatomically via the uncinate fascicle (UF), which connects prefrontal cortex and the anterior temporal lobe [5,6].”
Amygdaloid modulation of hypothalamic flight in cats.
Stokman, C. L. J., & Glusman, M. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0029128 · Cited by 24
Imaging of the superficial white matter in health and disease
Dyken, P. C. V., KHAN, A. R., & Palaniyappan, L. K. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00221 · Cited by 24
“…dissection is perhaps the most reliable evidence of the existence, course, and termination points of white matter fascicles ( Agrawal et al., 2011; Klingler & Gloor, 1960; Yendiki et al., 2022), making it a cornerstone of modern neuroanatomy ( Jitsuishi et al., 2020; Shinohara et al., 2020;…”
Background
Alterations in diffusion properties of white matter in Williams syndrome
Arlinghaus, L. R., Thornton‐Wells, T. A., Dykens, E. M., & Anderson, A. W. (2011) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2011.07.012 · Cited by 23
“The UF also contains connections between the amygdala and temporal lobe structures [53].”
Background
A White Matter Fiber Microdissection Study of the Anterior Perforated Substance and the Basal Forebrain: A Gateway to the Basal Ganglia?
Serra, C., Akeret, K., Maldaner, N., Staartjes, V. E., Regli, L., Baltsavias, G., & Krayenbühl, N. (2018) · Operative Neurosurgery · doi:10.1093/ons/opy345 · Cited by 23
The Relationship of Hallucinations to the Depth Structures of the Temporal Lobe
Weingarten, S. M., Cherlow, D. G., & Holmgren, E. (1977) · Acta neurochirurgica. Supplementum · doi:10.1007/978-3-7091-8482-0_27 · Cited by 23
What's your name again? A review of the superior longitudinal and arcuate fasciculus evolving nomenclature
Oliveira, J. V. M. P., Raquelo‐Menegassio, A. F., & Maldonado, I. L. (2021) · Clinical Anatomy · doi:10.1002/ca.23764 · Cited by 22
“Thirteen articles included in the present study described a one to three component organization (Klingler & Gloor, 1960; Türe et al., 1999; Türe et al., 2000; Catani et al., 2002; Peltier et al., 2006; Fernández-Miranda, Rhoton, AlvarezLinera, et al., 2008; Martino et al., 2011; Martino, Da…”
Background
Frontal and Insular Input to the Dorsolateral Temporal Pole in Primates: Implications for Auditory Memory
Parada, M. C., Ubero, M., Morris, R., Insausti, R., Mishkin, M., & Muñoz, M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01099 · Cited by 22
“In primates, the TP has dense connections with the amygdala, so strong that they form a distinct fasciculus (Klingler and Gloor, 1960).”
Background
The Balance between Negative and Positive Brain System Activity
Bovard, E. W. (1962) · Perspectives in biology and medicine · doi:10.1353/pbm.1963.0009 · Cited by 22
Transient Architectonic Features in the Basolateral Amygdala of the Human Fetal Brain
Ulfig, N., Setzer, M., & Bohl, J. R. E. (1998) · Cells Tissues Organs · doi:10.1159/000046489 · Cited by 21
“…and are mainly involved in vegetative regulation, the basolateral nuclei project to many iso- and allocortical areas and receive afferents from all unimodal and polysensory association cortices [Klingler and Gloor, 1960; Herzog and van Hoesen, 1976; Iwai and Yukie, 1987; Amaral et al., 1992].”
Background
Medial Pulvinar Stimulation in Temporal Lobe Epilepsy: A Literature Review and a Hypothesis Based on Neuroanatomical Findings
Κalamatianos, T., Mavrovounis, G., Skouras, P., Pandis, D., Fountas, K. N., & Stranjalis, G. (2023) · Cureus · doi:10.7759/cureus.35772 · Cited by 20
“Importantly, Klingler and Gloor in 1960, note that based on previous anatomical and electrophysiological data, the connections between the anterior temporal cortex and the pulvinar contain both ascending and descending fibers [30].”
BackgroundMethodInfluential
Diffusion tensor imaging analysis of long association bundles in the presence of an arteriovenous malformation
Bérubé, J., McLaughlin, N., Bourgouin, P. M., Beaudoin, G., & Bojanowski, M. W. (2007) · Journal of neurosurgery · doi:10.3171/jns-07/09/0509 · Cited by 20
Uncovering a Role for the Dorsal Hippocampal Commissure in Recognition Memory
Postans, M., Parker, G. D., Lundell, H., Ptito, M., Hamandi, K., Gray, W., Aggleton, J. P., Dyrby, T. B., Jones, D. K., & Winter, M. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz143 · Cited by 21
“The temporal pole and amygdala were ROIs that are known to project to or receive from contralateral structures via the AC, which was used as a comparison tract for our tractography analyses, as described below (Klingler and Gloor 1960; Turner et al. 1979; Demeter et al. 1985).”
BackgroundMethod

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

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

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