Morphometric and dendritic analysis of fascia dentata granule cells in human aging and senile dementia

Practical Nonparametric Statistics

Groggel, D. J., & Conover, W. J. (2000) · Technometrics · doi:10.2307/1271101 · Cited by 11,071 · see citing works

Untitled work

(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works

A New Clinical Scale for the Staging of Dementia

Hughes, C. P., Berg, L., Danziger, W., Coben, L. A., & Martin, R. L. (1982) · British Journal of Psychiatry · doi:10.1192/bjp.140.6.566 · Cited by 7,056 · see citing works

The Association Between Quantitative Measures of Dementia and of Senile Change in the Cerebral Grey Matter of Elderly Subjects

Blessed, G., Tomlinson, B. E., & Roth, M. (1968) · British Journal of Psychiatry · doi:10.1192/bjp.114.512.797 · Cited by 4,117 · see citing works

Practical Non-Parametric Statistics.

Brown, B. M., & Conover, W. J. (1981) · Biometrics · doi:10.2307/2530578 · Cited by 2,404 · see citing works

The Hippocampus as a Cognitive Map

Ranck, J. B. (1979) · American Journal of Psychiatry · doi:10.1176/ajp.136.10.1353 · Cited by 2,373 · see citing works

Alzheimer's disease: cell-specific pathology isolates the hippocampal formation.

Hyman, B. T., Van Hoesen, G. W., Damasio, A. R., & Barnes, C. L. (1984) · Science · doi:10.1126/science.6474172 · Cited by 2,268 · see citing works

Stereology of arbitrary particles. A review of unbiased number and size estimators and the presentation of some new ones, in memory of William R. Thompson.

Gundersen, H. J. G. (1986) · PubMed · Cited by 1,659 · see citing works

Practical Nonparametric Statistics

Conover, W. J. (1971) · Cited by 1,477 · see citing works

Stereology of arbitrary particles*

Gundersen, H. J. G. (1986) · Journal of Microscopy · doi:10.1111/j.1365-2818.1986.tb02764.x · Cited by 1,444 · see citing works

Pathological verification of ischemic score in differentiation of dementias

Rosen, W. G., Terry, R. D., Fuld, P. A., Katzman, R., & Peck, A. (1980) · Annals of Neurology · doi:10.1002/ana.410070516 · Cited by 1,273 · see citing works

A memory system in the monkey

Mishkin, M. (1982) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1982.0074 · Cited by 1,129 · see citing works

Some morphometric aspects of the brain in senile dementia of the alzheimer type

Terry, R. D., Peck, A., DeTeresa, R., Schechter, R., & Horoupian, D. S. (1981) · Annals of Neurology · doi:10.1002/ana.410100209 · Cited by 801 · see citing works

Neuronal loss, neurofibrillary tangles and granulovacuolar degeneration in the hippocampus with ageing and dementia: A quantitative study

Ball, M. J. (1977) · Acta Neuropathologica · doi:10.1007/bf00692056 · Cited by 639 · see citing works

The Human Central Nervous System: A Synopsis and Atlas

Nieuwenhuys, R., Voogd, J., & van Huijzen, C. (2012) · Medical Entomology and Zoology · Cited by 543 · see citing works

The impact of recent stereological advances on quantitative studies of the nervous system

Brændgaard, H., & Gundersen, H. J. G. (1986) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(86)90112-3 · Cited by 505 · see citing works

Plasticity of Hippocampal Circuitry in Alzheimer's Disease

Geddes, J. W., Monaghan, D. T., Cotman, C. W., Lott, I. T., Kim, R. C., & Chui, H. C. (1985) · Science · doi:10.1126/science.4071042 · Cited by 461 · see citing works

The Human Central Nervous System: A Synopsis and Atlas

Clayman, C. Β. (1979) · JAMA · doi:10.1001/jama.1979.03300140055030 · Cited by 332 · see citing works

Memory

Penfield, W. G. (1974) · Archives of Neurology · doi:10.1001/archneur.1974.00490390027001 · Cited by 330 · see citing works

Five types of basket cell in the hippocampal dentate gyrus: a combined Golgi and electron microscopic study

Ribak, C. E., & Seress, L. (1983) · Journal of Neurocytology · doi:10.1007/bf01181525 · Cited by 314 · see citing works

Some morphometric observations on the cerebral cortex and hippocampus in presenile Alzheimer's disease, senile dementia of Alzheimer type and Down's syndrome in middle age

Mann, D. M. A., Yates, P. O., & Marcyniuk, B. (1985) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(85)90129-7 · Cited by 240 · see citing works

Mild senile dementia of Alzheimer type: research diagnostic criteria, recruitment, and description of a study population.

van den Berg, L., Hughes, C. P., Coben, L. A., Danziger, W. L., Martin, R. L., & Knesevich, J. W. (1982) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.45.11.962 · Cited by 233 · see citing works

Quantitative evidence for selective dendritic growth in normal human aging but not in senile dementia

Buell, S. J., & Coleman, P. D. (1981) · Brain Research · doi:10.1016/0006-8993(81)90436-4 · Cited by 220 · see citing works

The metric analysis of three-dimensional dendritic tree patterns: a methodological review

Uylings, H. B. M., Ruiz‐Marcos, A., & van Pelt, J. (1986) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(86)90116-0 · Cited by 187 · see citing works

Morphometry of size/volume variables and comparison of their bivariate relations in the nervous system under different conditions

Uylings, H. B. M., van Eden, C. G., & Hofman, M. A. (1986) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(86)90111-1 · Cited by 184 · see citing works

Dendritic extent in human dentate gyrus granule cells in normal aging and senile dementia

Flood, D. G., Buell, S. J., Horwitz, G. J., & Coleman, P. D. (1987) · Brain Research · doi:10.1016/0006-8993(87)90027-8 · Cited by 164 · see citing works

Physiology and Pathology of Dendrites

Kreutzberg, G. W. (1975) · Medical Entomology and Zoology · Cited by 140 · see citing works

Granule cell dendritic spine density in the rat hippocampus varies with spine shape and location

Desmond, N. L., & Levy, W. B. (1985) · Neuroscience Letters · doi:10.1016/s0304-3940(85)80082-3 · Cited by 138 · see citing works

The Golgi Rapid Method in Clinical Neuropathology: The Morphologic Consequences of Suboptimal Fixation

Williams, R. S., Ferrante, R. J., & Caviness, V. S. (1978) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-197801000-00002 · Cited by 131 · see citing works

Age-related dendritic growth in dentate gyrus of human brain is followed by regression in the ‘oldest old’

Flood, D. G., Buell, S. J., Defiore, C. H., Horwitz, G. J., & Coleman, P. D. (1985) · Brain Research · doi:10.1016/0006-8993(85)91018-2 · Cited by 111 · see citing works

Chapter 14 Dendritic proliferation in the aging brain as a compensatory repair mechanism

Coleman, P. D., & Flood, D. G. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64307-1 · Cited by 91 · see citing works

Ordering methods in quantitative analysis of branching structures of dendritic trees.

Uylings, H. B. M., Smit, G. J., & Veltman, W. A. M. (1975) · PubMed · Cited by 89 · see citing works

Chapter 4 Dendritic Growth and The Control of Neuronal Form

Berry, M., McConnell, P., & Sievers, J. (1980) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60117-9 · Cited by 87 · see citing works

Golgi-Cox and Rapid Golgi Methods as Applied to Autopsied Human Brain Tissue

Buell, S. J. (1982) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198209000-00003 · Cited by 78 · see citing works

Dementia of the Alzheimer Type and Multi‐infarct Dementia

Bucht, G., Adolfsson, R., & Winblad, B. G. (1984) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1984.tb02233.x · Cited by 70 · see citing works

Diseases presenting as dementia.

Haase, G. R. (1971) · PubMed · Cited by 65 · see citing works

Neural Systems of the Non‐human Primate Forebrain Implicated in Memorya

Hoesen, G. W. V. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb37582.x · Cited by 64 · see citing works

An economical, semi‐automatic system for measuring cellular tree structures in three dimensions, with special emphasis on Golgi‐impregnated neurons

Overdijk, J., Uylings, H. B. M., Kuypers, K., & Kamstra, A. W. (1978) · Journal of Microscopy · doi:10.1111/j.1365-2818.1978.tb00137.x · Cited by 54 · see citing works

Chapter 20 Cell-specific pathology in neural systems of the temporal lobe in Alzheimer's disease

Hoesen, G. W. V., Hyman, B. T., & Damásio, A. R. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64313-7 · Cited by 54 · see citing works

Artifactual displacement of neuronal nucleoli in paraffin sections.

Cammermeyer, J. (1967) · PubMed · Cited by 45 · see citing works

Chapter 4 Age-related changes in Down syndrome brain and the cellular pathology of Alzheimer disease

Williams, R. S., & Matthysse, S. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64297-1 · Cited by 39 · see citing works

The influence of post-mortem fixation delay on the reliability of the Golgi silver impregnation

de Ruiter, J. P. (1983) · Brain Research · doi:10.1016/0006-8993(83)91317-3 · Cited by 36 · see citing works

Advances in the morphology of cells and tissues

Vidrio, E. A., & Galina, M. A. (1981) · A.R. Liss eBooks · Cited by 36 · see citing works

Quantitative analysis of dendritic branching pattern of granular cells from human dentate gyrus

Lindsay, R. D., & Scheibel, A. B. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90173-4 · Cited by 34 · see citing works

Basal lamina at the site of spinal cord injury in normal, immunotolerant and immunosuppressed rats

Feringa, E. R., Kowalski, T. F., & Vahlsing, H. L. (1985) · Neuroscience Letters · doi:10.1016/s0304-3940(85)80083-5 · Cited by 11 · see citing works

Morphometry of cortical dendrites.

Uylings, H. B. M., Parnavelas, J. G., & Walg, H. L. (1981) · PubMed · Cited by 7 · see citing works

Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?

Fiala, J. C., Spacek, J., & Harris, K. M. (2002) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00158-3 · Cited by 811 · see citing works

Neuron numbers and dendritic extent in normal aging and Alzheimer’s disease

Coleman, P. D., & Flood, D. G. (1987) · Neurobiology of Aging · doi:10.1016/0197-4580(87)90127-8 · Cited by 772 · see citing works

Reorganization of the morphology of hippocampal neurites and synapses after stress-induced damage correlates with behavioral improvement

Sousa, N., Lukoyanov, N. V., Madeira, M. D., Almeida, O. F. X., & Paula-Barbosa, M. M. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00050-6 · Cited by 758 · see citing works

Apolipoprotein E in animal models of CNS injury and in alzheimer's disease

Poirier, J. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90156-2 · Cited by 637 · see citing works

Dendritic Spine Abnormalities in Amyloid Precursor Protein Transgenic Mice Demonstrated by Gene Transfer and Intravital Multiphoton Microscopy

Spires, T. L., Meyer-Luehmann, M., Stern, E. A., McLean, P. J., Skoch, J., Nguyen, P. T., Bacskai, B. J., & Hyman, B. T. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1879-05.2005 · Cited by 550 · see citing works

Quantitative assessment of cortical synaptic density in Alzheimer's disease

Scheff, S. W., DeKosky, S. T., & Price, D. A. (1990) · Neurobiology of Aging · doi:10.1016/0197-4580(90)90059-9 · Cited by 446 · see citing works

The dendritic tree and brain disorders

Kulkarni, V. A., & Firestein, B. L. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.03.005 · Cited by 390 · see citing works

Synaptic slaughter in Alzheimer's disease

Coleman, P. (2003) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.09.001 · Cited by 351 · see citing works

Dendritic and Axonal Architecture of Individual Pyramidal Neurons across Layers of Adult Human Neocortex

Mohan, H., Verhoog, M. B., Doreswamy, K. K., Eyal, G., Aardse, R., Lodder, B. N., Goriounova, N. A., Asamoah, B., B. Brakspear, A. B. C., Groot, C., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv188 · Cited by 280 · see citing works

Prenatal development of neurons in the human prefrontal cortex. II. A quantitative Golgi study

Mrzljak, L., Uylings, H. B. M., Kostović, I., & van Eden, C. G. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903160408 · Cited by 316 · see citing works

Meta‐analysis of synaptic pathology in Alzheimer's disease reveals selective molecular vesicular machinery vulnerability

de Wilde, M. C., Overk, C., Sijben, J., & Masliah, E. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.12.005 · Cited by 273 · see citing works

Lifespan Alterations of Basal Dendritic Trees of Pyramidal Neurons in the Human Prefrontal Cortex: A Layer-Specific Pattern

Petanjek, Z., Judas, M., Kostovic, I., & Uylings, H. B. M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm124 · Cited by 273 · see citing works

Neuronal changes in normal human aging and Alzheimer's disease.

Uylings, H., & de Brabander, J. D. (2002) · Brain and Cognition · doi:10.1006/brcg.2001.1500 · Cited by 260 · see citing works

Minding the calcium store: Ryanodine receptor activation as a convergent mechanism of PCB toxicity

Pessah, I. N., Cherednichenko, G., & Lein, P. J. (2010) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.10.009 · Cited by 231 · see citing works

Dendritic spine loss in the hippocampus of young PDAPP and Tg2576 mice and its prevention by the ApoE2 genotype

Lanz, T. A., Carter, D. B., & Merchant, K. M. (2003) · Neurobiology of Disease · doi:10.1016/s0969-9961(03)00079-2 · Cited by 227 · see citing works

Spine density on neostriatal neurones changes with 6-hydroxydopamine lesions and with age

Ingham, C. A., Hood, S. H., & Arbuthnott, G. W. (1989) · Brain Research · doi:10.1016/0006-8993(89)91686-7 · Cited by 219 · see citing works

Impaired Spine Stability Underlies Plaque-Related Spine Loss in an Alzheimer's Disease Mouse Model

Spires-Jones, T. L., Meyer-Luehmann, M., Osetek, J. D., Jones, P. B., Stern, E. A., Bacskai, B. J., & Hyman, B. T. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.070055 · Cited by 189 · see citing works

Synaptic plasticity and cell cycle activation in neurons are alternative effector pathways: the 'Dr. Jekyll and Mr. Hyde concept' of Alzheimer's disease or the yin and yang of neuroplasticity

Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 188 · see citing works

The metric analysis of three-dimensional dendritic tree patterns: a methodological review

Uylings, H. B. M., Ruiz‐Marcos, A., & van Pelt, J. (1986) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(86)90116-0 · Cited by 187 · see citing works

Repeated confocal imaging of individual dendritic spines in the living hippocampal slice: evidence for changes in length and orientation associated with chemically induced LTP

Hosokawa, T., Rusakov, D., Bliss, T., & Fine, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05560.1995 · Cited by 187 · see citing works

The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders

Wen, T. H., Binder, D. K., Ethell, I. M., & Razak, K. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00270 · Cited by 170 · see citing works

Layer‐specific dendritic regression of pyramidal cells with ageing in the human prefrontal cortex

de Brabander, Kramers, & Uylings (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00137.x · Cited by 180 · see citing works

Dendritic extent in human dentate gyrus granule cells in normal aging and senile dementia

Flood, D. G., Buell, S. J., Horwitz, G. J., & Coleman, P. D. (1987) · Brain Research · doi:10.1016/0006-8993(87)90027-8 · Cited by 164 · see citing works

Microtubular reorganization and dendritic growth response in alzheimer's disease

McKee, A. C., Kowall, N. W., & Kosik, K. S. (1989) · Annals of Neurology · doi:10.1002/ana.410260511 · Cited by 159 · see citing works

Region‐specific age effects on AMPA sensitivity: Electrophysiological evidence for loss of synaptic contacts in hippocampal field CA1

Barnes, C. A., RAO, G. R., Foster, T. C., & McNaughton, B. L. (1992) · Hippocampus · doi:10.1002/hipo.450020413 · Cited by 154 · see citing works

Environmental lead exposure during early life alters granule cell neurogenesis and morphology in the hippocampus of young adult rats

Verina, T., Rohde, C. A., & Guilarte, T. R. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.040 · Cited by 150 · see citing works

GSK-3β overexpression causes reversible alterations on postsynaptic densities and dendritic morphology of hippocampal granule neurons in vivo

Llorens-Martı́n, M., Fuster-Matanzo, A., Teixeira, C. M., Jurado‐Arjona, J., Ulloa, F., DeFelipe, J., Rábano, A., Hernández, F., Soriano, E., & Ávila, J. (2013) · Molecular Psychiatry · doi:10.1038/mp.2013.4 · Cited by 133 · see citing works

Measures for quantifying dendritic arborizations

Uylings, H. B. M., & van Pelt, J. (2002) · Network Computation in Neural Systems · doi:10.1088/0954-898x_13_3_309 · Cited by 138 · see citing works

Plasticity of the dendritic spine

Horner, C. H. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90002-a · Cited by 123 · see citing works

The dendritic hypothesis for Alzheimer's disease pathophysiology

Cochran, J. N., Hall, A. M., & Roberson, E. D. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.12.004 · Cited by 114 · see citing works

Metal Ionophore Treatment Restores Dendritic Spine Density and Synaptic Protein Levels in a Mouse Model of Alzheimer's Disease

Adlard, P. A., Bica, L., White, A. R., Nurjono, M., Filiz, G., Crouch, P. J., Donnelly, P. S., Cappai, R., Finkelstein, D. I., & Bush, A. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017669 · Cited by 120 · see citing works

Postnatal maturation of layer V pyramidal neurons in the human prefrontal cortex. A quantitative Golgi analysis

Koenderink, M. J. T., & Uylings, H. B. M. (1995) · Brain Research · doi:10.1016/0006-8993(95)00206-6 · Cited by 116 · see citing works

Dendritic changes in Alzheimer's disease and factors that may underlie these changes

Anderton, B. H., Callahan, L. M., Coleman, P. D., Davies, P., Flood, D. G., Jicha, G. A., Ohm, T. G., & Weaver, C. L. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00022-7 · Cited by 111 · see citing works

Neuronal Structure is Altered by Amyloid Plaques

Spires‐Jones, T. L., & Hyman, B. T. (2004) · Reviews in the Neurosciences · doi:10.1515/revneuro.2004.15.4.267 · Cited by 107 · see citing works

Heat Shock Proteins and Autophagy Pathways in Neuroprotection: From Molecular Bases to Pharmacological Interventions

Penke, B., Bogár, F., Crul, T., Sántha, M., Tóth, M. E., & Vı́gh, L. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19010325 · Cited by 106 · see citing works

Increase in perforant path quantal size in aged F-344 rats

Foster, T. C., Barnes, C. A., RAO, G. R., & McNaughton, B. L. (1991) · Neurobiology of Aging · doi:10.1016/0197-4580(91)90071-q · Cited by 102 · see citing works

Postnatal maturation of the layer III pyramidal neurons in the human prefrontal cortex: a quantitative Golgi analysis

Koenderink, M. J. T., Uylings, H. B. M., & Mrzljak, L. (1994) · Brain Research · doi:10.1016/0006-8993(94)90387-5 · Cited by 98 · see citing works

Dendritic reorganisation in the basal forebrain under degenerative conditions and its defects in Alzheimer's disease. II. Ageing, Korsakoff's disease, Parkinson's disease, and Alzheimer's disease

Arendt, T., Brückner, M., Bigl, V., & Marcova, L. (1995) · The Journal of comparative neurology · doi:10.1002/cne.903510203 · Cited by 103 · see citing works

Understanding mental retardation in Down's syndrome using trisomy 16 mouse models

Galdzicki, Z., & Siarey, R. J. (2003) · Genes Brain & Behavior · doi:10.1034/j.1601-183x.2003.00024.x · Cited by 98 · see citing works

Excitatory amino acid binding sites in the hippocampal region of Alzheimer's disease and other dementias.

Penney, J. B., Maragos, W. F., Greenamyre, J. T., Debowey, D. L., Hollingsworth, Z. R., & Young, A. B. (1990) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.53.4.314 · Cited by 98 · see citing works

Region-specific stability of dendritic extent in normal human aging and regression in Alzheimer's disease. I. CA1 of hippocampus

Hanks, S. D., & Flood, D. G. (1991) · Brain Research · doi:10.1016/0006-8993(91)90493-f · Cited by 92 · see citing works

Reduced density of adenosine A1 receptors and preserved coupling of adenosine A1 receptors to G proteins in Alzheimer hippocampus: a quantitative autoradiographic study.

Ułas, J., Brunner, L., Nguyen, L., & Cotman, C. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90533-l · Cited by 98 · see citing works

Region-specific stability of dendritic extent in normal human aging and regression in Alzheimer's disease. II. Subiculum

Flood, D. G. (1991) · Brain Research · doi:10.1016/0006-8993(91)90494-g · Cited by 89 · see citing works

Granule cell loss and dendritic regrowth in the hippocampal dentate gyrus of the rat after chronic alcohol consumption

Cadete-Leite, A., Tavares, M. A., Uylings, H. B. M., & Paula-Barbosa, M. (1988) · Brain Research · doi:10.1016/0006-8993(88)90309-5 · Cited by 87 · see citing works

Structural changes in the hippocampal formation after long‐term alcohol consumption and withdrawal in the rat

PAULA‐BARBOSA, M. M., BRANDÃO, F., Madeira, M. D., & Cadete-Leite, A. (1993) · Addiction · doi:10.1111/j.1360-0443.1993.tb00807.x · Cited by 84 · see citing works

Apolipoprotein E, Synaptic Plasticity and Alzheimer's Disease

Poirier, J., Minnich, A., & Davignon, J. (1995) · Annals of Medicine · doi:10.3109/07853899509019253 · Cited by 82 · see citing works

Chapter 31 Chapter Hippocampal plasticity in normal aging and decreased plasticity in Alzheimer's disease

Flood, D. G., & Coleman, P. D. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61267-4 · Cited by 82 · see citing works

Neuronal alterations in patients with dementia: a Golgi study on biopsy samples

Ferrer, I., Guionnet, N., Cruz-Sánchez, F. F., & Tuñón, T. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90420-e · Cited by 82 · see citing works

The dentate gyrus in Alzheimer's disease

Ohm, T. G. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63039-8 · Cited by 78 · see citing works

Dendritic changes in visual pathways in glaucoma and other neurodegenerative conditions

Liu, M., Duggan, J., Salt, T. E., & Cordeiro, M. F. (2011) · Experimental Eye Research · doi:10.1016/j.exer.2011.01.014 · Cited by 78 · see citing works

The discovery of dendritic spines by Cajal in 1888 and its relevance in the present neuroscience

García-López, P., García‐Marín, V., & Freire, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.002 · Cited by 77 · see citing works

Morphological Changes of the Human Purkinje Cells and Deposition of Neuritic Plaques and Neurofibrillary Tangles on the Cerebellar Cortex of Alzheimer’s Disease

Mavroudis, I. A., Fotiou, D. F., Adipepe, L. F., Manani, M. G., Njau, S. N., Psaroulis, D., Costa, V., & Balogiannis, S. (2010) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/1533317510382892 · Cited by 74 · see citing works

Characterization of perforant path lesions in rodent models of memory and attention

Kirkby, D. L., & Higgins, G. A. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00087.x · Cited by 74 · see citing works

Immunohistochemical localization of caffeine-induced c-Fos protein expression in the rat brain

Bennett, H. J., & Semba, K. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19981109)401:1 · Cited by 41 · see citing works

Dendritic changes in the hippocampal formation of AIDS patients: a quantitative Golgi study

S�, M. J., Madeira, M. D., Ruela, C., Volk, B., Mota‐Miranda, A., & Paula-Barbosa, M. M. (2004) · Acta Neuropathologica · doi:10.1007/s00401-003-0781-3 · Cited by 72 · see citing works

Comparison of the regional expression of nicotinic acetylcholine receptor ?7 mRNA and [125I]-?-bungarotoxin binding in human postmortem brain

Breese, C. R., Adams, C. E., Logel, J., Drebing, C. J., Rollins, Y. D., Barnhart, M. M., Sullivan, B. F., DeMasters, B. K., Freedman, R., & Leonard, S. S. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971027)387:3 · Cited by 231 · see citing works

Prenatal stress induces learning deficits and is associated with a decrease in granules and CA3 cell dendritic tree size in rat hippocampus

Sharifabad, M. H., & Hadinedoushan, H. (2007) · Anatomical Science International · doi:10.1111/j.1447-073x.2007.00186.x · Cited by 68 · see citing works

Age‐related loss of synapses in the frontal cortex of SAMP10 mouse: A model of cerebral degeneration

Shimada, A., Keino, H., Satoh, M., Kishikawa, M., & Hosokawa, M. (2003) · Synapse · doi:10.1002/syn.10209 · Cited by 66 · see citing works

The Ever-Changing Morphology of Hippocampal Granule Neurons in Physiology and Pathology

Llorens-Martı́n, M., Rábano, A., & Ávila, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00526 · Cited by 61 · see citing works

Differential spine loss and regrowth of striatal neurons following multiple forms of deafferentation: a Golgi study

Cheng, H.-W., Rafols, J. A., Goshgarian, H. G., Anavi, Y., Tong, J., & McNeill, T. H. (1997) · Experimental Neurology · doi:10.1006/exnr.1997.6618 · Cited by 64 · see citing works

Evidence for altered dendritic spine compartmentalization in Alzheimer’s disease and functional effects in a mouse model

Androuin, A., Potier, B., Nägerl, U. V., Cattaert, D., Danglot, L., Thierry, M., Youssef, I., Triller, A., Duyckaerts, C. J., Hachimi, K. H. E., et al. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1847-6 · Cited by 59 · see citing works

Apolipoprotein E in the brain and its role in Alzheimer's disease.

Poirier, J. (1996) · PubMed Central · Cited by 60 · see citing works

Morphological variability is a characteristic feature of granule cells in the primate fascia dentata: A combined Golgi/electron microscope study

Seress, L., & Frotscher, M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930208 · Cited by 59 · see citing works

Is senile dementia of the Alzheimer type associated with hippocampal plasticity?

Represa, A., Duyckaerts, C. J., Tremblay, E. C., Hauw, J., & Ben‐Ari, Y. (1988) · Brain Research · doi:10.1016/0006-8993(88)90706-8 · Cited by 58 · see citing works

Decreased expression of N-methyl-D-aspartate receptor 1 messenger RNA in select regions of Alzheimer brain.

Ułas, J., & Cotman, C. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00023-7 · Cited by 54 · see citing works

Postmortem changes in brain cell structure: a reviewPreprint

Krassner, M. M., Kauffman, J., Sowa, A., Cialowicz, K. I., Walsh, S., Farrell, K. W., Crary, J. F., & McKenzie, A. T. (2023) · Free Neuropathology · doi:10.17879/freeneuropathology-2023-4790 · Cited by 64 · see citing works

Stereological evaluation and Golgi study of the sexual dimorphisms in the volume, cell numbers, and cell size in the medial preoptic nucleus of the rat

Madeira, M. D., Leal, S., & Paula-BARBOSA, M. M. (1999) · Journal of Neurocytology · doi:10.1023/a:1007076206828 · Cited by 45 · see citing works

Dendritic spine plasticity in hippocampus

Gazzaley, A. H., Kay, S., & Benson, D. L. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00021-0 · Cited by 45 · see citing works

Ultrastructure of neurofibrillary tangles in the cerebral cortex of sheep

Nelson, P. T., & Saper, C. B. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(94)00175-z · Cited by 45 · see citing works

The dendritic trees of neurons from the hippocampal formation of protein-deprived adult rats. A quantitative Golgi study

Andrade, J. P., Castanheira-Vale, A. J., Paz-Dias, P. G., Madeira, M. D., & Paula-Barbosa, M. M. (1996) · Experimental Brain Research · doi:10.1007/bf00229626 · Cited by 44 · see citing works

CaMKII-dependent dendrite ramification and spine generation promote spatial training-induced memory improvement in a rat model of sporadic Alzheimer's disease

Jiang, X., Chai, G., Wang, Z.-H., Hu, Y., Li, X., Ma, Z., Wang, Q., Wang, J., & Liu, G. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.10.018 · Cited by 37 · see citing works

Sexual dimorphism in the subiculum of the rat hippocampal formation

Andrade, J. P., Madeira, M. D., & Paula-Barbosa, M. M. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02605-6 · Cited by 39 · see citing works

Cytoarchitecture, neuronal composition, and entorhinal afferents of the flying fox hippocampus

Buhl, E., & Dann, J. F. (1991) · Hippocampus · doi:10.1002/hipo.450010203 · Cited by 36 · see citing works

Dendritic Pathology: An Overview of Golgi Studies in Man

Jagadha, V., & Becker, L. E. (1989) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100028493 · Cited by 36 · see citing works

Using curcumin to prevent structural and behavioral changes of medial prefrontal cortex induced by sleep deprivation in rats

Noorafshan, A., Karimi, F., Karbalay‐Doust, S., & Kamali, A. M. (2017) · EXCLI journal · doi:10.17179/excli2017-139 · Cited by 34 · see citing works

Chronic food restriction is associated with subtle dendritic alterations in granule cells of the rat hippocampal formation

Andrade, J. P., Lukoyanov, N., & Paula‐Barbosa, M. M. (2002) · Hippocampus · doi:10.1002/hipo.1102 · Cited by 33 · see citing works

Corticosterone replacement restores normal morphological features to the hippocampal dendrites, axons and synapses of adrenalectomized rats

Sousa, N., Madeira, M. D., & Paula-Barbosa, M. M. (1999) · Journal of Neurocytology · doi:10.1023/a:1007015321767 · Cited by 32 · see citing works

Loss of synapses in the entorhinal‐dentate gyrus pathway following repeated induction of electroshock seizures in the rat

Cardoso, A., Assunção, M., Andrade, J. P., Pereira, P. A., Madeira, M. D., Paula‐Barbosa, M. M., & Lukoyanov, N. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21474 · Cited by 31 · see citing works

Effect of Boswellia serrata gum resin on the morphology of hippocampal CA1 pyramidal cells in aged rat

Sharifabad, M. H., & Esfandiari, E. (2014) · Anatomical Science International · doi:10.1007/s12565-014-0228-z · Cited by 30 · see citing works

Protective effects of a catechin-rich extract on the hippocampal formation and spatial memory in aging rats

Rodrigues, J., Assunção, M., Lukoyanov, N., Cardoso, A., Carvalho, F. D., & Andrade, J. P. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.02.040 · Cited by 29 · see citing works

Cajal's Contributions to the Study of Alzheimer's Disease

García‐Marín, V., García-López, P., & Freire, M. (2007) · Journal of Alzheimer s Disease · doi:10.3233/jad-2007-12206 · Cited by 29 · see citing works

Molecular mechanisms mediating pathological plasticity in Huntington's disease and Alzheimer's disease

Spires‐Jones, T. L., & Hannan, A. J. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04275.x · Cited by 29 · see citing works

Metric Analysis of Hippocampal Granule Cell Dendritic Trees After Alcohol Withdrawal in Rats

Cadete-Leite, A., Tavares, M. A., Aives, M. C., Uylings, H. B. M., & Paula‐Barbosa, M. M. (1989) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1989.tb00433.x · Cited by 29 · see citing works

Environmental enrichment alters dentate granule cell morphology in oldest‐old rat

Darmopil, S., Petanjek, Z., Mohammed, A. H. S., & Bogdanović, N. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00560.x · Cited by 28 · see citing works

RanBP9 aggravates synaptic damage in the mouse brain and is inversely correlated to spinophilin levels in Alzheimer’s brain synaptosomes

Palavicini, J. P., Wang, H., Bianchi, E., Xu, S., Rao, J. S., Kang, D. E., & Lakshmana, M. K. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.183 · Cited by 28 · see citing works

The Hippocampal Neuro-Glio-Vascular Network: Metabolic Vulnerability and Potential Neurogenic Regeneration in Disease

Kirschen, G. W., Kéry, R., & Ge, S. (2017) · Brain Plasticity · doi:10.3233/bpl-170055 · Cited by 28 · see citing works

ESCRT, autophagy, and frontotemporal dementia

Lee, J., & Gao, F. (2008) · BMB Reports · doi:10.5483/bmbrep.2008.41.12.827 · Cited by 27 · see citing works

Role of Apolipoprotein E in Alzheimer’s Disease

Zannis, V. I., Zanni, E. E., Makrides, S. C., Kardassis, D., & Aleshkov, S. B. (1998) · Springer eBooks · doi:10.1007/978-1-4899-0133-0_13 · Cited by 26 · see citing works

Original article Sertraline and curcumin prevent stress-induced morphological changes of dendrites and neurons in the medial prefrontal cortex of rats

Noorafshan, A., Abdollahifar, M., Karbalay‐Doust, S., Asadi-Golshan, R., & Rashidiani-Rashidabadi, A. (2015) · Folia Neuropathologica · doi:10.5114/fn.2015.49976 · Cited by 22 · see citing works

Hypertrophy of the ageing rat medial preoptic nucleus

Madeira, M. D., Andrade, J. P., & Paula-Barbosa, M. M. (2000) · Journal of Neurocytology · doi:10.1023/a:1026598906739 · Cited by 22 · see citing works

Beneficial effect of Boswellia serrata gum resin on spatial learning and the dendritic tree of dentate gyrus granule cells in aged rats.

Sharifabad, M. H., Ardakani, R. K., & Hosseini-Sharifabad, A. (2016) · PubMed Central · Cited by 21 · see citing works

Progression of Alzheimer's disease parallels unusual structural plasticity of human dentate granule cells

Márquez‐Valadez, B., Rábano, A., & Llorens-Martı́n, M. (2022) · Acta Neuropathologica Communications · doi:10.1186/s40478-022-01431-7 · Cited by 20 · see citing works

HspB5/αB-crystallin increases dendritic complexity and protects the dendritic arbor during heat shock in cultured rat hippocampal neurons

Bartelt‐Kirbach, B., Moron, M., Glomb, M., Beck, C.-M., Weller, M.-P., & Golenhofen, N. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2219-9 · Cited by 20 · see citing works

A Morphometeric Study on CA3 Hippocampal Field in Young Rats Following Maternal Administration of Boswellia Serrata Resin During Gestation

Sharifabad, M. H., & Esfandiary, E. (2007) · Iranian journal of basic medical sciences. · doi:10.22038/ijbms.2007.5292 · Cited by 20 · see citing works

Enhanced but delayed axonal sprouting of the commissural/associational pathway following a combined entorhinal cortex/fimbria fornix lesion

Schauwecker, P. E., & McNeill, T. H. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903510311 · Cited by 20 · see citing works

Total number of neurons in the layers of the human entorhinal cortex

West, M. J., & Slomianka, L. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:1 · Cited by 57 · see citing works

Tangle-bearing neurons show more extensive dendritic trees than tangle-free neurons in area CA1 of the hippocampus in Alzheimer's disease

Gertz, H., Krüger, H., Patt, S., & Cervós‐Navarro, J. (1991) · Brain Research · doi:10.1016/0006-8993(91)91130-s · Cited by 20 · see citing works

Therapeutic Efficacy of Boric Acid Treatment on Brain Tissue and Cognitive Functions in Rats with Experimental Alzheimer’s Disease

Özdemir, Ç., Arslan, M., Küçük, A., Yığman, Z., & Dursun, A. D. (2023) · Drug Design Development and Therapy · doi:10.2147/dddt.s405963 · Cited by 18 · see citing works

Apolipoprotein E and Alzheimer's disease

Poirier, J., Nalbantoglu, J. N., Guillaume, D., & Bertrand, P. (1995) · Elsevier eBooks · doi:10.1016/b978-012286965-5/50014-5 · Cited by 18 · see citing works

Synaptopathy Mechanisms in ALS Caused by C9orf72 Repeat Expansion

Nishimura, A. L., & Arias, N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.660693 · Cited by 16 · see citing works

Dendritic atrophy in the dentate gyrus of the senescent rat

Geinisman, Y., Bondareff, W., & Dodge, J. T. (1978) · American Journal of Anatomy · doi:10.1002/aja.1001520305 · Cited by 81 · see citing works

Dendritic extent in human dentate gyrus granule cells in normal aging and senile dementia

Flood, D. G., Buell, S. J., Horwitz, G. J., & Coleman, P. D. (1987) · Brain Research · doi:10.1016/0006-8993(87)90027-8 · Cited by 164 · see citing works

Dendritic Growth in the Aged Human Brain and Failure of Growth in Senile Dementia

Buell, S. J., & Coleman, P. D. (1979) · Science · doi:10.1126/science.493989 · Cited by 475 · see citing works

Age-related dendritic growth in dentate gyrus of human brain is followed by regression in the ‘oldest old’

Flood, D. G., Buell, S. J., Defiore, C. H., Horwitz, G. J., & Coleman, P. D. (1985) · Brain Research · doi:10.1016/0006-8993(85)91018-2 · Cited by 111 · see citing works

Quantitative evidence for selective dendritic growth in normal human aging but not in senile dementia

Buell, S. J., & Coleman, P. D. (1981) · Brain Research · doi:10.1016/0006-8993(81)90436-4 · Cited by 220 · see citing works