-
1
-
-
77649244042
-
Synaptophysin immunoreactivity in the human hippocampus and neocortex from 6 to 41 weeks of gestation
-
Sarnat HB, Flores-Sarnat L, Trevenen CL. Synaptophysin immunoreactivity in the human hippocampus and neocortex from 6 to 41 weeks of gestation. J Neuropathol Exp Neurol. 2010; 69: 234-245.
-
(2010)
J Neuropathol Exp Neurol.
, vol.69
, pp. 234-245
-
-
Sarnat, H.B.1
Flores-Sarnat, L.2
Trevenen, C.L.3
-
2
-
-
0033004355
-
Synaptophysin immunocytochemistry with thermal intensification: a marker of terminal axonal maturation in the human fetal nervous system
-
Sarnat HB, Born DE. Synaptophysin immunocytochemistry with thermal intensification: a marker of terminal axonal maturation in the human fetal nervous system. Brain Dev. 1999; 21: 41-50.
-
(1999)
Brain Dev.
, vol.21
, pp. 41-50
-
-
Sarnat, H.B.1
Born, D.E.2
-
3
-
-
0034141205
-
Changing distribution patterns of synaptophysinimmunoreactive structures in the human dorsal striatum of the fetal brain
-
Ulfig N, Setzer M, Neudörfer F, Saretzki U. Changing distribution patterns of synaptophysinimmunoreactive structures in the human dorsal striatum of the fetal brain. Anat Rec. 2000; 258: 198-209.
-
(2000)
Anat Rec.
, vol.258
, pp. 198-209
-
-
Ulfig, N.1
Setzer, M.2
Neudörfer, F.3
Saretzki, U.4
-
4
-
-
84881503005
-
Synaptogenesis in the fetal corpus striatum, globus pallidus and substantia nigra. Correlations with striosomes of Graybiel and dyskinesias in premature infants
-
in press
-
Sarnat HB, Auer RN, Flores-Sarnat L. Synaptogenesis in the fetal corpus striatum, globus pallidus and substantia nigra. Correlations with striosomes of Graybiel and dyskinesias in premature infants. J Child Neurol. 2012; 27. in press.
-
(2012)
J Child Neurol.
, pp. 27
-
-
Sarnat, H.B.1
Auer, R.N.2
Flores-Sarnat, L.3
-
5
-
-
84879182785
-
Sequence of synaptogenesis in the human fetal cerebellar system Part 1. Guillain-Mollaret triangle (dentate- rubro-olivo-cerebellar circuit)
-
in press
-
Sarnat HB, Flores-Sarnat L, Auer R. N. Sequence of synaptogenesis in the human fetal cerebellar system. Part 1. Guillain-Mollaret triangle (dentate- rubro-olivo-cerebellar circuit). Dev Neurosci. 2013. in press.
-
(2013)
Dev Neurosci
-
-
Sarnat, H.B.1
Flores-Sarnat, L.2
Auer, R.N.3
-
6
-
-
84883312563
-
Sequence of synaptogenesis in the human fetal cerebellar system Part 2. Pontine nuclei and cerebellar cortex
-
in press
-
Sarnat HB, Flores-Sarnat L, Auer R. N. Sequence of synaptogenesis in the human fetal cerebellar system. Part 2. Pontine nuclei and cerebellar cortex. Dev Neurosci. 2013. in press.
-
(2013)
Dev Neurosci
-
-
Sarnat, H.B.1
Flores-Sarnat, L.2
Auer, R.N.3
-
7
-
-
0344237032
-
A 38,000-dalton membrane protein (p38) present in synaptic vesicles
-
Jahn R, Schiebler W, Ouimet C, Greengard P. A 38,000-dalton membrane protein (p38) present in synaptic vesicles. Proc Natl Acad Sci USA. 1985; 82: 4137-4141.
-
(1985)
Proc Natl Acad Sci USA.
, vol.82
, pp. 4137-4141
-
-
Jahn, R.1
Schiebler, W.2
Ouimet, C.3
Greengard, P.4
-
8
-
-
0022391791
-
Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles
-
Wiedenmann B, Franke WW. Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles. Cell. 1985; 41: 1017-1028.
-
(1985)
Cell.
, vol.41
, pp. 1017-1028
-
-
Wiedenmann, B.1
Franke, W.W.2
-
10
-
-
0031728633
-
Holoprosencephaly: a defect in brain patterning
-
Golden JA. Holoprosencephaly: a defect in brain patterning. J Neuropathol Exp Neurol. 1998; 57: 991-999.
-
(1998)
J Neuropathol Exp Neurol.
, vol.57
, pp. 991-999
-
-
Golden, J.A.1
-
11
-
-
0035570924
-
Neuropathologic research strategies in holoprosencephaly
-
Sarnat HB, Flores-Sarnat L. Neuropathologic research strategies in holoprosencephaly. J Child Neurol. 2001; 16: 918-931.
-
(2001)
J Child Neurol.
, vol.16
, pp. 918-931
-
-
Sarnat, H.B.1
Flores-Sarnat, L.2
-
12
-
-
84881484714
-
-
Sarnat HB (ed). MedLink. San Diego
-
Siebert JR. Holoprosencephaly. In: Sarnat HB (ed). MedLink. San Diego: www.MedLink.com; 2012.
-
(2012)
Holoprosencephaly
-
-
Siebert, J.R.1
-
13
-
-
0017741766
-
Holoprosencephaly in human embryos: epidemiologic studies of 150 cases
-
Matsunaga E, Shiota K. Holoprosencephaly in human embryos: epidemiologic studies of 150 cases. Teratology. 1977; 16: 261-272.
-
(1977)
Teratology.
, vol.16
, pp. 261-272
-
-
Matsunaga, E.1
Shiota, K.2
-
14
-
-
0035339735
-
Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England
-
Bullen PJ, Rankin JM, Robson SC. Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England. Am J Obstet Gynecol. 2001; 184: 1256-1262.
-
(2001)
Am J Obstet Gynecol.
, vol.184
, pp. 1256-1262
-
-
Bullen, P.J.1
Rankin, J.M.2
Robson, S.C.3
-
15
-
-
80053551866
-
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction
-
McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT. Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction. J Clin Endocrinol Metab. 2011; 96: E1709-E1718.
-
(2011)
J Clin Endocrinol Metab.
, vol.96
-
-
McCabe, M.J.1
Gaston-Massuet, C.2
Tziaferi, V.3
Gregory, L.C.4
Alatzoglou, K.S.5
Signore, M.6
Puelles, E.7
Gerrelli, D.8
Farooqi, I.S.9
Raza, J.10
Walker, J.11
Kavanaugh, S.I.12
Tsai, P.S.13
Pitteloud, N.14
Martinez-Barbera, J.P.15
Dattani, M.T.16
-
16
-
-
1842847054
-
Microscopic criteria to determine gestational age of the fetal and neonatal brain
-
García JH (ed) Louis: Mosby-Yearbook
-
Sarnat HB. Microscopic criteria to determine gestational age of the fetal and neonatal brain. In: García JH (ed). Neuropathology: The Diagnostic Approach. St. Louis: Mosby-Yearbook; 1997. p. 529-540.
-
(1997)
Neuropathology: The Diagnostic Approach. St
, pp. 529-540
-
-
Sarnat, H.B.1
-
17
-
-
79959924122
-
Development and evolution of the human neocortex
-
Lui JH, Hansen DV, Kriegstein AR. Development and evolution of the human neocortex. Cell. 2011; 146: 18-36.
-
(2011)
Cell.
, vol.146
, pp. 18-36
-
-
Lui, J.H.1
Hansen, D.V.2
Kriegstein, A.R.3
-
18
-
-
84881487497
-
Pathological spectrum of cerebral cortex disturbances in human holoprosencephaly.Disturbances of cortical development in human holoprosencephaly
-
abstract
-
Laure-Kamionowska M, Szymanska K, Taraszewska A, Ogonowska W, Klepacka T, Deregowski K. Pathological spectrum of cerebral cortex disturbances in human holoprosencephaly. Disturbances of cortical development in human holoprosencephaly. Folia Neuropathol. 2011; 49: 244. abstract.
-
(2011)
Folia Neuropathol.
, vol.49
, pp. 244
-
-
Laure-Kamionowska, M.1
Szymanska, K.2
Taraszewska, A.3
Ogonowska, W.4
Klepacka, T.5
Deregowski, K.6
-
19
-
-
0031934642
-
Neuronal nuclear antigen (NeuN): a marker of neuronal maturation in early human fetal nervous system
-
Sarnat HB, Nochlin D, Born DE. Neuronal nuclear antigen (NeuN): a marker of neuronal maturation in early human fetal nervous system. Brain Dev. 1998; 20: 88-94.
-
(1998)
Brain Dev.
, vol.20
, pp. 88-94
-
-
Sarnat, H.B.1
Nochlin, D.2
Born, D.E.3
-
20
-
-
0036048323
-
Calcium-binding proteins in the human developing brain
-
Ulfig N. Calcium-binding proteins in the human developing brain. Adv Anat Embryol Cell Biol 2002; 165(III-IX): 1-92.
-
(2002)
Adv Anat Embryol Cell Biol
, vol.165
, Issue.3-9
, pp. 1-92
-
-
Ulfig, N.1
-
21
-
-
72249086809
-
Calretinin immunoreactivity in focal cortical dysplasias and in non-malformed epileptic cortex
-
Barinka F, Druga R, Marusic P, Krsek P, Zamecnik J. Calretinin immunoreactivity in focal cortical dysplasias and in non-malformed epileptic cortex. Epilepsy Res. 2010; 88: 76-86.
-
(2010)
Epilepsy Res.
, vol.88
, pp. 76-86
-
-
Barinka, F.1
Druga, R.2
Marusic, P.3
Krsek, P.4
Zamecnik, J.5
-
22
-
-
77956183883
-
Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes
-
Marcorelles P, Laquerrière A, Adde-Michel C, Marret S, Saugier-Veber P, Beldjord C, Friocourt G. Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes. Acta Neuropathol. 2010; 120: 503-515.
-
(2010)
Acta Neuropathol.
, vol.120
, pp. 503-515
-
-
Marcorelles, P.1
Laquerrière, A.2
Adde-Michel, C.3
Marret, S.4
Saugier-Veber, P.5
Beldjord, C.6
Friocourt, G.7
-
23
-
-
84875178160
-
Radial micro-columnar cortical architecture: maturational arrest or cortical dysgenesis?
-
in press
-
Sarnat HB, Flores-Sarnat L. Radial micro-columnar cortical architecture: maturational arrest or cortical dysgenesis? Pediatr Neurol. 2013. in press.
-
(2013)
Pediatr Neurol
-
-
Sarnat, H.B.1
Flores-Sarnat, L.2
-
24
-
-
0141769719
-
An increase of hippocampal calretinin-immunoreactive neurons correlates with early febrile seizures in temporal lobe epilepsy
-
Blxümcke I, Beck H, Suter B, Hoffmann D, Födisch HJ, Wolf HK, Schramm J, Elger CE, Wiestler OD. An increase of hippocampal calretinin-immunoreactive neurons correlates with early febrile seizures in temporal lobe epilepsy. Acta Neuropathol. 1999; 97: 31-39.
-
(1999)
Acta Neuropathol.
, vol.97
, pp. 31-39
-
-
Blümcke, I.1
Beck, H.2
Suter, B.3
Hoffmann, D.4
Födisch, H.J.5
Wolf, H.K.6
Schramm, J.7
Elger, C.E.8
Wiestler, O.D.9
-
25
-
-
13344270381
-
Preservation of calretinin-immunoreactive neurons in the hippocampus of epilepsy patients with Ammon's horn sclerosis
-
Blümcke I, Beck H, Nitsch R, Eickhoff C, Scheffler B, Celio MR, Schramm J, Elger CE, Wolf HK, Wiestler OD. Preservation of calretinin-immunoreactive neurons in the hippocampus of epilepsy patients with Ammon's horn sclerosis. J Neuropathol Exp Neurol. 1996; 55: 329-341.
-
(1996)
J Neuropathol Exp Neurol.
, vol.55
, pp. 329-341
-
-
Blümcke, I.1
Beck, H.2
Nitsch, R.3
Eickhoff, C.4
Scheffler, B.5
Celio, M.R.6
Schramm, J.7
Elger, C.E.8
Wolf, H.K.9
Wiestler, O.D.10
-
26
-
-
0033755964
-
Molecular genetic classification of central nervous system malformations
-
Sarnat HB. Molecular genetic classification of central nervous system malformations. J Child Neurol. 2000; 15: 675-687. CrossRef
-
(2000)
J Child Neurol.
, vol.15
, pp. 675-687
-
-
Sarnat, H.B.1
-
27
-
-
76649095751
-
Axes and gradients of the neural tube and other criteria for an integrated morphological and molecular genetic classification of nervous system malformations
-
Edinburgh, London, NY, Toronto: Elsevier Sarnat HB, Curatolo P (eds),3-11
-
Flores-Sarnat L, Sarnat HB. Axes and gradients of the neural tube and other criteria for an integrated morphological and molecular genetic classification of nervous system malformations. In: Sarnat HB, Curatolo P (eds). Malformations of the Nervous System. Edinburgh, London, NY, Toronto: Elsevier; 2008. p. 87; 3-11.
-
(2008)
Malformations of the Nervous System
, pp. 87
-
-
Flores-Sarnat, L.1
Sarnat, H.B.2
-
28
-
-
84896327595
-
Developmental origin of patchy axonal connectivity in the neocortex: a computational model
-
Cereb Cortex; in press. e-pub ahead of print, doi:10:1093/cercor/bhs327
-
Bauer R, Zubler F, Hauri A, Muir DR, Douglas RJ. Developmental origin of patchy axonal connectivity in the neocortex: a computational model. Cereb Cortex. 2012; in press. e-pub ahead of print, doi:10:1093/cercor/bhs327.
-
(2012)
-
-
Bauer, R.1
Zubler, F.2
Hauri, A.3
Muir, D.R.4
Douglas, R.J.5
-
29
-
-
43249096303
-
Fetal ethanol exposure activates protein kinase-A and impairs Shh expression in prechordal mesoderm cells in the pathogenesis of holoprosencephaly
-
Aoto K, Shikata Y, Higashiyama D, Shiota K, Motoyama J. Fetal ethanol exposure activates protein kinase-A and impairs Shh expression in prechordal mesoderm cells in the pathogenesis of holoprosencephaly. Birth Defects Res A Clin Mol Teratol. 2008; 82: 224-231. CrossRefPart A
-
(2008)
Birth Defects Res A Clin Mol Teratol.
, vol.82
, pp. 224-231
-
-
Aoto, K.1
Shikata, Y.2
Higashiyama, D.3
Shiota, K.4
Motoyama, J.5
-
30
-
-
0037044287
-
Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain
-
Plawner LL, Delgado MR, Miller VS, Levey EB, Kinsman SL, Barkovich AJ, Simon EM, Clegg NJ, Sweet VT, Stashinko EE, Hahn JS. Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain. Neurology. 2002; 59: 1058-1066.
-
(2002)
Neurology.
, vol.59
, pp. 1058-1066
-
-
Plawner, L.L.1
Delgado, M.R.2
Miller, V.S.3
Levey, E.B.4
Kinsman, S.L.5
Barkovich, A.J.6
Simon, E.M.7
Clegg, N.J.8
Sweet, V.T.9
Stashinko, E.E.10
Hahn, J.S.11
-
31
-
-
0036931690
-
Holoprosencephaly: genetic, neuroradiological, and clinical advances
-
Hahn JS, Pinter JD. Holoprosencephaly: genetic, neuroradiological, and clinical advances. Semin Pediatr Neurol. 2002; 9: 309-319.
-
(2002)
Semin Pediatr Neurol.
, vol.9
, pp. 309-319
-
-
Hahn, J.S.1
Pinter, J.D.2
-
32
-
-
84881540648
-
Midline hypoplasias, Holoprosencephaly
-
Sarnat HB, Curatolo P (eds). (3rd series). Edinburgh: Elsevier
-
Hahn JS. Midline hypoplasias. Holoprosencephaly. In: Sarnat HB, Curatolo P (eds). Handbook of Clinical Neurology, Vol. 87 (3rd series). Edinburgh: Elsevier; 2008. p. 13-37.
-
(2008)
Handbook of Clinical Neurology
, vol.87
, pp. 13-37
-
-
Hahn, J.S.1
-
33
-
-
0642372558
-
Electroencephalography in holoprosencephaly: findings in children without epilepsy
-
Hahn JS, Delgado MR, Clegg NJ, Sparagana SP, Gerace KL, Barkovich AJ, Olson DM. Electroencephalography in holoprosencephaly: findings in children without epilepsy. Clin Neurophysiol. 2003; 114: 1908-1917.
-
(2003)
Clin Neurophysiol.
, vol.114
, pp. 1908-1917
-
-
Hahn, J.S.1
Delgado, M.R.2
Clegg, N.J.3
Sparagana, S.P.4
Gerace, K.L.5
Barkovich, A.J.6
Olson, D.M.7
-
34
-
-
84864258635
-
Neonates with seizures: what predicts development?
-
Painter MJ, Sun Q, Scher MS, Janosky J, Alvin J. Neonates with seizures: what predicts development?. J Child Neurol. 2012; 27: 1022-1026.
-
(2012)
J Child Neurol.
, vol.27
, pp. 1022-1026
-
-
Painter, M.J.1
Sun, Q.2
Scher, M.S.3
Janosky, J.4
Alvin, J.5
-
35
-
-
0029655880
-
Precocious cerebral development associated with agenesis of the corpus callosum in midfetal life: a transient syndrome?
-
Hori A. Precocious cerebral development associated with agenesis of the corpus callosum in midfetal life: a transient syndrome?. Acta Neuropathol. 1996; 91: 120-125.
-
(1996)
Acta Neuropathol.
, vol.91
, pp. 120-125
-
-
Hori, A.1
-
36
-
-
0026736312
-
Role of human fetal ependyma
-
Sarnat HB. Role of human fetal ependyma. Pediatr Neurol. 1992; 8: 163-178.
-
(1992)
Pediatr Neurol.
, vol.8
, pp. 163-178
-
-
Sarnat, H.B.1
-
37
-
-
0026585326
-
Regional differentiation of the human fetal ependyma: immunocytochemical markers
-
Sarnat HB. Regional differentiation of the human fetal ependyma: immunocytochemical markers. J Neuropathol Exp Neurol. 1992; 51: 58-75.
-
(1992)
J Neuropathol Exp Neurol.
, vol.51
, pp. 58-75
-
-
Sarnat, H.B.1
-
38
-
-
0033011476
-
An immunohistochemical study of Purkinje cells in a case of hereditary cerebellar cortical atrophy
-
Nakamura R, Kurita K, Kawanami T, Kato T. An immunohistochemical study of Purkinje cells in a case of hereditary cerebellar cortical atrophy. Acta Neuropathol. 1999; 97: 196-200.
-
(1999)
Acta Neuropathol.
, vol.97
, pp. 196-200
-
-
Nakamura, R.1
Kurita, K.2
Kawanami, T.3
Kato, T.4
-
39
-
-
34848902266
-
Pontocerebellar hypoplasia type 2: a neuropathological update
-
Barth PG, Aronica E, de Vries L, Nikkels PG, Scheper W, Hoozemans JJ, Poll-The BT, Troost D. Pontocerebellar hypoplasia type 2: a neuropathological update. Acta Neuropathol. 2007; 114: 373-386.
-
(2007)
Acta Neuropathol.
, vol.114
, pp. 373-386
-
-
Barth, P.G.1
Aronica, E.2
de Vries, L.3
Nikkels, P.G.4
Scheper, W.5
Hoozemans, J.J.6
Poll-The, B.T.7
Troost, D.8
|