-
1
-
-
33644554160
-
Agenesis of the corpus callosum: Clinical and genetic study in 63 young patients
-
Bedeschi MF, Bonaglia MC, Grasso R, et al. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients. Pediatr Neurol 2006;34:186-193.
-
(2006)
Pediatr Neurol
, vol.34
, pp. 186-193
-
-
Bedeschi, M.F.1
Bonaglia, M.C.2
Grasso, R.3
-
3
-
-
12344333585
-
Spectrum of corpus callosum agenesis
-
Sztriha L. Spectrum of corpus callosum agenesis. Pediatr Neurol 2005;32:94-101.
-
(2005)
Pediatr Neurol
, vol.32
, pp. 94-101
-
-
Sztriha, L.1
-
4
-
-
33646548244
-
Characteristics, associations and outcome of partial agenesis of the corpus callo-sum in the fetus
-
Volpe P, Paladini D, Resta M, et al. Characteristics, associations and outcome of partial agenesis of the corpus callo-sum in the fetus. Ultrasound Obstet Gynecol 2006;27: 509-516.
-
(2006)
Ultrasound Obstet Gynecol
, vol.27
, pp. 509-516
-
-
Volpe, P.1
Paladini, D.2
Resta, M.3
-
5
-
-
33750291247
-
Anomalies of the corpus callosum: An MR analysis of the phenotypic spectrum of associated malformations
-
Hetts SW, Sherr EH, Chao S, Gobuty S, Barkovich AJ. Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations. AJR Am J Roentgenol 2006;187:1343-1348.
-
(2006)
AJR Am J Roentgenol
, vol.187
, pp. 1343-1348
-
-
Hetts, S.W.1
Sherr, E.H.2
Chao, S.3
Gobuty, S.4
Barkovich, A.J.5
-
6
-
-
0004289354
-
-
Philadelphia: Lip-pincott Williams & Wilkins
-
Barkovich AJ. Pediatric Neuroimaging. Philadelphia: Lip-pincott Williams & Wilkins; 2005.
-
(2005)
Pediatric Neuroimaging
-
-
Barkovich, A.J.1
-
8
-
-
0035936638
-
Callosal agenesis with cyst: A better understanding and new classification
-
Barkovich AJ, Simon EM, Walsh CA. Callosal agenesis with cyst: a better understanding and new classification. Neurology 2001;56:220-227.
-
(2001)
Neurology
, vol.56
, pp. 220-227
-
-
Barkovich, A.J.1
Simon, E.M.2
Walsh, C.A.3
-
9
-
-
84876796027
-
Embryology and malformations of the fore-brain commissure
-
Sarnat HB, Curatolo P, eds St. Louis: Elsevier
-
Sarnat HB. Embryology and malformations of the fore-brain commissure. In: Sarnat HB, Curatolo P, eds. Malformations of the Nervous System. St. Louis: Elsevier; 2008:67.
-
(2008)
Malformations of the Nervous System
, pp. 67
-
-
Sarnat, H.B.1
-
10
-
-
0031820684
-
Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance
-
Al-Gazali L, Bakalinova D. Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance. Clin Dysmorphol 1998;7:177-184.
-
(1998)
Clin Dysmorphol
, vol.7
, pp. 177-184
-
-
Al-Gazali, L.1
Bakalinova, D.2
-
11
-
-
0034983846
-
Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26
-
Bayoumi R, Saar K, Lee YA, et al. Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26. J Med Genet 2001;38:369-373.
-
(2001)
J Med Genet
, vol.38
, pp. 369-373
-
-
Bayoumi, R.1
Saar, K.2
Lee, Y.A.3
-
12
-
-
41849109879
-
A new autosomal recessive syndrome of ocular colobo-mas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family
-
Al-Gazali L, Hertecant J, Algawi K, El Teraifi H, Dattani M. A new autosomal recessive syndrome of ocular colobo-mas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family. Am J Med Genet A 2008;146:813-819.
-
(2008)
Am J Med Genet A
, vol.146
, pp. 813-819
-
-
Al-Gazali, L.1
Hertecant, J.2
Algawi, K.3
El Teraifi, H.4
Dattani, M.5
-
13
-
-
65649142979
-
Reliability study of white matter rating scale for the dementia and disability in Thai Elderly Project
-
Chawalparit O, Wonglaksanapimon S, Songsaeng D, Saenanarong V. Reliability study of white matter rating scale for the dementia and disability in Thai Elderly Project. J Med Assoc Thai 2009;92:543-547.
-
(2009)
J Med Assoc Thai
, vol.92
, pp. 543-547
-
-
Chawalparit, O.1
Wonglaksanapimon, S.2
Songsaeng, D.3
Saenanarong, V.4
-
14
-
-
27644515103
-
An evidence-based causative classification system for acute ischemic stroke
-
Ay H, Furie KL, Singhal A, Smith WS, Sorensen AG, Koroshetz WJ. An evidence-based causative classification system for acute ischemic stroke. Ann Neurol 2005;58:688-697.
-
(2005)
Ann Neurol
, vol.58
, pp. 688-697
-
-
Ay, H.1
Furie, K.L.2
Singhal, A.3
Smith, W.S.4
Sorensen, A.G.5
Koroshetz, W.J.6
-
16
-
-
0141855225
-
Agenesis of corpus callosum: Prenatal diagnosis and prognosis
-
Moutard ML, Kieffer V, Feingold J, et al. Agenesis of corpus callosum: prenatal diagnosis and prognosis. Childs Nerv Syst 2003;19:471-476.
-
(2003)
Childs Nerv Syst
, vol.19
, pp. 471-476
-
-
Moutard, M.L.1
Kieffer, V.2
Feingold, J.3
-
17
-
-
4844229901
-
Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human
-
Richards LJ, Plachez C, Ren T. Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human. Clin Genet 2004;66:276-289.
-
(2004)
Clin Genet
, vol.66
, pp. 276-289
-
-
Richards, L.J.1
Plachez, C.2
Ren, T.3
-
18
-
-
32144434924
-
Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain
-
Ren T, Anderson A, Shen WB, et al. Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain. Anat Rec A Discov Mol Cell Evol Biol 2006;288:191-204.
-
(2006)
Anat Rec A Discov Mol Cell Evol Biol
, vol.288
, pp. 191-204
-
-
Ren, T.1
Anderson, A.2
Shen, W.B.3
-
19
-
-
0345107244
-
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): One gene leads to many phenotypes
-
Sherr EH. The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes. Curr Opin Pediatr 2003;15:567-571.
-
(2003)
Curr Opin Pediatr
, vol.15
, pp. 567-571
-
-
Sherr, E.H.1
-
20
-
-
0021749738
-
The An-dermann syndrome: Agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy
-
Larbrisseau A, Vanasse M, Brochu P, Jasmin G. The An-dermann syndrome: agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy. CanJ Neurol Sci 1984;11:257-261.
-
(1984)
CanJ Neurol Sci
, vol.11
, pp. 257-261
-
-
Larbrisseau, A.1
Vanasse, M.2
Brochu, P.3
Jasmin, G.4
-
21
-
-
14644402393
-
Aicardi syndrome
-
Aicardi J. Aicardi syndrome. Brain Dev 2005;27:164-171.
-
(2005)
Brain Dev
, vol.27
, pp. 164-171
-
-
Aicardi, J.1
-
22
-
-
27644494079
-
Genomic microar-ray analysis identifies candidate loci in patients with corpus callosum anomalies
-
Sherr EH, Owen R, Albertson DG, et al. Genomic microar-ray analysis identifies candidate loci in patients with corpus callosum anomalies. Neurology 2005;65:1496-1498.
-
(2005)
Neurology
, vol.65
, pp. 1496-1498
-
-
Sherr, E.H.1
Owen, R.2
Albertson, D.G.3
-
23
-
-
34547786100
-
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum
-
Boland E, Clayton-Smith J, Woo VG, et al. Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum. Am J Hum Genet 2007;81:292-303.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 292-303
-
-
Boland, E.1
Clayton-Smith, J.2
Woo, V.G.3
-
24
-
-
31944443357
-
Pure direct duplication (12) (q24.1->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies
-
Doco-Fenzy M, Mauran P, Lebrun JM, et al. Pure direct duplication (12) (q24.1->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies. Am J Med Genet A 2006;140:212-221.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 212-221
-
-
Doco-Fenzy, M.1
Mauran, P.2
Lebrun, J.M.3
-
25
-
-
0036922442
-
Agenesis and dysgenesis of the corpus callosum
-
Davila-Gutierrez G. Agenesis and dysgenesis of the corpus callosum. Semin Pediatr Neurol 2002;9:292-301.
-
(2002)
Semin Pediatr Neurol
, vol.9
, pp. 292-301
-
-
Davila-Gutierrez, G.1
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