LJ Richards, C Plachez, T Ren - Clinical genetics, 2004 - s04-2.qbi.uq.edu.au LJ Richards, C Plachez and T Ren The University of Maryland School of Medicine,
Department of Anatomy and Neurobiology and Programs in Neuroscience and Membrane
Biology, Baltimore, MD, USA Key words: axon guidance – cingulate cortex ... Cited by 52 - Related articles - View as HTML - BL Direct - All 6 versions
TL Rosser, MT Acosta, RJ Packer - Pediatric neurology, 2002 - Elsevier Aicardi syndrome is an X-linked-dominant condition characterized by infantile
spasms, agenesis of the corpus callosum, and chorioretinal lacunae. We reviewed
the Aicardi Syndrome Foundation's compilation of family-based, ... Cited by 34 - Related articles - All 8 versions
MAK Glasmacher, VR Sutton, B Hopkins, T … - Journal of child neurology, 2007 - jcn.sagepub.com Aicardi syndrome is associated with moderate to severe developmental delay,
although mildly affected patients have also been reported. 7,8,10-12 Because the
syndrome is rare, most descriptions of its clinical characteristics rely on ... Cited by 13 - Related articles - BL Direct - All 9 versions
RT Chan, HH Chan, HB Collin - Clinical & experimental optometry: journal of the …, 2002 - ncbi.nlm.nih.gov Morning glory syndrome is a congenital optic disc anomaly in which much of the
excavated colobomatous optic disc is filled with glial tissue. Ocular
complications may include strabismus, reduced visual acuity and retinal ... Cited by 11 - Related articles - BL Direct - All 4 versions
A Matlary, T Prescott, B Tvedt, K Lindberg, A … - Clinical dysmorphology, 2004 - journals.lww.com Aicardi syndrome (OMIM 304050) is an X-linked dominant condition with a possible
molecular basis located in Xp22-Xp23. The syndrome typically includes the triad
of infantile spasms, punched out chorioretinal lacunae and agenesis of the ... Cited by 11 - Related articles - BL Direct - All 3 versions
S Grosso, G Lasorella, A Russo, P Galluzzi, G … - Brain and Development, 2007 - Elsevier Aicardi syndrome is a congenital disorder characterized by severe psychomotor
retardation, corpus callosum agenesis, chorioretinal lacunae, and early-onset
infantile spasms. The prognosis is generally poor for children with the ... Cited by 1 - Related articles - All 14 versions
KEG Tamez, RR Bonito, ÉCO Correa, RC … - Medicina Universitaria, 2007 - medigraphic.com Se informa el caso de un recién nacido de sexo femenino que padecía
microftalmia derecha, microcórnea, coloboma del iris, crisis convulsivas,
agenesia de cuerpo calloso, hidrocefalia no activa y quiste ... Related articles - All 6 versions
S Génomique - scd.uhp-nancy.fr Page 1. AVERTISSEMENT Ce document est le fruit d'un long travail approuvé par
le jury de soutenance et mis à disposition de l'ensemble de la ... Related articles - View as HTML