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kw.\*:("Corpus callosum agenesis")

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Patterned Neuropathologic Events Occurring in hyh Congenital Hydrocephalic Mutant MicePAEZ, Patricia; BATIZ, Luis-Federico; ROALES-BUJAN, Ruth et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 12, pp 1082-1092, issn 0022-3069, 11 p.Article

Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8FEENSTRA, I; VAN RAVENSWAAIJ, C. M. A; VAN DER KNAAP, M. S et al.Neuropediatrics. 2006, Vol 37, Num 2, pp 83-87, issn 0174-304X, 5 p.Article

Spectrum of corpus callosum agenesisSZTRIHA, Laszlo.Pediatric neurology. 2005, Vol 32, Num 2, pp 94-101, issn 0887-8994, 8 p.Article

Partial Agenesis of Corpus Callosum in Sanjad-Sakati Syndrome (p-ACC)ALGHASAB, Naif; JANATI, A. Bruce; KHAN, Aslam et al.Canadian journal of neurological sciences. 2012, Vol 39, Num 6, pp 833-834, issn 0317-1671, 2 p.Article

Dandy-Walker syndrome and corpus callosum agenesis in 5p deletionVIALARD, F; ROBYR, R; HILLION, Y et al.Prenatal diagnosis. 2005, Vol 25, Num 4, pp 311-313, issn 0197-3851, 3 p.Article

Prenatal MR Diffusion Tractography in a Fetus with Complete Corpus Callosum AgenesisMEODED, A; PORETTI, A; TEKES, A et al.Neuropediatrics. 2011, Vol 42, Num 3, pp 122-123, issn 0174-304X, 2 p.Article

Neuroendoscopic management of interhemispheric cysts in childrenCINALLI, Giuseppe; PERETTA, Paola; MAGGI, Giuseppe et al.Journal of neurosurgery. Pediatrics. 2006, Vol 105, Num 3, pp 194-202, issn 1933-0707, 9 p.Article

A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesisANDRIEUX, Joris; CUVELLIER, Jean-Christophe; DUBAN-BEDU, Bénédicte et al.European journal of medical genetics. 2008, Vol 51, Num 1, pp 87-91, issn 1769-7212, 5 p.Article

MYELOLIPOMATOUS CHANGE IN AN INTERHEMISPHERIC LIPOMA ASSOCIATED WITH CORPUS CALLOSUM AGENESIS : CASE REPORT. CommentarySURI, Vaishali; SHARMA, Mehar C; SURI, Ashish et al.Neurosurgery. 2008, Vol 62, Num 3, pp 745-745, issn 0148-396X, 1 p.Article

Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum : case report and review of the literatureANDRIEUX, Joris; DEVISME, Louise; VALAT, Anne-Sylvie et al.European journal of medical genetics. 2005, Vol 48, Num 2, pp 199-206, issn 1769-7212, 8 p.Article

Interstitial Deletion 1q42 in a Patient With Agenesis of Corpus Callosum: Phenotype―Genotype Comparison to the 1q41q42 Microdeletion Suggests a Contiguous 1q4 SyndromeFILGES, Isabel; RÖTHLISBERGER, Benno; BOESCH, Nemya et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 4, pp 987-993, issn 1552-4825, 7 p.Article

Aicardi Syndrome : Follow-Up Investigation of Swedish Children Born in 1975-2002PALMER, L; ZETTERLUND, B; HARD, A.-L et al.Neuropediatrics. 2007, Vol 38, Num 4, pp 188-192, issn 0174-304X, 5 p.Article

Corpus Callosum Agenesis, Severe Mental Retardation, Epilepsy, and Dyskinetic Ouadriparesis Due To a Novel Mutation in the Homeodomain of ARXCONTI, Valerio; MARINI, Carla; GANA, Simone et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 4, pp 892-897, issn 1552-4825, 6 p.Article

Identification of Genomic Loci Contributing to Agenesis of the Corpus CallosumO'DRISCOLL, Mary C; BLACK, Graeme C. M; CLAYTON-SMITH, Jill et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 9, pp 2145-2159, issn 1552-4825, 15 p.Article

Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters : The Chudley-McCullough syndromeMATTEUCCI, Fabio; TARANTINO, Enrico; BIANCHI, Maria Cristina et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 11, pp 1183-1188, issn 1552-4825, 6 p.Article

Corpus Callosum Agenesis in Trisomy 8pll.23 and Monosomy 4q34 Because of Maternal TranslocationISIK, Ugur; BASARAN, Seher; DEHGAN, Tahir et al.Pediatric neurology. 2008, Vol 39, Num 1, pp 55-57, issn 0887-8994, 3 p.Article

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisBAALA, Lekbir; BRIAULT, Sylvain; ATTIE-BITACH, Tania et al.Nature genetics. 2007, Vol 39, Num 4, pp 454-456, issn 1061-4036, 3 p.Article

Chromosome lq42 deletion and agenesis of the corpus callosumPUTHURAN, Mani J; ROWLAND-HILL, Christopher A; SIMPSON, J et al.American journal of medical genetics. 2005, Vol 138A, Num 1, pp 68-69, issn 0148-7299, 2 p.Article

Rare Combination of Gelastic Epilepsy, Agenesis of the Corpus Callosum, and HamartomaCHEN, Chia-Chun; LIN, Yu-Ting; CHANG, Wen-Cheng et al.Pediatric neurology. 2011, Vol 45, Num 4, pp 265-267, issn 0887-8994, 3 p.Article

Agénésie du corps calleux révélée par une encéphalocèle = Corpus callous agenesis revealed by an encephaloceleKAM, L; DAO, F; DIALLO, O et al.Journal de pédiatrie et de puériculture. 2007, Vol 20, Num 2, pp 74-77, issn 0987-7983, 4 p.Article

Agenesis of the corpus callosum : Clinical and genetic study in 63 young patientsBEDESCHI, Maria Francesca; BONAGLIA, Maria Clara; BASSI, Maria Teresa et al.Pediatric neurology. 2006, Vol 34, Num 3, pp 186-193, issn 0887-8994, 8 p.Article

Clinical and molecular characteristics of 1qter microdeletion syndrome : delineating a critical region for corpus callosum agenesis/hypogenesisVAN BON, B. W. M; KOOLEN, D. A; NOVARA, F et al.Journal of medical genetics. 2008, Vol 45, Num 6, pp 346-354, issn 0022-2593, 9 p.Article

Agenesis of the corpus callosum : Lessons from humans and miceKAMNASARAN, Deepak.Clinical and investigative medicine. 2005, Vol 28, Num 5, pp 267-282, issn 0147-958X, 16 p.Article

Comprehension of humor in primary agenesis of the corpus callosumBROWN, Warren S; PAUL, Lynn K; SYMINGTON, Melissa et al.Neuropsychologia. 2005, Vol 43, Num 6, pp 906-916, issn 0028-3932, 11 p.Article

Assessment of Pericallosal Arteries by Color Doppler Ultrasonography at 11-14 Weeks: An Early Marker of Fetal Corpus Callosum Development in Normal Fetuses and Agenesis in Cases with Chromosomal AnomaliesDIAZ-GUERRERO, L; GIUGNI-CHALBAUD, G; SOSA-OLAVARRIA, A et al.Fetal diagnosis and therapy. 2013, Vol 34, Num 2, pp 85-89, issn 1015-3837, 5 p.Article

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