Results 131 to 140 of about 167,788,531 (210)

Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach. [PDF]

Front Genet
Khadija B, Abdallah HH, Slimani W, Bennour A, Dimassi S, Soyah N, Benzarti A, Rjiba K, Dahleb W, Kammoun M, Hannechi H, Khelifa HB, Khouja NG, Boughamoura L, Kraoua I, Triki C, Tej A, Mathlouthi J, Guith A, Abroug S, Kebaili R, Bouaziz MA, Soua H, Sboui E, Hadded S, Ziadi R, Monastiri K, Ben Hamida H, Ghanmi M, Hassayoun S, Sfar MT, Saad A, Depienne C, Mougou-Zerelli S.   +33 more
europepmc   +1 more source

Isolated Agenesis of the Splenium of the Corpus Callosum Associated With Autism Spectrum Disorder: A Rare and Clinically Relevant Association. [PDF]

Cureus
Ibanez Escalante CR, Goker HD, Bernad PG.   +2 more
europepmc   +1 more source

Microcephaly, Agenesis of the Corpus Callosum, and Suspected Blake Pouch Cyst Presenting With Failure to Thrive in an Infant. [PDF]

Cureus
Ingram H, Knighton K, Skalka N, Chappell D.   +3 more
europepmc   +1 more source

Familial corpus callosum agenesis.

The Turkish journal of pediatrics, 1978
E Ozdirim, Y Renda
openaire   +2 more sources

Incidentally Identified Open-Lip Schizencephaly in an Adult With Schizoaffective Disorder: A Case Report. [PDF]

Clin Case Rep
Bhattessa S, Pokhrel S, Pokharel U, Neupane P.   +3 more
europepmc   +1 more source

Expanding the clinical and molecular spectrum of TUBB2B through distinct variants identified across multiple families. [PDF]

HGG Adv
Beheshti ST, Jolly A, Saad AK, Du H, Westerfield LE, Munderloh C, Kalra D, Wu Y, Chen Y, Gingras MC, Jhangiani SN, Yilmaz S, Zaki MS, Calame DG, Pehlivan D, Gibbs RA, Lewis RA, Lupski JR, Posey JE.   +18 more
europepmc   +1 more source

Fetal Cortical Layers and Midline Histological Alterations in the BTBR Mouse Model of Neurodevelopmental Disorders. [PDF]

Biology (Basel)
Czyrska J, Poznański P, Bernat A, Winiarczyk D, Ziętek MM, Sampino S.   +5 more
europepmc   +1 more source

A lethal form of ASCC3 disease: Severe global developmental delay, axial hypotonia, hypoplasia of corpus callosum, hypothyroidism, and micropenis. [PDF]

HGG Adv
Narkis G, Dolgin V, Sued-Hendrickson S, Zahran J, Kanengisser-Pines B, Smooha-Schechter G, Carmon L, Shorer Z, Michaelovsky A, Birk OS.   +9 more
europepmc   +1 more source

Incidental Diagnosis of Complete Agenesis of the Corpus Callosum in a 62-Year-Old Man Presenting With Dizziness. [PDF]

Cureus
Pande LJ, Sharron K, Singh D, Brini G, Woolf S.   +4 more
europepmc   +1 more source

Clinical outcomes and neurodevelopmental outcome of prenatally diagnosed agenesis of corpus callosum in single center of Korea. [PDF]

Obstet Gynecol Sci, 2017
Kim SE, Jang HI, Chang KH, Sung JH, Lee J, Lee J, Choi SJ, Oh SY, Roh CR, Kim JH.   +9 more
europepmc   +1 more source