Results 201 to 210 of about 17,723 (256)

Shapiro Syndrome: A Case Report. [PDF]

Cureus
Motsara M.
europepmc   +1 more source

Complete corpus callosum agenesis

, 2013
openaire   +1 more source

RTN4IP1 mutation and endocrine failure: clinical features and possible benefits of coenzyme Q10. [PDF]

Endocr Connect
Digitale Selvaggio L, Allosso F, Errico M, Grande G, Yousaf M, Torella A, Nigro V, Pasquali D, Telethon Undiagnosed Diseases Program Study Group.   +8 more
europepmc   +1 more source

Prevalence of epilepsy and structural brain anomalies in spina bifida aperta. [PDF]

Childs Nerv Syst
Koomen LR, Dremmen M, Kik C, van den Berg R, Dronkers W, Eggink AJ, DeKoninck PLJ, Veldhuijzen van Zanten SEM, Deprest J, Eelkman Rooda OHJ, Koudijs S, Spoor JKH.   +11 more
europepmc   +1 more source

Agenesis of corpus callosum

, 2017
openaire   +1 more source

Glial interactions in the formation and plasticity of the corpus callosum. [PDF]

Front Cell Neurosci
Czyrska J, Ziętek MM, Bernat A, Sampino S.   +3 more
europepmc   +1 more source

Complete corpus callosum agenesis

, 2018
openaire   +1 more source

A case of central sleep apnea in an adult with agenesis of the corpus callosum. [PDF]

Respir Med Case Rep
Cabriada-Nuño V, Castro-Quintas S, Urrutia-Gajate A, Tijero-Merino B.   +3 more
europepmc   +1 more source

Role of foeral MRI in the diagnosis and prognosis of cerebral ventriculomegaly assessed by prenatal ultrasonography [PDF]

, 2014
Maria Inês Moreira Vieites Branco
core  

Assessing the clinical application value of SNP-array in fetal central nervous system malformations. [PDF]

Hum Genomics
Li W, Su J, Lu W, Tang X, Zhou C, Lan Y, Wei Y, Huang L, Luo J, Ou S, Tan S, Wei S, Jiang Y, Su J, Wang L, Huang M, Luo J, Huang P.   +17 more
europepmc   +1 more source