Results 121 to 130 of about 17,723 (256)

1 Early Development of Adaptive Skills in Young Children with Agenesis of the Corpus Callosum: A Comparison to Monogenetic and Neurodevelopmental Conditions [PDF]

, 2023
Lauren D Haisley, Lana Hantzch, Jasmin Turner, Kelly N. Botteron, Stephen R. Dager, Annette Estes, Lisa Flake, Heather C. Hazlett, Robert T. Schultz, Joseph Piven, Lynn K. Paul, Jed T. Elison   +11 more
openalex   +1 more source

Frontal subcutaneous lipoma associated with large interhemispheric lipoma and corpus callosum agenesis. [PDF]

Radiol Case Rep, 2022
Rana D, Kulkarni S, Zuberi J, Berlin F.
europepmc   +1 more source

Corpus Callosum Agenesis [PDF]

, 2020
openaire   +2 more sources

A selective defect in the glial wedge as part of the neuroepithelium disruption in hydrocephalus development in the mouse hyh model is associated with complete corpus callosum dysgenesis

Frontiers in Cellular Neuroscience
IntroductionDysgenesis of the corpus callosum is present in neurodevelopmental disorders and coexists with hydrocephalus in several human congenital syndromes.
Luis-Manuel Rodríguez-Pérez, Luis-Manuel Rodríguez-Pérez, Javier López-de-San-Sebastián, Isabel de Diego, Aníbal Smith, Ruth Roales-Buján, Antonio J. Jiménez, Antonio J. Jiménez, Patricia Paez-Gonzalez, Patricia Paez-Gonzalez   +9 more
doaj   +1 more source

Agenesis of the Corpus Callosum [PDF]

American Journal of Obstetrics and Gynecology, 2020
Siegfried, Rotmensch, Ana, Monteagudo
openaire   +2 more sources

Effect of corpus callosum agenesis on the language network in children and adolescents. [PDF]

Brain Struct Funct, 2021
Bartha-Doering L, Schwartz E, Kollndorfer K, Fischmeister FPS, Novak A, Langs G, Werneck H, Prayer D, Seidl R, Kasprian G.   +9 more
europepmc   +1 more source

Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities. [PDF]

Am J Hum Genet, 2021
Jeanne M, Demory H, Moutal A, Vuillaume ML, Blesson S, Thépault RA, Marouillat S, Halewa J, Maas SM, Motazacker MM, Mancini GMS, van Slegtenhorst MA, Andreou A, Cox H, Vogt J, Laufman J, Kostandyan N, Babikyan D, Hancarova M, Bendova S, Sedlacek Z, Aldinger KA, Sherr EH, Argilli E, England EM, Audebert-Bellanger S, Bonneau D, Colin E, Denommé-Pichon AS, Gilbert-Dussardier B, Isidor B, Küry S, Odent S, Redon R, Khanna R, Dobyns WB, Bézieau S, Honnorat J, Lohkamp B, Toutain A, Laumonnier F.   +40 more
europepmc   +1 more source

Aicardi syndrome: Clinical spectrum of a rare disorder

Journal of Family Medicine and Primary Care
Aicardi syndrome is a rare genetic syndrome reported exclusively in females, with reported incidence of approximately 1 in 1.1 lakh live births. The clinical condition comprises of triad of infantile spasms, and mental retardation with neuroimaging ...
Sunisha Jakhar, Dinkar Yadav, Kapil Bhalla, Komal Jindal, Rohan Acharya   +4 more
doaj   +1 more source

A Case of a Newborn with Agenesis of the Corpus Callosum Complicated with Ocular Albinism [PDF]

, 2016
Michiko Miki, Makiko Miyamoto, Tatsuma Mitsutsuji, H. Watanabe, Kazuhiro Shimizu, Junko Matsuo, Masahiro Tonari, Teruyo Kida, Jun Sugasawa, Tsunehiko Ikeda   +9 more
openalex   +1 more source

A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis. [PDF]

Child Neurol Open, 2021
Şenbil N, Arslan Z, Sayın Kocakap DB, Bilgili Y.   +3 more
europepmc   +1 more source