Results 161 to 170 of about 3,402 (231)

Case Report: A case of complex cortical dysplasia with central precocious puberty onset. [PDF]

Front Pediatr
Guo C, Chen C, Wang X, Lin K, Guo J, Ge P.   +5 more
europepmc   +1 more source

Supplementary Material for: Nonmosaic Trisomy 19p13.3p13.2 Resulting from a Rare Unbalanced t(Y;19)(q12;p13.2) Translocation in a Patient with Pachygyria and Polymicrogyria

, 2020
Daniel Martínez Anaya, Leilani Hernandez, Ariadna González del Ángel, Miguel Angel Alcántara‐Ortigoza, Verónica Ulloa Avilés, Patricia Pérez‐Vera   +5 more
openalex   +2 more sources

The oculocerebrorenal syndrome of Lowe: an update [PDF]

, 2016

core   +1 more source

Pyloric Stenosis in a Patient with CEDNIK Syndrome. [PDF]

Cureus
Potesta MA, Aldana V, Patel S.
europepmc   +1 more source

Lissencephaly–pachygyria masquerading as leukodystrophy on magnetic resonance imaging brain

, 2017
AnilVasudev Israni, Anirban Mandal
openalex   +2 more sources

Selective Fetal Growth Restriction Leading to Cerebral Injury in Monochorionic Twins: A Case Report. [PDF]

Cureus
Campos P, Matos AR, Ferraz A, Henriques R.   +3 more
europepmc   +1 more source

Corpus Callosotomy for Atonic Drop Seizures in Bilateral Malformations of Cortical Development: A Systematic Review of Literature. [PDF]

Cureus
Kosco E, Back W, Lucarelli V, Acharya A, Waack A, Schroeder J.   +5 more
europepmc   +1 more source

Two-Compound Heterozygous Deletions Affecting <i>TUBGCP6</i> in a Patient with Microcephaly and Ocular Abnormalities and in an Unborn Sibling with Abnormal Sulcation. [PDF]

Mol Syndromol
Pal S, Kulshrestha S, Garg N, Gupta D, Gupta ND, Puri RD.   +5 more
europepmc   +1 more source

MICROCEPHALY A CLINICAL-GENETIC AND NEUROLOGIC APPROACH [PDF]

, 2013
Alongi, A, Antona, V, Ballacchino, A, Consiglio, V, CORSELLO, Giovanni, GIUFFRE, Mario, Graziano, F, PIRO, Ettore, VECCHIO, Davide   +8 more
core  

Nucleotide Variants of the BH4 Biosynthesis Pathway Gene and the Risk of Orofacial Clefts [PDF]

core   +1 more source