Results 181 to 190 of about 3,402 (231)

Double Cortex Syndrome: An Unusual Cause of Seizures. [PDF]

Cureus
Nedday S, Naji Y, Assardoun M, Laadami S, Adali N.   +4 more
europepmc   +1 more source

Emergent responsive neurostimulation in pediatric super-refractory epilepsia partialis continua. [PDF]

Ann Clin Transl Neurol
Hadar PN, Nanda P, Walsh KG, McLaren J, Geffrey A, Simon M, Kahle K, Richardson RM, Chu CJ.   +8 more
europepmc   +1 more source

A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the Literature. [PDF]

Mol Syndromol
Talea A, Bayat S, Khan GS, Pak N, Aziz-Ahari S, Sinaei R, Tavasoli AR, Ashrafi MR, Heidari M.   +8 more
europepmc   +1 more source

Connecting neurodevelopment to neurodegeneration: a spotlight on the role of kinesin superfamily protein 2A (KIF2A). [PDF]

Neural Regen Res
Ruiz-Reig N, Hakanen J, Tissir F.
europepmc   +1 more source

A novel mouse model for <i>LAMA2</i>-related muscular dystrophy with analysis of molecular pathogenesis and clinical phenotype. [PDF]

Elife
Tan D, Liu Y, Luo H, Shen Q, Long X, Xu L, Liu J, Zhong NA, Zhang H, Xiong H.   +9 more
europepmc   +1 more source

HJV mutations causing hemochromatosis: variable phenotypic expression in a pair of twins. [PDF]

Haematologica
Vadivelan A, Zhang S, Srole DN, Marcus EA, Neto GC, Nemeth E, Ganz T, De Oliveira S.   +7 more
europepmc   +1 more source

Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement [PDF]

core   +1 more source

Unilateral schizencephaly open lip with septo optic dysplasia in adult woman with glaucoma: A rare case. [PDF]

Radiol Case Rep
Aristiady EB, Mahmudah R, Mulyono A.
europepmc   +1 more source

Prenatal Diagnosis of Hemimegalencephaly Using Radiological Methods: A Case Report. [PDF]

Cureus
Mejia M, Vargas Arango S, Vargas Vélez S, Pimiento Figueroa J.   +3 more
europepmc   +1 more source