Results 181 to 190 of about 17,135 (242)

Retrospective evaluation of cerebral fissure depths by magnetic resonance imaging in fetuses with isolated ventriculomegaly. [PDF]

BMC Pregnancy Childbirth
Bozbay N, Duymuş AC, Sağlam RN, Ateş F, Durmaz MS, Koplay M, Örgül G, Pekin AT.   +7 more
europepmc   +1 more source

Unilateral Task, Bilateral Response: An Acquired Movement Disorder in a Child With Chiari Malformation Type III and Syringomyelia

Annals of the Child Neurology Society
Aysha Arshad, John R. Crawford
doaj   +1 more source

Intraventricular iron causes severe hydrocephalus - a model of severe neonatal hydrocephalus. [PDF]

Fluids Barriers CNS
Kim KM, Cheetham-West AO, Ahmed MR, Phillips M, Malkovskiy AV, Pothineni VR, Brewer KD, Patel CB, Rajadas J, Mahaney KB.   +9 more
europepmc   +1 more source

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad. [PDF]

Medicine (Baltimore)
Al-Bustanji R, AlRababah BK, Rumman MSA, Abukhaled Y, Al-Rabadi N, Younis HKB, Ghalyon G, Al-Tawalbeh S, Aloudat O, Alrashdan MMM, Yamin MT, Maaita M, Salah AKD, Satari A.   +13 more
europepmc   +1 more source

Peripheral immunity patterns, imaging features, and clinical outcomes in patients with gait impairment and ventriculomegaly on brain MRI. [PDF]

Front Aging Neurosci
Espinoza-Vinces C, Aviles-Olmos I, Núñez-Córdoba JM, Jiménez-Vázquez M, Calvo-Imirizaldu M, Montoya-Murillo G, Martí-Andrés G, Arbizu J, Luquin MR.   +8 more
europepmc   +1 more source

Prenatal detection of Gorlin-Goltz syndrome: a case report and focused review of the literature. [PDF]

Front Med (Lausanne)
Oelmeier K, Horváth J, Vogtmann R, Meyer-Wittkopf M, Möllers M, Schmitz R, Oberste KM, Willy D.   +7 more
europepmc   +1 more source

Distinguishing Intraventricular Hemorrhage From Infectious Etiologies in Febrile Late Preterm Neonates: Case Studies in Antibiotic Stewardship. [PDF]

Cureus
Kapinos A, Rhoads S, Yossuck P, Gunasekaran V.   +3 more
europepmc   +1 more source

Prenatal Characterization of Houge-Janssens Syndrome Type 2: A Case Report and Systematic Review of Fetal Phenotypes Associated With PPP2R1A Mutations. [PDF]

Mol Genet Genomic Med
Hu J, Pang J, Zhou L, Kuang H, Yu W, Peng Y.   +5 more
europepmc   +1 more source

<i>DLL1</i> haploinsufficiency in prenatal brain anomalies: a retrospective analysis of 6q terminal deletions. [PDF]

Front Genet
Ge T, Lin X, Tian X, Song X, Zhou B, Hui L, Wang X, Zhang Z, Zhang C.   +8 more
europepmc   +1 more source