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American Journal of Medical Genetics. Part A|January 11, 2016
Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?Beyhan Tüysüz, Adife Gülhan Ercan-Sencicek, Nur Canpolat, et al.
Surgical Neurology|February 12, 2008
Neuroprotective effects of Ac.YVAD.cmk on experimental spinal cord injury in ratsAlper Karaoğlan, Ekrem Kaya, Osman Akdemir, et al.
The Journal of Pediatrics|October 21, 2009
COL4A1 mutation in preterm intraventricular hemorrhageKaya Bilguvar, Michael L DiLuna, Matthew J Bizzarro, et al.
Nature Communications|March 27, 2014
Spontaneous tumour regression in keratoacanthomas is driven by Wnt/retinoic acid signalling cross-talkGiovanni Zito, Ichiko Saotome, Zongzhi Liu, et al.
Molecular Syndromology|November 13, 2025
Novel PIBF1 Pathogenic Variant in Three Siblings with Joubert Syndrome Type 33Busra Aynekin, Bahadır M Samur, Ummu Gulsum Ozgul Gumus, et al.
Neuropediatrics|October 20, 2015
Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral NeuropathyHuseyin Per, Mehmet Canpolat, Ayşe Kaçar Bayram, et al.
Journal of Child Neurology|March 16, 2026
Periodic Genetic Reanalysis Identifies a Novel De Novo <i>NOTCH1</i> Variant: A Case ReportEylul Aydin, Aybike S Bulut, Berkay Yildiz, et al.
Brain : a Journal of Neurology|January 17, 2025
Spreading depolarization triggers pro- and anti-inflammatory signalling: a potential link to headacheZeynep Kaya, Nevin Belder, Melike Sever-Bahçekapılı, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2015
A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenonAyşe Kaçar Bayram, Hüseyin Per, Jennifer Quon, et al.
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