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Frontiers in Neurology|August 7, 2025
Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohortUla Arkar Silan, Ana Trebše, Jernej Kovač, et al.
Journal of Clinical Medicine|October 27, 2022
The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic NeuropathySanja Petrovic Pajic, Luka Lapajne, Bor Vratanar, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|December 21, 2016
Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN StudyPeter A Mossey, Julian Little, Regine Steegers-Theunissen, et al.
HGG Advances|October 27, 2025
Splicing and frameshift variants in QSER1 may be involved in developmental phenotypesMegan C Fischer, Linda M Reis, Jerica Lenberg, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 9, 2024
Earlier age of symptom onset in younger generation of familial cases of multiple sclerosisAleksa Jovanovic, Tatjana Pekmezovic, Sarlota Mesaros, et al.
Human Reproduction (Oxford, England)|June 14, 2024
An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproductionAntonio Capalbo, Guido de Wert, Lidewij Henneman, et al.
Bosnian Journal of Basic Medical Sciences|February 12, 2021
Sirtuin 1 rs7069102 polymorphism is associated with diabetic nephropathy in patients with type 2 diabetes mellitusJernej Letonja, Matej Završnik, Jana Makuc, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|June 13, 2006
No association of CCR5delta32 gene mutation with multiple sclerosis in Croatian and Slovenian patientsSmiljana Ristić, Luca Lovrecić, Nada Starcević-Cizmarević, et al.
Multiple Sclerosis and Related Disorders|December 30, 2023
Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control studyAleksa Jovanovic, Tatjana Pekmezovic, Sarlota Mesaros, et al.
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