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Molecular Syndromology|May 27, 2026
PHRINL Syndrome: A Case of Infantile Cataract and CardiomyopathyAliye Gülbahçe, Adnan Deniz, İsmihan Merve Tekin, et al.
Endocrine|February 2, 2025
Etiology, presentation, and outcomes of hyperprolactinemia due to pituitary masses in children and adolescentsFatih Kilci, Emre Sarikaya, Nurhan Özcan Murat, et al.
Journal of Pediatric Genetics|May 9, 2024
Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based ReviewAdnan Deniz, Sinan Çomu, Mesut Güngör, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 3, 2023
Probable association between mRNA COVID-19 vaccine and opsoclonus-myoclonus-ataxia syndromeAdnan Deniz, Defne Alikılıç, Merve Öztürk, et al.
The Turkish Journal of Pediatrics|May 22, 2026
Leber hereditary optic neuropathy (LHON) in a 6-year-old boy with a transient spinal cord lesionAnıl Gök, Gökçe Cırdı, Adnan Deniz, et al.
Multiple Sclerosis and Related Disorders|April 22, 2017
Long-term clinical and radiologic follow-up of Schilder's diseaseHülya Maraş Genç, Bülent Kara, Emek Uyur Yalçın, et al.
Neurogenetics|February 17, 2025
20 years of ROBO3-related horizontal gaze palsy with progressive scoliosis: a mini-reviewEhab Y Harahsheh, Lauren E Moxley, Matu Al-Amin, et al.
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