Items where Author is "Sharbaf, F. G."
 | Up a level |
(2026) Bi-allelic TPP1 variants in neuronal ceroid lipofuscinosis 2: clinical findings from an Iranian cohort of 20 patients, founder effect, and in silico analyses. Human Genetics. p. 19. ISSN 0340-6717
(2025) Genetically Confirmed Hyperoxaluria in Iranian Children-A Multicenter Survey. Iranian Journal of Kidney Diseases. pp. 200-205. ISSN 1735-8582
(2023) Validity of the Adrogué-Madias Formula for the Management of Acute Dysnatremias in Critically Ill Children. Pediatric Emergency Care. pp. 707-714. ISSN 0749-5161
(2021) Chronic Kidney Disease in Iran: First Report of the National Registry in Children and Adolescences. Urology Journal. pp. 122-130. ISSN 1735-1308