Items where Author is "Moravej, H."

Article

(2025) Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation. Journal of Medical Genetics. p. 12. ISSN 0022-2593

(2025) Comprehensive Iranian guidelines for the diagnosis and management of maple syrup urine disease: an evidence- and consensus- based approach. Orphanet Journal of Rare Diseases. p. 11.

(2025) Evaluation of the safety and efficacy of biosimilar recombinant growth hormone in children with growth hormone deficiency: non-inferiority, randomized, parallel, multicentric and Phase III trial. Expert opinion on drug safety. pp. 111-119. ISSN 1744-764X (Electronic) 1474-0338 (Linking)

(2024) The immunopathological landscape of human pre-TCRa deficiency: From rare to common variants. Science. ISSN 00368075 (ISSN)

(2024) The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants. Science. p. 19. ISSN 0036-8075

(2023) Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from Iran. Indian Pediatrics. pp. 193-196. ISSN 0019-6061

(2022) Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion). HUMAN MUTATION. E1-E23. ISSN 1059-7794 1098-1004 J9 - HUM MUTAT

(2022) Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion). Human mutation. e1-e23. ISSN 1098-1004 (Electronic) 1059-7794 (Linking)

(2021) Optimal Frequency to Screen Celiac Disease amongst Patients with Type 1 Diabetes Mellitus: A Multicenter Study. PRIMARY CARE DIABETES. pp. 1100-1103. ISSN 1751-9918 1878-0210 J9 - PRIM CARE DIABETES

(2021) Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus. FRONTIERS IN NEUROLOGY. ISSN 1664-2295 J9 - FRONT NEUROL