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Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis.
Albaramki J, Dmour H, Shboul M, Bonnard C, Venkatesh B, Odeh R. Albaramki J, et al. Among authors: odeh r. Turk J Pediatr. 2019;61(1):130-133. doi: 10.24953/turkjped.2019.01.022. Turk J Pediatr. 2019. PMID: 31559735 Free article.
Albaramki J, Dmour H, Shboul M, Bonnard C, Venkatesh B, Odeh R. Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis. ...
Albaramki J, Dmour H, Shboul M, Bonnard C, Venkatesh B, Odeh R. Recessive mutation in GALNT3 causes hyperphosphatemic familial …
IPEX syndrome: an easily-missed diagnosis of a life threatening condition.
Alassaf A, Odeh R. Alassaf A, et al. Among authors: odeh r. Turk J Pediatr. 2019;61(3):424-427. doi: 10.24953/turkjped.2019.03.016. Turk J Pediatr. 2019. PMID: 31916722 Free article.
Alassaf A, Odeh R. IPEX syndrome: an easily-missed diagnosis of a life threatening condition. ...
Alassaf A, Odeh R. IPEX syndrome: an easily-missed diagnosis of a life threatening condition. ...
Frequency, Clinical Characteristics and Predictors of Ketoacidosis at Diagnosis of Type One Diabetes Mellitus in Children and Adolescents from Jordan.
Odeh R, Gharaibeh L, Daher A, Albaramki J, Ashour B, Al Barakat F, Dahabreh D, Hadadin H, Melhem T, Alassaf A. Odeh R, et al. J Clin Res Pediatr Endocrinol. 2023 Feb 27;15(1):46-54. doi: 10.4274/jcrpe.galenos.2022.2022-5-8. Epub 2022 Oct 20. J Clin Res Pediatr Endocrinol. 2023. PMID: 36264035 Free PMC article.
96 results