O. Hamiel

Bone age in the 21st century: is Greulich and Pyle’s atlas accurate for Israeli children?

I. Eshed, M. Soudack, A. Ben-Shlush, 2012, Pediatric Radiology.

A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant

Yonatan Yeshayahu, A. Nicholas, N. Schoenmakers, 2019, Journal of clinical research in pediatric endocrinology.

Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial

A. Eliakim, M. Phillip, T. Battelino, 2020, The Journal of clinical endocrinology and metabolism.

Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant.

M. Upadhyaya, M. Frydman, O. Hamiel, 1993, The Journal of pediatrics.

Abstract: P386 CONSERVATIVE TREATMENT OF L-ASPARGINASE-ASSOCIATED LIPID ABNORMALITIES IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

D. Harats, A. Toren, B. Bielorai, 2009 .

Israeli guidelines for the management of hypercholesterolemia in children and adolescents. Report of the pediatric association expert group

D. Harats, R. Shamir, H. Cohen, 2010 .

A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant

Yonatan Yeshayahu, A. Nicholas, N. Schoenmakers, 2021, Journal of Clinical Research in Pediatric Endocrinology.