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    Results: 3

    1.

    Autosomal recessive familial neurohypophyseal diabetes insipidus - onset in early infancy.

    Abu-Libdeh A, Levy-Khademi F, Abdulhadi-Atwan M, Bosin E, Korner M, White P, Zangen D.

    Eur J Endocrinol. 2009 Nov 6. [Epub ahead of print]PMID: 19897608 [PubMed - as supplied by publisher]Related articles

    2.

    Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.

    Abdulhadi-Atwan M, Bushman J, Tornovsky-Babaey S, Perry A, Abu-Libdeh A, Glaser B, Shyng SL, Zangen DH.

    Diabetes. 2008 Jul;57(7):1935-40. Epub 2008 Apr 4. Erratum in: Diabetes. 2008 Sep;57(9):2552. Bushmann, Jeremy [corrected to Bushman, Jeremy]. PMID: 18390792 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Role of a founder c.201_202delCT mutation and new phenotypic features of congenital lipoid adrenal hyperplasia in Palestinians.

    Abdulhadi-Atwan M, Jean A, Chung WK, Meir K, Ben Neriah Z, Stratigopoulos G, Oberfield SE, Fennoy I, Hirsch HJ, Bhangoo A, Ten S, Lerer I, Zangen DH.

    J Clin Endocrinol Metab. 2007 Oct;92(10):4000-8. Epub 2007 Jul 31.PMID: 17666473 [PubMed - indexed for MEDLINE]Related articlesFree article

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