Abu-Libdeh A - Search Results

1

Optimizing health care for individuals with Down syndrome in Israel.

Wexler ID, Abu-Libdeh A, Kastiel Y, Nimrodi A, Kerem E, Tenenbaum A. Wexler ID, et al. Isr Med Assoc J. 2009 Nov;11(11):655-9. Isr Med Assoc J. 2009. PMID: 20108550 Free article.

2

Euthyroid submedian free T4 and subclinical hypothyroidism may have a detrimental clinical effect in Down syndrome.

Tenenbaum A, Lebel E, Malkiel S, Kastiel Y, Abulibdeh A, Zangen DH. Tenenbaum A, et al. Horm Res Paediatr. 2012;78(2):113-8. doi: 10.1159/000342075. Epub 2012 Aug 23. Horm Res Paediatr. 2012. PMID: 22922417 Clinical Trial.

3

Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel.

Blumenfeld O, Dichtiar R, Shohat T; Israel IDDM Registry Study Group (IIRSG). Blumenfeld O, et al. Pediatr Diabetes. 2014 Sep;15(6):422-7. doi: 10.1111/pedi.12101. Epub 2013 Nov 27. Pediatr Diabetes. 2014. PMID: 24283719

4

Iatrogenic Cushing Syndrome due to Intranasal Dexamethasone.

Rottenstreich A, Wexler ID, Abu-Libdeh A, Berkun Y. Rottenstreich A, et al. Clin Pediatr (Phila). 2015 Oct;54(12):1215-7. doi: 10.1177/0009922814563927. Epub 2014 Dec 21. Clin Pediatr (Phila). 2015. PMID: 25533884 No abstract available.

5

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. Abdulhadi-Atwan M, et al. Diabetes. 2008 Jul;57(7):1935-40. doi: 10.2337/db08-0159. Epub 2008 Apr 4. Diabetes. 2008. PMID: 18390792 Free PMC article.

6

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

Abu Libdeh A, Levy-Khademi F, Abdulhadi-Atwan M, Bosin E, Korner M, White PC, Zangen DH. Abu Libdeh A, et al. Eur J Endocrinol. 2010 Feb;162(2):221-6. doi: 10.1530/EJE-09-0772. Epub 2009 Nov 6. Eur J Endocrinol. 2010. PMID: 19897608

7

XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.

Zangen D, Kaufman Y, Zeligson S, Perlberg S, Fridman H, Kanaan M, Abdulhadi-Atwan M, Abu Libdeh A, Gussow A, Kisslov I, Carmel L, Renbaum P, Levy-Lahad E. Zangen D, et al. Am J Hum Genet. 2011 Oct 7;89(4):572-9. doi: 10.1016/j.ajhg.2011.09.006. Epub 2011 Sep 29. Am J Hum Genet. 2011. PMID: 21963259 Free PMC article.

8

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress.

Weinberg-Shukron A, Abu-Libdeh A, Zhadeh F, Carmel L, Kogot-Levin A, Kamal L, Kanaan M, Zeligson S, Renbaum P, Levy-Lahad E, Zangen D. Weinberg-Shukron A, et al. J Med Genet. 2015 Sep;52(9):636-41. doi: 10.1136/jmedgenet-2015-103078. Epub 2015 Jun 12. J Med Genet. 2015. PMID: 26070314

9

GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome.

Danielpur L, Sohn YS, Karmi O, Fogel C, Zinger A, Abu-Libdeh A, Israeli T, Riahi Y, Pappo O, Birk R, Zangen DH, Mittler R, Cabantchik ZI, Cerasi E, Nechushtai R, Leibowitz G. Danielpur L, et al. J Clin Endocrinol Metab. 2016 Oct;101(10):3592-3599. doi: 10.1210/jc.2016-2240. Epub 2016 Jul 26. J Clin Endocrinol Metab. 2016. PMID: 27459537

10

Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.

Pode-Shakked N, Blau A, Pode-Shakked B, Tiosano D, Weintrob N, Eyal O, Zung A, Levy-Khademi F, Tenenbaum-Rakover Y, Zangen D, Gillis D, Pinhas-Hamiel O, Loewenthal N, de Vries L, Landau Z, Rachmiel M, Abu-Libdeh A, Eliakim A, Strich D, Koren I, German A, Sack J, Almashanu S. Pode-Shakked N, et al. J Clin Endocrinol Metab. 2019 Aug 1;104(8):3172-3180. doi: 10.1210/jc.2018-02468. J Clin Endocrinol Metab. 2019. PMID: 30865229

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