Al-Hadidy A - Search Results

1

Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?

Akawi NA, Ali BR, Hamamy H, Al-Hadidy A, Al-Gazali L. Akawi NA, et al. Among authors: al hadidy a. Am J Med Genet A. 2011 Jun;155A(6):1236-45. doi: 10.1002/ajmg.a.34009. Epub 2011 May 5. Am J Med Genet A. 2011. PMID: 21548126

2

Cockayne syndrome in 2 siblings.

Hamamy HA, Daas HA, Shegem NS, Al-Hadidy AM, Ajlouni K. Hamamy HA, et al. Saudi Med J. 2005 May;26(5):875-9. Saudi Med J. 2005. PMID: 15951889

3

Consanguinity and genetic disorders. Profile from Jordan.

Hamamy HA, Masri AT, Al-Hadidy AM, Ajlouni KM. Hamamy HA, et al. Saudi Med J. 2007 Jul;28(7):1015-7. Saudi Med J. 2007. PMID: 17603701

4

Griscelli syndrome type 2: a rare and lethal disorder.

Masri A, Bakri FG, Al-Hussaini M, Al-Hadidy A, Hirzallah R, de Saint Basile G, Hamamy H. Masri A, et al. Among authors: al hadidy a. J Child Neurol. 2008 Aug;23(8):964-7. doi: 10.1177/0883073808315409. Epub 2008 Apr 10. J Child Neurol. 2008. PMID: 18403584

5

Brachydactyly type B1: report of a family with de novo ROR2 mutation.

Hamamy H, Saleh N, Oldridge M, Al-Hadidy A, Ajlouni K. Hamamy H, et al. Clin Genet. 2006 Dec;70(6):538-40. doi: 10.1111/j.1399-0004.2006.00719.x. Clin Genet. 2006. PMID: 17101003 No abstract available.

6

Familial short fifth metacarpals and insulin resistance.

Hyari M, Hamamy H, Barham M, Al-Hadidy A, Ajlouni K. Hyari M, et al. Skeletal Radiol. 2006 Sep;35(9):702-5. doi: 10.1007/s00256-005-0939-2. Epub 2005 Aug 13. Skeletal Radiol. 2006. PMID: 16132981

7

Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling.

Tian J, Ling L, Shboul M, Lee H, O'Connor B, Merriman B, Nelson SF, Cool S, Ababneh OH, Al-Hadidy A, Masri A, Hamamy H, Reversade B. Tian J, et al. Among authors: al hadidy a. Am J Hum Genet. 2010 Dec 10;87(6):768-78. doi: 10.1016/j.ajhg.2010.11.005. Am J Hum Genet. 2010. PMID: 21129727 Free PMC article.

8

Cenani-Lenz syndactyly with facial dysmorphism, hypothyroidism, and renal hypoplasia: a case report.

Jarbhou H, Hamamy H, Al-Hadidy A, Ajlouni K. Jarbhou H, et al. Among authors: al hadidy a. Clin Dysmorphol. 2008 Oct;17(4):269-70. doi: 10.1097/MCD.0b013e328306a6ed. Clin Dysmorphol. 2008. PMID: 18978656 No abstract available.

9

Hereditary multiple exostoses with pseudoaneurysm.

Al-Hadidy AM, Al-Smady MM, Haroun AA, Hamamy HA, Ghoul SM, Shennak AO. Al-Hadidy AM, et al. Cardiovasc Intervent Radiol. 2007 May-Jun;30(3):537-40. doi: 10.1007/s00270-005-0334-3. Cardiovasc Intervent Radiol. 2007. PMID: 17225974

10

Congenital pseudoarthrosis associated with venous malformation.

Al-Hadidy A, Haroun A, Al-Ryalat N, Hamamy H, Al-Hadidi S. Al-Hadidy A, et al. Skeletal Radiol. 2007 Jun;36 Suppl 1:S15-8. doi: 10.1007/s00256-006-0175-4. Epub 2006 Sep 12. Skeletal Radiol. 2007. PMID: 16967289

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