Al-Odaib A - Search Results

1

A novel X-linked disorder with developmental delay and autistic features.

Kaya N, Colak D, Albakheet A, Al-Owain M, Abu-Dheim N, Al-Younes B, Al-Zahrani J, Mukaddes NM, Dervent A, Al-Dosari N, Al-Odaib A, Kayaalp IV, Al-Sayed M, Al-Hassnan Z, Nester MJ, Al-Dosari M, Al-Dhalaan H, Chedrawi A, Gunoz H, Karakas B, Sakati N, Alkuraya FS, Gascon GG, Ozand PT. Kaya N, et al. Ann Neurol. 2012 Apr;71(4):498-508. doi: 10.1002/ana.22673. Epub 2011 Dec 28. Ann Neurol. 2012. PMID: 22213401

2

A simple, rapid test for the differential diagnosis of glycogen storage disease type 3.

Bhuiyan J, Al Odaib AN, Ozand PT. Bhuiyan J, et al. Clin Chim Acta. 2003 Sep;335(1-2):21-6. doi: 10.1016/s0009-8981(03)00234-1. Clin Chim Acta. 2003. PMID: 12927680

3

A new era for preventive genetic programs in the Arabian Peninsula.

Al-Odaib AN, Abu-Amero KK, Ozand PT, Al-Hellani AM. Al-Odaib AN, et al. Saudi Med J. 2003 Nov;24(11):1168-75. Saudi Med J. 2003. PMID: 14647548 Review.

4

Multiple displacement amplification on single cell and possible PGD applications.

Hellani A, Coskun S, Benkhalifa M, Tbakhi A, Sakati N, Al-Odaib A, Ozand P. Hellani A, et al. Mol Hum Reprod. 2004 Nov;10(11):847-52. doi: 10.1093/molehr/gah114. Epub 2004 Oct 1. Mol Hum Reprod. 2004. PMID: 15465849

5

Preimplantation genetic diagnosis for Niemann-Pick disease type B.

Hellani A, Schuchman EH, Al-Odaib A, Al Aqueel A, Jaroudi K, Ozand P, Coskun S. Hellani A, et al. Prenat Diagn. 2004 Dec 15;24(12):943-8. doi: 10.1002/pd.1050. Prenat Diagn. 2004. PMID: 15612058

6

3-Methylcrotonyl-CoA carboxylase deficiency. A long-term outcome.

Al-Odaib A, Rashed M, Page T, Nyhan W, Ozand PT. Al-Odaib A, et al. Saudi Med J. 2006 May;27(5):732-3. Saudi Med J. 2006. PMID: 16680273 No abstract available.

7

Hormonal levels of leptin, insulin, ghrelin, and neuropeptide Y in lean, overweight, and obese Saudi females.

Daghestani MH, Ozand PT, Al-Himadi AR, Al-Odaib AN. Daghestani MH, et al. Saudi Med J. 2007 Aug;28(8):1191-7. Saudi Med J. 2007. PMID: 17676200

8

Identification of Gaucher disease mutations found in Saudi Arabia.

Kaya N, Al-Zahrani F, Al-Odaib A, Rahbeeni Z, Al-Hassnan Z, Al-Sharif F, Ozand P, Al-Sayed M. Kaya N, et al. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):200-1. doi: 10.1016/j.bcmd.2008.05.002. Epub 2008 Jun 30. Blood Cells Mol Dis. 2008. PMID: 18586535 No abstract available.

9

Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia.

Kaya N, Al-Owain M, Albakheet A, Colak D, Al-Odaib A, Imtiaz F, Coskun S, Al-Sayed M, Al-Hassnan Z, Al-Zaidan H, Meyer B, Ozand P. Kaya N, et al. Eur J Med Genet. 2008 Nov-Dec;51(6):558-65. doi: 10.1016/j.ejmg.2008.08.001. Epub 2008 Aug 26. Eur J Med Genet. 2008. PMID: 18790721

10

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.

Kaya N, Imtiaz F, Colak D, Al-Sayed M, Al-Odaib A, Al-Zahrani F, Al-Mubarak BR, Al-Owain M, Al-Dhalaan H, Chedrawi A, Al-Hassnan Z, Coskun S, Sakati N, Ozand P, Meyer BF. Kaya N, et al. Genet Med. 2008 Sep;10(9):675-84. doi: 10.1097/gim.0b013e31818337a8. Genet Med. 2008. PMID: 18978679 Free article.

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