Ozand PT - Search Results

1

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. Among authors: ozand pt. Saudi Med J. 2003 Nov;24(11):1168-75. Saudi Med J. 2003. PMID: 14647548 Review.

2

Recently available techniques applicable to genetic problems in the Middle East.

Ozand PT, Odaib AA, Sakati N, Al-Hellani AM. Ozand PT, et al. Community Genet. 2005;8(1):44-7. doi: 10.1159/000083338. Community Genet. 2005. PMID: 15767755 Review.

3

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. Among authors: ozand pt. Saudi Med J. 2006 May;27(5):732-3. Saudi Med J. 2006. PMID: 16680273 No abstract available.

4

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. Among authors: ozand pt. Saudi Med J. 2007 Aug;28(8):1191-7. Saudi Med J. 2007. PMID: 17676200

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

Glutaric aciduria yype 1: First reported cases in three Saudi patients.

Coates R, Rashed M, Rahbeeni Z, Al-Garawi S, Al-Odaib AN, Sakati N, Gascon G, Worthen H, Ozand PT. Coates R, et al. Among authors: ozand pt. Ann Saudi Med. 1994 Jul;14(4):316-21. doi: 10.5144/0256-4947.1994.316. Ann Saudi Med. 1994. PMID: 17586927 Free PMC article.

7

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

8

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

9

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. Among authors: ozand pt. Clin Chim Acta. 2003 Sep;335(1-2):21-6. doi: 10.1016/s0009-8981(03)00234-1. Clin Chim Acta. 2003. PMID: 12927680

10

Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy.

Bosley TM, Abu-Amero KK, Ozand PT. Bosley TM, et al. Among authors: ozand pt. Neurology. 2004 Oct 12;63(7):1305-8. doi: 10.1212/01.wnl.0000140696.34117.95. Neurology. 2004. PMID: 15477560

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