Al-Odaib A - Search Results

1

Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders.

Alfadhel M, Al Othaim A, Al Saif S, Al Mutairi F, Alsayed M, Rahbeeni Z, Alzaidan H, Alowain M, Al-Hassnan Z, Saeedi M, Aljohery S, Alasmari A, Faqeih E, Alwakeel M, AlMashary M, Almohameed S, Alzahrani M, Migdad A, Al-Dirbashi OY, Rashed M, Alamoudi M, Jacob M, Alahaidib L, El-Badaoui F, Saadallah A, Alsulaiman A, Eyaid W, Al-Odaib A. Alfadhel M, et al. Among authors: al odaib a. J Paediatr Child Health. 2017 Jun;53(6):585-591. doi: 10.1111/jpc.13469. Epub 2017 Mar 24. J Paediatr Child Health. 2017. PMID: 28337809

2

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.

3

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.

4

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

5

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.

6

Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implications.

Al-Hassnan ZN, Imtiaz F, Al-Amoudi M, Rahbeeni Z, Al-Sayed M, Al-Owain M, Al-Zaidan H, Al-Odaib A, Rashed MS. Al-Hassnan ZN, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S263-7. doi: 10.1007/s10545-010-9143-1. Epub 2010 Jun 22. J Inherit Metab Dis. 2010. PMID: 20567907

7

Preimplantation genetic diagnosis in Saudi Arabia: parents' experience and attitudes.

Alsulaiman A, Al-Odaib A, Al-Rejjal R, Hewison J. Alsulaiman A, et al. Prenat Diagn. 2010 Aug;30(8):753-7. doi: 10.1002/pd.2532. Prenat Diagn. 2010. PMID: 20593451

8

Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia.

Kaya N, Colak D, Al-Bakheet A, Al-Younes B, Tulbah S, Daghestani M, Al-Mutairi F, Al-Amoudi M, Al-Odaib A, Al-Aqeel AI. Kaya N, et al. Gene. 2013 Jan 25;513(2):297-300. doi: 10.1016/j.gene.2012.09.097. Epub 2012 Oct 9. Gene. 2013. PMID: 23063737

9

Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening.

Al-Sulaiman A, Kondkar AA, Saeedi MY, Saadallah A, Al-Odaib A, Abu-Amero KK. Al-Sulaiman A, et al. Among authors: al odaib a. Biomed Res Int. 2015;2015:718674. doi: 10.1155/2015/718674. Epub 2015 Oct 12. Biomed Res Int. 2015. PMID: 26543864 Free PMC article.

10

Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.

Zou M, Alzahrani AS, Al-Odaib A, Alqahtani MA, Babiker O, Al-Rijjal RA, BinEssa HA, Kattan WE, Al-Enezi AF, Al Qarni A, Al-Faham MSA, Baitei EY, Alsagheir A, Meyer BF, Shi Y. Zou M, et al. Among authors: al odaib a. J Clin Endocrinol Metab. 2018 May 1;103(5):1889-1898. doi: 10.1210/jc.2017-02202. J Clin Endocrinol Metab. 2018. PMID: 29546359

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