Ozand PT - Search Results

1

Novel mitochondrial DNA transversion mutation in transfer ribonucleic acid for leucine 2 (CUN) in a patient with the clinical features of MELAS.

Abu-Amero KK, Ozand PT, Al-Dhalaan H. Abu-Amero KK, et al. Among authors: ozand pt. J Child Neurol. 2006 Nov;21(11):971-2. doi: 10.1177/08830738060210110601. J Child Neurol. 2006. PMID: 17092464

2

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

3

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.

4

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. Among authors: ozand pt. Ann Neurol. 2012 Apr;71(4):498-508. doi: 10.1002/ana.22673. Epub 2011 Dec 28. Ann Neurol. 2012. PMID: 22213401

5

Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways.

Colak D, Al-Dhalaan H, Nester M, Albakheet A, Al-Younes B, Al-Hassnan Z, Al-Dosari M, Chedrawi A, Al-Owain M, Abudheim N, Al-Alwan L, Al-Odaib A, Ozand P, Inan MS, Kaya N. Colak D, et al. Genomics. 2011 Jan;97(1):19-28. doi: 10.1016/j.ygeno.2010.09.004. Epub 2010 Oct 8. Genomics. 2011. PMID: 20934504 Free article.

6

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.

7

Novel mutation in GLRB in a large family with hereditary hyperekplexia.

Al-Owain M, Colak D, Al-Bakheet A, Al-Hashmi N, Shuaib T, Al-Hemidan A, Aldhalaan H, Rahbeeni Z, Al-Sayed M, Al-Younes B, Ozand PT, Kaya N. Al-Owain M, et al. Among authors: ozand pt. Clin Genet. 2012 May;81(5):479-84. doi: 10.1111/j.1399-0004.2011.01661.x. Epub 2011 Apr 7. Clin Genet. 2012. PMID: 21391991

8

Sanfilippo type D presenting with acquired language disorder but without features of mucopolysaccharidosis.

Ozand PT, Thompson JN, Gascon GG, Sarvepalli SB, Rahbeeni Z, Nester MJ, Brismar J. Ozand PT, et al. J Child Neurol. 1994 Oct;9(4):408-11. doi: 10.1177/088307389400900415. J Child Neurol. 1994. PMID: 7822734

9

GM1 gangliosidosis type 2 in two siblings.

Gascon GG, Ozand PT, Erwin RE. Gascon GG, et al. Among authors: ozand pt. J Child Neurol. 1992 Apr;7 Suppl:S41-50. doi: 10.1177/08830738920070010711. J Child Neurol. 1992. PMID: 1588015

10

Organic acidurias: a review. Part 2.

Ozand PT, Gascon GG. Ozand PT, et al. J Child Neurol. 1991 Oct;6(4):288-303. doi: 10.1177/088307389100600402. J Child Neurol. 1991. PMID: 1940129 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

181 results

Search Page

Filters