Al-Dhalaan H - 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. J Child Neurol. 2006 Nov;21(11):971-2. doi: 10.1177/08830738060210110601. J Child Neurol. 2006. PMID: 17092464

2

Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.

Aldosary M, Al-Bakheet A, Al-Dhalaan H, Almass R, Alsagob M, Al-Younes B, AlQuait L, Mustafa OM, Bulbul M, Rahbeeni Z, Alfadhel M, Chedrawi A, Al-Hassnan Z, AlDosari M, Al-Zaidan H, Al-Muhaizea MA, AlSayed MD, Salih MA, AlShammari M, Faiyaz-Ul-Haque M, Chishti MA, Al-Harazi O, Al-Odaib A, Kaya N, Colak D. Aldosary M, et al. Among authors: al dhalaan h. OMICS. 2020 Mar;24(3):160-171. doi: 10.1089/omi.2019.0192. Epub 2020 Feb 27. OMICS. 2020. PMID: 32105570

3

Muscle phosphofructokinase deficiency with neonatal seizures and nonprogressive course.

Al-Hassnan ZN, Al Budhaim M, Al-Owain M, Lach B, Al-Dhalaan H. Al-Hassnan ZN, et al. J Child Neurol. 2007 Jan;22(1):106-8. doi: 10.1177/0883073807299968. J Child Neurol. 2007. PMID: 17608317

4

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. Among authors: al dhalaan h. Genet Med. 2008 Sep;10(9):675-84. doi: 10.1097/gim.0b013e31818337a8. Genet Med. 2008. PMID: 18978679

5

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report.

Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW. Abu-Amero KK, et al. Among authors: al dhalaan h. J Med Case Rep. 2009 Oct 15;3:77. doi: 10.1186/1752-1947-3-77. J Med Case Rep. 2009. PMID: 19946553 Free PMC article.

6

Sphingolipid activator protein B deficiency: report of 9 Saudi patients and review of the literature.

Al-Hassnan ZN, Al Dhalaan H, Patay Z, Faqeih E, Al-Owain M, Al-Duraihem A, Faiyaz-Ul-Haque M. Al-Hassnan ZN, et al. Among authors: al dhalaan h. J Child Neurol. 2009 Dec;24(12):1513-9. doi: 10.1177/0883073809341269. J Child Neurol. 2009. PMID: 19955343 Review.

7

Vanishing white matter in Saudi Arabia.

Otaif MY, Al-Muhaizea MA, Al-Jofan F, Al-Dhalaan H. Otaif MY, et al. Neurosciences (Riyadh). 2008 Oct;13(4):433-6. Neurosciences (Riyadh). 2008. PMID: 21063376

8

Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII.

Kaya N, Aldhalaan H, Al-Younes B, Colak D, Shuaib T, Al-Mohaileb F, Al-Sugair A, Nester M, Al-Yamani S, Al-Bakheet A, Al-Hashmi N, Al-Sayed M, Meyer B, Jungbluth H, Al-Owain M. Kaya N, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):826-34. doi: 10.1002/ajmg.b.31227. Epub 2011 Aug 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21812104

9

Propionic acidemia associated with visual hallucinations.

Shuaib T, Al-Hashmi N, Ghaziuddin M, Megdad E, Abebe D, Al-Saif A, Doubi A, Aldhalaan H, Abouzied ME, Al-Owain M. Shuaib T, et al. J Child Neurol. 2012 Jun;27(6):799-803. doi: 10.1177/0883073811426929. Epub 2011 Dec 7. J Child Neurol. 2012. PMID: 22156789

10

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: al dhalaan h. Ann Neurol. 2012 Apr;71(4):498-508. doi: 10.1002/ana.22673. Epub 2011 Dec 28. Ann Neurol. 2012. PMID: 22213401

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