Al Hassnan ZN - Search Results

1

Profound biotinidase deficiency in a child with predominantly spinal cord disease.

Chedrawi AK, Ali A, Al Hassnan ZN, Faiyaz-Ul-Haque M, Wolf B. Chedrawi AK, et al. Among authors: al hassnan zn. J Child Neurol. 2008 Sep;23(9):1043-8. doi: 10.1177/0883073808318062. Epub 2008 Jul 21. J Child Neurol. 2008. PMID: 18645204

2

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. Among authors: al budhaim m, al owain m, al dhalaan h. J Child Neurol. 2007 Jan;22(1):106-8. doi: 10.1177/0883073807299968. J Child Neurol. 2007. PMID: 17608317

3

Rapid UPLC-MS/MS method for routine analysis of plasma pristanic, phytanic, and very long chain fatty acid markers of peroxisomal disorders.

Al-Dirbashi OY, Santa T, Rashed MS, Al-Hassnan Z, Shimozawa N, Chedrawi A, Jacob M, Al-Mokhadab M. Al-Dirbashi OY, et al. J Lipid Res. 2008 Aug;49(8):1855-62. doi: 10.1194/jlr.D800019-JLR200. Epub 2008 Apr 25. J Lipid Res. 2008. PMID: 18441019 Free article.

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. Genet Med. 2008 Sep;10(9):675-84. doi: 10.1097/gim.0b013e31818337a8. Genet Med. 2008. PMID: 18978679 Free article.

5

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.

Faiyaz-Ul-Haque M, Al-Owain M, Al-Dayel F, Al-Hassnan Z, Al-Zaidan H, Rahbeeni Z, Al-Sayed M, Balobaid A, Cluntun A, Toulimat M, Abalkhail H, Peltekova I, Zaidi SH. Faiyaz-Ul-Haque M, et al. Eur J Pediatr. 2009 Dec;168(12):1467-71. doi: 10.1007/s00431-009-0953-9. Epub 2009 Mar 4. Eur J Pediatr. 2009. PMID: 19259699

6

Variant late infantile neuronal ceroid lipofuscinosis (CLN6 gene) in Saudi Arabia.

Al-Muhaizea MA, Al-Hassnan ZN, Chedrawi A. Al-Muhaizea MA, et al. Among authors: al hassnan zn. Pediatr Neurol. 2009 Jul;41(1):74-6. doi: 10.1016/j.pediatrneurol.2009.01.012. Pediatr Neurol. 2009. PMID: 19520283 Review.

7

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 duraihem a, al owain m, al dhalaan h. J Child Neurol. 2009 Dec;24(12):1513-9. doi: 10.1177/0883073809341269. J Child Neurol. 2009. PMID: 19955343 Review.

8

Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria.

Zaidi SH, Faiyaz-Ul-Haque M, Shuaib T, Balobaid A, Rahbeeni Z, Abalkhail H, Al-Abdullatif A, Al-Hassnan Z, Peltekova I, Al-Owain M. Zaidi SH, et al. Clin Genet. 2012 Jun;81(6):563-70. doi: 10.1111/j.1399-0004.2011.01690.x. Epub 2011 May 18. Clin Genet. 2012. PMID: 21517828

9

Novel V97G ASAH1 mutation found in Farber disease patients: unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system.

Chedrawi AK, Al-Hassnan ZN, Al-Muhaizea M, Colak D, Al-Younes B, Albakheet A, Tulba S, Kaya N. Chedrawi AK, et al. Among authors: al muhaizea m, al younes b, al hassnan zn. Brain Dev. 2012 May;34(5):400-4. doi: 10.1016/j.braindev.2011.07.003. Epub 2011 Sep 3. Brain Dev. 2012. PMID: 21893389

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. 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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