Al Tassan NA - Search Results

1

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.

Bohlega SA, Al-Mubarak BR, Alyemni EA, Abouelhoda M, Monies D, Mustafa AE, Khalil DS, Al Haibi S, Abou Al-Shaar H, Faquih T, El-Kalioby M, Tahir AI, Al Tassan NA. Bohlega SA, et al. Among authors: al tassan na, al mubarak br, al haibi s. BMC Res Notes. 2016 Jun 7;9:295. doi: 10.1186/s13104-016-2102-7. BMC Res Notes. 2016. PMID: 27268037 Free PMC article.

2

Congential fibrosis of the extraocular muscles type I (CFEOM1) on the Arabian Peninsula.

Khan AO, Khalil DS, Al-Tassan NA. Khan AO, et al. Among authors: al tassan na. Ophthalmic Genet. 2008 Mar;29(1):25-8. doi: 10.1080/13816810701850058. Ophthalmic Genet. 2008. PMID: 18363169

3

Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.

Morales J, Al-Sharif L, Khalil DS, Shinwari JM, Bavi P, Al-Mahrouqi RA, Al-Rajhi A, Alkuraya FS, Meyer BF, Al Tassan N. Morales J, et al. Am J Hum Genet. 2009 Nov;85(5):558-68. doi: 10.1016/j.ajhg.2009.09.011. Am J Hum Genet. 2009. PMID: 19836009 Free PMC article.

4

Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus.

Khan AO, Khalil DS, Al-Sharif LJ, Al-Tassan NA. Khan AO, et al. Among authors: al tassan na, al sharif lj. Ophthalmic Genet. 2009 Dec;30(4):206-7. doi: 10.3109/13816810903183613. Ophthalmic Genet. 2009. PMID: 19852579 No abstract available.

5

Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles.

Khan AO, Khalil DS, Al Sharif LJ, Al-Ghadhfan FE, Al Tassan NA. Khan AO, et al. Among authors: al tassan na, al ghadhfan fe, al sharif lj. Ophthalmology. 2010 Jan;117(1):154-8. doi: 10.1016/j.ophtha.2009.06.029. Epub 2009 Nov 5. Ophthalmology. 2010. PMID: 19896199

6

Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.

Khan AO, Shinwari J, Omar A, Al-Sharif L, Khalil DS, Alanazi M, Al-Amri A, Al Tassan N. Khan AO, et al. Mol Vis. 2011 Jan 20;17:218-24. Mol Vis. 2011. PMID: 21264235 Free PMC article.

7

Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.

Bohlega SA, Shinwari JM, Al Sharif LJ, Khalil DS, Alkhairallah TS, Al Tassan NA. Bohlega SA, et al. Among authors: al tassan na, al sharif lj. BMC Med Genet. 2011 Feb 16;12:27. doi: 10.1186/1471-2350-12-27. BMC Med Genet. 2011. PMID: 21324166 Free PMC article.

8

The optic nerve head in congenital fibrosis of the extraocular muscles.

Khan AO, Shinwari J, Omar A, Khalil D, Al-Anazi M, Al-Amri A, Al-Tassan NA. Khan AO, et al. Among authors: al anazi m, al tassan na, al amri a. Ophthalmic Genet. 2011 Sep;32(3):175-80. doi: 10.3109/13816810.2011.567318. Epub 2011 Mar 31. Ophthalmic Genet. 2011. PMID: 21449832

9

Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3).

Khan AO, Shinwari J, Abu Dhaim N, Khalil D, Al Sharif L, Al Tassan N. Khan AO, et al. Mol Vis. 2011 Apr 19;17:971-6. Mol Vis. 2011. PMID: 21541264 Free PMC article.

10

Prolonged pursuit by optokinetic drum testing in asymptomatic female carriers of novel FRMD7 splice mutation c.1050 +5 G>A.

Khan AO, Shinwari J, Al-Sharif L, Khalil DS, Al Tassan N. Khan AO, et al. Arch Ophthalmol. 2011 Jul;129(7):936-40. doi: 10.1001/archophthalmol.2011.166. Arch Ophthalmol. 2011. PMID: 21746984

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