Garzozi HJ - Search Results

1

Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa.

Collin RW, Safieh C, Littink KW, Shalev SA, Garzozi HJ, Rizel L, Abbasi AH, Cremers FP, den Hollander AI, Klevering BJ, Ben-Yosef T. Collin RW, et al. Among authors: garzozi hj. Am J Hum Genet. 2010 May 14;86(5):783-8. doi: 10.1016/j.ajhg.2010.03.016. Epub 2010 Apr 15. Am J Hum Genet. 2010. PMID: 20398884 Free PMC article.

2

A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.

Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T. Auslender N, et al. Among authors: garzozi hj. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5431-8. doi: 10.1167/iovs.07-0736. Invest Ophthalmol Vis Sci. 2007. PMID: 18055789

3

A novel splice-site mutation of TULP1 underlies severe early-onset retinitis pigmentosa in a consanguineous Israeli Muslim Arab family.

Abbasi AH, Garzozi HJ, Ben-Yosef T. Abbasi AH, et al. Among authors: garzozi hj. Mol Vis. 2008 Apr 21;14:675-82. Mol Vis. 2008. PMID: 18432314 Free PMC article.

4

Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mapping.

Benayoun L, Spiegel R, Auslender N, Abbasi AH, Rizel L, Hujeirat Y, Salama I, Garzozi HJ, Allon-Shalev S, Ben-Yosef T. Benayoun L, et al. Among authors: garzozi hj. Am J Med Genet A. 2009 Feb 15;149A(4):650-6. doi: 10.1002/ajmg.a.32634. Am J Med Genet A. 2009. PMID: 19140180

5

[Ophthalmology in the Middle East from antiquity to the twentieth century].

Abbasi AH, Garzozi HJ. Abbasi AH, et al. Among authors: garzozi hj. Harefuah. 2008 Jun;147(6):547-52, 572. Harefuah. 2008. PMID: 18693634 Hebrew.

6

[Ophthalmology in the Holy Land].

Abbasi AH, Garzozi HJ. Abbasi AH, et al. Among authors: garzozi hj. Harefuah. 2009 Feb;148(2):125-9, 138. Harefuah. 2009. PMID: 19627043 Hebrew.

7

Prenatal diagnosis of dacryocystocele.

Abbasi AH, Haj N, Nseir T, Garzozi HJ. Abbasi AH, et al. Among authors: garzozi hj. Eye (Lond). 2007 Dec;21(12):1537-8. doi: 10.1038/sj.eye.6702994. Epub 2007 Oct 5. Eye (Lond). 2007. PMID: 17917684 No abstract available.

8

A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts.

Pras E, Raz J, Yahalom V, Frydman M, Garzozi HJ, Pras E, Hejtmancik JF. Pras E, et al. Among authors: garzozi hj. Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1940-5. doi: 10.1167/iovs.03-1117. Invest Ophthalmol Vis Sci. 2004. PMID: 15161861

9

A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.

Pras E, Pras E, Bakhan T, Levy-Nissenbaum E, Lahat H, Assia EI, Garzozi HJ, Kastner DL, Goldman B, Frydman M. Pras E, et al. Among authors: garzozi hj. Isr Med Assoc J. 2001 Aug;3(8):559-62. Isr Med Assoc J. 2001. PMID: 11519376

10

[The effects of hormone replacement therapy (HRT) on the human eye].

Lang Y, Lang N, Ben-Ami M, Garzozi H. Lang Y, et al. Harefuah. 2002 Mar;141(3):287-91, 313, 312. Harefuah. 2002. PMID: 11944225 Review. Hebrew.

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