Selwa Al-Hazzaa

Selwa Al-Hazzaa

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Selwa Al-Hazzaa

Selwa Al-Hazzaa

Publications by authors named "Selwa Al-Hazzaa"

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18Publications

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Asymmetrical Ocular Manifestations of Nephropathic Cystinosis; A Case Report.

Am J Case Rep 2019 Sep 4;20:1308-1313. Epub 2019 Sep 4.

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741281PMC
September 2019

Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.

Int J Pediatr Otorhinolaryngol 2018 May 14;108:17-21. Epub 2018 Feb 14.

Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

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https://linkinghub.elsevier.com/retrieve/pii/S01655876183008
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http://dx.doi.org/10.1016/j.ijporl.2018.02.016DOI Listing
May 2018

Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center.

Am J Case Rep 2018 Apr 28;19:500-504. Epub 2018 Apr 28.

Department of Ophthalmology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.12659/AJCR.908036DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944404PMC
April 2018

Etiology of optic atrophy: a prospective observational study from Saudi Arabia.

Ann Saudi Med 2017 May-Jun;37(3):232-239

Dr. Joyce N. Mbekeani, Department of Surgery (Ophthalmology),, Jacobi Medical Center,, 5N, 1400 Pelham Parkway, Bronx NY 10461, USA, T: 718-918-4784;, F: 718-918-7379, ORCID: http://orcid.org/0000-0002-8801-4110.

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http://dx.doi.org/10.5144/0256-4947.2017.232DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150579PMC
March 2018

Papillary tumor of the pineal region presenting with Foster Kennedy sign.

Hematol Oncol Stem Cell Ther 2015 Sep 7;8(3):140-2. Epub 2015 Jul 7.

Department of Anatomical Pathology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.hemonc.2015.06.002DOI Listing
September 2015

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.

Nat Cell Biol 2015 Aug 13;17(8):1074-1087. Epub 2015 Jul 13.

Section of Ophthalmology and Neuroscience, Leeds Institutes of Molecular Medicine, University of Leeds, Leeds, LS9 7TF, UK.

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http://www.nature.com/articles/ncb3201
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http://dx.doi.org/10.1038/ncb3201DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536769PMC
August 2015

Signet ring cell adenocarcinoma and bilateral leptomeningeal involvement of optic nerve sheaths.

J Neuroophthalmol 2015 Jun;35(2):162-4

Department of Ophthalmology (JNM), North Bronx Health Network; Department of Ophthalmology & Visual Sciences (JNM), Albert Einstein College of Medicine of Yeshiva University, Bronx, New York; Departments of Ophthalmology (MQH, SAAH), Pathology (AMT), Gynecologic Oncology (SHH), and Neuro-radiology (MAD), King Faisal Specialist Hospital, Riyadh, Saudi Arabia; and the Al Faisal University College of Medicine (SAAH), Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1097/WNO.0000000000000236DOI Listing
June 2015

LOXL3, encoding lysyl oxidase-like 3, is mutated in a family with autosomal recessive Stickler syndrome.

Hum Genet 2015 Apr 7;134(4):451-3. Epub 2015 Feb 7.

Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03, PO BOX 3354, Riyadh, 11211, Saudi Arabia.

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http://link.springer.com/10.1007/s00439-015-1531-z
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http://dx.doi.org/10.1007/s00439-015-1531-zDOI Listing
April 2015

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.

Eur J Med Genet 2014 May-Jun;57(6):253-8. Epub 2014 Apr 21.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O.Box 3354, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1016/j.ejmg.2014.04.004DOI Listing
February 2015

COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.

Int J Pediatr Otorhinolaryngol 2014 Mar 18;78(3):427-32. Epub 2013 Dec 18.

Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.ijporl.2013.12.008DOI Listing
March 2014

Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.

Am J Hum Genet 2013 Mar 28;92(3):387-91. Epub 2013 Feb 28.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.ajhg.2013.01.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591839PMC
March 2013

Homozygous null mutation in ODZ3 causes microphthalmia in humans.

Genet Med 2012 Nov 5;14(11):900-4. Epub 2012 Jul 5.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1038/gim.2012.71DOI Listing
November 2012

Progression of age-related macular degeneration after cataract surgery.

Arch Ophthalmol 2009 Nov;127(11):1412-9

Department of Preventive Medicine, Stony Brook University School of Medicine, USA.

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http://dx.doi.org/10.1001/archophthalmol.2009.152DOI Listing
November 2009