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Ophthalmic Genetics|April 11, 2012
Familial spherophakia with short stature caused by a novel homozygous ADAMTS17 mutationArif O Khan, Mohammed A Aldahmesh, Huda Al-Ghadeer, et al.
Gastroenterology and Hepatology From Bed to Bench|November 22, 2019
Resolved HBV behavior during the treatment of chronic HCV infection with direct-acting antiviralsSalem Y Mohamed, Baasim A Gaballah, Hany Mohamed Elsadek, et al.
Human Mutation|March 15, 2012
Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locusMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.
Current Gerontology and Geriatrics Research|September 27, 2013
Mental health problems and sociodemographic correlates in elderly medical inpatients in a university hospital in egyptEmam M Esmayel, Mohsen M Eldarawy, Mohamed M Hassan, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 21, 2011
Familial juvenile glaucoma with underlying homozygous p.G61E CYP1B1 mutationsArif O Khan, Lama Al-Abdi, Jawahir Y Mohamed, et al.
The British Journal of Ophthalmology|March 9, 2012
The distinct ophthalmic phenotype of Knobloch syndrome in childrenArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.
The Egyptian Journal of Immunology|September 30, 2015
Detection of Cytotoxic T-Lymphocyte Associated Antigen-4 Gene Polymorphism in Type 1 Diabetes MellitusRoshdan M Arafa, Somaya M Desouky, Sherin M Emam, et al.
Journal of Gastrointestinal Cancer|March 3, 2018
Prognostic Value of Cyclin D1 and CD44 Expression in Gastric AdenocarcinomaHanaa M Ibrahim, Abeer M AbdElbary, Salem Y Mohamed, et al.
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