Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maaly Abdel Fattah"'
Autor:
Joyce N. Mbekeani, Maaly Abdel Fattah, David M. Poulsen, Selwa Al Hazzaa, M. Anas Dababo, Abdelmoneim Eldali, Manzoor Ahmed
Publikováno v:
Annals of Saudi Medicine, Vol 37, Iss 3, Pp 232-239 (2017)
BACKGROUND: Optic atrophy (OA) represents permanent retinal ganglion cell loss warranting study to establish etiology. OBJECTIVES: To describe neurogenic causes of OA. DESIGN: Prospective, observational. SETTING: Tertiary care center, Riyadh, Saudi A
Externí odkaz:
https://doaj.org/article/9292a6faf84a41939535b4618659f6a5
Publikováno v:
European Journal of Ophthalmology. 32:2604-2614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae715e10e4cb79072826b925b2ec3c0e
https://doi.org/10.1177/11206721211055620
https://doi.org/10.1177/11206721211055620
Autor:
Randa M. Al Nounou, Mohammed Asif Dogar, Maaly Abdel Fattah, Joyce N. Mbekeani, Wahiba Chebbo
Publikováno v:
Journal of Neuro-Ophthalmology. 36:73-77
Bilateral, simultaneous optic nerve sheath infiltration as a manifestation of leukemia relapse is very rare. A 45-year-old woman with chronic myelogenous leukemia was successfully treated to cytogenetic bone marrow remission 1 year previously and mai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef3779a4cb447cd92b8e5d49a576b13
https://doi.org/10.1097/wno.0000000000000326
https://doi.org/10.1097/wno.0000000000000326
Autor:
Gheid Abuharb, Abeer Al-Mostafa, Rabab Allam, Zahra Al-Sahlawi, Maaly Abdel-Fattah, Hamad Al-Zaidan, Alain Verloes, Khushnooda Ramzan, Michael Nester, Faiqa Imtiaz, Ola Khalifa
Publikováno v:
European Journal of Medical Genetics. 58:293-299
Donnai-Barrow syndrome (DBS; MIM 222448) is characterized by typical craniofacial anomalies (major hypertelorism with bulging eyes), high grade myopia, deafness and low molecular weight proteinuria. The disorder results from mutations in the low dens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21e0e6bed2f9bce89a37785a8e2e3f2
https://doi.org/10.1016/j.ejmg.2014.12.008
https://doi.org/10.1016/j.ejmg.2014.12.008
Autor:
David M Poulsen, Maaly Abdel Fattah, Selwa A. Al Hazzaa, M Anas Dababo, Joyce N. Mbekeani, Manzoor Ahmed, Abdelmoneim Eldali
Publikováno v:
Annals of Saudi Medicine, Vol 37, Iss 3, Pp 232-239 (2017)
BACKGROUND: Optic atrophy (OA) represents permanent retinal ganglion cell loss warranting study to establish etiology. OBJECTIVES: To describe neurogenic causes of OA. DESIGN: Prospective, observational. SETTING: Tertiary care center, Riyadh, Saudi A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50a32bd20abee70329bb4f361fe2b2a7
https://pubmed.ncbi.nlm.nih.gov/28578363
https://pubmed.ncbi.nlm.nih.gov/28578363