Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Majed al Obailan"'
Autor:
Abdullah I. Almater, Jawaher Jehad Alwatban, Arwa Z. Alromaih, Motazz Alarfaj, Majed Al-Obailan
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 1, Pp 292-296 (2022)
Idiopathic intracranial hypertension (IIH) is a poorly understood condition, and its presentation can coexist with other diseases. Simultaneous IIH and Duane retraction syndrome (DRS) type 1 have never been reported to coexist in an adult patient. He
Externí odkaz:
https://doaj.org/article/e14be7adad394b268829aed83291854b
Autor:
Majed Al-Obailan, A.K. Daif, Ahmed M. Abu El-Asrar, Abdulrahman F AlBloushi, Nayef F Al-Swaina, Abdulsalam M Dheyab
Publikováno v:
European Journal of Ophthalmology. 31:482-490
Purpose: To describe the clinical findings and outcomes in patients who presented with uveitis associated with multiple sclerosis. Methods: Retrospective review of 20 patients (38 eyes). Results: The most frequent ocular finding was multifocal elonga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d55957ebc6d8150f7a4013a69abc6cec
https://doi.org/10.1177/1120672120904667
https://doi.org/10.1177/1120672120904667
Publikováno v:
Neuroophthalmology
Wernicke’s encephalopathy (WE) is an acute neuropsychiatric syndrome resulting from thiamine deficiency (vitamin B(1)). It is characterised classically by a triad of ophthalmoplegia, confusion, and ataxia. WE is classically associated with alcoholi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb3698a147b6c5023a6e19eae6147d5
https://europepmc.org/articles/PMC9762834/
https://europepmc.org/articles/PMC9762834/
Publikováno v:
Saudi Journal of Ophthalmology
Saudi Journal of Ophthalmology, Vol 33, Iss 3, Pp 203-208 (2019)
Saudi Journal of Ophthalmology, Vol 33, Iss 3, Pp 203-208 (2019)
Purpose: To study clinical and histopathological findings of corneal opacification caused by thickened epithelium leading to reduced vision and topographical changes and to evaluate the outcome of its removal. Methods: Twelve patients (17 eyes) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c1023e958c264a9dec076b81da2a81
http://europepmc.org/articles/PMC6819717
http://europepmc.org/articles/PMC6819717
Publikováno v:
Neuro-Ophthalmology. 34:297-300
Of 237 patients seen in the Neuro-Ophthalmology Division of the Jules Stein Eye Institute 1986–2009, coded as “congenital optic nerve anomaly”, 13 demonstrated focal superonasal flattening of the optic disc margin and nerve fibre layer thinning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0554e2b9fe68efa2347fd24554718946
https://doi.org/10.3109/01658107.2010.494327
https://doi.org/10.3109/01658107.2010.494327
Autor:
Majed Alkharashi, Abdullah S. Al-Kharashi, Altaf A. Kondkar, Khaled K. Abu-Amero, Majed Al-Obailan
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 43:332-333
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf50952b5cab5b1fdd1a439ab5f6496
https://doi.org/10.1017/cjn.2015.345
https://doi.org/10.1017/cjn.2015.345
Autor:
Anthony C. Arnold, Gorkem Bilgin, Harry V. Vinters, Majed Al-Obailan, Laura Bonelli, Ben J. Glasgow
Publikováno v:
Neuro-ophthalmology (Aeolus Press), vol 38, iss 6
Primary optic nerve gliomas are most commonly benign pilocytic astrocytomas (World Health Organization [WHO] Grade I) occurring in childhood and following an indolent course. Malignant optic gliomas occur in adulthood and follow an extremely aggressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef6169ccaa80cae5fafe400379515d9
https://europepmc.org/articles/PMC5131714/
https://europepmc.org/articles/PMC5131714/
Autor:
Thomas M. Bosley, Ibrahim A. Alorainy, Abdulkarim Al Hussain, Majed al Obailan, Ali Hellani, Khaled K. Abu-Amero, Mustafa A. Salih, Ghassan Zidan
Publikováno v:
Ophthalmic genetics. 31(1)
To correlate the clinical phenotype with the genotype of a boy with a terminal deletion of chromosome 6q and to compare these observations to previous reports of 6q deletions and review of the literature.Careful clinical evaluation, conventional cyto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5464a82bd5057ab8706c119583ac85e
https://pubmed.ncbi.nlm.nih.gov/20141352
https://pubmed.ncbi.nlm.nih.gov/20141352
Publikováno v:
Saudi Journal of Ophthalmology. (3-4):203-209
Keratoconus is a disease causing increased steepening of the cornea resulted in irregular astigmatism. Treatment options are Glasses, Hard contact lenses, Cross linking, Intracorneal Segments insertion, Refractive surgery (Gilda et al., 2008), or Ker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15888113960aeeb5c7c904ef88ec9eb2
Autor:
Alarfaj, Motazz A.1,2 (AUTHOR) motazz.alarfaj@gmail.com, Almadhi, Nada H.1 (AUTHOR), Al-Amry, Mohammad1 (AUTHOR), Almater, Abdullah I.3 (AUTHOR), Al-Obailan, Majed1,3 (AUTHOR)
Publikováno v:
Neuro-Ophthalmology. Dec2022, Vol. 46 Issue 6, p409-412. 4p.