Ali M Hellani
Overview
Explore the profile of Ali M Hellani including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
45
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Recent Articles
1.
Abu-Amero K, Kondkar A, Hellani A, Bosley T, Khan A
Neurosciences (Riyadh)
. 2016 Jan;
21(1):72-4.
PMID: 26818173
No abstract available.
2.
Mohamed S, Elkholy S, El-Meleagy E, Abu-Amero K, Hellani A
Ann Saudi Med
. 2014 Oct;
34(3):217-21.
PMID: 25266181
Background And Objectives: The prevalence of maturity-onset diabetes of the young (MODY) in Saudi population remains unknown, and data on molecular etiology of this condition is limited. Therefore, the present...
3.
Bosley T, Alorainy I, Oystreck D, Hellani A, Seidahmed M, Faki Osman M, et al.
Can J Neurol Sci
. 2014 Jan;
41(1):42-8.
PMID: 24384336
Background: We review clinical, neuroimaging, and genetic information on six individuals with isolated sulfite oxidase deficiency (ISOD). Methods: All patients were examined, and clinical records, biochemistry, neuroimaging, and sulfite oxidase...
4.
Abu-Amero K, Kondkar A, Hellani A, Oystreck D, Khan A, Bosley T
Ophthalmic Genet
. 2013 Sep;
36(2):99-104.
PMID: 24001015
Background: To evaluate possible monogenic and chromosomal anomalies in a patient with unilateral Duane retraction syndrome and modest dysmorphism. Materials And Methods: Clinical evaluation, sequencing of candidate genes, and array...
5.
Abu-Amero K, Kondkar A, Al Otaibi A, Alorainy I, Khan A, Hellani A, et al.
Ophthalmic Genet
. 2013 Aug;
36(1):14-20.
PMID: 23952617
Background: To evaluate possible monogenic and chromosomal anomalies in a patient with unilateral Duane retraction syndrome, modest dysmorphism, cerebral white matter abnormalities, and normal cognitive function. Materials And Methods: Performing...
6.
Abu-Amero K, Kondkar A, Salih M, Al-Husain M, Al Shammari M, Zeidan G, et al.
Ophthalmic Genet
. 2013 Feb;
34(4):249-53.
PMID: 23406309
Background: To carefully assess the phenotype and genotype of a patient with partial mosaic trisomy 8 with particular attention to ophthalmologic features. Methods: Ophthalmologic and neuro-ophthalmologic examination; neuroimaging; conventional karyotyping;...
7.
Salih M, Bosley T, Alorainy I, Sabry M, Rashed M, Al-Yamani E, et al.
Can J Neurol Sci
. 2012 Dec;
40(1):109-12.
PMID: 23250141
No abstract available.
8.
Hellani A, Akoum S, Fadel E, Yousef H, Abu-Amero K
Saudi Med J
. 2012 Oct;
33(10):1059-64.
PMID: 23047205
Objective: To devise a new and simple technique to help select normal embryos that are human leukocyte antigen (HLA) matched to their affected siblings for diseases, such as beta-thalassemia or...
9.
Abu-Amero K, Hellani A, Al Mansouri S, Kalantan H, Al-Muammar A
Mol Vis
. 2011 Apr;
17:822-6.
PMID: 21528002
Purpose: To determine whether patients with sporadic, non-familial keratoconus and no pathogenic mutations in the visual system homeobox 1 (VSX1) gene have evidence of chromosomal copy number alterations. Methods: Twenty...
10.
Abu-Amero K, Faletra F, Gasparini P, Parentin F, Pensiero S, Alorainy I, et al.
Ophthalmic Genet
. 2011 Apr;
32(4):212-6.
PMID: 21510772
Background: To describe clinical and genetic observations in a patient with horizontal gaze palsy and progressive scoliosis (HGPPS) without identified mutations in the ROBO3 gene. Materials And Methods: Neurologic and...