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M.A. Sabry
Observed names:
M A Sabry,
M. A. Sabry,
Mohamed A. Sabry
Institution:
Saad Specialist Hospital
Observed institutions:
Harvard University,
King Faisal Specialist Hospital & Research Centre,
Saad Specialist Hospital,
Massachusetts General Hospital,
Birmingham Children's Hospital,
Medical Genetics Center,
Ibn Sina Hospital
show all 7
OpenAlex ID:
A5103457874
Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome?
1997
·
S. Farah
, M. A. Sabry
, et al.
·
Clinical Genetics
·
24
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency
2005
·
M.Z. Seidahmed
, E.A. Alyamani
, et al.
·
American Journal of Medical Genetics Part A
·
23
Profile of Chromosomal Abnormalities in the Al Jahra Region of Kuwait
1999
·
R.L. Al-Naggar
, S.A. Mady
, et al.
·
Medical Principles and Practice
·
18
Neurologic Injury in Isolated Sulfite Oxidase Deficiency
2014
·
Thomas M. Bosley
, Ibrahim A. Alorainy
, et al.
·
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
·
17
PDF
Marinesco-Sjögren syndrome in a Bedouin family
2009
·
S. Farah
, M. A. Sabry
, et al.
·
Acta Neurologica Scandinavica
·
17
PDF
Successful long‐term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutation
2004
·
J. M. Stoler
, M. A. Sabry
, et al.
·
Journal of Inherited Metabolic Disease
·
17
Cutis Verticis Gyrata-Mental Deficiency syndrome: report of a case with unusual neuroradiological findings
1998
·
S Farah
, Tl Farag
, et al.
·
Clinical Dysmorphology
·
17
Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: new entity?
1997
·
S. Farah
, M.A. Sabry
, et al.
·
Clinical Neurology and Neurosurgery
·
14
Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome.
1998
·
M A Sabry
, M Zaki
, et al.
·
Journal of Medical Genetics
·
12
PDF
Craniofacial dyssynostosis with cryptorchidism and normal stature
1998
·
N.A. Al-Torki
, M.A. Sabry
, et al.
·
American Journal of Medical Genetics
·
10
Chromosome 15q11‐13 region and the autistic disorder
1998
·
M A Sabry
, T I Farag
·
Journal of Intellectual Disability Research
·
5
Phenylketonuria in Four Bedouin Sibs
2008
·
M.A. Mubashir
, T.I. Farag
, et al.
·
Medical Principles and Practice
·
1
Triophthalmia and facial clefting: a case report.
1998
·
S M Tayel
, M A Sabry
, et al.
·
Journal of Medical Genetics
·
1
PDF
Sjögren-Larsson Syndrome: Clinical and Neuroradiological Findings in an Institutionalized Bedouin Patient
2008
·
S. Farah
, M. Rudwan
, et al.
·
Medical Principles and Practice
Clustering of Major Chromosomal Abnormalities among Azoospermic Males in Kuwait: A Study of 280 Patients
2008
·
M.A. Sabry
, A.A. Al-Othman
, et al.
·
Medical Principles and Practice
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Works count:
15
Citation count:
176
H-index:
10
I10-index:
10
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