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Mahmoud Fawzi Elsaid
Mahmoud Fawzi Elsaid
Verified email at hamad.qa
Title
Cited by
Cited by
Year
Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study
COVIDSurg Collaborative
Anaesthesia 76 (6), 748-758, 2021
555*2021
SARS-CoV-2 infection and venous thromboembolism after surgery: an international prospective cohort study.
C COVIDSurg, C GlobalSurg
Anaesthesia 77 (1), 28-39, 2022
1002022
Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia
MF Elsaid, N Chalhoub, T Ben‐Omran, P Kumar, H Kamel, K Ibrahim, ...
Annals of neurology 81 (1), 68-78, 2017
822017
Recurrence risk after a first febrile convulsion
MS Bessisso, MF Elsaid, NA Almula, NK Kadomi, SH Zeidan, SB Azzam, ...
Saudi medical journal 22 (3), 254-258, 2001
742001
Autosomal recessive inheritance of GLUT1 deficiency syndrome
J Klepper, H Scheffer, MF Elsaid, EJ Kamsteeg, M Leferink, T Ben-Omran
Neuropediatrics 40 (05), 207-210, 2009
712009
A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population
MF El‐Said, R Badii, MS Bessisso, N Shahbek, MG El‐Ali, M El‐Marikhie, ...
Human mutation 27 (7), 719-719, 2006
612006
Effects of pre‐operative isolation on postoperative pulmonary complications after elective surgery: an international prospective cohort study
COVIDSurg Collaborative, GlobalSurg Collaborative, D Nepogodiev, ...
Anaesthesia 76 (11), 1454-1464, 2021
432021
Gene therapy for spinal muscular atrophy: the Qatari experience
HG Ali, K Ibrahim, MF Elsaid, RB Mohamed, MIA Abeidah, AO Al Rawwas, ...
Gene Therapy 28 (10), 676-680, 2021
402021
Altered PLP1 splicing causes hypomyelination of early myelinating structures
SH Kevelam, JR Taube, RML van Spaendonk, E Bertini, K Sperle, ...
Annals of clinical and translational neurology 2 (6), 648-661, 2015
352015
Neuro-imaging evaluation after the first afebrile seizure in children: A retrospective observational study
R Al-Shami, AM Khair, M Elseid, K Ibrahim, A Al-Ahmad, A Elsetouhy, ...
Seizure 43, 26-31, 2016
342016
Pattern of headache in school children in the State of Qatar.
MS Bessisso, A Bener, MF Elsaid, FA Al-Khalaf, KA Huzaima
Saudi medical journal 26 (4), 566-570, 2005
332005
W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report
L Elsaadany, M El-Said, R Ali, H Kamel, T Ben-Omran
BMC Medical Genetics 17, 1-6, 2016
322016
Novel hypomyelinating leukoencephalopathy affecting early myelinating structures
ME Steenweg, NI Wolf, JH Schieving, MF Elsaid, RL Friederich, ...
Archives of neurology 69 (1), 125-128, 2012
282012
Acute bacterial meningitis in Qatar
MF Elsaid, AA Flamerzi, MS Bessisso, SS Elshafie
Saudi medical journal 27 (2), 198, 2006
282006
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy
S Lakhani, R Doan, M Almureikhi, JN Partlow, M Al Saffar, MF Elsaid, ...
European Journal of Medical Genetics 60 (5), 245-249, 2017
252017
Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance
P Kumar, M Al-Shafai, WA Al Muftah, N Chalhoub, MF Elsaid, AA Aleem, ...
BMC Research Notes 7, 1-13, 2014
202014
Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum
MF Elsaid, H Kamel, N Chalhoub, NA Aziz, K Ibrahim, T Ben-Omran, ...
Am J Med Genet A 164 (6), 1614-1617, 2014
202014
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant
AA Aleem, MF Elsaid, N Chalhoub, A Chakroun, KAS Mohamed, ...
Neuromuscular Disorders 30 (6), 457-471, 2020
192020
NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup
MF Elsaid, K Ibrahim, N Chalhoub, A Elsotouhy, N El Mudehki, ...
BMC Medical Genetics 18, 1-7, 2017
182017
Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency?
MF Elsaid, A Bener, M Lindner, M Alzyoud, N Shahbek, MO Abdelrahman, ...
Molecular genetics and metabolism 92 (1-2), 100-103, 2007
182007
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