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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
H Gacaferi, GS Collaborative, COVIDSurg Collaborative
Anaesthesia 76 (6), 2021
534*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
792017
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
692009
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
692001
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
692001
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
602006
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
602006
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
422021
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
372021
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
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
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
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
322016
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
Acute bacterial meningitis in Qatar
MF Elsaid, AA Flamerzi, MS Bessisso, SS Elshafie
Saudi medical journal 27 (2), 198, 2006
282006
Acute bacterial meningitis in Qatar
MF Elsaid, AA Flamerzi, MS Bessisso, SS Elshafie
Saudi medical journal 27 (2), 198, 2006
282006
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
262012
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
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