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Mahmoud M Qouqas
Observed names:
Mahmoud M. Qouqas,
Mahmoud Qouqas
Institution:
Hebron University
Observed institution:
Hebron University
ORCID:
0009-0007-1988-1820
Observed ORCID:
0009-0007-1988-1820
OpenAlex ID:
A5099104182
Deficiency of adenosine deaminase 2 leading to recurrent Hodgkin lymphoma: A case report
2024
·
Anas Manhal
, Mahmoud M Qouqas
, et al.
·
SAGE Open Medical Case Reports
·
5
Rare case of respiratory syncytial virus induced myocarditis in a neonate: A case report
2025
·
Lema S K Jaber
, Mo'ath Abu-hamdeh
, et al.
·
World Journal of Clinical Pediatrics
·
1
PDF
Pancrelipase as Adjunctive Therapy in Severe SCOT Deficiency: A Case of a Novel OXCT1 Gene Deletion
2025
·
Mo'ath Abu Hamdeh
, Lema Jaber
, et al.
·
JIMD Reports
·
1
PDF
Assessment of mental health and coping mechanisms among adolescents in Palestine: a cross-sectional study
2026
·
Anas Hussien
, Ahmad Fasfoos
, et al.
·
BMC Psychology
Seropositive rheumatoid arthritis in osteogenesis imperfecta type XI (FKBP10 mutation): first case report and literature review
2026
·
Anas Manhal
, Jamal Abdallah
, et al.
·
Orphanet Journal of Rare Diseases
PDF
Dry synovitis, RF-negative: a rare entity distinct from juvenile idiopathic arthritis
2025
·
Raghad Dghaish
, Mahmoud Qouqas
, et al.
·
Rheumatology Advances in Practice
PDF
Succinyl-Coa:3-Ketoacid-Coa Transferase (Scot) Deficiency in Infancy: A Case Report of Metabolic Disorder Linked to a Novel Oxct1 Deletion Mutation
2024
·
Mo'ath Abu Hamdeh
, Jamal Abdallah
, et al.
·
SSRN Electronic Journal
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Works count:
7
Citation count:
7
H-index:
1
I10-index:
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