Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Daoud, Ali Mohamed"'
Autor:
Hanane Charaf, Rachida Zahraoui, Mouna Soualhi, Nezha Rguig, Jamal Eddine Bourkadi, Daoud Ali Mohamed, Nasser Ittimad
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-8 (2022)
Abstract Background Granulomatosis with polyangiitis is a systemic inflammatory disease characterized by necrotizing vasculitis that affects small- and medium-sized blood vessels. Granulomatous inflammation affects the lungs, ears, nose, and throat,
Externí odkaz:
https://doaj.org/article/f938a64270bf46a3867f440f76e0f4d2
Autor:
Daoud Ali Mohamed MhD, Amarkak Waiss MhD, Behyamet Onka MhD, Walid Mohamed MhD, Nazik Allali PhD, Latifa Chat PhD, Siham El Haddad PhD
Publikováno v:
Global Pediatric Health, Vol 8 (2021)
Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypox
Externí odkaz:
https://doaj.org/article/6f7d3ee3d65745c7b9c294ac5a806bd5
Autor:
Daoud Ali Mohamed MD, Arthur Semedo MD, Boris Adeyemi MD, Leila Hessissen MD, Maria El Kababri PhD, Nazik Allali PhD, Latifa Chat PhD, Siham El Haddad MD
Publikováno v:
Global Pediatric Health, Vol 8 (2021)
Chemotherapy may be responsible for central and/or peripheral neurotoxicity. These neurological complications are frequent but little known. Some molecules are more providers, responsible for acute or late complications, sometimes not reversible. Som
Externí odkaz:
https://doaj.org/article/124e8f6eb1f7416795cef6a168b11af4
Publikováno v:
Case Reports in Radiology, Vol 2021 (2021)
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare disorder associated with brain iron accumulation caused by a recessive mutation in pantothenate kinase 2 gene (PANK2). We present a case of an 11 year-old boy presenting extrapyramidal
Externí odkaz:
https://doaj.org/article/9dec0ab840b9478da4df65a67ff13e13
Publikováno v:
International Journal of Case Reports and Images. 13:160-163
No Abstract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9caadfbf4bd1b0f42612c1b3fa33af33
https://doi.org/10.5348/101351z01an2022ci
https://doi.org/10.5348/101351z01an2022ci
Autor:
Firdaous Touarsa, Daoud Ali Mohamed, Behyamet Onka, Soufiane Rostoum, Najwa Ech-Cherif El Kettani, Meriem Fikri, Mohamed Jiddane
Publikováno v:
BJR|case reports. 8
Aceruloplasminemia is a rare autosomal recessive disorder of iron accumulation in the brain. It is one of the subtypes of Neurodegeneration with brain iron accumulation and is characterized by the uniform involvement of all basal ganglia, thalami, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b28be4db6a28e0f5653a918801a44281
https://doi.org/10.1259/bjrcr.20220035
https://doi.org/10.1259/bjrcr.20220035
Autor:
Behyamet Onka, Daoud ali Mohamed, Romeo Thierry Tessi Yehouenou, Boris Adeyemi, Wend-Yam Mohammed Traore, Mbina Mbougou Kevin arthur, Hounayda Jerguigue, Rachida Latib, Youssef Omor
Publikováno v:
BJR|case reports. 8
lynch syndrome (LS) is an autosomal dominant genetic disorder with incomplete penetration caused by a germline mutation in one of the genes of the deoxyribonucleic acid (DNA) mismatch repair system (MMR) namely: mutL homolog 1 (MLH1), mutS homolog 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5ea64d9e1062beee3d60b5fd1611d69
https://doi.org/10.1259/bjrcr.20210230
https://doi.org/10.1259/bjrcr.20210230
Autor:
Fatima Zohra Benmoula, Behyamet Onka, Wend-Yam Mohamed Traore, Ittimade Nassar, Daoud Ali Mohamed, Selma Khouchoua, Nabil Moatassim Billah
Publikováno v:
BJR|case reports. 7
The hydatid cyst is a worldwide anthropozoonosis, which constitutes a health issue in Northern Africa. It may involve any organ, but it mostly affects the liver. This often asymptomatic disease can lead to multiple complications. Among them, spontane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::667fd2af079aa33c51d59a646edf8ec3
https://doi.org/10.1259/bjrcr.20210087
https://doi.org/10.1259/bjrcr.20210087
Autor:
Abide, Zakaria, Daoud, Ali Mohamed, Latib, Rachida, Omor, Youssef, Mahdi, Youssef, Khannoussi, Basma EL
Publikováno v:
In Radiology Case Reports August 2023 18(8):2810-2813
Autor:
Nazik Allali, Latifa Chat, Daoud Ali Mohamed, Siham El Haddad, Behyamet Onka, Walid Mohamed, Amarkak Waiss
Publikováno v:
Global Pediatric Health
Global Pediatric Health, Vol 8 (2021)
Global Pediatric Health, Vol 8 (2021)
Pulmonary Arteriovenous Malformations (PAVMs) are structurally abnormal vascular communications between pulmonary arteries and pulmonary veins, which bypass the normal capillary bed and cause a low resistance right-to-left shunt with refractory hypox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c30065406a2c2cf44e5f7858d9c8adb7
https://doi.org/10.1177/2333794x211051186
https://doi.org/10.1177/2333794x211051186