Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Salwa A Musa"'
Autor:
Asma Deeb, Jean-Pierre Chanoine, Jamal Raza, Amanda Rowlands, Abdulsalam Abu-Libdeh, Asmahane Ladjouze, Rasha T Hamza, Salwa A Musa, Farida Jennane, Bouferoua Fadila, Delileche Hana, Djahlat Larbi, Noumi Mustapha, Haya Alkhayyat, Abdourahman Douksie, Ali Rabbani, Ali Al-Jumaili, Rasha Odeh, Hessa Alkandari, Hala Tfayli, Suleiman Abusrewil, Millad Ghawil, Aisha Al senani, Fawziya Alkhalaf, Abdelhadi Habeb, Noman Ahmad, Omer Elshareef, Mohamed Abdullah, Olivia Al-Hassan, Dima Karah, Mongia Hachicha, Mohammed Alshakka
Publikováno v:
BMJ Global Health, Vol 6, Iss 10 (2021)
Congenital adrenal hyperplasia (CAH), if untreated, carries high morbidity and mortality. A higher incidence of CAH is expected in countries where consanguinity is common, such as in the countries of the WHO Eastern Mediterranean Region (EMRO). CAH i
Externí odkaz:
https://doaj.org/article/56dbc542be5c46a880a38a1bb10953e1
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-6 (2023)
Abstract Background Hyaline fibromatosis syndrome is a rare progressive autosomal recessive connective tissue disorder caused by a mutation in the ANTXR2/CMG2 gene. According to its severity, patients may present with skin nodules or visceral infiltr
Externí odkaz:
https://doaj.org/article/862ab6473bb04e0d88c284f387f5cbf7
Autor:
Ghassan Faisal Fadlalbari, Salwa Abdelbagi Musa, Samar Sabir Hassan, Areej Ahmed Ibrahim, Mohamed Ahmed Abdullah
Publikováno v:
Pan African Medical Journal. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a11f527c5d4a6d5e3e9b6bd25e941a04
https://doi.org/10.11604/pamj.2023.44.86.35649
https://doi.org/10.11604/pamj.2023.44.86.35649
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(7)
Objectives Delayed puberty is a common presentation to endocrine clinics, with adult height, sexual capability and fertility being the main concerns for the child and his/her family. Presentation is variable including short stature and/or absence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d297b5edd2dc592fb63620ab4e199efc
https://pubmed.ncbi.nlm.nih.gov/35671155
https://pubmed.ncbi.nlm.nih.gov/35671155
Autor:
Renson O Mukhwana, Salwa A. Musa, Mohamed A. Abdullah, Samar Sabir Hassan, Omer Babiker, Areej A. Ibrahim
Publikováno v:
Sudan J Paediatr
There is paucity of reported information regarding aetiology and clinical profile of hypopituitarism from resource-limited countries particularly in populations with high rates of consanguineous marriages. Here, we are reporting the first data on thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6016d3dfe32c4e1cb6d305c107c36be3
https://europepmc.org/articles/PMC8025993/
https://europepmc.org/articles/PMC8025993/
Autor:
Areej A. Ibrahim, Marlies Kempers, Mohamed A. Abdullah, Dorien Lugtenberg, Salwa A. Musa, Asmahan Tajelsir Abdallah, Samar Sabir Hassan
Publikováno v:
Pan African Medical Journal, 40
The Pan African Medical Journal
Pan African Medical Journal; Vol. 40 No. 1 (2021)
The Pan African Medical Journal
Pan African Medical Journal; Vol. 40 No. 1 (2021)
Contains fulltext : 243931.pdf (Publisher’s version ) (Open Access) Neonatal hyperparathyroidism is a rare disease caused by a homozygous inactivating mutation in the calcium sensing receptor gene. It presents early in life with life threatening ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f92bafdbb5e5f60d7859b3ac95f02a
https://hdl.handle.net/2066/243931
https://hdl.handle.net/2066/243931
Autor:
Asmahan T. Basheer, Ali M E Arabi, Areej A. Ibrahim, Samar Sabir Hassan, Mohamed A. Abdullah, Matthew B. Johnson, Salwa A. Musa
Publikováno v:
International Journal of Pediatric Endocrinology
BackgroundFanconi-Bickel syndrome (FBS) is a rare condition of carbohydrate metabolism, caused by a recessive defect in the facilitative glucose transporter GLUT2 encoded by theSLC2A2gene and characterized by a wide spectrum of phenotypical features.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5155156b93e1373f9b28b3e33f4fcb5b
https://pubmed.ncbi.nlm.nih.gov/33292488
https://pubmed.ncbi.nlm.nih.gov/33292488
Endocardiomiofibrose idiopática complicada com a realização de procedimento invasivo: relato de caso
Publikováno v:
Revista Eletrônica Acervo Científico. 9:e3286
Esse artigo buscou relatar e discutir sobre um caso de cardiomiopatia restritiva por endocardiomiofibrose. Paciente do sexo feminino, 63 anos, procedente do interior estado do Amazonas (AM), foi diagnosticada com cardiomiopatia restritiva por endocar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63afeba4d000ae53e0c0f5d767e4b793
https://doi.org/10.25248/reac.e3286.2020
https://doi.org/10.25248/reac.e3286.2020