Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mohammed, Fazalullah"'
Autor:
Allen W. Root, Saif Al-Yaarubi, John P. Cannon, Alicia Diaz-Thomas, Pallavi Iyer, Mohammed Fazalullah, Frank B. Diamond, Almundher Al-Maawali, O. Thomas Mueller
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 27(9-10)
BACKGROUND Neonatal severe primary hyperparathyroidism (NSHPT, MIM 239200) is most often an isolated disorder that is due to biallelic inactivating mutations in the CASR, the gene encoding the calcium sensing receptor; NSHPT is inherited from parents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fc5922cf5a3cd9e308a1bef4bafb1a0
https://pubmed.ncbi.nlm.nih.gov/24854525
https://pubmed.ncbi.nlm.nih.gov/24854525
Autor:
Roshan, Koul, Amna, Al-Futaisi, Alexander, Chacko, Mohammed, Fazalullah, Susan Al, Nabhani, Salah, Al-Awaidy, Suleiman, Al-Busaidy, Salim, Al-Mahrooqi
Publikováno v:
Oman medical journal. 23(3)
To find the incidence, clinical pattern and outcome of Guillain-Barre syndrome in the Sultanate of Oman in children less than 15 years of age.All children under fifteen years with acute flaccid paralysis were admitted to identify the underlying cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8685fc9f9298354f24d4b4611204c3d5
https://pubmed.ncbi.nlm.nih.gov/22359705
https://pubmed.ncbi.nlm.nih.gov/22359705