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1978 1
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2002 1
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2013 3
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2017 4
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31 results

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Page 1
Systemic Lupus Erythematosus and Cardiovascular Diseases: A Systematic Review.
Nor MA, Ogedegbe OJ, Barbarawi A, Ali AI, Sheikh IM, Yussuf FM, Adam SM, Hassan OA, Tabowei G, Jimoh A, Mejulu EO, Cheema AY. Nor MA, et al. Among authors: adam sm. Cureus. 2023 May 21;15(5):e39284. doi: 10.7759/cureus.39284. eCollection 2023 May. Cureus. 2023. PMID: 37346216 Free PMC article. Review.
Impact of A Multidisciplinary Team Discussion for Genetic Lung Fibrosis.
Franco G, Ba I, Nathan N, Guerin C, Lassus A, Kannengiesser C, Froidure A, Manali E, Bunel V, Bonniaud P, Bouvry D, Debray MP, Juge PA, Epaud R, Louvrier C, Plessier A, de Fontbrune FS, Wémeau-Stervinou L, Adam SM, Chabrol A, Maurac A, Savale L, Montani D, Raynal C, Konyukh M, Mageau A, Crestani B, Cottin V, de Becdelièvre A, Borie R; Respifil and OrphaLung. Franco G, et al. Among authors: adam sm. Respirology. 2025 Jun;30(6):523-532. doi: 10.1111/resp.70039. Epub 2025 Mar 26. Respirology. 2025. PMID: 40134350 Free PMC article.
MALARIA: A GENERAL MINIREVIEW WITH REFERENCE TO EGYPT.
Ahmad Saleh AM, Adam SM, Ibrahim AM, Morsy TA. Ahmad Saleh AM, et al. Among authors: adam sm. J Egypt Soc Parasitol. 2016 Apr;46(1):35-48. doi: 10.12816/0026148. J Egypt Soc Parasitol. 2016. PMID: 27363039 Review.
A bio-inspired heterodinuclear hydrogenase CoFe complex.
Sun L, Adam SM, Mokdad W, David R, Milet A, Artero V, Duboc C. Sun L, et al. Among authors: adam sm. Faraday Discuss. 2022 May 18;234(0):34-41. doi: 10.1039/d1fd00085c. Faraday Discuss. 2022. PMID: 35188161
Diffuse panbronchiolitis and IgA nephropathy.
Tossier C, Pilette C, Guilleminault L, Buchler M, de Muret A, Diot P, Adam SM. Tossier C, et al. Among authors: adam sm. Am J Respir Crit Care Med. 2014 Jan 1;189(1):106-9. doi: 10.1164/rccm.201307-1381LE. Am J Respir Crit Care Med. 2014. PMID: 24381993 No abstract available.
International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4.
Yildiz I, Sagliker Y, Demirhan O, Tunc E, Inandiklioglu N, Tasdemir D, Acharya V, Zhang L, Golea O, Sabry A, Ookalkar DS, Capusa C, Radulescu D, Garneata L, Mircescu G, Ben Maiz H, Chen CH, Prado Rome J, Benzegoutta M, Paylar N, Eyuboglu K, Karatepe E, Esenturk M, Yavascan O, Grzegorzevska A, Shilo V, Mazdeh MM, Francesco RC, Gouda Z, Adam SM, Emir I, Ocal F, Usta E, Kiralp N, Sagliker C, Ozkaynak PS, Sagliker HS, Bassuoni M, Sekin O. Yildiz I, et al. Among authors: adam sm. J Ren Nutr. 2012 Jan;22(1):157-61. doi: 10.1053/j.jrn.2011.10.030. J Ren Nutr. 2012. PMID: 22200434 Review.
31 results