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A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.
J Hum Genet. 2013 Jul;58(7):480-9. doi: 10.1038/jhg.2013.27. Epub 2013 Apr 18.
J Hum Genet. 2013.
PMID: 23595123
Novel mutations underlying nephrogenic diabetes insipidus in Arab families.
Carroll P, Al-Mojalli H, Al-Abbad A, Al-Hassoun I, Al-Hamed M, Al-Amr R, Butt AI, Meyer BF.
Carroll P, et al. Among authors: al hassoun i.
Genet Med. 2006 Jul;8(7):443-7. doi: 10.1097/01.gim.0000223554.46981.7a.
Genet Med. 2006.
PMID: 16845277
Free article.
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A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family.
Al-Hamed M, Sayer JA, Al-Hassoun I, Aldahmesh MA, Meyer B.
Al-Hamed M, et al. Among authors: al hassoun i.
NDT Plus. 2010 Dec;3(6):545-8. doi: 10.1093/ndtplus/sfq149. Epub 2010 Aug 26.
NDT Plus. 2010.
PMID: 25949463
Free PMC article.
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Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.
Gee HY, Otto EA, Hurd TW, Ashraf S, Chaki M, Cluckey A, Vega-Warner V, Saisawat P, Diaz KA, Fang H, Kohl S, Allen SJ, Airik R, Zhou W, Ramaswami G, Janssen S, Fu C, Innis JL, Weber S, Vester U, Davis EE, Katsanis N, Fathy HM, Jeck N, Klaus G, Nayir A, Rahim KA, Al Attrach I, Al Hassoun I, Ozturk S, Drozdz D, Helmchen U, O'Toole JF, Attanasio M, Lewis RA, Nürnberg G, Nürnberg P, Washburn J, MacDonald J, Innis JW, Levy S, Hildebrandt F.
Gee HY, et al. Among authors: al hassoun i.
Kidney Int. 2014 Apr;85(4):880-7. doi: 10.1038/ki.2013.450. Epub 2013 Nov 20.
Kidney Int. 2014.
PMID: 24257694
Free PMC article.
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Clinical significance of IgM deposition in pediatric minimal change disease.
Al Romaili DM, Al-Hussain TO, Awad HS, Saadeh SA, Al-Hassoun IA, Al-Shareef TA.
Al Romaili DM, et al. Among authors: al hassoun ia.
Int J Pediatr Adolesc Med. 2019 Dec;6(4):146-150. doi: 10.1016/j.ijpam.2019.09.001. Epub 2019 Sep 12.
Int J Pediatr Adolesc Med. 2019.
PMID: 31890840
Free PMC article.
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