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Year Number of Results
1999 1
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2007 2
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2011 2
2012 2
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2016 6
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57 results

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Page 1
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.
Buerger F, Salmanullah D, Liang L, Gauntner V, Krueger K, Qi M, Sharma V, Rubin A, Ball D, Lemberg K, Saida K, Merz LM, Sever S, Issac B, Sun L, Guerrero-Castillo S; Nephrotic Syndrome Study Network (NEPTUNE); Gomez AC, McNulty MT, Sampson MG, Al-Hamed MH, Saleh MM, Shalaby M, Kari J, Fawcett JP, Hildebrandt F, Majmundar AJ. Buerger F, et al. medRxiv [Preprint]. 2024 Mar 21:2024.03.17.24303374. doi: 10.1101/2024.03.17.24303374. medRxiv. 2024. PMID: 38562757 Free PMC article. Preprint.
Cystic fibrosis in a child from Syria.
Wahab AA, Janahi IA, Hebi S, al-Hamed M, Kambouris M. Wahab AA, et al. Ann Trop Paediatr. 2002 Mar;22(1):53-5. doi: 10.1179/027249302125000157. Ann Trop Paediatr. 2002. PMID: 11926050 Review.
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia.
Sheikh F, Alajlan H, Albanyan M, Alruwaili H, Alawami F, Sumayli S, Al Gazlan S, Abu Awwad S, Al-Dhekri H, Al-Saud B, Arnaout R, Alrayes H, Sayes N, Al-Hamed MH, Al-Mousa H, AlShareef S, Alazami AM. Sheikh F, et al. J Clin Immunol. 2023 Feb;43(2):479-484. doi: 10.1007/s10875-022-01399-y. Epub 2022 Nov 8. J Clin Immunol. 2023. PMID: 36348183
Novel pathogenic MAPKBP1 variant in a family with nephronophthisis.
Al-Hamed MH, Alzaidan H, Hussein M, Albaik L, Qari A, Sayer JA, Imtiaz F. Al-Hamed MH, et al. Clin Kidney J. 2020 Jun 24;14(2):728-730. doi: 10.1093/ckj/sfaa090. eCollection 2021 Feb. Clin Kidney J. 2020. PMID: 33623699 Free PMC article. No abstract available.
57 results