Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 2
2014 1
2016 4
2017 1
2019 2
2020 4
2021 4
2022 6
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

22 results

Results by year

Filters applied: . Clear all
Page 1
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.
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. Among authors: al hamed mh. 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
Favorable Effects of Octreotide in Congenital Chloride Diarrhea Associated With CKD.
Hussein MH, Alsohaibani F, Alrubaysh A, Al-Hamed MH, Alabdaljabar MS, Ullah A. Hussein MH, et al. Among authors: al hamed mh. Kidney Int Rep. 2022 Jun 16;7(9):2112-2115. doi: 10.1016/j.ekir.2022.06.004. eCollection 2022 Sep. Kidney Int Rep. 2022. PMID: 36090494 Free PMC article. No abstract available.
A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families.
Olinger E, Alawi IA, Al Riyami MS, Salmi IA, Molinari E, Faqeih EA, Al-Hamed MH, Barroso-Gil M, Powell L, Al-Hussaini AA, Rahim KA, Almontashiri NAM, Miles C, Shril S, Hildebrandt F, Consortium GER, Wilson IJ, Sayer JA. Olinger E, et al. Among authors: al hamed mh. Hum Mutat. 2021 Oct;42(10):1221-1228. doi: 10.1002/humu.24251. Epub 2021 Jul 26. Hum Mutat. 2021. PMID: 34212438 Free PMC article.
Recessive, Deleterious Variants in SMG8 Expand the Role of Nonsense-Mediated Decay in Developmental Disorders in Humans.
Alzahrani F, Kuwahara H, Long Y, Al-Owain M, Tohary M, AlSayed M, Mahnashi M, Fathi L, Alnemer M, Al-Hamed MH, Lemire G, Boycott KM, Hashem M, Han W, Al-Maawali A, Al Mahrizi F, Al-Thihli K, Gao X, Alkuraya FS. Alzahrani F, et al. Among authors: al hamed mh. Am J Hum Genet. 2020 Dec 3;107(6):1178-1185. doi: 10.1016/j.ajhg.2020.11.007. Epub 2020 Nov 25. Am J Hum Genet. 2020. PMID: 33242396 Free PMC article.
22 results