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Page 1
Complications of intravascular intrauterine transfusion for Rh alloimmunization.
Alkhaibary A, Ali M, Tulbah M, Al-Nemer M, Khan RM, Al Mugbel M, Al Sahan N, Hassounah MM, Alshammari W, Kurdi WI. Alkhaibary A, et al. Among authors: al nemer m. Ann Saudi Med. 2021 Nov-Dec;41(6):313-317. doi: 10.5144/0256-4947.2021.313. Epub 2021 Dec 2. Ann Saudi Med. 2021. PMID: 34873935 Free PMC article.
Chorioangioma: a single tertiary care center retrospective study.
Saeed B, Tulbah A, Bintalib M, De Vol EB, Almogbel S, BaAli M, Bukhari H, Foudaneel M, Almutairi J, Mahfodh MB, Tulbah M, Alnemer M, Kurdi W. Saeed B, et al. J Perinat Med. 2023 Feb 23;51(5):664-674. doi: 10.1515/jpm-2021-0085. Print 2023 Jun 27. J Perinat Med. 2023. PMID: 36809315
Observational cohort study of perinatal outcomes of women with COVID-19.
Al-Hajjar S, Ibrahim L, Kurdi W, Tulbah M, Alnemer M, Bin Jabr M, Elsaidawi W, Binmanee A, Ali M, Bukhari H, Altuwaijri L, Allaboon R, Alghamdi R, Saeed B, Adi Y, Alhamlan F. Al-Hajjar S, et al. J Infect Public Health. 2022 Dec;15(12):1503-1507. doi: 10.1016/j.jiph.2022.11.007. Epub 2022 Nov 11. J Infect Public Health. 2022. PMID: 36427409 Free PMC article.
Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel.
Al-Hamed MH, Kurdi W, Alsahan N, Alabdullah Z, Abudraz R, Tulbah M, Alnemer M, Khan R, Al-Jurayb H, Alahmed A, Tahir AI, Khalil D, Edwards N, Al Abdulaziz B, Binhumaid FS, Majid S, Faquih T, El-Kalioby M, Abouelhoda M, Altassan N, Monies D, Meyer B, Sayer JA, Albaqumi M. Al-Hamed MH, et al. J Med Genet. 2016 May;53(5):338-47. doi: 10.1136/jmedgenet-2015-103469. Epub 2016 Feb 9. J Med Genet. 2016. PMID: 26862157 Free PMC article.
Molecular autopsy in maternal-fetal medicine.
Shamseldin HE, Kurdi W, Almusafri F, Alnemer M, Alkaff A, Babay Z, Alhashem A, Tulbah M, Alsahan N, Khan R, Sallout B, Al Mardawi E, Seidahmed MZ, Meriki N, Alsaber Y, Qari A, Khalifa O, Eyaid W, Rahbeeni Z, Kurdi A, Hashem M, Alshidi T, Al-Obeid E, Abdulwahab F, Ibrahim N, Ewida N, El-Akouri K, Al Mulla M, Ben-Omran T, Pergande M, Cirak S, Al Tala S, Shaheen R, Faqeih E, Alkuraya FS. Shamseldin HE, et al. Genet Med. 2018 Apr;20(4):420-427. doi: 10.1038/gim.2017.111. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28749478 Free article.
Lethal variants in humans: lessons learned from a large molecular autopsy cohort.
Shamseldin HE, AlAbdi L, Maddirevula S, Alsaif HS, Alzahrani F, Ewida N, Hashem M, Abdulwahab F, Abuyousef O, Kuwahara H, Gao X; Molecular Autopsy Consortium; Alkuraya FS. Shamseldin HE, et al. Genome Med. 2021 Oct 13;13(1):161. doi: 10.1186/s13073-021-00973-0. Genome Med. 2021. PMID: 34645488 Free PMC article.
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F. Al-Hamed MH, et al. Hum Genet. 2022 Jan;141(1):101-126. doi: 10.1007/s00439-021-02406-9. Epub 2021 Dec 1. Hum Genet. 2022. PMID: 34853893
21 results