Al Balwi MA - Search Results

1

Prevalence of Associated Endocrine Diseases in Patients with Neurofibromatosis Type 1.

Alshahrani A, Abuoliat Z, Alshahrani AS, Al Balwi MA. Alshahrani A, et al. Among authors: al balwi ma. Avicenna J Med. 2022 Feb 18;12(1):16-20. doi: 10.1055/s-0041-1742197. eCollection 2022 Jan. Avicenna J Med. 2022. PMID: 35586386 Free PMC article.

2

Prevalence of mixed hepatitis C virus (HCV) genotypes among recently diagnosed dialysis patients with HCV infection.

Al Balwi MA. Al Balwi MA. Saudi J Kidney Dis Transpl. 2011 Jul;22(4):712-6. Saudi J Kidney Dis Transpl. 2011. PMID: 21743215

3

Prevalence of BRCA1 and BRCA2 Mutations Among High-Risk Saudi Patients With Breast Cancer.

Abulkhair O, Al Balwi M, Makram O, Alsubaie L, Faris M, Shehata H, Hashim A, Arun B, Saadeddin A, Ibrahim E. Abulkhair O, et al. J Glob Oncol. 2018 Aug;4:1-9. doi: 10.1200/JGO.18.00066. J Glob Oncol. 2018. PMID: 30199306 Free PMC article.

4

Genetic Profile of Epidermolysis Bullosa Cases in King Abdulaziz Medical City, Riyadh, Saudi Arabia.

Alharthi R, Alnahdi MA, Alharthi A, Almutairi S, Al-Khenaizan S, AlBalwi MA. Alharthi R, et al. Front Genet. 2022 Feb 10;12:753229. doi: 10.3389/fgene.2021.753229. eCollection 2021. Front Genet. 2022. PMID: 35222512 Free PMC article.

5

The prevalence of CCR5-Δ32 mutation in a cohort of Saudi stem cell donors.

Alarifi M, Al-Amro F, Alalwan A, Al-Turki A, Fakhoury H, Atallah N, Al-Muallimi M, Al-Balwi M, Alzahrani M, Alaskar A, Hajeer A, Jawdat D. Alarifi M, et al. HLA. 2017 Nov;90(5):292-294. doi: 10.1111/tan.13100. Epub 2017 Aug 28. HLA. 2017. PMID: 28731615

6

HLA class II polymorphism in Saudi patients with multiple sclerosis.

Al Jumah M, Kojan S, Al Shehri AM, Al Balwi M, Al Abdulkarim I, Masuadi EM, Alhaidan Y, Alabdulrahman A, Fakhoury HM, Hajeer AH. Al Jumah M, et al. HLA. 2018 Jan;91(1):17-22. doi: 10.1111/tan.13173. Epub 2017 Dec 11. HLA. 2018. PMID: 29131543

7

Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening.

Alfadhel M, Umair M, Almuzzaini B, Alsaif S, AlMohaimeed SA, Almashary MA, Alharbi W, Alayyar L, Alasiri A, Ballow M, AlAbdulrahman A, Alaujan M, Nashabat M, Al-Odaib A, Altwaijri W, Al-Rumayyan A, Alrifai MT, Alfares A, AlBalwi M, Tabarki B. Alfadhel M, et al. Ann Clin Transl Neurol. 2019 Oct;6(10):2097-2103. doi: 10.1002/acn3.50898. Epub 2019 Sep 26. Ann Clin Transl Neurol. 2019. PMID: 31557427 Free PMC article.

8

Clinical course of myeloproliferative leukaemia virus oncogene (MPL) mutation-associated familial thrombocytosis: a review of 64 paediatric and adult patients.

Al-Harbi T, Al-Zahrani M, Al-Balwi M, Al-Hazmi A, Alsuhaibani A, Aljafn N, Alsumari F, Aleshaiwi L, Alsuhibani A, Alqasim O, Ahmad N. Al-Harbi T, et al. Br J Haematol. 2021 Sep;194(5):893-898. doi: 10.1111/bjh.17624. Epub 2021 Jun 15. Br J Haematol. 2021. PMID: 34131895

9

Pro106Leu MPL mutation is associated with thrombocytosis and a low risk of thrombosis, splenomegaly and marrow fibrosis.

Alzahrani M, Al Turki S, Al Rajban W, Alshalati F, Almodaihsh F, Abuelgasim KA, Alahmari B, Al Bogami T, Ali O, Al Harbi T, AlBalwi MA, Alotaibi M, Aleem A, Al Asker A, Al Mugairi A. Alzahrani M, et al. Platelets. 2022 Nov 17;33(8):1220-1227. doi: 10.1080/09537104.2022.2091773. Epub 2022 Jul 5. Platelets. 2022. PMID: 35791502

10

Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia.

Alfadhel M, Benmeakel M, Hossain MA, Al Mutairi F, Al Othaim A, Alfares AA, Al Balwi M, Alzaben A, Eyaid W. Alfadhel M, et al. Among authors: al mutairi f, al balwi m, al othaim a. Orphanet J Rare Dis. 2016 Sep 15;11(1):126. doi: 10.1186/s13023-016-0510-3. Orphanet J Rare Dis. 2016. PMID: 27629047 Free PMC article.

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