AlBalwi MA - Search Results

1

Ichthyosis Prematurity Syndrome: A Rare Form but Easily Recognizable Ichthyosis.

Al-Khenaizan S, AlSwailem A, AlBalwi MA. Al-Khenaizan S, et al. Among authors: albalwi ma. Case Rep Dermatol. 2021 Sep 21;13(3):470-473. doi: 10.1159/000519035. eCollection 2021 Sep-Dec. Case Rep Dermatol. 2021. PMID: 34720920 Free PMC article.

2

A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient.

Ayoub N, Al-Khenaizan S, Sonbol H, Albreakan R, AlSufyani M, AlBalwi M. Ayoub N, et al. Int J Dermatol. 2015 Jun;54(6):e233-5. doi: 10.1111/ijd.12770. Epub 2015 Jan 20. Int J Dermatol. 2015. PMID: 25601417 No abstract available.

3

Peeling of skin as presenting manifestation in congenital disorders of glycosylation.

Almutairi M, Al-Khenaizan S, Al Sufiani F, Al Balwi M, Al Mutairi F. Almutairi M, et al. J Dermatol. 2020 Sep;47(9):e335-e336. doi: 10.1111/1346-8138.15459. Epub 2020 Jun 11. J Dermatol. 2020. PMID: 32525245 No abstract available.

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. Among authors: albalwi ma. Front Genet. 2022 Feb 10;12:753229. doi: 10.3389/fgene.2021.753229. eCollection 2021. Front Genet. 2022. PMID: 35222512 Free PMC article.

5

Coexistence of chronic myeloid leukemia and diffuse large B-cell lymphoma with antecedent chronic lymphocytic leukemia: a case report and review of the literature.

Abuelgasim KA, Rehan H, Alsubaie M, Al Atwi N, Al Balwi M, Alshieban S, Almughairi A. Abuelgasim KA, et al. J Med Case Rep. 2018 Mar 11;12(1):64. doi: 10.1186/s13256-018-1612-4. J Med Case Rep. 2018. PMID: 29524963 Free PMC article. Review.

6

Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome.

Ababneh FK, AlSwaid A, Youssef T, Al Azzawi M, Crosby A, AlBalwi MA. Ababneh FK, et al. Among authors: albalwi ma. Am J Med Genet A. 2013 Dec;161A(12):3155-60. doi: 10.1002/ajmg.a.36160. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 24039075

7

Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial.

Arabi YM, Al-Balwi M, Hajeer AH, Jawdat D, Sadat M, Al-Dorzi HM, Tamim H, Afesh L, Almashaqbeh W, Alkadi H, Alwadaani D, UdayaRaja GK, Abdulkareem IBA, Al-Dawood A. Arabi YM, et al. Sci Rep. 2018 Dec 20;8(1):17984. doi: 10.1038/s41598-018-36007-w. Sci Rep. 2018. PMID: 30573851 Free PMC article. Clinical Trial.

8

Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children.

Alhaidan Y, Larsen MJ, Schou AJ, Stenlid MH, Al Balwi MA, Christesen HT, Brusgaard K. Alhaidan Y, et al. Sci Rep. 2020 Feb 7;10(1):2114. doi: 10.1038/s41598-020-58845-3. Sci Rep. 2020. PMID: 32034166 Free PMC article.

9

The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort.

Al Ammari M, AlBalwi M, Sultana K, Alabdulkareem IB, Almuzzaini B, Almakhlafi NS, Aldrees M, Alghamdi J. Al Ammari M, et al. Sci Rep. 2020 Jul 15;10(1):11613. doi: 10.1038/s41598-020-68519-9. Sci Rep. 2020. PMID: 32669629 Free PMC article.

10

Congenital duplication of the palm syndrome.

Al-Qattan MM, Eyaid W, Al-Balwi M. Al-Qattan MM, et al. Ann Plast Surg. 2007 Sep;59(3):341-3. doi: 10.1097/01.sap.0000251486.89375.03. Ann Plast Surg. 2007. PMID: 17721228

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

95 results

Search Page