Al Shibli A - Search Results

1

Bradycardia following oral corticosteroid use: case report and literature review.

Al Shibli A, Al Attrach I, Hamdan MA. Al Shibli A, et al. Among authors: al attrach i. Arab J Nephrol Transplant. 2012 Jan;5(1):47-9. Arab J Nephrol Transplant. 2012. PMID: 22283866 Review.

2

Lupus cystitis in an Omani girl.

Al-Shibli A, Al-Salam S, Bernieh B, Matta H, Al Attrach I. Al-Shibli A, et al. Among authors: al salam s, al attrach i. Saudi J Kidney Dis Transpl. 2010 Sep;21(5):943-6. Saudi J Kidney Dis Transpl. 2010. PMID: 20814138

3

Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia.

Al-Shibli A, Al Attrach I, Willems PJ. Al-Shibli A, et al. Among authors: al attrach i. Pediatr Nephrol. 2011 Jul;26(7):1167-70. doi: 10.1007/s00467-011-1835-8. Epub 2011 Mar 12. Pediatr Nephrol. 2011. PMID: 21399899

4

Systemic lupus erythematosus with severe nephritis that mimicked Henoch-Schoenlein purpura.

Al-Attrach I, Al-Shibli A, Al-Riyami L, Al-Salam S. Al-Attrach I, et al. Among authors: al salam s, al shibli a, al riyami l. Arab J Nephrol Transplant. 2011 Sep;4(3):159-61. doi: 10.4314/ajnt.v4i3.71029. Arab J Nephrol Transplant. 2011. PMID: 22026341

5

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): report of three cases with a novel mutation in CLDN19 gene.

Al-Shibli A, Konrad M, Altay W, Al Masri O, Al-Gazali L, Al Attrach I. Al-Shibli A, et al. Among authors: al gazali l, al attrach i, al masri o. Saudi J Kidney Dis Transpl. 2013 Mar;24(2):338-44. doi: 10.4103/1319-2442.109601. Saudi J Kidney Dis Transpl. 2013. PMID: 23538362

6

Uric acid excretion in rotavirus gastro-enteritis.

Al-Shibli A, Al Tatari H, Al Ameri A, Ghatasheh G, Issah M, Al Attrach I, Narchi H. Al-Shibli A, et al. Among authors: al ameri a, al attrach i, al tatari h. Paediatr Int Child Health. 2014 Feb;34(1):19-23. doi: 10.1179/2046905513Y.0000000077. Epub 2013 Dec 6. Paediatr Int Child Health. 2014. PMID: 23921092

7

Mild phenotypic expression of a heterozygous mutation in NPHS1 gene.

Al-Shibli A, Al Kaabi S, Abou Najab I. Al-Shibli A, et al. Among authors: al kaabi s. Arab J Nephrol Transplant. 2014 May;7(2):137-8. Arab J Nephrol Transplant. 2014. PMID: 25366512 No abstract available.

8

Unusual Presentation of a Hemiplegic Migraine in a Seven-Year-Old Child: A Case Report.

Alebaji MB, Ani MA, Rozieh SA, Al Shibli AI. Alebaji MB, et al. Among authors: al shibli ai. Cureus. 2023 Mar 27;15(3):e36726. doi: 10.7759/cureus.36726. eCollection 2023 Mar. Cureus. 2023. PMID: 37123759 Free PMC article.

9

Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations.

Al Shibli A, Narchi H. Al Shibli A, et al. World J Methodol. 2015 Jun 26;5(2):55-61. doi: 10.5662/wjm.v5.i2.55. eCollection 2015 Jun 26. World J Methodol. 2015. PMID: 26140272 Free PMC article.

10

Hyponatraemia and neurological complications in children admitted with bronchiolitis.

Al Shibli A, Abukhater D, Al Kuwaiti N, Noureddin MB, Al Harbi M, Al Kaabi A, Al Kaabi S, Hamie M, Al Amri A, Narchi H. Al Shibli A, et al. Among authors: al kaabi a, al harbi m, al kuwaiti n, al amri a, al kaabi s. Paediatr Int Child Health. 2016 Aug;36(3):175-80. doi: 10.1080/20469047.2016.1162390. Epub 2016 Apr 15. Paediatr Int Child Health. 2016. PMID: 27079908

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