Mohammad Shagrani
Overview
Explore the profile of Mohammad Shagrani including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
296
Followers
0
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Recent Articles
1.
Maddirevula S, Shagrani M, Ji A, Horne C, Young S, Mather L, et al.
Genet Med
. 2024 Aug;
26(11):101231.
PMID: 39132680
Purpose: Pediatric cholestasis is the phenotypic expression of clinically and genetically heterogeneous disorders of bile acid synthesis and flow. Although a growing number of monogenic causes of pediatric cholestasis have...
2.
Felzen A, van Wessel D, Gonzales E, Thompson R, Jankowska I, Shneider B, et al.
JHEP Rep
. 2023 Jan;
5(2):100626.
PMID: 36687469
Background & Aims: Bile salt export pump (BSEP) deficiency frequently necessitates liver transplantation in childhood. In contrast to two predicted protein truncating mutations (PPTMs), homozygous p.D482G or p.E297G mutations are...
3.
Shagrani M, Kumar K, Baker A, Al-Awwami M, Alhussaini H, Almanea H, et al.
Transplant Direct
. 2022 Dec;
8(12):e1353.
PMID: 36479277
Methods: From November 2010 to June 2015, 176 children aged 0.2-to18 y were transplanted in the King Faisal Specialist Hospital and Research Center. Out of those, 19 children were transplanted...
4.
Thompson R, Arnell H, Artan R, Baumann U, Calvo P, Czubkowski P, et al.
Lancet Gastroenterol Hepatol
. 2022 Jul;
7(9):830-842.
PMID: 35780807
Background: Progressive familial intrahepatic cholestasis (PFIC) is a group of inherited paediatric liver diseases resulting from mutations in genes that impact bile secretion. We aimed to evaluate the effects of...
5.
Schulze M, Zidan A, Sturdevant M, Aljudaibi S, Shagrani M, Bzeizi K, et al.
Transplant Direct
. 2022 May;
8(6):e1332.
PMID: 35557991
Methods: Between January 2012 and September 2021, 20 donors with SCT were reviewed for age, gender, relation to the recipient, hemoglobin, hemoglobin S (HbS), surgical approach, intensive care unit stay,...
6.
Shamseldin H, Shaheen R, Ewida N, Bubshait D, Alkuraya H, Almardawi E, et al.
Genet Med
. 2022 Apr;
24(4):966.
PMID: 35394428
No abstract available.
7.
Zakaria H, Alobthani S, Elsarawy A, Saleh Y, Zidan A, Alabbad S, et al.
Pediatr Transplant
. 2021 Jun;
25(6):e14044.
PMID: 34076330
Background: There are still controversies in using the large left lateral segment in pediatrics LT, with the possibility of the problem of LFS grafts, and the use of monosegmental or...
8.
van Wessel D, Thompson R, Gonzales E, Jankowska I, Shneider B, Sokal E, et al.
Hepatology
. 2021 Mar;
74(2):892-906.
PMID: 33666275
Background And Aims: Mutations in ATPase phospholipid transporting 8B1 (ATP8B1) can lead to familial intrahepatic cholestasis type 1 (FIC1) deficiency, or progressive familial intrahepatic cholestasis type 1. The rarity of...
9.
Maddirevula S, Shamseldin H, Sirr A, AlAbdi L, Lo R, Ewida N, et al.
Front Genet
. 2021 Jan;
11:580484.
PMID: 33456446
There is a growing interest in standardizing gene-disease associations for the purpose of facilitating the proper classification of variants in the context of Mendelian diseases. One key line of evidence...
10.
van Wessel D, Thompson R, Gonzales E, Jankowska I, Sokal E, Grammatikopoulos T, et al.
J Hepatol
. 2020 Feb;
73(1):84-93.
PMID: 32087350
Background & Aims: Mutations in ABCB11 can cause deficiency of the bile salt export pump (BSEP), leading to cholestasis and end-stage liver disease. Owing to the rarity of the disease,...