Ibrahim Elsharkawi
Overview
Explore the profile of Ibrahim Elsharkawi including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
13
Citations
82
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Skotko B, Garza Flores A, Elsharkawi I, Patsiogiannis V, McDonough M, Verda D, et al.
Am J Med Genet A
. 2022 Nov;
191(2):518-525.
PMID: 36426646
Detecting obstructive sleep apnea (OSA) is important to both prevent significant comorbidities in people with Down syndrome (DS) and untangle contributions to other behavioral and mental health diagnoses. However, laboratory-based...
2.
Elsharkawi I, Wongkittichote P, Daniel E, Starosta R, Ueda K, Ng B, et al.
J Inherit Metab Dis
. 2022 Oct;
46(1):92-100.
PMID: 36214423
Congenital disorders of glycosylation (CDG) are a group of heterogeneous inherited metabolic disorders affecting posttranslational protein modification. DDOST-CDG, caused by biallelic pathogenic variants in DDOST which encodes dolichyl-diphospho-oligosaccharide-protein glycosyltransferase, a...
3.
Said J, Pithadia D, Snyder E, Elsharkawi I, Lin A, Lilly E
J Am Acad Dermatol
. 2021 Oct;
87(2):476-479.
PMID: 34688825
No abstract available.
4.
Uguen K, Krysiak K, Audebert-Bellanger S, Redon S, Benech C, Viora-Dupont E, et al.
Clin Genet
. 2021 Jun;
100(4):386-395.
PMID: 34164801
13q12.3 microdeletion syndrome is a rare cause of syndromic intellectual disability. Identification and genetic characterization of patients with 13q12.3 microdeletion syndrome continues to expand the phenotypic spectrum associated with it....
5.
Kan S, Elsharkawi I, Le S, Prill H, Mangini L, Cooper J, et al.
Mol Genet Metab
. 2021 Apr;
133(2):185-192.
PMID: 33839004
Mucopolysaccharidosis IIIB (MPS IIIB, Sanfilippo syndrome type B) is caused by a deficiency in α-N-acetylglucosaminidase (NAGLU) activity, which leads to the accumulation of heparan sulfate (HS). MPS IIIB causes progressive...
6.
Kitcharoensakkul M, Aluri J, Elsharkawi I, Steed A, Putnam C, Swayampakula A, et al.
J Clin Immunol
. 2021 Mar;
41(6):1352-1355.
PMID: 33712943
No abstract available.
7.
Chung J, Donelan K, Macklin E, Schwartz A, Elsharkawi I, Torres A, et al.
Genet Med
. 2020 Nov;
23(1):236.
PMID: 33169000
No abstract available.
8.
Chung J, Donelan K, Macklin E, Schwartz A, Elsharkawi I, Torres A, et al.
Genet Med
. 2020 Sep;
23(1):163-173.
PMID: 32879436
Purpose: We sought to determine if a novel online health tool, called Down Syndrome Clinic to You (DSC2U), could improve adherence to national Down syndrome (DS) guidelines. We also sought...
9.
Elsharkawi I, Parambath D, Saber-Ayad M, Khan A, El-Serafi A
Hum Cell
. 2019 Nov;
33(1):1-9.
PMID: 31755075
Diabetes is a worldwide health problem with increasing incidence. The current management modalities did not succeed to decrease comorbidities. This study aimed at enhancing the regenerative solution for diabetes by...
10.
Karaa A, Elsharkawi I, Clapp M, Balcells C
Mitochondrion
. 2018 Jul;
46:214-220.
PMID: 29990538
A retrospective survey assessed the gynecologic, obstetric and fertility history of 103 women with mitochondrial disease (MD)/dysfunction (Md) aged 16 to 75 who had previously been pregnant. Most participants (34%)...