Mahmut Coker
Overview
Explore the profile of Mahmut Coker 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
96
Citations
720
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Yoldas Celik M, Canda E, Yazici H, Erdem F, Yuksel Yanbolu A, Aykut A, et al.
J Bone Miner Metab
. 2025 Jan;
PMID: 39827430
Introduction: Gaucher disease (GD) is a lysosomal storage disorder causing systemic and skeletal complications. This study evaluates bone health in adult GD type 1 patients, focusing on skeletal complications, bone...
2.
Yoldas Celik M, Yazici H, Erdem F, Yuksel Yanbolu A, Canda E, Sezer E, et al.
Pediatr Int
. 2024 Dec;
66(1):e15832.
PMID: 39697013
Background: Niemann-Pick type C (NPC) disease is a lysosomal storage disease with visceral organ involvement and neurological and psychiatric symptoms. This study presents the clinical and laboratory findings of NPC...
3.
Yoldas Celik M, Canda E, Yazici H, Erdem F, Yuksel Yanbolu A, Atik Altinok Y, et al.
Eur J Pediatr
. 2024 Dec;
184(1):72.
PMID: 39658645
Conclusion: The study underscores the importance of early diagnosis and intervention to mitigate severe neurological outcomes. Our findings highlight the need for incorporating GA1 into newborn screening programs to ensure...
4.
Canbay E, Canda E, Yazici H, Kasikci G, Durmaz B, Copur O, et al.
Lipids Health Dis
. 2024 Nov;
23(1):374.
PMID: 39538217
Aim: Elevated levels of cholesterol in the bloodstream, also referred to as hypercholesterolemia, pose a significant risk for the onset of cardiovascular and cerebrovascular diseases. Oxysterols, cholesterol-derived oxidized compounds that...
5.
Yazici H, Erdem F, Canda E, Ucar S, Coker M
J Clin Lipidol
. 2024 Nov;
19(1):167-172.
PMID: 39532566
Background: Autosomal recessive hypercholesterolemia (ARH) is an ultrarare dyslipidemia caused by variants in the LDLRAP1 gene. Clinically, this condition is indistinguishable from other homozygous familial hypercholesterolemia (HoFH). Case: We present...
6.
Korkmaz I, Ucar S, Onay H, Yildirim Sozmen E, Coker M, Palamar M
Turk J Ophthalmol
. 2024 Jun;
54(3):127-132.
PMID: 38940325
Objectives: To report ocular manifestations in patients with Fabry disease (FD) from a tertiary eye care center in Türkiye. Materials And Methods: This prospective, cross-sectional study included 30 eyes of...
7.
Ucar S, Atik Altinok Y, Mansuroglu Y, Canda E, Yazici H, Yoldas Celik M, et al.
J Inherit Metab Dis
. 2024 Apr;
47(5):1001-1017.
PMID: 38623712
Dietary lipid manipulation has recently been proposed for managing glycogen storage disease (GSD) type IIIa. This study aimed to evaluate the myopathic, cardiac, and metabolic status, physical activity, growth, and...
8.
Yoldas Celik M, Canda E, Yazici H, Erdem F, Yuksel Yanbolu A, Atik Altinok Y, et al.
Nutr Metab Cardiovasc Dis
. 2024 Mar;
34(7):1798-1806.
PMID: 38503616
Background And Aim: APO CII, one of several cofactors which regulate lipoprotein lipase enzyme activity, plays an essential role in lipid metabolism. Deficiency of APO CII is an ultra-rare autosomal...
9.
Canbay E, Sezer E, Canda E, Yazici H, Ucar S, Coker M, et al.
ACS Omega
. 2024 Feb;
9(7):7621-7633.
PMID: 38405530
Galactosemia is an inherited disease that occurs as a result of insufficient or no synthesis of some enzymes (GALT, GALK, and GALE) in galactose metabolism. Failure to make an early...
10.
Yazici H, Ak G, Yoldas Celik M, Erdem F, Yuksel Yanbolu A, Er E, et al.
J Pediatr Endocrinol Metab
. 2023 Nov;
37(1):33-41.
PMID: 37925743
Objectives: Carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive disorder of long-chain fatty acid oxidation. Three clinical phenotypes, lethal neonatal form, severe infantile hepatocardiomuscular form, and myopathic form,...