Mehmet Gunduz
Overview
Explore the profile of Mehmet Gunduz including associated specialties, affiliations and a list of published articles.
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Articles
245
Citations
2917
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0
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Recent Articles
1.
Civelek-Urey B, Kasapkara C, Biberoglu G, Oktem R, Gunduz M, Kireker-Koylu O, et al.
Klin Padiatr
. 2024 Sep;
PMID: 39321830
Lysosomal storage disorders (LSD) are a group of inherited inborn metabolism errors that are characterized by a deficiency in the lysosomal enzyme. In patients with suspected lipid storage disorders, confirmation...
2.
Yilmaz B, Ceylan A, Gunduz M, Uzun O, Kucukcongar Yavas A, Bilginer Gurbuz B, et al.
Eur J Pediatr
. 2023 Dec;
183(3):1341-1351.
PMID: 38141137
Biotinidase deficiency (BD) is an autosomal recessive inherited metabolic disorder which results from the inability of biotin-dependent carboxylase enzymes to function due to the release and absorption of biotin, leading...
3.
Okulu E, Hirfanoglu I, Satar M, Erdeve O, Koc E, Ozlu F, et al.
PLoS One
. 2023 Dec;
18(12):e0295759.
PMID: 38096201
Background: Hypoxic ischemic encephalopathy (HIE) is a significant cause of mortality and short- and long-term morbidities. Therapeutic hypothermia (TH) has been shown to be the standard care for HIE of...
4.
Gunduz M, Gunduz B, Tubas F, Dulkadir R, Cakir B, Camurdan A, et al.
Epileptic Disord
. 2023 Nov;
26(1):79-89.
PMID: 37930114
Objective: Paroxysmal non-epileptic events (PNEs) are a group of disorders that may be misdiagnosed as epilepsy. This study has aimed to assess the knowledge and practices of family physicians and...
5.
Gunduz M, Yuksel Gudek Y, Kasapkara C
Orphanet J Rare Dis
. 2023 Jul;
18(1):179.
PMID: 37415155
Aim: The implementation of newborn screening programs for inborn errors of metabolism has advanced the diagnosis and management of affected infants and undoubtedly improved their outcomes. We aimed to determine...
6.
Kasapkara C, Ceylan A, Yilmaz D, Kireker Koylu O, Yurek B, Civelek Urey B, et al.
Mol Syndromol
. 2023 Feb;
14(1):30-34.
PMID: 36777709
Introduction: Neuronal ceroid lipofuscinoses (NCLs) are a broad class of inherited lysosomal storage disorders. Known mutations in at least 13 different genes can result in NCL with variable ages of...
7.
Akcora-Yildiz D, Ozkan T, Ozen M, Gunduz M, Sunguroglu A, Beksac M
Mol Biol Rep
. 2022 Dec;
50(2):1565-1573.
PMID: 36515823
Background: Multiple myeloma (MM), characterized by extensive genomic instability and aberrant DNA damage repair, is a plasma cell malignancy due to the excessive proliferation of monoclonal antibody-producing plasma cells in...
8.
Kayikci O, Mehtap O, Sari I, Demirkan F, Beyan C, Cetin G, et al.
Turk J Haematol
. 2022 Jun;
39(3):170-177.
PMID: 35678126
Objective: Peripheral T-cell lymphomas (PTCLs) are an uncommon and quite heterogeneous group of disorders, representing only 10%-15% of all non-Hodgkin lymphomas. Although both molecular and clinical studies have increased in...
9.
Ceran F, Akinci S, Ucar M, Korkmaz G, Gunduz M, Cavdarli B, et al.
Turk J Haematol
. 2022 May;
39(3):196-203.
PMID: 35620443
Objective: Achieving an early molecular response (EMR) is crucial for improving the prognosis of patients with chronic myeloid leukemia (CML). The halving time (HT) and reduction ratio (RR) of transcript...
10.
Islamoglu M, Dokur M, Uysal B, Gunduz M
Turk J Emerg Med
. 2022 May;
22(2):111-113.
PMID: 35529027
Coronavirus disease-2019 continues to have a serious impact in countries with the effect of new variant viruses emerging with mutations. While the effectiveness and protection of the vaccine have been...