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Mesut Parlak
Observed names:
M Parlak,
Parlak Mesut
Institution:
Akdeniz University
Observed institutions:
Ministry of Health,
Akdeniz University,
Pediatric Nephrology of Alabama,
Akdeniz University Hospital,
Antalya Eğitim ve Araştırma Hastanesi,
Gaziantep University
show all 6
ORCID:
0000-0001-9692-8396
Observed ORCID:
0000-0001-9692-8396
OpenAlex ID:
A5043765535
A Combination of Nifedipine and Octreotide Treatment in an Hyperinsulinemic Hypoglycemic Infant
2014
·
Erdem Durmaz
, Sarah E. Flanagan
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
26
PDF
Serum anti-Müllerian hormone levels in euthyroid adolescent girls with Hashimoto's thyroiditis: relationship to antioxidant status
2016
·
Onur Erol
, Mesut Parlak
, et al.
·
European Journal of Obstetrics & Gynecology and Reproductive Biology
·
25
The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population
2019
·
Ayca Dundar
, Ruslan Bayramov
, et al.
·
Molecular Biology Reports
·
15
A novel splice site mutation of the beta subunit gene of epithelial sodium channel (ENaC) in one Turkish patient with a systemic form of pseudohypoaldosteronism type 1
2012
·
Cagla Serpil Dogan
, Durmaz Erdem
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
11
Psychiatric Disorders and Peer-Victimization in Children and Adolescents With Growth Hormone Deficiency
2022
·
Özge Gizli Çoban
, Aynur Bedel
, et al.
·
Clinical Pediatrics
·
9
Effects of the Gonadotropin-Releasing Hormone Agonist Therapy on Growth and Body Mass Index in Girls with Idiopathic Central Precocious Puberty
2022
·
Z Donbaloglu
, A Bedel
, et al.
·
Acta Endocrinologica (Bucharest)
·
9
Try235Phe homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Turkish patient
2014
·
Mesut Parlak
, Erdem Durmaz
, et al.
·
Annals of Saudi Medicine
·
8
Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche
2016
·
Mesut Parlak
, Doğa Türkkahraman
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
7
PDF
Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder
2025
·
Berna Singin
, Zeynep Donbaloğlu
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
6
PDF
Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population
2019
·
Sema Hepsen
, Erman Cakal
, et al.
·
Gynecological Endocrinology
·
6
High-Dose Hook Effect in 17-Hydroxyprogesterone Assay in a Patient with 21-Hydroxylase Deficiency
2015
·
Mesut Parlak
, Hamit Yaşar Ellidağ
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
6
PDF
Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism?
2020
·
Ayşe Balat
, Mesut Parlak
, et al.
·
The Turkish Journal of Pediatrics
·
4
PDF
Gene Expression and Promoter Region Polymorphisms of Interleukin-10 in Meningitis Patients
2011
·
Serdar Öztuzcu
, Ecir Ali Çakmak
, et al.
·
Genetic Testing and Molecular Biomarkers
·
4
Can monocyte to HDL ratio be used as an inflammatory marker in children with familial mediterranean fever?
2019
·
Hatice Güneş
, Fatma Duksal
, et al.
·
Annals of Medical Research
·
3
B-Mode Gray Scale Histogram Value in Diagnosis of Adolescent Patients with Hashimoto Thyroiditis
2017
·
Bulent Cekic
, Ilhan Nahit Mutlu
, et al.
·
Istanbul Medical Journal
·
3
Growth Hormone Therapy in Neurosecretory Dysfunction
2025
·
Ebru Barsal Çetiner
, Zeynep Donbaloğlu
, et al.
·
Turkish Archives of Pediatrics
·
2
PDF
A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene
2024
·
Berna Singin
, Zeynep Donbaloğlu
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
1
PDF
Evaluation of fractal dimension and panoramic radiomorphometric indices in children and adolescents with type 1 diabetes mellitus: A retrospective study
2024
·
Humeyra Tercanli Alkis
, Burcu Yagmur
, et al.
·
1
PDF
Genotype–Phenotype Spectrum of Non‐Syndromic Monogenic Obesity in a National Paediatric Cohort
2026
·
Ahmet Kahveci
, Selin Uzun Karauzum
, et al.
·
Pediatric Obesity
The contribution of end-tidal carbon dioxide monitoring to the management of pediatric patients with diabetic ketoacidosis
2025
·
Ozlem Tolu Kendir
, Ceren Kahraman
, et al.
·
The American Journal of Emergency Medicine
Symptomatic Cerebral Infarction: A Rare Complication of Diabetic Ketoacidosis
2018
·
Gamze Çelmeli
, Mesut Parlak
, et al.
·
57th Annual ESPE
Does Sodium and Potassium Intake Contribute to Hypertension in Children
2018
·
Elif Çomak
, Meltem Bozkurt
, et al.
Serum Neurokinin B Level can be Used to Differentiate Central Precocious Puberty from Premature Thelarche
2015
·
Mesut Parlak
, Doğa Türkkahraman
, et al.
·
54th ESPE Meeting (ESPE 2015)
High-Dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-Hydroxylase Deficiency
2015
·
Mesut Parlak
, Doğa Türkkahraman
, et al.
·
54th ESPE Meeting (ESPE 2015)
Prognostic Effect Of Convertional Treatment In Pediatric Dilated Cardiomyopathy
2009
·
Osman Başpınar
, Metin Kılınç
, et al.
·
European Journal of Therapeutics
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Works count:
25
Citation count:
146
H-index:
7
I10-index:
4
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