Evaluation of the Association between Precocious Puberty and Obesity

Autor: Recep Polat

Publikováno v: Sakarya Tıp Dergisi, Vol 12, Iss 4, Pp 659-663 (2022)

Objective: The marked variation in the timing of puberty despite similar living conditions shows that many factors are effective in determining the onset of puberty. Many factors, such as genetic and environmental factors, stress, socioeconomic statu

Externí odkaz: https://doaj.org/article/c4829c07e17a4433a98e0a4a524aa497

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome in Two Siblings: Same Mutation But Different Clinical Manifestations at Onset

Autor: Gülay Karagüzel, Recep Polat, Mehtap H. Abul, Alper Han Cebi, Fazıl Orhan

Publikováno v: JCRPE, Vol 14, Iss 3, Pp 361-365 (2022)

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is an early onset systemic autoimmune genetic disorder caused by mutation of the forkhead box protein 3 (FOXP3) gene. Enteropathy, endocrinopathy and skin manifestations

Externí odkaz: https://doaj.org/article/afb5bc8aca7141629c8bbb1d449c4f84

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

Autor: Damla Gökşen, Ediz Yeşilkaya, Samim Özen, Yılmaz Kor, Erdal Eren, Özlem Korkmaz, Merih Berberoğlu, Gülay Karagüzel, Eren Er, Ayhan Abacı, Olcay Evliyaoğlu, Emine Demet Akbaş, Edip Ünal, Semih Bolu, Özlem Nalbantoğlu, Ahmet Anık, Meltem Tayfun, Muammer Büyükinan, Saygın Abalı, Gülay Can Yılmaz, Deniz Kör, Elif Söbü, Zeynep Şıklar, Recep Polat, Şükran Darcan

Publikováno v: JCRPE, Vol 13, Iss 4, Pp 433-438 (2021)

Objective:Monogenic diabetes is a heterogeneous disease that causes functional problems in pancreatic beta cells and hyperglycemia. The aim of this study was to determine the clinical and laboratory features, the admission characteristics and distrib

Externí odkaz: https://doaj.org/article/d246cab85ec94663b4edadd4a7d45387

Spondyloenchondrodysplasia Due to Mutation in ACP5 Gene Presenting with Nephrotic Syndrome: A Case Report

Autor: Recep Polat, Öner Özdemir

Publikováno v: Aktuelle Rheumatologie. 47:517-522

Spondyloenchondrodysplasia (SPENCD) with immune dysregulation (SPENCDI) is a rare autosomal recessive inherited immuno-osseous dysplasia characterized by spondylo-metaphyseal enchondromas, along with immune dysregulation ranging from immunodeficiency

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9689fe165189a71c9bf298b879fcb83
https://doi.org/10.1055/a-1806-0918

Salivary macrophage activation-related chemokines and mitogen-activated kinase kinase (MAPKK)-degrading proteolytic activity in type 1 diabetes mellitus

Autor: Neslihan Yilmaz, Recep Polat, Mervi Gürsoy, Wendy Kaman, Elif Gül Aydin, Dareen Fteita, Dogukan Yilmaz, Floris Bikker, Ulvi Kahraman Gürsoy

Publikováno v: Yilmaz, N, Polat, R, Gürsoy, M, Kaman, W, Gül Aydin, E, Fteita, D, Yilmaz, D, Bikker, F & Gürsoy, U K 2023, ' Salivary macrophage activation-related chemokines and mitogen-activated kinase kinase (MAPKK)-degrading proteolytic activity in type 1 diabetes mellitus ', Journal of Periodontology . https://doi.org/10.1002/JPER.22-0314
Journal of Periodontology. John Wiley & Sons Inc.

Background: This cross-sectional study aimed to evaluate salivary concentrations of macrophage activation-related chemokines and mitogen-activated kinase kinase (MAPKK)-degrading proteolytic activity in children and adolescents with and without type

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef507e002e9315bc0b9b395bcf35e1b0
https://doi.org/10.1002/JPER.22-0314