Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Turkan Turgay"'
Publikováno v:
Romanian Neurosurgery, Vol 37, Iss 3 (2023)
Background: Alkaptonuria is a rare metabolic autosomal recessive disorder. Its aetiology involves homogentisate 1,2 dioxygenase (HGD) deficiency resulting in homogentisic acid accumulation in the connective tissues (ochronosis). The classic triad of
Externí odkaz:
https://doaj.org/article/e88fd084796d43c9be9e53a089dc59c0
Publikováno v:
Acta Orthopaedica et Traumatologica Turcica, Vol 54, Iss 6, Pp 591-595 (2020)
Externí odkaz:
https://doaj.org/article/dfa13c5abc3f4533a6ef23fa7c6b2324
Publikováno v:
Türk Osteoporoz Dergisi, Vol 26, Iss 2, Pp 127-131 (2020)
Objective:This study investigates the role of ATG16L1 rs2241880, ATG10 rs1864183 and ATG5 rs2245214 gene polymorphisms, which are involved in autophagosome formation, in the susceptibility to postmenopausal osteoporosis (PMO) disease.Materials and Me
Externí odkaz:
https://doaj.org/article/ae17013426c4479baf3689d8831aa69e
Publikováno v:
Archives of Breast Cancer (2021)
Background: The aim of this study was to examine the clinical characteristics and quality of life (QOL) of patients with BCRL (breast cancer-related lymphedema). Methods: In this cross-sectional descriptive study, patients' characteristics such as ag
Externí odkaz:
https://doaj.org/article/8c8ad4a27ff24dd59927dc1ac6e0652b