Zobrazeno 1 - 10
of 92
pro vyhledávání: ''
Autor:
Maria Claudia Nogueira Zerbini, Vanessa Petry Helena, Madson Q. Almeida, Maria Del Pilar Estevez Diz, Vania Balderrama Brondani, Ana O. Hoff, Amanda Meneses Ferreira, Ana Claudia Latronico, Berenice B. Mendonca, Helaine Charchar, Maria Candida Barisson Villares Fragoso, Luiz Antonio Senna Leite
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 190:250-255
Background The TP53 p.R337H germline mutation is highly prevalent among children with adrenocortical tumors (ACTs) from South and Southeast Brazil. However, the prevalence of other tumors of the Li-Fraumeni syndrome (LFS) and Li-Fraumeni-like syndrom
Autor:
Parvin Mirmiran, Maryam Mahdavi, Golaleh Asghari, Carol L. Wagner, Fereidoun Azizi, Pooneh Dehghan, Emad Yuzbashian, Farhad Hosseinpanah, Maryam Tohidi, Tirang R. Neyestani
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 188:117-123
Evidence on the association of vitamin D and parathyroid hormone (PTH) with cardiovascular risk factors in the young is limited. We therefore assessed the relationships of circulating vitamin D and PTH concentrations and subclinical atherosclerosis i
Autor:
Fortune Kohen, Naftali Stern, Asaf Aizic, Dalia Somjen, Orli Sharon, Elena Izkhakov, Esther Knoll, Dan M. Fliss
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 182:81-86
Background Sorafenib improves progression-free survival in patients with progressive radioactive iodine-refractory differentiated thyroid carcinoma, but causes severe side effects. Estrogens may accelerate thyroid carcinoma cell growth. Our group rec
Autor:
Wencui Wang, Zhihan Wan, Zuwei Yang, Lei Ye, Shouyue Sun, Haorong Li, Guang Ning, Yan Qi, Sichang Zheng, Rulai Han
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 211
Context Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive genetic diseases caused by genetic deficiency in nine genes encoding steroidogenesis enzymes and cofactors. Objective To establish a targeted next-generation sequencing (N
Autor:
Heinrich Schmidt, Christian Lottspeich, Meike Neuner, Nicole Reisch, Matthias K. Auer, Luisa Paizoni, James Hawley, Martin Bidlingmaier, Brian G. Keevil
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 212
Context Hypothalamus-pituitary-gonadal (HPG)-axis disturbances are a common phenomenon in patients with classic congenital adrenal hyperplasia (CAH). 11-oxygenated androgens have been suggested to play a role in this context. Design Cross-sectional s
Autor:
Shaun Sabico, Yousef Al-Saleh, Malak Nawaz Khan Khattak, Syed Danish Hussain, Mohammed Y. Al-Harbi, Naji Aljohani, Mohammed Ghouse Ahmed Ansari, Nasser M. Al-Daghri, Majed S. Alokail
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 212
Widespread vitamin D deficiency (serum 25-hydroxyvitamin D 50 nmol/L) in Saudi Arabia (SA) has been documented, yet a time trend is needed to establish where the prevalence is headed. This study aims to fill this gap.This cross-sectional series (N =
Autor:
Mohammed M. Al-Harbi, Shaun Sabico, Yousef Al-Saleh, Abdulaziz M. Al-Othman, Naji Aljohani, Mohammed Ghouse Ahmed Ansari, Sunil J. Wimalawansa, Hanan Alfawaz, Majed S. Alokail, Nasser M. Al-Daghri
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 180:23-28
Vitamin D deficiency is rampant in the Middle East, even in children and adolescents. This study was designed to investigate the effects of different vitamin D repletion strategies commonly used on serum vitamin D levels of Saudi adolescents. Study d
Autor:
Cláudia dos Santos Cople-Rodrigues, Felipe Vogt Cureau, Kênia Mara Baiocchi de Carvalho, Beatriz D'Agord Schaan, Denise Tavares Giannini, Cecília Lacroix de Oliveira, Maria Cristina Caetano Kuschnir, Katia Vergetti Bloch
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 199
Vitamin D plays a role in bone and metabolic health in life long, however hypovitaminosis D is common in different settings. The aim of this study was to describe vitamin D status among adolescents from a large sunny country and analyze associated fa
Autor:
Laura Coleman, Kimberley Franks, Peter N. Le Souëf, Meredith L Borland, Ingrid A. Laing, Katharine Leiter, Leesa Harris
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 201
Single nucleotide polymorphisms (SNPs) of the vitamin D receptor (VDR) gene have shown linkage and association with asthma development in multiple cohort studies. However, the majority of investigations have focused on asthma phenotypes in cohorts wi
Autor:
Larry Ke, Sarah P. Garnett, Xiaoying Liu, Kaye E. Brock, Louise A. Baur, Christopher T. Cowell, Rebecca S. Mason
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 177:270-277
As the prevalence of obesity appears to be increasing in Australia's youth the overall objective of this study was to examine serum 25-hydroxyvitamin D (25OHD) concentrations in a cohort of 8-year-olds (n=249) followed up at age 15 (n=162) and explor