Suchergebnisse - "17,20-lyase"

PubPharm (95)

1

A Case of 17α-hydroxylase/17,20-lyase Deficiency Diagnosed at 45 Years of Age with Hyperaldosteronism

enthalten in: Internal medicine (Tokyo, Japan) | 2024

von Ikeya, A. | Yamashita, M. | Kakizawa, K. | +5

2

A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX : a case report and literature review

enthalten in: Blood pressure | 2023

von Chen, H. | Chen, Y. | Mao, H. | +2

3

Full-term live birth in a woman with 17α-hydroxylase and 17,20-lyase deficiency with assisted reproductive technology : a case report

enthalten in: BMC women's health | 2023

von Xi, S. | Yang, X. | Shan, X. | +1

4

Full-term live birth in a woman with 17α-hydroxylase and 17,20-lyase deficiency with assisted reproductive technology: a case report

enthalten in: BMC women's health | 2023

von Xi, S. | Yang, X. | Shan, X. | +1

5

Endocrine profiles and cycle characteristics of infertile 17α-hydroxylase/17,20-lyase Deficiency Patients undergoing assisted Reproduction Treatment : a retrospective cohort study

enthalten in: Journal of ovarian research | 2023

von Pan, P. | Zheng, L. | Huang, J. | +5

6

Endocrine profiles and cycle characteristics of infertile 17α-hydroxylase/17,20-lyase Deficiency Patients undergoing assisted Reproduction Treatment: a retrospective cohort study

enthalten in: Journal of ovarian research | 2023

von Pan, P. | Zheng, L. | Huang, J. | +5

7

Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China

enthalten in: Journal of clinical research in pediatric endocrinology | 2023

von Li, Y. | Han, T. | Wang, Y. | +3

8

A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review

in: Blood Pressure | 2023

von Heye Chen | Yingting Chen | Hongxian Mao | +2

9

Excess dietary zinc drives a Cushing's-like syndrome in ovariectomized mice - Implications for postmenopausal obesity

enthalten in: Biochemical and biophysical research communications | 2022

von Zhao, Y. | Wang, Y. | Hu, L. | +11

10

A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency

enthalten in: International journal of environmental research and public health | 2022

von Saltarelli, M. | Ferrante, R. | Marcello, F. | +7

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