Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1472-6823
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency ; volume:20 ; number:1 ; day:21 ; month:9 ; year:2020 ; pages:1-6 ; date:12.2020
BMC endocrine disorders ; 20, Heft 1 (21.9.2020), 1-6, 12.2020
- Creator
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Xiang, Chenyu
Han, Minmin
Zhang, Yi
Yin, Jianhong
Pei, Li’e
Yang, Jing
Liu, Yunfeng
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12902-020-00625-1
- URN
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urn:nbn:de:101:1-2020110821160941721315
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:31 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Xiang, Chenyu
- Han, Minmin
- Zhang, Yi
- Yin, Jianhong
- Pei, Li’e
- Yang, Jing
- Liu, Yunfeng
- SpringerLink (Online service)
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Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients
Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report
Congenital adrenal hyperplasia
Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients
Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency