Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: BMC Endocrine Disorders 18 (2018).
- Keyword
-
-
- Event
-
Veröffentlichung
- (where)
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Erlangen
- (who)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (when)
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2018
- Creator
- URN
-
urn:nbn:de:bvb:29-opus4-100933
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:44 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Dörr, Helmuth-Günther
- Wollmann, Hartmut A.
- Hauffa, Berthold P.
- Wölfle, Joachim
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Time of origin
- 2018
Other Objects (12)
Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Congenital adrenal hyperplasia
Effects of Congenital Adrenal Hyperplasia (CAH) and Biological Sex on Brain Size
Novel therapeutic approaches for Congenital Adrenal Hyperplasia
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Congenital leptin deficiency : lacking so much more than just satiety
Molecular basis of the heterogeneity in congenital sucrase-isomaltase deficiency
Impact of prolyl-4-hydroxylase deficiency on liver regeneration and sepsis
Optimisation of congenital adrenal hyperplasia therapy in paediatric and foetal populations by leveraging pharmacometrics
Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Congenital adrenal hyperplasia
Effects of Congenital Adrenal Hyperplasia (CAH) and Biological Sex on Brain Size
Novel therapeutic approaches for Congenital Adrenal Hyperplasia
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Congenital leptin deficiency : lacking so much more than just satiety
Molecular basis of the heterogeneity in congenital sucrase-isomaltase deficiency
Impact of prolyl-4-hydroxylase deficiency on liver regeneration and sepsis
Optimisation of congenital adrenal hyperplasia therapy in paediatric and foetal populations by leveraging pharmacometrics
Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Congenital adrenal hyperplasia
Effects of Congenital Adrenal Hyperplasia (CAH) and Biological Sex on Brain Size
Novel therapeutic approaches for Congenital Adrenal Hyperplasia
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Congenital leptin deficiency : lacking so much more than just satiety
Molecular basis of the heterogeneity in congenital sucrase-isomaltase deficiency
Impact of prolyl-4-hydroxylase deficiency on liver regeneration and sepsis