- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1720-8386
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
POR polymorphisms are associated with 21 hydroxylase deficiency ; day:5 ; month:3 ; year:2021 ; pages:1-8
Journal of endocrinological investigation ; (5.3.2021), 1-8
- Creator
-
Pecori Giraldi, F.
Einaudi, S.
Sesta, A.
Verna, F.
Messina, M.
Manieri, C.
Menegatti, E.
Ghizzoni, L.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s40618-021-01527-2
- URN
-
urn:nbn:de:101:1-2021041821112539993154
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:46 AM CEST
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
- Pecori Giraldi, F.
- Einaudi, S.
- Sesta, A.
- Verna, F.
- Messina, M.
- Manieri, C.
- Menegatti, E.
- Ghizzoni, L.
- SpringerLink (Online service)
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Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2
HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Impact of prolyl-4-hydroxylase deficiency on liver regeneration and sepsis
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Coexistence of 21 Hydroxylase Deficiency and Autoimmune Adrenalitis: A Case Report
Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Successful treatment of infantile oxysterol 7α-hydroxylase deficiency with oral chenodeoxycholic acid
Investigation of protein stability as underlying molecular pathology in 21-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
Dopamine beta-hydroxylase deficiency
An unusual presentation of tyrosine hydroxylase deficiency
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2
HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Impact of prolyl-4-hydroxylase deficiency on liver regeneration and sepsis
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Coexistence of 21 Hydroxylase Deficiency and Autoimmune Adrenalitis: A Case Report
Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Successful treatment of infantile oxysterol 7α-hydroxylase deficiency with oral chenodeoxycholic acid
Investigation of protein stability as underlying molecular pathology in 21-hydroxylase deficiency