Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1752-1947
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report ; volume:13 ; number:1 ; day:30 ; month:7 ; year:2019 ; pages:1-4 ; date:12.2019
Journal of medical case reports ; 13, Heft 1 (30.7.2019), 1-4, 12.2019
- Urheber
-
Mikami, Yukiko
Takai, Yasushi
Obata-Yasuoka, Mana
Kumagai, Ryo
Yagyu, Hiroaki
Shigematsu, Kosuke
Huang, Haipeng
Uemura, Nozomi
Shinsaka, Mamiko
Saitoh, Masahiro
Baba, Kazunori
Seki, Hiroyuki
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13256-019-2166-9
- URN
-
urn:nbn:de:101:1-2019120813002274945964
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:46 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Mikami, Yukiko
- Takai, Yasushi
- Obata-Yasuoka, Mana
- Kumagai, Ryo
- Yagyu, Hiroaki
- Shigematsu, Kosuke
- Huang, Haipeng
- Uemura, Nozomi
- Shinsaka, Mamiko
- Saitoh, Masahiro
- Baba, Kazunori
- Seki, Hiroyuki
- SpringerLink (Online service)
Ähnliche Objekte (12)
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency
An unusual presentation of tyrosine hydroxylase deficiency
Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
POR polymorphisms are associated with 21 hydroxylase deficiency
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency
An unusual presentation of tyrosine hydroxylase deficiency
Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
POR polymorphisms are associated with 21 hydroxylase deficiency
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency
An unusual presentation of tyrosine hydroxylase deficiency
Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene