(Q44610199)

4 December 2017

title

17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies (English)

1 reference

4 December 2017

1 reference

C Scaroni

1

1 reference

4 December 2017

A Biason

2

1 reference

4 December 2017

G Carpenè

3

1 reference

4 December 2017

G Opocher

4

1 reference

4 December 2017

F Mantero

5

1 reference

4 December 2017

publication date

1 February 1991

1 reference

Journal of Endocrinological Investigation

4 December 2017

published in

1 reference

4 December 2017

volume

14

1 reference

4 December 2017

issue

2

1 reference

4 December 2017

page(s)

99-108

1 reference

https://scigraph.springernature.com/pub.10.1007/bf03350278

4 December 2017

exact match

0 references

cites work

17-hydroxylation deficiency in man

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Control of Aldosterone in 17&alpha;-Hydroxylase Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Male pseudohermaphroditism due to 17α-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Studies in a phenotypic female with 17-α-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Combined 17a- and 18-Hydroxylase Deficiency Associated with Complete Male Pseudohermaphroditism and Hypoaldosteronism*

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Congenital adrenal hyperplasia. (1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Microdroplet Assay of Human Serum Cytotoxins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03350278

Hypogonadism and mineralocorticoid excess. The 17-hydroxylase deficiency syndrome

21 January 2018

1 reference

12 December 2020

A New Male Pseudohermaphroditism Associated with Hypertension due to a Block of 17α-Hydroxylation

1 reference

12 December 2020

Indications for study of adrenal function by measurement of the cortisol secretion rate

1 reference

12 December 2020

17-Hydroxylase deficiency. Apropos of a case

1 reference

12 December 2020

Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries

1 reference

12 December 2020

Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis

1 reference

12 December 2020

Primary amenorrhoea with hypertension due to 17-hydroxylase deficiency. Therapy with dexamethasone and ethinyloestradiol

1 reference

12 December 2020

The deficiency of 17-hydroxylase: a cause of growth and puberty retardation in the girl. One case

1 reference

12 December 2020

Free urinary cortisol radioimmunoassay (application in the diagnosis of adrenal diseases)

1 reference

12 December 2020

17 alpha-Hydroxylase deficiency. A combination of hydroxylation defect and reversible blockade in aldosterone biosynthesis

1 reference

12 December 2020

Zona fasciculata origin of 18-hydroxycorticosterone in the chronically suppressed zona glomerulosa

1 reference

12 December 2020

17-Alpha-hydroxylase deficiency of the gonads and adrenals in a male pseudohermaphrodite.

1 reference

12 December 2020

No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

1 reference

12 December 2020

Studies of the C-21 and C-19 Steroids and HLA Genotyping in Siblings and Parents of Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*

1 reference

12 December 2020

Renin-angiotensin-aldosterone system: a long-term follow-up study in 17 alpha-hydroxylase deficiency syndrome (17OHDS)

1 reference

12 December 2020

Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency

1 reference

12 December 2020

Arterial hypertension, hypokalemic alkalosis and male pseudohermaphroditism caused by 17 alpha-hydroxylase deficiency

1 reference

12 December 2020

17α-Hydroxylase Deficiency: Mineralocorticoid Hormone Profiles in an Affected Family*

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03350278

1 reference

release_zcytloqcuvfmdb2hdc3saux3xa

4 December 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zcytloqcuvfmdb2hdc3saux3xa

24 November 2022

mapped directly with Wikidata item

1 reference