(Q34329934)

1 August 2017

title

Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism (English)

1 reference

1 August 2017

Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism* (English)

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

15 October 2023

1 reference

1 reference

Gordon-Holmes syndrome

1 reference

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

15 October 2023

2

Opitz JM

1 reference

1 August 2017

G. Neuhäuser

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1149314

26 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1149314

26 August 2022

publication date

1 May 1975

1 reference

full work available at URL

1 August 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1975.tb00353.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1975.tb00353.x/fullpdf

15 October 2023

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

15 October 2023

1 reference

1 August 2017

volume

7

1 reference

1 August 2017

issue

5

1 reference

1 August 2017

page(s)

426-434

1 reference

Pallido-cerebello-olivary degeneration with eunuchoidism

1 August 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

A new familial syndrome with ataxia, hearing loss, and mental retardation. Report of three brothers

15 October 2023

4

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Wernicke's encephalopathy and cardiomyopathy in a boy with Friedreich's ataxia.

15 October 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

An atypical hereditary spinocerebellar syndrome. A clinical and genetic study

15 October 2023

9

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Seminiferous tubule dysgenesis (Klinefelter's syndrome) associated with familiar cerebellar ataxia

15 October 2023

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

The olivopontocerebellar atrophies: a review

15 October 2023

21

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

FAMILIAL CEREBELLAR ATAXIA AND HYPOGONADISM

15 October 2023

27

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Cerebellar ataxia and total albinism: a kindred suggesting pleitotropism or linkage

15 October 2023

32

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Anomalies of form and function in Friedreich's ataxia

15 October 2023

34

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Some unusual findings in a family with Friedreich's ataxia

15 October 2023

36

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

The primary spino-cerebellar atrophies and their associated defects, with a study of the foot deformity.

15 October 2023

38

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

Familial hypogonadotrophic eunuchoidism with cerebellar ataxia

15 October 2023

42

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)

15 October 2023

43

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00353.X

15 October 2023

Identifiers

0 references

1 reference