(Q39585231)

English

Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a family

scientific article published on January 1979

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a family (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

author name string

P Khoubesserian

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

N van Regemorter

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

O Ohrn-Degueldre

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

D Toussaint

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

N Telerman-Toppet

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

C Coërs

6

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

publication date

1 January 1979

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

222

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1-10

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Some comments on the histochemical characterization of muscle adenosine triphosphatase.

1 reference

https://api.crossref.org/works/10.1007%2FBF00313262

21 January 2018

Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1007%2FBF00313262

21 January 2018

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

1 reference

https://api.crossref.org/works/10.1007%2FBF00313262

21 January 2018

Myotonic pupils in Charcot-Marie-Tooth disease. Successful relief of symptoms with 0.025% pilocarpine

1 reference

https://api.crossref.org/works/10.1007%2FBF00313262

21 January 2018

THE PERONEAL TYPE OF MUSCULAR ATROPHY: WITH AN ACCOUNT OF A FAMILY GROUP OF CASES

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A histochemical method for the demonstration of diphosphopyridine nucleotide diaphorase

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The vital staining of muscle biopsies with methylene blue

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurological signs in a normal population

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motor innervation and fiber type pattern in amyotrophic lateral sclerosis and in Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Normal and pathological structural variations of the myoneural junction]

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Charcot-Marie-Tooth disease with Leber optic atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of certain traits accompanying some inherited neurological disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/93622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00313262

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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