(Q36780943)

English

Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen).

scientific article published on April 1993

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen). (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

0 references

1 reference

based on heuristic

inferred from title

Werdnig–Hoffmann disease

1 reference

based on heuristic

inferred from title

author name string

A Thieme

1

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

B Mitulla

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

F Schulze

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

A W Spiegler

4

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

publication date

1 April 1993

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

91

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

295-297

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00218278

0 references

Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A hungarian study on Werdnig-Hoffmann disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cluster of acute infantile spinal muscular atrophy (Werdnig-Hoffmann disease) in a limited area of Reunion Island

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile and juvenile spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical, epidemiological and genetic study of hereditary motor neuropathies in Benghazi, Libya

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nosology of the spinal muscular atrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00218278

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

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