(Q53287659)

English

Psychosocial issues that face patients with Charcot-Marie-Tooth disease: the role of genetic counseling.

scientific article published in August 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

Psychosocial issues that face patients with Charcot-Marie-Tooth disease: the role of genetic counseling. (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

author name string

Angela Arnold

1

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

Meriel McEntagart

2

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

David S Younger

3

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

publication date

1 August 2005

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

Journal of Genetic Counseling

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

14

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

4

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

307-318

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

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%2FS10897-005-0760-Z

21 January 2018

Serious genetic disorders: can or should they be defined?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Disability, coping and quality of life in individuals with muscular dystrophy: a prospective study over five years.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

based on heuristic

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The illness experience of adult persons with muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Prenatal diagnosis of Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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The Charcot-Marie-Tooth syndrome: perceptions of disability and projected use of DNA diagnostic tests

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Charcot-Marie-Tooth disease and related peripheral neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Genetically determined neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

based on heuristic

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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and results

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

based on heuristic

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Disease course of Charcot-Marie-Tooth disease type 2: a 5-year follow-up study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overview of Charcot-Marie-Tooth disease type 1A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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A clinical review of Charcot-Marie-Tooth

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047093

12 December 2020

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Identifiers

10.1007/S10897-005-0760-Z

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 May 2018

http://europepmc.org/abstract/MED/16047093

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