Klinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's disease (Q36180810)

12 August 2017

0 references

Klinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's disease (English)

1 reference

progressive muscular atrophy

12 August 2017

Klinefelter's syndrome

1 reference

based on heuristic

inferred from title

1 reference

1 reference

Pedro Enrique Jiménez Caballero

series ordinal

1

1 reference

12 August 2017

1 July 2012

1 reference

Annals of Indian Academy of Neurology

12 August 2017

1 reference

12 August 2017

15

1 reference

12 August 2017

3

1 reference

12 August 2017

227-229

1 reference

The history of progressive muscular atrophy: syndrome or disease?

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Sporadic lower motor neuron disease with adult onset: classification of subtypes

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Distinguishing clinical and electrodiagnostic features of X-linked bulbospinal neuronopathy

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

X-chromosome inactivation in mammals

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Benign neurogenic amyotrophy in Klinefelter's syndrome

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy's disease

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Genetic diagnosis of Werdnig-Hoffmann disease: a problem for application to prenatal diagnosis.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3424807

Familiar spastic paraplegia presenting in a boy with Klinefelter syndrome--case report

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22919202

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4103/0972-2327.99730

1 reference

12 August 2017

1 reference

PMC publication ID

3424807

12 August 2017

PubMed publication ID

22919202

1 reference

PMC publication ID

3424807