(Q24515487)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

title

Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

0 references

1

1 reference

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3 October 2019

author name string

R Michelucci

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

P Genton

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

J F Pellissier

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

J Roger

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

language of work or name

English

0 references

publication date

1 February 1989

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

Journal of Neurology, Neurosurgery and Psychiatry

3 October 2019

published in

1 reference

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3 October 2019

volume

52

1 reference

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3 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

page(s)

262-265

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

Clinical and electroencephalographic investigations in myoclonic cerebellar dyssynergia

3 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

MYOCLONUS AND ATAXIA OCCURING IN A FAMILY.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

The clinical incidence of myoclonus.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Myoclonus and the Electroencephalogram, a Review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Familial myoclonic epilepsy with ataxia and neuropathy with additional features of Friedreich's ataxia and peroneal muscular atrophy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Short-latency somatosensory evoked potentials (SEPs) in dyssynergia cerebellaris myoclonica (author's transl)

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

The clinical features of mitochondrial myopathy.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Progressive myoclonic epilepsy, nerve deafness and spinal muscular atrophy.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Mitochondria1 encephalomyopathy with decreased succinate-cytochrome c reductase activity

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032517

Familial myoclonus and ataxia. Pathophysiologic implications

29 November 2018

1 reference

12 December 2020

Myoclonic cerebellar dyssynergy (Ramsay Hunt syndrome)

1 reference

12 December 2020

1 reference

12 December 2020

[Electroencephalographic study of myoclonic cerebellar dyssynergia with epilepsy (Ramsay-Hunt syndrome)]

1 reference

12 December 2020

Deficient intestinal absorption of l-tryptophan in progressive myoclonus epilepsy without Lafora bodies

1 reference

12 December 2020

[An autopsy case of degenerative type myoclonus epilepsy associated with Friedreich's ataxia and mitochondrial myopathy (author's transl)]

1 reference

12 December 2020

[Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)]

1 reference

12 December 2020

Myoclonus, ataxia, and hypoventilation: response to L-5-hydroxytryptophan

1 reference

12 December 2020

Myoclonus, cerebellar disorder, neuropathy, mitochondria1 myopathy, and ACTH deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.52.2.262

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2703843%20AND%20SRC:MED&resulttype=core&format=json

3 October 2019

1 reference