(Q28346777)

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Hyperekplexia in neonates

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scholarly article

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Europe PubMed Central

Hyperekplexia in neonates (English)

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author name string

V Praveen

1

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S K Patole

2

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J S Whitehall

3

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language of work or name

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publication date

September 2001

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Postgraduate Medical Journal

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77

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911

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570-2

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Hyperekplexia-like syndromes without mutations in the GLRA1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

A novel mutation (Gln266-->His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

Mutational analysis of familial and sporadic hyperekplexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

Startle disease: an avoidable cause of sudden infant death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

20 March 2017

"JUMPING FRENCHMEN OF MAINE." MYRIACHIT.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

A FAMILY WITH EMOTIONALLY PRECIPITATEED "DROP SEIZURES"

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Startle disease or hyperekplexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

The resolution of the Latah paradox.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Hyperexplexia: an inherited disorder of the startle response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Startle disease or hyperekplexia: further delineation of the syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Hyperekplexia: a syndrome of pathological startle responses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Startle disorders of man: hyperekplexia, jumping and startle epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Sudden death and paroxysmal autonomic dysfunction in stiff-man syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

The cardiorespiratory control hypothesis for sudden infant death syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

29 September 2017

Spectroscopic imaging of frontal neuronal dysfunction in hyperekplexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperekplexia and trismus due to brainstem encephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Symptomatic hyperekplexia occurring as a result of pontine infarction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Posttraumatic movement disorders after moderate or mild head injury.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperekplexia: abnormal startle response due to glycine receptor mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

The startle and orienting reactions in man. A study of their characteristics and habituation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperexplexia or stiff baby syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperekplexia: pedigree studies in two families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperekplexia and sudden neonatal death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

2 June 2018

Hyperekplexia: a rare differential of neonatal fits described in a developing country

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

27 November 2018

Hyperekplexia in a patient with a brainstem vascular anomaly.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

27 November 2018

Hyperexplexia: not hereditary stiff-baby syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

27 November 2018

The startle disease or hyperekplexia. Pathological surprise reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757896

27 November 2018

The effects of clonazepam and vigabatrin in hyperekplexia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperekplexia, a cause of neonatal apnea: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete heart block in nonfamilial hyperekplexia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperekplexia as cause of abnormal intrauterine movements

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperekplexia associated with apnea and sudden infant death syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physiological abnormalities in hereditary hyperekplexia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital stiff-man syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperekplexia exacerbated by occlusion of posterior thalamic arteries

1 reference

https://pubmed.ncbi.nlm.nih.gov/11524514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/PMJ.77.911.570

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release_gdbof2n7u5ch5amggslyoejt2m

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