(Q67259686)

English

On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands

scientific article published on 01 July 1973

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

generalized epilepsy

1 reference

based on heuristic

inferred from title

author name string

T Tsuboi

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

W Christian

2

1 reference

Europe PubMed Central

PubMed publication ID

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11 September 2019

publication date

1 July 1973

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

19

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Europe PubMed Central

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11 September 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

155-182

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Prevention in epileptic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary aspects of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and social aspects of the epilepsies of childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centrencephalic Myoclonic-Astatic Petit Mal1– Clinical and genetic investigations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the genetic prognosis of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetical background of common diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myoclonus. Clinical significance and an approach to classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of epilepsy in its clinical, social and genetic aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Observations on so-called genetic epilepsy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PROGNOSIS OF "PURE" PETIT MAL; A FOLLOW-UP STUDY

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The development of the electroencephalogram in normal children and adolescents from the age of 1 through 21 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discrimination between mulifactorial inheritance with threshold effect and two-allele single-locus hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The clinical classification of pyknolepsy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The factor of inheritance in convulsive disorders in childhood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the inheritance of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epilepsy as a mental hygiene problem.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is idiopathic convulsive disorder partially sex-linked?

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The petit mal epilepsies; their treatment with tridione

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics and epilepsy: a model from critical path analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY CHARACTERISTICS OF FAMILIAL TEMPORAL-CENTRAL FOCAL EPILEPSY

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Clinical and electroencephalographic family studies on pyknolepsy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial occurrence of focal temporal electroencephalographic abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of photosensitive epilepsy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EVIDENCE FOR A GENETIC ETIOLOGY OF TEMPORAL-CENTRAL ABNORMALITIES IN FOCAL EPILEPSY.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary components in epileptic patients. Electroencephalogram family studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[EEG studies of relatives of idiopathic epilepsy patients]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EEG studies of relatives of probands with focal epilepsy who have been treated surgically

1 reference

https://pubmed.ncbi.nlm.nih.gov/4200688

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282192

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4200688%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

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