Literature DB >> 3123238

Epilepsy with primarily generalized myoclonic-astatic seizures: a genetically determined disease.

H Doose1, W K Baier.   

Abstract

This paper presents case reports of patients suffering from myoclonic-astatic and stimulus-sensitive myoclonic seizures, respectively. It gives details of clinical and EEG data in the pertinent families. This is discussed in the context of controversial nosographic concepts of epilepsies with myoclonic seizures, and of the results of extensive family investigations. The findings demonstrate the decisive importance of hereditary factors in the pathogenesis of myoclonic and myoclonic-astatic epilepsy, the genetic background of which is probably polygenic.

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Year:  1987        PMID: 3123238     DOI: 10.1007/bf02467351

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  5 in total

1.  Centrencephalic myoclonic-astatic petit mal. Clinical and genetic investigation.

Authors:  H Doose; H Gerken; R Leonhardt; E Völzke; C Völz
Journal:  Neuropadiatrie       Date:  1970-08

2.  Myoclonic epilepsies of childhood.

Authors:  J Aicardi; J J Chevrie
Journal:  Neuropadiatrie       Date:  1971-10

3.  [The benign myoclonic epilepsy of infancy (author's transl)].

Authors:  C Dravet; M Bureau
Journal:  Rev Electroencephalogr Neurophysiol Clin       Date:  1981-12

Review 4.  [Severe infant myoclonic epilepsy (author's transl)].

Authors:  B Dalla Bernardina; G Capovilla; M B Gattoni; V Colamaria; S Bondavalli; M Bureau
Journal:  Rev Electroencephalogr Neurophysiol Clin       Date:  1982-04

5.  Childhood epileptic encephalopathy with diffuse slow spike-waves (otherwise known as "petit mal variant") or Lennox syndrome.

Authors:  H Gastaut; J Roger; R Soulayrol; C A Tassinari; H Régis; C Dravet; R Bernard; N Pinsard; M Saint-Jean
Journal:  Epilepsia       Date:  1966-06       Impact factor: 6.740

  5 in total
  3 in total

1.  Myoclonic dystonia.

Authors:  S M Pueschel; J H Friedman; T Shetty
Journal:  Childs Nerv Syst       Date:  1992-03       Impact factor: 1.475

2.  Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures.

Authors:  Gemma L Carvill; Jacinta M McMahon; Amy Schneider; Matthew Zemel; Candace T Myers; Julia Saykally; John Nguyen; Angela Robbiano; Federico Zara; Nicola Specchio; Oriano Mecarelli; Robert L Smith; Richard J Leventer; Rikke S Møller; Marina Nikanorova; Petia Dimova; Albena Jordanova; Steven Petrou; Ingo Helbig; Pasquale Striano; Sarah Weckhuysen; Samuel F Berkovic; Ingrid E Scheffer; Heather C Mefford
Journal:  Am J Hum Genet       Date:  2015-04-09       Impact factor: 11.025

3.  Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Authors:  Rikke S Møller; Thomas V Wuttke; Ingo Helbig; Carla Marini; Katrine M Johannesen; Eva H Brilstra; Ulvi Vaher; Ingo Borggraefe; Inga Talvik; Tiina Talvik; Gerhard Kluger; Laurence L Francois; Gaetan Lesca; Julitta de Bellescize; Susanne Blichfeldt; Nicolas Chatron; Nils Holert; Julia Jacobs; Marielle Swinkels; Cornelia Betzler; Steffen Syrbe; Marina Nikanorova; Candace T Myers; Line H G Larsen; Sabina Vejzovic; Manuela Pendziwiat; Sarah von Spiczak; Sarah Hopkins; Holly Dubbs; Yuan Mang; Konstantin Mukhin; Hans Holthausen; Koen L van Gassen; Hans A Dahl; Niels Tommerup; Heather C Mefford; Guido Rubboli; Renzo Guerrini; Johannes R Lemke; Holger Lerche; Hiltrud Muhle; Snezana Maljevic
Journal:  Neurology       Date:  2017-01-04       Impact factor: 9.910

  3 in total

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