1

Step 1

Dube C. M. et al. Febrile seizures. Mechanisms and relationship to epilepsy

2

Step 2

Volkers L. et al. Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation

3

Step 3

Dong Z.-F. et al. Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1

4

Step 4

Chen R. et al. Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

5

Step 5

Berg A. T. Are febrile seizures provoked by a rapid rise in temperature?

6

Step 6

Volkers L. et al. Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

7

Step 7

Ogiwara I. et al. Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons. A Circuit Basis for Epileptic Seizures in Mice

8

Step 8

Yu F. H. et al. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

9

Step 9

Mantegazza M. et al. Mutations of Ion Channels in Genetic Epilepsies

10

Step 10

Bechi G. et al. Pure haploinsufficiency for Dravet syndrome NaV1.1 (SCN1A) sodium channel truncating mutations

1

Step 1

Dube C. M. et al. Febrile seizures. Mechanisms and relationship to epilepsy

2

Step 2

Volkers L. et al. Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation

3

Step 3

Dong Z.-F. et al. Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1

4

Step 4

Chen R. et al. Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

5

Step 5

Berg A. T. Are febrile seizures provoked by a rapid rise in temperature?

6

Step 6

Volkers L. et al. Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

7

Step 7

Ogiwara I. et al. Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons. A Circuit Basis for Epileptic Seizures in Mice

8

Step 8

Yu F. H. et al. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

9

Step 9

Mantegazza M. et al. Mutations of Ion Channels in Genetic Epilepsies

10

Step 10

Bechi G. et al. Pure haploinsufficiency for Dravet syndrome NaV1.1 (SCN1A) sodium channel truncating mutations

03 January 2016 31 December 2016
The goal is overdue by 2683 days
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Goal abandoned

The author does not write in the goal 7 years 5 months 8 days

Goal author

Роман Душкин

Russia

46 years old

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General

Перевести в 2016 году не менее 10 статей по неврологии, эпилептологии, биохимии, фармакологии и прочим подобным темам

К сожалению, на русском языке практически нет современных и качественных источников информации по таким интересным для меня темам, как:

  1. Неврология
  2. Эпилептология
  3. Биохимия
  4. Генетика
  5. Фармакология
  6. Персональная медицина

Поэтому необходимо искать самые интересные описания исследований и переводить их. Перевод улучшает понимание и позволяет более вдумчиво прочесть источник.

Цель будет дополняться по мере поиска и добавления в список источников, необходимых к переводу.

 Goal Accomplishment Criteria

До конца 2016 года переведено 10 статей, переводы опубликованы и отрекламированы

 Personal resources

Время, Энтузиазм

 Goal ecological compatibility

Переводы требуются мне для саморазвития и получения новейших знаний в областях интереса

  1. Dube C. M. et al. Febrile seizures. Mechanisms and relationship to epilepsy

  2. Volkers L. et al. Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation

  3. Dong Z.-F. et al. Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1

  4. Chen R. et al. Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

  5. Berg A. T. Are febrile seizures provoked by a rapid rise in temperature?

  6. Volkers L. et al. Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

  7. Ogiwara I. et al. Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons. A Circuit Basis for Epileptic Seizures in Mice

  8. Yu F. H. et al. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

  9. Mantegazza M. et al. Mutations of Ion Channels in Genetic Epilepsies

  10. Bechi G. et al. Pure haploinsufficiency for Dravet syndrome NaV1.1 (SCN1A) sodium channel truncating mutations

  • 2303
  • 03 January 2016, 18:21

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