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Benign familial neonatal convulsions

✍ Scribed by Takebe, Yukinao; Chiba, Chikara; Kimura, Shigeru


Book ID
122405449
Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
403 KB
Volume
5
Category
Article
ISSN
0387-7604

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Benign familial neonatal convulsions
✍ Arts, W.F.M.; Halley, D.J.J.; Lindhout, D. πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 English βš– 119 KB
Electroclinical signs of benign neonatal
✍ Dr. E. Hirsch; A. Velez; F. Sellal; B. Maton; A. Grinspan; A. Malafosse; C. Mare πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 566 KB

## Abstract Benign neonatal familial convulsions comprise a distinct epileptic syndrome with a autosomal mode of transmission. The electroclinical signs of seizures in this syndrome are not yet well defined. In 3 children from two families presenting with benign neonatal familial convulsions, 14 se

Benign infantile familial convulsions ar
✍ Dr. A. Malafosse; C. Beck; H. Bellet; M. Di Capua; O. Dulac; B. Echenne; L. Fusc πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 480 KB πŸ‘ 1 views

Benign infantile familial convulsions (BIFC) and benign familial neonatal convulsions (BFNC) are two forms of familial convulsions having an age of onset within the first year of life. The gene responsible for BFNC has been mapped to chromosome 20q in the close vicinity of D20S19 and D20S20 markers.