## Background and procedure: The etiology of familial hemophagocytic lymphohistiocytosis (fhl), which is characterized by fever, hepatosplenomegaly, pancytopenia, and coagulopathy, remains unknown. we analyzed 43 fhl patients, all with affected siblings, in 18 families who were identified during th
Multicenter study of paroxysmal dyskinesias in Japan—Clinical and pedigree analysis
✍ Scribed by Shinichiro Nagamitsu; Toyojiro Matsuishi; Kiyoshi Hashimoto; Yushiro Yamashita; Masao Aihara; Katsunori Shimizu; Masashi Mizuguchi; Hiroko Iwamoto; Shinji Saitoh; Yukiko Hirano; Hirohisa Kato; Yukio Fukuyama; Morimi Shimada
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 37 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0885-3185
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