๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

High incidence of factor XI deficiency in Gaucher's disease

โœ Scribed by A. Berrebi; S. D. H. Malnick; E. J. Vorst; D. Stein

Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
118 KB
Volume
40
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Combined hereditary factor XI (plasma th
Combined hereditary factor XI (plasma thromboplastin antecedent) deficiency, von Willebrand's disease, and xeroderma pigmentosum in a Japanese family
โœ Masayuki Sano; Hidehiko Saito; Yoshinori Shimamoto; Isamu Sugiura; Haruhiko Ohts ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 369 KB ๐Ÿ‘ 1 views

## H.S., I.S.) Japan We report a 28-year-old-Japanese male who had a skin tumor derived from variant type xeroderma pigmentosum (XP), combined with factor XI (FXI) deficiency and type llB von Willebrand's disease (vWd). The patient had abnormal bleeding history on tooth extraction. FXI clotting ac

High incidence of treatment failure with
High incidence of treatment failure with vincristine, etoposide, epirubicin, and prednisolone chemotherapy with successful salvage in childhood Hodgkin disease
โœ Ekert, Henry; Toogood, Ian; Downie, Peter; Smith, Peter J.; Macfarlane, S.; Whit ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 68 KB ๐Ÿ‘ 2 views

Background and Procedure. In an attempt to further reduce the long-term toxicity of chemotherapy for childhood Hodgkin disease (HD), the Australian and New Zealand Children's Cancer Study Group between 1990 and 1996 enrolled 53 children with biopsy-proven and imaging-staged HD into a chemotherapyonl