𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Familial Hodgkin's disease a clinical and laboratory investigation

✍ Scribed by Susan J. Robertson; James T. Lowman; Seymour Grufferman; Donna Kostyu; Charles M. Der Van Horst; Thomas J. Matthews; Michael J. Borowitz; Sandra H. Bigner


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
605 KB
Volume
59
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Familial longevity and prognosis in Hodg
✍ Magnus BjΓΆrkholm; Christina Wedelin; GΓΆran Holm; Bertil Essy-Ehsing πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 English βš– 472 KB πŸ‘ 2 views
Hla in familial hodgkin's disease. Resul
✍ William H. Marshall; John M. Barnard; Sharon K. Buehler; Joyce Crumley; Bodil La πŸ“‚ Article πŸ“… 1977 πŸ› John Wiley and Sons 🌐 French βš– 412 KB

## Abstract A familial aggregate of seven cases of Hodgkin's disease (HD) has been investigated by HLA typing. Over 600 people in the immediate population (__i.e__. about half) have been HLA typed and haplotypes have been obtained for 95% of them. It was expected that the cases would share a partic

Familial eosinophilia: Clinical and labo
✍ Lin, Albert Y.; Nutman, Thomas B.; Kaslow, David; Mulvihill, John J.; Fontaine, πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 69 KB

We describe a five-generation kindred with familial eosinophilia (FE; MIM131400), characterized by the occurrence of sustained eosinophilia of unidentifiable cause in multiple relatives. The inheritance pattern is consistent with an autosomal dominant pattern. Among 52 related subjects studied, 19 w

HLA antigens in familial Hodgkin's disea
✍ Mark H. Greene; Elisabeth A. McKeen; Frederick P. Li; William A. Blattner; Josep πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 French βš– 352 KB

## Abstract In a study of 13 families prone to Hodgkin's disease, the probands showed significant excesses of the HLA antigens Bw35 (7 cases) and Bw37 (3 cases). Although based on a small number of patients, the results suggest that immunogenetic mechanisms account at least partly for the familial

Intracranial Hodgkin's disease in two pa
✍ Ashigbi, Michael Y.; Venkatraj, Usha; Agarwal, Veneeta; Bello, Jackie; Wiernik, πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 366 KB πŸ‘ 2 views

Intracranial Hodgkin's disease is very rare and is often a terminal event. The case of a 33-year-old man who relapsed in the anterior pituitary gland without other evidence of disease 6 months after extended field radiation therapy for Stage IIA Hodgkin's disease is presented. He remains well with n