𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Idiopathic multicentric osteolysis: Report of two new cases and a review of the literature

✍ Scribed by Barr, R. J. ;Hughes, A. E. ;Mollan, R. A. B. ;Nevin, N. C.

Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
113 KB
Volume
32
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Acquired hypertrichosis lanuginosa. Repo
Acquired hypertrichosis lanuginosa. Report of two new cases and a review of the literature
✍ Michael K. Samson; Thomas R. Buroker; Michael D. Henderson; Laurence H. Baker; V πŸ“‚ Article πŸ“… 1975 πŸ› John Wiley and Sons 🌐 English βš– 253 KB πŸ‘ 1 views

Hypertrichosis lanuginosa is a pathologic state characterized by an excessive, new growth of fine, fetal hair. Two cases of hypertrichosis languinosa with malignancy (lymphoma and uterine cancer) are presented and added to the 9 in the literature. Lymphoma and uterine cancer are previously unreporte

Cyclophosphamide-induced cardiomyopathy.
Cyclophosphamide-induced cardiomyopathy. A report of two cases and review of the english literature
✍ Barry A. Mills; Raymond W. Roberts πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 English βš– 327 KB πŸ‘ 1 views

Fatal cardiomyopathy developed in two patients receiving cyclophosphamide in preparation for bone marrow transplantation. Both patients had normal EKGs prior to receiving cyclophosphamide in total doses of 168 mg/kg (case 1) and 144 mgkg (case 2) and subsequently developed loss of voltage and ST-T w

The management of unicentric and multice
The management of unicentric and multicentric Castleman's disease : A report of 16 cases and a review of the literature
✍ Wilbur B. Bowne; Jonathan J. Lewis; Daniel A. Filippa; Ruben Niesvizky; Ari D. B πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 385 KB πŸ‘ 1 views

## Background: Castleman's disease (cd), or angiofollicular lymph node hyperplasia, creates both diagnostic and therapeutic dilemmas for most physicians. for patients with this rare and poorly understood disease, the optimal therapy is unknown. the authors report their experience during the years 1