๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Cytogenetic studies in sideroblastic anemia

โœ Scribed by Mogens Krogh Jensen; Margareta Mikkelsen


Publisher
John Wiley and Sons
Year
1976
Tongue
English
Weight
310 KB
Volume
37
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Meme biosynthesis in sideroblastic anemi
โœ Aarne V.O. Fasanen; Mirjam Salmi; Pekka Vuopio; Raimo Tenhunen ๐Ÿ“‚ Article ๐Ÿ“… 1980 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 660 KB
Sideroblastic anemia terminating in myel
โœ Dr. Daniel F. Lukowicz; Thomas J. Myers; Joseph A. Grasso; Maurice M. Albala ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 753 KB

## Abstract Two patients with primary acquired sideroblastic anemia who eventually developed myelofibrosis with myeloid metaplasia are reported. Splenectomy was performed in one patient because of increasing blood transfusion requirements, and splenic histology revealed both myeloid metaplasia and

Sideroblastic anemias: Variations on imp
โœ Koc, Sibel; Harris, John W. ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 28 KB

Sideroblastic anemias are caused by a diversity of hereditary, congenital, or acquired disorders. Criteria used in describing sideroblastic anemias vary widely among standard medical textbooks and even so have been imprecisely applied in the literature. Recent discoveries concerning the basic pathop

Sideroblastic anemia terminating in chro
โœ Bandieri, E.; Di Donato, C.; Artioli, F.; Carapezzi, C.; Luppi, M.; Artusi, T.; ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 164 KB ๐Ÿ‘ 2 views

## Case of Schwachman's Syndrome With Intermittent Neutropenia and Lymphocyte Subset Disturbances To the Editor: Schwachman's syndrome, a familial disease transmitted as an autosomal-recessive trait, is characterized by moderate chronic neutropenia, marked marrow hypocellularity, occasional thromb