๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Lymphocyte phenotype and function in chronically transfused children with sickle cell disease

โœ Scribed by Winfred Wang; Henry Herrod; Gerald Presbury; Judith Wilimas


Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
571 KB
Volume
20
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Patterns of hepatic iron distribution in
โœ Nilesh R. Ghugre; Ignacio Gonzalez-Gomez; Ellen Butensky; Leila Noetzli; Roland ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 190 KB ๐Ÿ‘ 2 views

## Abstract Patients with sickle cell disease (SCD) appear to be at lower risk of endocrinopathies and cardiac dysfunction than those with thalassemia major (TM). Circulating redox active iron is lower in these patients, possibly due to increased systemic inflammation and circulating cytokines. Hep

Erythrocytapheresis for chronically tran
โœ Sylvia T. Singer; Keith Quirolo; Kuai Nishi; Ekua Hackney-Stephens; Cherie Evans ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 54 KB

Cerebrovascular accident (CVA) is a major complication of sickle cell disease during childhood. Long-term transfusion reduces the hemoglobin S level and generally prevents recurrent stroke, but it also results in progressive iron overload that requires regular chelation therapy. Erythrocytapheresis

Lung function in infants with sickle cel
โœ Anastassios C. Koumbourlis; Anne Hurlet-Jensen; Michael R. Bye ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 58 KB ๐Ÿ‘ 2 views

We performed pulmonary function testing in 20 infants (11 male and 9 female; ages 3-30 months) with sickle cell disease to assess whether abnormal lung function develops early in life. Respiratory system compliance (C rs ) and resistance (R rs ) were measured by the passive occlusion technique, func