## Abstract Richter syndrome (RS) represents the clinicoβpathologic transformation of chronic lymphocytic leukaemia (CLL) to an aggressive lymphoma, most commonly diffuse large Bβcell lymphoma (DLBCL). The clinical definition of RS is heterogeneous, and encompasses at least two biologically differe
Rett syndrome: new clinical and molecular insights
β Scribed by Williamson, Sarah L; Christodoulou, John
- Book ID
- 110026583
- Publisher
- Nature Publishing Group
- Year
- 2006
- Tongue
- English
- Weight
- 219 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1018-4813
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The presentation and clinical diagnosis of Rett syndrome at various ages and stages are reviewed. In addition to the classical form, variability in phenotype between different atypical Rett forms is given. Obligatory, supportive, and differential diagnostic criteria are summarized. Long-term follow-
An analysis of all aphidicolin-inducible breakpoints has been carried out in PHA stimulated T-lymphocytes of five patients with classical Rett syndrome, their mothers and a group of age matched controls. Observed breakpoints were divided into two groups: common, rare, and those recorded by others bu