## Abstract Movement disturbances are common in dementia disorders and are a central feature of the clinical classification criteria of CreutzfeldtβJakob disease (CJD). Polymorphism at codon 129 of the prion protein gene is known to determine the clinical picture of CJD. The frequency and character
Microelectrophoresis in the differential diagnosis of proteinuric diseases
β Scribed by Dr. Michael H. Weber; Kyung-Sun Cheong (Kim); Klaus-Joachim Schott; Volker Neuholff
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 899 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
We present our approach to the diagnosis of pediatric neurotransmitter diseases exemplified by the differential diagnosis of children presenting with dystonia. This approach is based upon the primary aim of early diagnosis of treatable conditions and the need for a logical series of investigations.
The utility of immunohistochemical staining for leukocyte common antigen (LCA) in the differential diagnosis of Hodgkin's disease was studied in a series of 42 cases of Hodgkin's and non-Hodgkin's lymphoma and compared with Leu M-1, a proposed marker for Reed-Sternberg cells. LCA staining of neoplas
## Background: The objective of the study was to evaluate the diagnostic accuracy of recently developed antiglycan serological tests in clinical practice for the diagnosis of Crohn's disease. ## Methods: This study was a cohort analysis of both clinical and biochemical parameters of patients wi
## Abstract Renal involvement in lipid storage diseases is well recognized. Electron microscopy or chemical analysis of urinary sediment has been used for the diagnosis of these diseases. Urine cytology, supplemented by cytochemistry, polarization, and autofluorescence, helped us in the diagnosis o