Detection of different forms of variant transthyretin (Met30) in cerebrospinal fluid
- 1 December 1997
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 238 (3) , 123-126
- https://doi.org/10.1016/s0304-3940(97)00868-9
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Transthyretin amyloidosis: A new mutation associated with dementiaAnnals of Neurology, 1997
- Post translational modification of serum TTRNeuromuscular Disorders, 1996
- LIVER TRANSPLANTATION IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY FOLLOW-UP OF THE FIRST 20 SWEDISH PATIENTSTransplantation, 1995
- Change in Variant Transthyretin Levels in Patients with Familial Amyloidotic Polyneuropathy Type I Following Liver TransplantationBiochemical and Biophysical Research Communications, 1995
- Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosisThe Lancet, 1993
- FAMILIAL AMYLOID POLYNEUROPATHY ASSOCIATED WITH THE TRANSTHYRETIN CYS114 GENE IN A JAPANESE KINDREDBrain, 1992
- Homozygosity for the transthyretin‐Met30‐gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequencesClinical Genetics, 1992
- New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysisBiochemical and Biophysical Research Communications, 1991
- Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniquesBiochemical and Biophysical Research Communications, 1984
- The Concentration of Prealbumin in Cerebrospinal Fluid (CSF), Indicator of CSF Circulation DisordersEuropean Neurology, 1983