Results 171 to 180 of about 319,403 (201)

[Late onset of type I familial amyloid neuropathy: results of biopsy from accessory salivary glands].

Revue neurologique, 1999
Familial amyloidotic polyneuropathy (FAP) type I is usually characterized by onset in the third decade, autonomic nervous system failure, and heart block conduction occurring after the onset of neurological symptoms. A 74-year-old woman, with past medical history of a third degree heart block treated by a pace-maker, was hospitalized because of an ...
A, Mackowiak, T, Stojkovic, J F, Hurtevent, C A, Maurage, P, Vermersch   +4 more
openaire   +1 more source

3D Blockage Mapping for Identifying Familial Point Mutations in Single Amyloid‐β Peptides with a Nanopore

Angewandte Chemie - International Edition, 2022
Yitao Long
exaly  

Recent progress in Lynch syndrome and other familial colorectal cancer syndromes

Ca-A Cancer Journal for Clinicians, 2018
Patrick M Boland, Matthew Yurgelun, Clement Richard Boland   +2 more
exaly  

Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2011
Masahiro Iijima, Haruki Koike
exaly  

S.I.4 Therapeutic approaches for familial amyloid neuropathies

Neuromuscular Disorders, 2011
openaire   +1 more source

Familial amyloid polyneuropathy: mechanisms leading to nerve degeneration

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2003
Gérard Said
exaly  

Serum transthyretin monomer in patients with familial amyloid polyneuropathy

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2001
Fuyuki Kametani, Yoshiki Sekijima, Kei Maruyama   +2 more
exaly  

P21-17 Early detection of small-fiber neuropathy in familial amyloid polyneuropathy patients

Clinical Neurophysiology, 2010
I.S. Conceicao, J.F. Castro, J.P. Costa, M.A. de Carvalho   +3 more
openaire   +1 more source

Long-term quantitative evaluation of liver transplantation in familial amyloid polyneuropathy (Portuguese V30M)

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2002
Mamede de Carvalho, Carla Bentes
exaly  

Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 1990
C P Maury
exaly