Počet záznamov: 1
neuropatie amyloidné
SYS d017772 LBL 00000cx--j2200000---45-- 005 20240119200207.9 100 $a 19930630asloy0103----ba0 152 $b mesh 250 $a neuropatie amyloidné $x BL $x CF $x CI $x CL $x CN $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 1994 $8 eng 300 1-
$a Amyloidosis (1967-1993) $8 eng 300 1-
$a Peripheral Nervous System Diseases (1967-1993) $8 eng 330 1-
$a Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) $8 eng 450 $a Neuropathies, Amyloid $5 e $8 eng 450 $a neuropatie amyloidové $5 e $8 slo 450 $a neuropatie spôsobené amyloidózou $5 e $8 slo 450 $a neuropatie amyloidné, sekundárne $5 e $8 slo 450 $a polyneuropatie amyloidné $5 e $8 slo 686 $a C10.668.829.050 686 $a C18.452.845.500.050 750 $a Amyloid Neuropathies $8 eng 801 -0
$a US $b DNLM $c 19930630 801 -2
$a SK $b BA006 $c 20020410 801 -2
$a SK $b BA006 $c 20150601 820 $a coord IM with specific neurol dis (IM) or specific nerve (IM); /genet: consider also AMYLOID NEUROPATHIES, FAMILIAL $8 eng 980 $x M
Počet záznamov: 1