Number of the records: 1
neuropatie amyloidné familiárne
SYS d028227 LBL 00000nz--a2200000o--4500 005 20250606215437.8 008 010725|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C10.574.500.050 065 $a C10.668.829.050.050 065 $a C16.320.400.050 065 $a C16.320.565.176.050 065 $a C18.452.648.176.050 065 $a C18.452.845.500.050.050 065 $a C18.452.845.500.075.050 066 $a 01 $c 03 150 $a neuropatie amyloidné familiárne $x BL $x CF $x CI $x CL $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 $2 slo 450 $w v $a Familial Amyloid Polyneuropathies $2 eng 450 $w v $a polyneuropatie amyloidové familiárne $2 slo 450 $w v $a Wohlwill-Andradov syndróm $2 slo 450 $w v $a Wohlwill-Corino Andradov syndróm $2 slo 665 $a 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001 $2 eng 665 $a Amyloid Neuropathies (1994-2001) $2 eng 665 $a Amyloidosis (1967-1993) $2 eng 665 $a Peripheral Nervous System Diseases (1967-1993) $2 eng 680 9-
$i Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. $2 eng 750 -2
$a Amyloid Neuropathies, Familial $2 eng 980 $x M
Number of the records: 1