DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1993 • 791 citations

Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1A

1992 • 295 citations

HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES. ELECTROPHYSIOLOGICAL AND HISTOPATHOLOGICAL ASPECTS

1972 • 241 citations

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

1992 • 140 citations

Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study

1993 • 98 citations

Hereditary compression syndrome of peripheral nerves

1965 • 40 citations

Conduction block in hereditary neuropathy with susceptibility to pressure palsies

1987 • 35 citations

FAMILIAL RECURRENT POLYNEUROPATHY: A FAMILY AND A SURVEY

1972 • 32 citations

Quantitative measurement of duplicated DNA as a diagnostic test for Charcot-Marie-Tooth disease type 1a

1993 • 25 citations

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1

1993 • 23 citations