Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1991 • 1,293 citations

Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP)

1991 • 813 citations

THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND II

1980 • 805 citations

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1991 • 587 citations

The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A

1992 • 497 citations

QUALITATIVE AND QUANTITATIVE MORPHOLOGY OF HUMAN SURAL NERVE AT DIFFERENT AGES

1985 • 436 citations

Neuropathy associated with monoclonal gammopathies of undetermined significance

1991 • 230 citations

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1989 • 198 citations

The clinical spectrum of peripheral neuropathies associated with benign monoclonal IgM, IgG and IgA paraproteinaemia

1991 • 188 citations

De-novo mutation in hereditary motor and sensory neuropathy type I

1992 • 160 citations

Prednisone-responsive hereditary motor and sensory neuropathy.

1982 • 121 citations

Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)

1992 • 45 citations

Polyneuropathies Associated with Plasma Cell Dyscrasias

1987 • 41 citations

Polyneuropathies Associated with Plasma Cell Dyscrasias

1987 • 16 citations