HMSN III phenotype due to homozygous expression of a dominant HMSN II gene

Neurology ◽

10.1212/wnl.42.11.2201 ◽

1992 ◽

Vol 42 (11) ◽

pp. 2201-2201 ◽

Author(s):

A. Sghirlanzoni ◽

D. Pareyson ◽

M. R. Balestrini ◽

E. Bellone ◽

E. Berta ◽

...

Keyword(s):

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HMSN II (CMT2) and Miscellaneous Inherited System Atrophies of Nerve Axon: Clinical–Molecular Genetic Correlates

Peripheral Neuropathy ◽

10.1016/b978-0-7216-9491-7.50076-4 ◽

2005 ◽

pp. 1717-1751 ◽

Author(s):

CHRISTOPHER J. KLEIN ◽

PETER J. DYCK

Keyword(s):

Molecular Genetic ◽

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Hereditary motor and sensory neuropathy type II (HMSN-II) and neurogenic muscle hypertrophy: a case report and literature review

The Italian Journal of Neurological Sciences ◽

10.1007/bf00831570 ◽

1998 ◽

Vol 19 (3) ◽

pp. 184-188 ◽

Author(s):

M. Maurelli ◽

E. Candeloro ◽

M. T. Egitto ◽

E. Alfonsi

Keyword(s):

Case Report ◽

Literature Review ◽

Muscle Hypertrophy ◽

Sensory Neuropathy ◽

Type Ii ◽

Hereditary Motor ◽

Hmsn Ii ◽

Motor And Sensory Neuropathy

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2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2–HMSN II) and Distal Hereditary Motor Neuropathy (Distal HMN–Spinal CMT)

Neuromuscular Disorders ◽

10.1016/s0960-8966(98)00025-x ◽

1998 ◽

Vol 8 (6) ◽

pp. 426-431 ◽

Author(s):

Peter De Jonghe ◽

Vincent Timmerman ◽

Christine Van Broeckhoven

Keyword(s):

International Workshop ◽

Motor Neuropathy ◽

Charcot Marie Tooth ◽

Hereditary Motor ◽

Hereditary Motor Neuropathy ◽

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