Latest papers

Charcot spine in a person with congenital insensitivity to pain with anhydrosis: a case report of re-diagnosis.

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.

A molecular genetic update of inherited distal motor neuropathies.

The pitfalls of profoundly effective analgesic therapies.

Hereditary sensory neuropathy type I.

Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report.

[Hereditary neuropathy with liability to pressure palsies (HNPP) in hand surgery: reminds and warn against a usually unrecognised disease].

Hereditary sensory and autonomic neuropathy type I in a Chinese family: British C133W mutation exists in the Chinese.

Distal truncation of KCC3 in non-French Canadian HMSN/ACC families.

Spinal anesthesia in a patient with congenital insensitivity to pain with anhidrosis.

A case of herpes zoster in a child with congenital insensitivity to pain with anhidrosis.

Sorting out the inherited neuropathies.

Autonomic peripheral neuropathy.

Hereditary sensory and autonomic neuropathies: types II, III, and IV.

ALS in a patient with hereditary neuropathy with liability to pressure palsy.

Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up.

Early involvement of the spinal cord in diabetic peripheral neuropathy.

Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings.

Respiratory failure in infants due to spinal muscular atrophy with respiratory distress type 1.

[Hand involvement in Thevenard's disease: a new phlegmonous form. An exceptional case report].