Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Two causes of demyelinating neuropathy in one patient: CMT1A and POEMS syndrome.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques - 1 Aug 2007

Chahin Nizar, Zeldenrust Steven R, Amrami Kimberly K, Engelstad Janean K, Dyck P James B

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Antibodies, Monoclonal, Humanized
Share to Bevacizumab
Share to Charcot-Marie-Tooth Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Demyelinating Diseases

Share to Inheritance Patterns

Share to Melphalan

Share to Peripheral Nerves

Share to Peripheral Nervous System Diseases

Source

Identifiers

PMID: 17803044
DOI: 10.1017/s0317167100006892

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Two causes of demyelinating neuropathy in one patient: CMT1A and POEMS syndrome.PMID 17803044Read ↗

A Patient With DNMT1 Gene Mutation Presenting With Polyneuropathy, Hearing Loss, and Personality Changes.Semantic proximity Read ↗

Persistent CNS dysfunction in a boy with CMT1XSemantic proximity Read ↗

Novel mutation of the myelin P0 gene in a CMT1B family.Semantic proximity Read ↗

Mutations of the same sequence of the myelin P0 gene causing two different phenotypes.Semantic proximity Read ↗

Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.Semantic proximity Read ↗

Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutation.Semantic proximity Read ↗

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.Semantic proximity Read ↗

Mutations in the plasma cell clone identify mechanism of polyneuropathy in a case of POEMS syndrome associated with Castleman disease and multiple myeloma.Semantic proximity Read ↗

Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene.Semantic proximity Read ↗

A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia.Semantic proximity Read ↗

Nerve ultrasound in patients with CMT1C: description of 3 cases.Semantic proximity Read ↗

Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.