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

Uncompacted myelin lamellae in peripheral nerve biopsy.

Ultrastructural pathology - 1 Jan 2000

Vital Claude, Vital Anne, Bouillot Sandrine, Favereaux Alexandre, Lagueny Alain, Ferrer Xavier, Brechenmacher Christiane, Petry Klaus G

Abstract excerpt

Since 1979, the authors have studied 49 peripheral nerve biopsies presenting uncompacted myelin lamellae (UML). Based on the ultrastructural pattern of UML they propose a 3-category classification. The first category includes cases displaying regular UML, which was observed in 43 cases; it was more frequent in 9 cases with polyneuropathy organomegaly endocrinopathy m-protein skin changes (POEMS) syndrome as well...

Read the complete abstract on PubMed

Topics

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

Share to Charcot-Marie-Tooth Disease
Share to Lymphoma, B-Cell

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Myelin-Associated Glycoprotein

Share to Myelin P0 Protein

Share to Myelin Sheath

Share to Paraproteinemias

Share to Peripheral Nerves

Share to Peripheral Nervous System Diseases

Source

Identifiers

PMID: 12554530
DOI: 10.1080/01913120309941

Genes

MAG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Uncompacted myelin lamellae in peripheral nerve biopsy.PMID 12554530Read ↗

Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.Semantic proximity Read ↗

Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero.Semantic proximity Read ↗

Novel pathologic findings in patients with Pelizaeus-Merzbacher disease.Semantic proximity Read ↗

Molecular structure and function of myelin protein P0 in membrane stackingSemantic proximity Read ↗

How Does Protein Zero Assemble Compact Myelin?Semantic proximity Read ↗

Identification of PMD subgroups using a myelination score for PMD.Semantic proximity Read ↗

Uncompacted inner myelin lamellae in inherited tendency to pressure palsy.Semantic proximity Read ↗

Myelin: keeping nerves well wrapped up.Semantic proximity Read ↗

Ultrastructural Distribution of PMP22 in Charcot-Marie-Tooth Disease Type 1ASemantic proximity Read ↗

Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Axon damage in CMT due to mutation in myelin protein P0.Semantic proximity Read ↗

Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report.Semantic proximity Read ↗

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