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

[Case of LGMD2A (calpainopathy) clinically presenting as Miyoshi distal myopathy].

Rinsho shinkeigaku = Clinical neurology - 1 Sept 2008

Shirafuji Toshihiko, Otsuka Yoshihisa, Kobessho Hiroshi, Minami Narihiro, Hayashi Yukiko, Nishino Ichizo, Kanda Fumio

Abstract excerpt

We reported a 23-year-old woman with distal myopathy and highly elevated serum creatine kinase (CK) caused by calpainopathy. Although muscle weakness was not evident, a muscle CT scan revealed replacement by adipose tissue in the medial head of the gastrocnemius. The gluteus maximus and biceps fe...

Read the complete abstract on PubMed

Topics

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

Share to Calpain
Share to Creatine Kinase
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Distal Myopathies

Share to Muscle Proteins

Share to Muscle, Skeletal

Share to Muscular Dystrophies, Limb-Girdle

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 19048948
DOI: 10.5692/clinicalneurol.48.651

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19048948-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Case of LGMD2A (calpainopathy) clinically presenting as Miyoshi distal myopathy].PMID 19048948Read ↗

[A case of LGMD2A identified with both western blot analysis and immunostaining of calpain 3 in biopsied muscle].Semantic proximity Read ↗

[Calpainopathies: state of the art and therapeutic perspectives].Semantic proximity Read ↗

[LGMD2A(calpain 3 deficiency)].Semantic proximity Read ↗

Experiences in the molecular genetic and histopathological evaluation of calpainopathies.Semantic proximity Read ↗

[Recent advances in limb-girdle muscular dystrophy research].Semantic proximity Read ↗

The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B).Semantic proximity Read ↗

[A male patient with adult-onset sporadic calpainopathy presenting with hypertrophy of the upper extremities].Semantic proximity Read ↗

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.Semantic proximity Read ↗

[Miyoshi distal muscular dystrophy (Miyoshi myopathy)].Semantic proximity Read ↗

Calpain-3 mutations in Turkey.Semantic proximity Read ↗

[Muscular dystrophy and calpain].Semantic proximity Read ↗

[A patient with distal muscular dystrophy without mutations in dysferlin gene but with abnormal dysferlin localization in muscle fibers].Semantic proximity Read ↗

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