Welander distal myopathy outside the Swedish population: Phenotype and genotype

Neuromuscular Disorders

Volumn 12, Issue 6, 2002, Pages 544-547

  Von Tell, Désirée ^a   Somer, Hannu ^b   Udd, Bjarne ^c   Edström, Lars ^a   Borg, Kristian ^a   Åhlberg, Gabrielle ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c VAASA CENTRAL HOSPITAL   (Finland)

Author keywords

Genotype; Phenotype; Swedish population; Welander distal myopathy

Indexed keywords

MARKER;

ADULT; AGED; ARTICLE; CHROMOSOME 2P; CLINICAL ARTICLE; CONTROLLED STUDY; DISTAL MYOPATHY; EXTENSOR MUSCLE; FEMALE; FINLAND; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN TISSUE; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; SWEDEN;

AGE OF ONSET; AGED; AGED, 80 AND OVER; CHROMOSOME ABERRATIONS; FEMALE; FINLAND; GENOTYPE; HAPLOTYPES; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MUSCULAR DISEASES; MUTATION; PEDIGREE; PHENOTYPE; SWEDEN;

EID: 0036315171     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(01)00338-8     Document Type: Article

References (9)

1. Myopathia distalis tarda hereditaria
2. Genetic linkage of Welander distal myopathy to chromosome 2p13
3. Welander's distal myopathy: Clinical, neurophysiological and muscle biopsy observations in young and middle-aged adults with early symptoms
4. Histochemical and histopatological changes in skeletal muscles in late-onset hereditary myopathy (Welander)
5. Neurogenic involvement in distal myopathy (Welander)
6. Distribution of muscle degeneration in Welander distal myopathy-a magnetic resonance and muscle biopsy study
7. Rapid examination of muscle tissue: An improved trichrome method for fresh-frozen biopsy sections
8. The specificity of the histochemical method of adenosine triphosphatase
9. Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies