15 results on '"Udd B"'
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2. ‘Pathognomonic’ muscle imaging findings in DNAJB6 mutated LGMD1D
3. Altered expression and splicing of Ca2+ metabolism genes in myotonic dystrophies DM1 and DM2
4. Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients
5. Normal muscle MRI does not preclude increased connective tissue in muscle of recessive myotonia congenita
6. Myopathies caused by homozygous titin mutations: limb-girdle muscular dystrophy 2J and variations of phenotype
7. Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients
8. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration
9. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases: EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases
10. Do carriers of POLG mutation W748S have disease manifestations?
11. Zaspopathy in a large classic late-onset distal myopathy family
12. Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy
13. Enrichment of the R77C α-sarcoglycan gene mutation in finnish LGMD2D patients
14. Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy
15. High prevalence of Kennedy's disease in Western Finland - is the syndrome underdiagnosed?
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