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Article title matches
- Category:Desmin-related myopathy (54 bytes)
1: List of pages with the keyword Desmin-related myopathy - Category:Myopathy (39 bytes)
1: List of pages with the keyword Myopathy
Page text matches
- 2ald (2,878 bytes)
10: ...tic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.<ref... - 4ald (3,551 bytes)
11: ...tic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.<ref... - 9f4g (4,289 bytes)
11: ...MAN] Amyotrophic lateral sclerosis;Inclusion body myopathy with Paget disease of bone and frontotemporal dem... - 9f5d (4,282 bytes)
11: ...MAN] Amyotrophic lateral sclerosis;Inclusion body myopathy with Paget disease of bone and frontotemporal dem... - 9oyo (2,399 bytes)
10: ...r neuron disease;Autosomal dominant mitochondrial myopathy with exercise intolerance;Amyotrophic lateral scl... - 9oyq (2,393 bytes)
10: ...r neuron disease;Autosomal dominant mitochondrial myopathy with exercise intolerance;Amyotrophic lateral scl... - 9oys (2,398 bytes)
10: ...r neuron disease;Autosomal dominant mitochondrial myopathy with exercise intolerance;Amyotrophic lateral scl... - 9oyw (2,394 bytes)
10: ...r neuron disease;Autosomal dominant mitochondrial myopathy with exercise intolerance;Amyotrophic lateral scl... - 2uzi (7,478 bytes)
11: ...ef> Defects in HRAS are the cause of congenital myopathy with excess of muscle spindles (CMEMS) [MIM:[http... - 7lmz (6,605 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln0 (6,605 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln1 (6,604 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln2 (6,647 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln3 (6,647 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln4 (6,644 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln5 (6,663 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 7ln6 (6,662 bytes)
11: ...N] Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal... - 2clc (7,685 bytes)
11: ...ef> Defects in HRAS are the cause of congenital myopathy with excess of muscle spindles (CMEMS) [MIM:[http... - 2cl6 (7,714 bytes)
11: ...ef> Defects in HRAS are the cause of congenital myopathy with excess of muscle spindles (CMEMS) [MIM:[http... - 2cld (7,557 bytes)
11: ...ef> Defects in HRAS are the cause of congenital myopathy with excess of muscle spindles (CMEMS) [MIM:[http...
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