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Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. [electronic resource] by
- Hirano, M
- Silvestri, G
- Blake, D M
- Lombes, A
- Minetti, C
- Bonilla, E
- Hays, A P
- Lovelace, R E
- Butler, I
- Bertorini, T E
Producer: 19940524
In:
Neurology vol. 44
Availability: No items available.
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13.
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Multifocal motor neuropathy with conduction block: is it a distinct clinical entity? [electronic resource] by
- Lange, D J
- Trojaborg, W
- Latov, N
- Hays, A P
- Younger, D S
- Uncini, A
- Blake, D M
- Hirano, M
- Burns, S M
- Lovelace, R E
Producer: 19920423
In:
Neurology vol. 42
Availability: No items available.
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14.
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Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. [electronic resource] by
- Wilhelmsen, K C
- Blake, D M
- Lynch, T
- Mabutas, J
- De Vera, M
- Neystat, M
- Bernstein, M
- Hirano, M
- Gilliam, T C
- Murphy, P L
- Sola, M D
- Bonilla, E
- Schotland, D L
- Hays, A P
- Rowland, L P
Producer: 19960611
In:
Annals of neurology vol. 39
Availability: No items available.
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