Found: 6
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Coexistent hereditary and inflammatory neuropathy.
- Published in:
- Brain: A Journal of Neurology, 2004, v. 127, n. 1, p. 193, doi. 10.1093/brain/awh017
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- Publication type:
- Article
Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons.
- Published in:
- Annals of Neurology, 2006, v. 60, n. 2, p. 253
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- Publication type:
- Article
A novel RAB7 mutation associated with ulcero‐mutilating neuropathy.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 4, p. 586, doi. 10.1002/ana.20281
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- Publication type:
- Article
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 15, p. 1839, doi. 10.1093/hmg/ddg192
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- Publication type:
- Article
Binding of [3H]-5-hydroxytryptamine to human coronary artery and bypass graft vessels.
- Published in:
- Cardiovascular Research, 1996, v. 31, n. 5, p. 800, doi. 10.1016/S0008-6363(96)00029-6
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- Publication type:
- Article