Found: 7
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Clinical heterogeneity in two pedigrees with the 3243 bp tRNA<sup>Leu(UUR)</sup> mutation of mitochondrial DNA.
- Published in:
- Acta Neurologica Scandinavica, 1995, v. 91, n. 1, p. 62, doi. 10.1111/j.1600-0404.1995.tb05845.x
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- Publication type:
- Article
Controlled and uncontrolled thrombocytosis. Its clinical role in essential thrombocythemia.
- Published in:
- 1988
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- Publication type:
- journal article
Chronic Paroxysmal Hemicrania-Tic Syndrome.
- Published in:
- Headache: The Journal of Head & Face Pain, 2000, v. 40, n. 8, p. 682, doi. 10.1046/j.1526-4610.2000.040008682.x
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- Publication type:
- Article
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
- Published in:
- 2005
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- Publication type:
- Journal Article
LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene.
- Published in:
- Brain: A Journal of Neurology, 2005, v. 128, n. 4, p. 732
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- Publication type:
- Article
Gangliosides and Guillain-Barré Syndrome: The Spanish Data.
- Published in:
- Neuroepidemiology, 1993, v. 12, n. 5, p. 251, doi. 10.1159/000110325
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- Publication type:
- Article
Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion.
- Published in:
- 2001
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- Publication type:
- journal article