Found: 9
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Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus.
- Published in:
- Diabetic Medicine, 2001, v. 18, n. 8, p. 685, doi. 10.1046/j.1464-5491.2001.00530-2.x
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- Publication type:
- Article
Warfarin maintenance dose associated with genetic polymorphisms of CYP2C9.
- Published in:
- Hippokratia, 2017, v. 21, n. 2, p. 93
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- Publication type:
- Article
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia.
- Published in:
- Clinical Genetics, 2017, v. 92, n. 5, p. 534, doi. 10.1111/cge.13008
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- Publication type:
- Article
A Novel Missense Mutation in Human TTF-2 (FKHL15) Gene Associated with Congenital Hypothyroidism But Not Athyreosis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 10, p. 4183, doi. 10.1210/jc.2006-0405
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- Publication type:
- Article
Clinicopathological and genetic study of early-onset demyelinating neuropathy.
- Published in:
- 2004
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- Publication type:
- Journal Article
X-linked Charcot-Marie-Tooth disease and multiple sclerosis.
- Published in:
- Journal of Neurology, 2007, v. 254, n. 7, p. 953, doi. 10.1007/s00415-006-0324-7
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- Publication type:
- Article
High frequency of GJA12/ GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 1, p. 66, doi. 10.1111/j.1399-0004.2012.01846.x
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- Publication type:
- Article
Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 396, doi. 10.1034/j.1399-0004.2000.580511.x
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- Publication type:
- Article
Reply.
- Published in:
- Muscle & Nerve, 2012, v. 46, n. 2, p. 296, doi. 10.1002/mus.23328
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- Publication type:
- Article