Found: 15
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Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
- Published in:
- International Journal of Neuropsychopharmacology, 2004, v. 7, n. 2, p. 183, doi. 10.1017/s146114570400416x
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- Article
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts.
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- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-57
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- Article
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts.
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- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-57
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- Article
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
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- Nature Genetics, 2005, v. 37, n. 10, p. 1044, doi. 10.1038/ng1649
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- Article
Reply.
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- Muscle & Nerve, 2011, v. 44, n. 2, p. 303, doi. 10.1002/mus.22122
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- Article
REPORT of a novel mutation in the PMP22 gene causing an axonal neuropathy.
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- Muscle & Nerve, 2011, v. 43, n. 4, p. 605, doi. 10.1002/mus.21973
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- Article
Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy.
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- Journal of Neurology, 2010, v. 257, n. 11, p. 1864, doi. 10.1007/s00415-010-5624-2
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- Article
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.
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- Human Genetics, 2018, v. 137, n. 11/12, p. 911, doi. 10.1007/s00439-018-1952-6
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- Article
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.
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- European Journal of Human Genetics, 1999, v. 7, n. 8, p. 920, doi. 10.1038/sj.ejhg.5200384
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- Article
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C.
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- NeuroMolecular Medicine, 2019, v. 21, n. 2, p. 182, doi. 10.1007/s12017-019-08534-w
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- Article
Enhanced Rapid-Onset Cortical Plasticity in CADASIL as a Possible Mechanism of Preserved Cognition.
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- Cerebral Cortex, 2011, v. 21, n. 12, p. 2774, doi. 10.1093/cercor/bhr071
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- Article
Specific pattern of early white-matter changes in pure hereditary spastic paraplegia.
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- Movement Disorders, 2010, v. 25, n. 12, p. 1986, doi. 10.1002/mds.23211
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- Article
A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.
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- Movement Disorders, 2010, v. 25, n. 4, p. 413, doi. 10.1002/mds.22949
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- Article
Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1421952
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- Article
Interaction of BDNF and COMT Polymorphisms on Paired-Associative Stimulation-Induced Cortical Plasticity.
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- Journal of Neuroscience, 2012, v. 32, n. 13, p. 4553, doi. 10.1523/JNEUROSCI.6010-11.2012
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- Article