Found: 8
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Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 5, p. 273, doi. 10.1038/jhg.2013.15
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- Publication type:
- Article
Identification of <i>ATP1A3</i> Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056120
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- Article
Sporadic VACTERL Association in a Japanese Family with Sjögren-Larsson Syndrome.
- Published in:
- 2013
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- Case Study
Clinical and genetic investigation of 17 Japanese patients with hyperekplexia.
- Published in:
- Developmental Medicine & Child Neurology, 2015, v. 57, n. 4, p. 372, doi. 10.1111/dmcn.12617
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- Publication type:
- Article
Reversible infantile respiratory chain deficiency: A clinical and molecular study.
- Published in:
- Annals of Neurology, 2010, v. 68, n. 6, p. 845, doi. 10.1002/ana.22111
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- Publication type:
- Article
Self-limited lupus-like presentation of human parvovirus B19 infection in a 1-year-old girl.
- Published in:
- Pediatrics International, 2009, v. 51, n. 3, p. 411, doi. 10.1111/j.1442-200X.2009.02829.x
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- Article
Acute Disseminated Encephalomyelitis: The Time Until Diagnosis and Its Subsequent Course in Children.
- Published in:
- Journal of Child Neurology, 2014, v. 29, n. 1, p. 28, doi. 10.1177/0883073812465013
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- Publication type:
- Article
Finger Cold-Induced Vasodilatation, Sympathetic Skin Response, and R-R Interval Variation in Patients With Progressive Spinal Muscular Atrophy.
- Published in:
- Journal of Child Neurology, 2005, v. 20, n. 11, p. 871, doi. 10.1177/08830738050200110301
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- Publication type:
- Article