Found: 11
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Everolimus Treatment for an Early Infantile Subependymal Giant Cell Astrocytoma With Tuberous Sclerosis Complex.
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- Journal of Child Neurology, 2015, v. 30, n. 9, p. 1192, doi. 10.1177/0883073814544703
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- Article
In response to terminology and prognosis of Dravet syndrome.
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- Epilepsia (Series 4), 2014, v. 55, n. 6, p. 943, doi. 10.1111/epi.12640
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- Article
Long-term course of Dravet syndrome: A study from an epilepsy center in Japan.
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- Epilepsia (Series 4), 2014, v. 55, n. 4, p. 528, doi. 10.1111/epi.12532
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- Article
CDKL5 alterations lead to early epileptic encephalopathy in both genders.
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- Epilepsia (Series 4), 2011, v. 52, n. 10, p. 1835, doi. 10.1111/j.1528-1167.2011.03174.x
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- Article
Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome.
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- Epilepsia (Series 4), 2011, v. 52, n. 6, p. 1144, doi. 10.1111/j.1528-1167.2011.03053.x
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- Article
Mortality in Dravet syndrome: Search for risk factors in Japanese patients.
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- Epilepsia (Series 4), 2011, v. 52, p. 50, doi. 10.1111/j.1528-1167.2011.03002.x
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- Article
Quantification of BK polyoma viruria in Japanese children and adults with hemorrhagic cystitis complicating stem cell transplantation.
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- Journal of Medical Virology, 2008, v. 80, n. 12, p. 2108, doi. 10.1002/jmv.21328
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- Article
Quantification of adenovirus species B and C viremia by real‐time PCR in adults and children undergoing stem cell transplantation.
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- Journal of Medical Virology, 2007, v. 79, n. 3, p. 278, doi. 10.1002/jmv.20796
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- Article
Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 561, doi. 10.1038/jhg.2011.58
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- Article
Occurrence of the African subgroup (Ia) of BK polyomavirus in younger Japanese children.
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- Microbiology & Immunology, 2009, v. 53, n. 6, p. 319, doi. 10.1111/j.1348-0421.2009.00129.x
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- Article
Ambroxol chaperone therapy for neuronopathic Gaucher disease: A pilot study.
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- Annals of Clinical & Translational Neurology, 2016, v. 3, n. 3, p. 200, doi. 10.1002/acn3.292
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- Article