Found: 72
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Guillain-Barré syndrome after rtPA therapy for acute stroke.
- Published in:
- 2010
- By:
- Publication type:
- case study
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Cerebrospinal fluid biomarkers in progranulin mutations carriers.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer's Disease: Genetics and Expression Analysis.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
- Published in:
- 2011
- By:
- Publication type:
- journal article
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype.
- Published in:
- Scientific Reports, 2016, p. 21301, doi. 10.1038/srep21301
- By:
- Publication type:
- Article
Persistent inflammation, immunosuppression and catabolism syndrome (PICS) in critically ill children is associated with clinical outcomes: a prospective longitudinal study.
- Published in:
- Journal of Human Nutrition & Dietetics, 2021, v. 34, n. 2, p. 365, doi. 10.1111/jhn.12798
- By:
- Publication type:
- Article
IgD Multiple Myeloma Paraproteinemia as a Cause of Myositis.
- Published in:
- Neurology Research International, 2010, p. 1, doi. 10.1155/2010/808474
- By:
- Publication type:
- Article
Stem cell therapy in stroke.
- Published in:
- Cellular & Molecular Life Sciences, 2009, v. 66, n. 5, p. 757, doi. 10.1007/s00018-008-8346-1
- By:
- Publication type:
- Article
CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133<sup>+</sup> stem cells.
- Published in:
- Cellular & Molecular Life Sciences, 2009, v. 66, n. 4, p. 697, doi. 10.1007/s00018-009-8652-2
- By:
- Publication type:
- Article
Nomadic beekeeper movements create the potential for widespread disease in the honeybee industry.
- Published in:
- Australian Veterinary Journal, 2014, v. 92, n. 8, p. 283, doi. 10.1111/avj.12198
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- Publication type:
- Article
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis.
- Published in:
- Molecular Biology & Evolution, 2012, v. 29, n. 6, p. 1599, doi. 10.1093/molbev/mss002
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- Publication type:
- Article
Session 6 PFO.
- Published in:
- Medical & Surgical Pediatrics / Pediatria Medica e Chirurgica, 2009, v. 31, n. 1, p. 36
- By:
- Publication type:
- Article
Synaptotagmin 13 is neuroprotective across motor neuron diseases.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 5, p. 837, doi. 10.1007/s00401-020-02133-x
- By:
- Publication type:
- Article
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency.
- Published in:
- Acta Neuropathologica, 2003, v. 105, n. 6, p. 537, doi. 10.1007/s00401-002-0654-1
- By:
- Publication type:
- Article
Vagus nerve stimulation in treatment-resistant depression. Long-term clinical outcomes.
- Published in:
- European Psychiatry, 2021, v. 64, p. S492, doi. 10.1192/j.eurpsy.2021.1316
- By:
- Publication type:
- Article
P01-199 - Selective DNA methylation of BDNF promoter and nociceptin gene in bipolar disorder
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Intra-aortic injection of myoblasts in mdx mice: genetic and technetium-99m cell labeling and biodistribution.
- Published in:
- 1997
- By:
- Publication type:
- journal article
In vivo biolistic technique in control and mdx dystrophic mice.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiency.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Efficacy and tolerability of eperisone and baclofen in spastic palsy: a double-blind randomized trial.
- Published in:
- Advances in Therapy, 2009, v. 26, n. 5, p. 563, doi. 10.1007/s12325-009-0031-8
- By:
- Publication type:
- Article
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.
- Published in:
- Genes & Immunity, 2010, v. 11, n. 6, p. 497, doi. 10.1038/gene.2010.18
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- Publication type:
- Article
A population genetics study of the Familial Mediterranean Fever gene: evidence of balancing selection under an overdominance regime.
- Published in:
- Genes & Immunity, 2009, v. 10, n. 8, p. 678, doi. 10.1038/gene.2009.59
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- Publication type:
- Article
The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine.
- Published in:
- Neurological Sciences, 2011, v. 32, p. 141, doi. 10.1007/s10072-011-0517-4
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- Publication type:
- Article
Guillain–Barré syndrome after rtPA therapy for acute stroke.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 6, p. 867, doi. 10.1007/s10072-010-0259-8
- By:
- Publication type:
- Article
Candidate gene analysis of semaphorins in patients with Alzheimer's disease.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Genetics and neurobiology of frontotemporal lobar degeneration.
- Published in:
- Neurological Sciences, 2006, v. 27, p. s32, doi. 10.1007/s10072-006-0543-9
- By:
- Publication type:
- Article
Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene.
- Published in:
- Human Genetics, 2010, v. 128, n. 6, p. 577, doi. 10.1007/s00439-010-0884-6
- By:
- Publication type:
- Article
Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy.
- Published in:
- Acta Neurologica Scandinavica, 2012, v. 126, n. 2, p. 77, doi. 10.1111/j.1600-0404.2012.01661.x
- By:
- Publication type:
- Article
Painful sensory neuropathy and dysimmunity: is there a relation?
- Published in:
- 2004
- By:
- Publication type:
- Abstract
Poems syndrome: role of two angiogenic factors, VEGF and EPO.
- Published in:
- 2004
- By:
- Publication type:
- Abstract
Retroviral vectors for gene therapy of Duchenne muscular dystrophy.
- Published in:
- Neurological Sciences, 2000, v. 21, p. S925, doi. 10.1007/s100720070005
- By:
- Publication type:
- Article
Retroviral vectors for gene therapy of Duchenne muscular dystrophy.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene.
- Published in:
- 2009
- By:
- Publication type:
- Report
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
- Published in:
- Journal of Inherited Metabolic Disease, 1999, v. 22, n. 6, p. 762, doi. 10.1023/A:1005572906807
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- Publication type:
- Article
Genetic polymorphisms for the study of multifactorial stroke.
- Published in:
- Human Mutation, 2008, v. 29, n. 6, p. 776, doi. 10.1002/humu.20666
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- Publication type:
- Article
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL.
- Published in:
- Human Mutation, 2006, v. 27, n. 6, p. 600, doi. 10.1002/humu.9426
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- Publication type:
- Article
Mutational analysis of the AGL gene: Five novel mutations in GSD III patients <FN ID="fn1">Communicated by William S. Sly</FN><FN ID="fn2">Online Citation: Human Mutation, Mutation in Brief #648 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/648.pdf</FN>
- Published in:
- Human Mutation, 2003, v. 22, n. 4, p. 337, doi. 10.1002/humu.9177
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- Publication type:
- Article
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL.
- Published in:
- Human Mutation, 2002, v. 20, n. 6, p. 480, doi. 10.1002/humu.9093
- By:
- Publication type:
- Article
Low Doses of Ketazolam in Anxiety: A Double-Blind, Placebo-Controlled Study.
- Published in:
- Neuropsychobiology, 1988, v. 20, n. 2, p. 74, doi. 10.1159/000118476
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- Publication type:
- Article
Growth factors in ischemic stroke.
- Published in:
- Journal of Cellular & Molecular Medicine, 2011, v. 15, n. 8, p. 1645, doi. 10.1111/j.1582-4934.2009.00987.x
- By:
- Publication type:
- Article
A novel mutation in the [beta]-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
Novel Twinkle ( PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 9, p. 1384, doi. 10.1007/s00415-008-0926-3
- By:
- Publication type:
- Article
Transient response to immune therapies in post-irradiation lumbosacral radiculoplexopathy.
- Published in:
- Journal of Neurology, 2004, v. 251, n. 4, p. 488, doi. 10.1007/s00415-004-0405-4
- By:
- Publication type:
- Article
Efficacy and tolerability of eperisone in patients with spastic palsy: a cross-over, placebo-controlled dose-ranging trial.
- Published in:
- European Review for Medical & Pharmacological Sciences, 2009, v. 13, n. 5, p. 365
- By:
- Publication type:
- Article
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 2, p. 157, doi. 10.1111/j.1399-0004.2011.01717.x
- By:
- Publication type:
- Article
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 2, p. 150, doi. 10.1111/j.1399-0004.2011.01624.x
- By:
- Publication type:
- Article
Novel splice-site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophy.
- Published in:
- Clinical Genetics, 2010, v. 78, n. 5, p. 432, doi. 10.1111/j.1399-0004.2010.01417.x
- By:
- Publication type:
- Article
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
- Published in:
- 2009
- By:
- Publication type:
- Letter