about
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity geneUFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeMutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisDefining the role of the Bcl-2 family proteins in Huntington's diseaseLoss of huntingtin-mediated BDNF gene transcription in Huntington's diseasePhase II/III randomized trial of TCH346 in patients with ALSThe survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisA genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.Blood pressure and LDL-cholesterol targets for prevention of recurrent strokes and cognitive decline in the hypertensive patient: design of the European Society of Hypertension-Chinese Hypertension League Stroke in Hypertension Optimal Treatment ranEndovascular management of symptomatic cerebral malperfusion due to carotid dissection after type A aortic dissection repair.Consistent bone marrow-derived cell mobilization following repeated short courses of granulocyte-colony-stimulating factor in patients with amyotrophic lateral sclerosis: results from a multicenter prospective trial.A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.Motor neurone metabolism.Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyMutational analysis of TARDBP in neurodegenerative diseasesIntracerebroventricular administration of human umbilical cord blood cells delays disease progression in two murine models of motor neuron degeneration.C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisParaoxonase gene mutations in amyotrophic lateral sclerosis.Longitudinal tracking of human fetal cells labeled with super paramagnetic iron oxide nanoparticles in the brain of mice with motor neuron diseaseOligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations.Parkin regulates kainate receptors by interacting with the GluK2 subunitDiscovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS.Weight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options.TDP-43 is recruited to stress granules in conditions of oxidative insult.Extramotor damage is associated with cognition in primary lateral sclerosis patientsStem therapy for ALS: hope and reality.Novel mutations support a role for Profilin 1 in the pathogenesis of ALS.Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Stem cell therapy for neurodegenerative diseases: the issue of transdifferentiation.Impaired expression of insulin-like growth factor-1 system in skeletal muscle of amyotrophic lateral sclerosis patients.Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse modelThe role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementiaStem cell transplantation in multiple sclerosis: safety and ethics.Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group.Dose dependent side effect of superparamagnetic iron oxide nanoparticle labeling on cell motility in two fetal stem cell populationsAnalysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortHuntington's disease: the current state of research with peripheral tissues.
P50
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P50
description
hulumtues
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researcher
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հետազոտող
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name
Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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Vincenzo Silani
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P1053
P-4421-2017
P106
P1153
7006146949
P21
P214
2062148705742537080004
P31
P3829
P496
0000-0002-7698-3854
P735
P7859
viaf-2062148705742537080004