about
Guillain-Barré syndrome following the 2009 pandemic monovalent and seasonal trivalent influenza vaccination campaigns in Spain from 2009 to 2011: outcomes from active surveillance by a neurologist network, and records from a country-wide hospital diVAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis.Clinical study of 39 patients with atypical lacunar syndrome.Plasma metabolome and skin proteins in Charcot-Marie-Tooth 1A patientsDiagnosis of Charcot-Marie-Tooth disease.Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigen.MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational study.[Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].Long-term outcome in chronic inflammatory demyelinating polyneuropathy patients treated with intravenous immunoglobulin: a retrospective study.[Sequential heart and liver transplantation for familial amyloid polyneuropathy].Observational study of patients in Spain with amyotrophic lateral sclerosis: correlations between clinical status, quality of life, and dignity.Identification of two novel KIF5A mutations in hereditary spastic paraplegia associated with mild peripheral neuropathy.Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy.Causes of neuropathy in patients referred as "Idiopathic neuropathy".Two Spanish families with Charcot-Marie-Tooth type 2A: clinical, electrophysiological and molecular findings.Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTClinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodiesClinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish populationA novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotypeNeurological picture. Multifocal acquired demyelinating sensory and motor neuropathy presenting as idiopathic hypertrophic brachial neuropathyNumb chin syndrome as an early symptom of primary and secondary vasculitisCharcot-Marie-Tooth disease with intermediate conduction velocities caused by a novel mutation in the MPZ geneVery early electrodiagnostic findings in Guillain-Barré syndromeCharcot-Marie-tooth diseaseCharacterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia[Recommendations regarding diagnosis and treatment of transthyretin familial amyloid polyneuropathy.Grupo de Estudio y Tratamiento de la Polineuropatía Amiloidótica Familiar por Transtiretina (GETPAF-TTR)]A deep intronic splice variant advises reexamination of presumably dominant SPG7 Cases
P50
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P50
description
investigador
@es
researcher
@en
name
Carlos Casasnovas
@en
Carlos Casasnovas
@nl
type
label
Carlos Casasnovas
@en
Carlos Casasnovas
@nl
altLabel
Carlos Casasnovas Pons
@en
prefLabel
Carlos Casasnovas
@en
Carlos Casasnovas
@nl
P106
P31
P496
0000-0003-1170-2676