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JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
Rivista
Codice:
E094684
ISSN:
1085-9489
Dati Generali
Dati Generali
Pubblicazioni (43)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A GENOMIC APPROACH TO IDENTIFY NEW GENES RESPONSIBLE FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY
Articolo
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2
Articolo
A novel homozygous mutation in the MTMR2 gene in two siblings with 'hypermyelinating neuropathy'
Articolo
AUTOPHAGY INDUCTION AS A THERAPEUTIC STRATEGY FOR DEMYELINATING CMT1A NEUROPATHIES
Abstract
Abnormal Schwann cell-axon interaction in EBF-2 "knock out" mice
Abstract
BIOMATERIAL TO PROMOTE NERVE REGENERATION: TOWARDS CLINICAL TRIALS
Articolo
Balance exercise in patients with chronic sensory ataxic neuropathy: a pilot study.
Articolo
CHARCOT-MARIE-TOOTH DISEASE TYPE 4B: A MULTICENTRE RETROSPECTIVE STUDY
Abstract
CLINICAL AND MOLECULAR CHARACTERIZATION OF A COHORT OF PATIENTS WITH DISTAL MOTOR NEUROPATHY
Abstract
CLINICAL CHARACTERIZATION OF A PATIENT CARRYING HINT1 MUTATION
Contributo in Atti di convegno
CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE
Articolo
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION
Articolo
CYTOSKELETON AND PERIPHERAL NERVE MYELINATION: A NOVEL ROLE FOR VIMENTIN
Abstract
DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES
Abstract
DEVELOPMENT AND OPTIMIZATION OF A PROTOCOL FOR RNA EXTRACTION FROM HUMAN SKIN BIOPSY OF PATIENTS AFFECTED BY PAINFUL AND PAINLESS PERIPHERAL NEUROPATHY
Articolo
DLG1 COORDINATES A HOMEOSTATIC CONTROL OF MYELINATION VIA SEC8 AND MTMR2 INTERACTION
Articolo
DLG1 IS A NEGATIVE REGULATOR OF SCHWANN CELL MYELINATION
Abstract
Disruption of MTMR2 in Schwann cells produces CMT4B1-like neuropathy with myelin outfoldings
Abstract
EFFICIENT LENTIVIRAL GENE DELIVERY TO SCHWANN CELLS
Abstract
Expanding the phenotype of neuromuscular disorders: NGS reveals new genes responsible for recessive motor neuropathies
Abstract
GENERATION OF SENSORY NEURONS AND SCHWANN CELLS FROM HUMAN-IPS CELLS OF CMT PATIENTS: A SUITABLE TOOL TO TEST NEW DEVELOPING DRUGS
Abstract
GENOMIC APPROACH FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY
Abstract
HEREDITARY NEURALGIC AMYOTROPHY: A CASE REPORT
Articolo
HIGH POROSITY COLLAGEN TUBE: AN INNOVATIVE MEDICAL DEVICE FOR NERVE REGENERATION
Articolo
IN VIVO CORNEAL CONFOCAL MICROSCOPY IN PATIENTS WITH GUILLAIN-BARRE SYNDROME
Abstract
IT'S TOO EASY TO MAKE IT SIMPLE: HNPP DIAGNOSIS
Articolo
LOSS OF FIG4 IN BOTH SCHWANN CELLS AND MOTOR NEURONS CONTRIBUTES TO CMT4J NEUROPATHY
Abstract
LYMPHOMATOUS NEUROPATHY: CLINICAL AND PATHOLOGICAL HETEROGENEITY
Articolo
MODULATION OF NEUREGULIN 1 TYPE III PATHWAY TO TREAT HEREDITARY DEMYELINATING NEUROPATHIES
Abstract
MTMR2 phospholipid phosphatase and membrane trafficking in Schwann cells
Abstract
Meeting Report: 2013 Peripheral Nerve Society Biennial Meeting, Saint-Malo, France, June 29-July 3, 2013
Articolo
Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly
Abstract
Nerve pathology in animal models of neuropathies
Articolo
Recent advances in the treatment of Charcot-Marie-Tooth neuropathies
Articolo
Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies
Abstract
SEVEN EXAMPLES OF EXPANDABLE CLINICAL SPECTRUM OF NEUROMUSCULAR GENES
Abstract
SINGLE-FIBER ELECTROMYOGRAPHY STUDY OF RECOVERY AFTER NERVE CRUSH AND CARDIOTOXIN MUSCLE INJURY IN EXPERIMENTAL MOUSE MODEL
Articolo
SKIN BIOPSY IN ANIMAL MODELS OF HEREDITARY NEUROPATHIES
Articolo
STIMULATED SINGLE-FIBER ELECTROMYOGRAPHY EVALUATION OF AXONAL REGENERATION IN ANIMAL MODELS
Articolo
TRAFFICKING THROUGH THE ENDO-LYSOSOMAL AXIS REGULATES MYELINATION AND REPAIR IN THE PERIPHERAL NERVOUS SYSTEM
Abstract
VOCAL CORD PARALYSIS IN CHARCOT-MARIE-TOOTH TYPE 4B1 DISEASE ASSOCIATED WITH A NOVEL MUTATION IN THE MYOTUBULARIN-RELATED PROTEIN 2 GENE: A CASE REPORT AND REVIEW OF THE LITERATURE
Abstract
VOCAL CORD PARALYSIS IN CHARCOT-MARIE-TOOTH TYPE 4B1 DISEASE ASSOCIATED WITH A NOVEL MUTATION IN THE MYOTUBULARIN-RELATED PROTEIN 2 GENE: A CASE REPORT AND REVIEW OF THE LITERATUREPPP
Contributo in Atti di convegno
understanding the consequences of chronic inflammatory demyelinating polyradiculoneuropathy from impairments to activity and participation restrictions and reduced quality of life:ICE study
Articolo
No Results Found
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