نتائج البحث

Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases.

• Authors : Padua L; Department of Neurosciences, Institute of Neurology, UCSC University, Largo F. Vito 1, 00168, Rome, Italy. ; Briani C

Subjects: Surveys and Questionnaires*; Neuralgia/Neuralgia/Neuralgia/*diagnosis ; Pain Measurement/Pain Measurement/Pain Measurement/*methods

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2009 Apr; Vol. 30 (2), pp. 99-106. DatePublisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited

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Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families.

• Authors : Mazzeo A; Department of Neurosciences, Psychiatry and Anaesthesiology University of Messina, Messina, Italy. ; Muglia M

Subjects: Amino Acid Substitution/Amino Acid Substitution/Amino Acid Substitution/*genetics ; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

• Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2008 Nov; Vol. 118 (5), pp. 328-32. Date of Electronic Publication: 2008 Apr 12.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutation.

• Authors : Cafforio G; Department of Neuroscience O U of Neurology, S Chiara Hospital, University of Pisa, Pisa, Italy.; Calabrese R

Subjects: GTP-Binding Protein gamma Subunits/GTP-Binding Protein gamma Subunits/GTP-Binding Protein gamma Subunits/*genetics ; Hereditary Sensory and Motor Neuropathy/Hereditary Sensory and Motor Neuropathy/Hereditary Sensory and Motor Neuropathy/*genetics ; Movement Disorders/Movement Disorders/Movement Disorders/*genetics

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2008 Jun; Vol. 29 (3), pp. 189-91. DatePublisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited

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Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study.

• Authors : Padua L; Aprile I ...

Subjects: Disability Evaluation*; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*epidemiology ; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*psychology

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2008 Jun; Vol. 29 (3), pp. 157-62. DatePublisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited

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Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy.

• Authors : Di Stefano, Vincenzo¹ (AUTHOR) ; Prinzi, Francesco¹ (AUTHOR) ; Luigetti, Marco^2,3 (AUTHOR)

• Source: Brain Sciences (2076-3425). May2023, Vol. 13 Issue 5, p805. 10p.

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Curare l'uomo, non il sintomo: la promozione della salute sessuale nella sclerosi multipla secondo l'approccio integrato.

• Authors : Dasara, Eloisa¹ ; Todaro, Elisabetta²

• Source: Rivista di Sessuologia Clinica. 2020, Vol. 26 Issue 2, p23-45. 23p.

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AxoGen, Inc. Makes First Commercial Shipment of Avance(r) Nerve Graft to Distributor in Italy.

Subjects: SHIPMENT of goods; NERVE grafting; AUTOGRAFTSITALYAXOGEN Inc.

• Source: Biomedical Market Newsletter; 7/19/2012, Vol. 21, p1-2, 2p

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An Italian multicenter retrospective-prospective observational study on neurological manifestations of COVID-19 (NEUROCOVID).

• Authors : Ferrarese C; Silani V ...

Subjects: Betacoronavirus*; Coronavirus Infections/Coronavirus Infections/Coronavirus Infections/*epidemiology ; Coronavirus Infections/Coronavirus Infections/Coronavirus Infections/*therapy

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2020 Jun; Vol. 41 (6), pp. 1355-1359. Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited

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A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.

• Authors : Nicolaou P; Neurogenetics Department, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.; Cianchetti C

Subjects: Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*genetics ; RNA Splice Sites/RNA Splice Sites/RNA Splice Sites/*genetics ; Ubiquitin-Protein Ligases/Ubiquitin-Protein Ligases/Ubiquitin-Protein Ligases/*geneticsCharcot-Marie-Tooth disease, Type 2B

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2013 Feb; Vol. 21 (2), pp. 190-4. Date of Electronic Publication: 2012 Jul 11.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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