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Results 1 to 13 of 13

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Gain of Glycosylation: A New Pathomechanism of Myelin Protein Zero MutationsPRADA, Valeria; PASSALACQUA, Mario; SHY, Michael et al.Annals of neurology. 2012, Vol 71, Num 3, pp 427-431, issn 0364-5134, 5 p.Article

Phenotypic characterization of hypomyelination and congenital cataractBIANCHERI, Roberta; ZARA, Federico; UZIEL, Graziella et al.Annals of neurology. 2007, Vol 62, Num 2, pp 121-127, issn 0364-5134, 7 p.Article

Peripheral nerves : a target for the action of neuroactive steroidsMELCANGI, Roberto C; CAVARRETTA, Ilaria T. R; BALLABIO, Marinella et al.Brain research reviews. 2005, Vol 48, Num 2, pp 328-338, issn 0165-0173, 11 p.Conference Paper

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractZARA, Federico; BIANCHERI, Roberta; PEDEMONTE, Marina et al.Nature genetics. 2006, Vol 38, Num 10, pp 1111-1113, issn 1061-4036, 3 p.Article

Does parkin play a role in the peripheral nervous system? A family reportABBRUZZESE, Giovanni; PIGULLO, Simona; AJMAR, Franco et al.Movement disorders. 2004, Vol 19, Num 8, pp 978-981, issn 0885-3185, 4 p.Article

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1ANOBBIO, Lucilla; MANCARDI, Gianluigi; GRANDIS, Marina et al.Annals of neurology. 2001, Vol 50, Num 1, pp 47-55, issn 0364-5134Article

Impaired Expression of Ciliary Neurotrophic Factor in Charcot-Marie-Tooth Type 1 A NeuropathyNOBBIO, Lucilla; FIORESE, Fulvia; VIGO, Tiziana et al.Journal of neuropathology and experimental neurology. 2009, Vol 68, Num 5, pp 441-455, issn 0022-3069, 15 p.Article

GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal featuresBIANCHERI, Roberta; ZARA, Federico; MINETTI, Carlo et al.Journal of neurology. 2006, Vol 253, Num 9, pp 1234-1235, issn 0340-5354, 2 p.Article

Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patientsGRANDIS, Marina; NOBBIO, Lucilla; ABBRUZZESE, Michele et al.Muscle & nerve. 2001, Vol 24, Num 5, pp 622-629, issn 0148-639XArticle

PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot-Marie-Tooth 1A biomarkerNOBBIO, Lucilla; VISIGALLI, Davide; RADICE, Davide et al.Brain. 2014, Vol 137, pp 1614-1620, issn 0006-8950, 7 p., 6Article

Relapses after treatment with rituximab in a patient with multiple sclerosis and anti-myelin-associated glycoprotein polyneuropathyBENEDETTI, Luana; FRANCIOTTA, Diego; VIGO, Tiziana et al.Archives of neurology (Chicago). 2007, Vol 64, Num 10, pp 1531-1533, issn 0003-9942, 3 p.Article

Autologous stem cell transplantation as rescue therapy in malignant forms of multiple sclerosisMANCARDI, Giovanni Luigi; MURIALDO, Alessandra; COMI, Giancarlo et al.Multiple sclerosis. 2005, Vol 11, Num 3, pp 367-371, issn 1352-4585, 5 p.Article

Progressive multifocal leukoencephalopathy in an adult patient with ICF syndromeCOLUCCI, Monica; COCITO, Leonardo; CAPELLO, Elisabetta et al.Journal of the neurological sciences. 2004, Vol 217, Num 1, pp 107-110, issn 0022-510X, 4 p.Article

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