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N Nardocci

Showing results (41-50 of 49) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 15, 2011
Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosisL Chiapparini, G Uziel, C Vallinoto, et al.
Neurogenetics|July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndromeA Catania, R Battini, T Pippucci, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2008
Impaired body movement representation in DYT1 mutation carriersM Fiorio, M Gambarin, G Defazio, et al.
European Journal of Neurology|May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystoniasA Albanese, F Asmus, K P Bhatia, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
Acta Neuropathologica|July 1, 1997
Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspectsR Barresi, V Confalonieri, M Lanfossi, et al.
Nature Genetics|December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13T D Taylor, M Litt, P Kramer, et al.
Journal of Neurology|December 6, 2012
Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory studyD Martino, A Gajos, V Gallo, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 15, 2011
Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosisL Chiapparini, G Uziel, C Vallinoto, et al.
Neurogenetics|July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndromeA Catania, R Battini, T Pippucci, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2008
Impaired body movement representation in DYT1 mutation carriersM Fiorio, M Gambarin, G Defazio, et al.
European Journal of Neurology|May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystoniasA Albanese, F Asmus, K P Bhatia, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
Acta Neuropathologica|July 1, 1997
Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspectsR Barresi, V Confalonieri, M Lanfossi, et al.
Nature Genetics|December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13T D Taylor, M Litt, P Kramer, et al.
Journal of Neurology|December 6, 2012
Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory studyD Martino, A Gajos, V Gallo, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Pageof 5