Search Results - "Cocozza S"

Interactive data analysis and clustering of genomic data.

Authors: Ciaramella, A. Cocozza, S. Iorio, F.

Source: Neural Networks; March/April 2008, Vol. 21 Issue 2/3, p368-378, 11p

Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex^®.

Authors: Carotenuto, A. Iodice, R. Petracca, M. et al.

Source: Acta Neurologica Scandinavica. Apr2017, Vol. 135 Issue 4, p442-448. 7p.

Subjects: Multiple sclerosis treatment, Motor neurons, Spasticity, Pyramidal tract, Neural circuitry, Electrophysiology, Statistical correlation

Friedreich's ataxia: from the patient to the gene.

Authors: Filla, A. Cocozza, S. De Michele, G.

Source: Neurological Sciences. May2001 Supplement 1, Vol. 22, pS21. 5p. 1 Diagram, 1 Graph.

Subjects: Friedreich's ataxia, Pathological physiology

Diffuse brain connectivity changes in Charcot–Marie–Tooth type 1a patients: a resting‐state functional magnetic resonance imaging study.

Authors: Pontillo, G. Tozza, S. Perillo, T. et al.

Source: European Journal of Neurology. Jan2021, Vol. 28 Issue 1, p305-313. 9p.

Subjects: Functional magnetic resonance imaging, Diagnostic imaging, Functional connectivity, Visual cortex, Peripheral nervous system

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The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families.

Authors: Lieto, M. Riso, V. Galatolo, D. et al.

Source: European Journal of Neurology. Mar2020, Vol. 27 Issue 3, p498-505. 8p. 3 Diagrams, 1 Chart.

Subjects: Spinocerebellar ataxia, Peripheral nervous system, Cerebellar ataxia, Movement disorders, Cerebral atrophy, Pyramidal tract

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Grey:white matter ratio at diagnosis and the risk of 10-year multiple sclerosis progression.

Authors: Moccia, M. Quarantelli, M. Lanzillo, R. et al.

Source: European Journal of Neurology. Jan2017, Vol. 24 Issue 1, p195-204. 10p.

Subjects: Multiple sclerosis diagnosis, Multiple sclerosis risk factors, White matter (Nerve tissue), Gray matter (Nerve tissue), Magnetic resonance imaging of the brain, Neurodegeneration

Comment on: Zhang et al. Peroxisome proliferator-activated receptor γ polymorphism Pro12Ala is associated with nephropathy in type 2 diabetes: evidence from meta-analysis of 18 studies. Diabetes Care 2012;35:1388-1393.

Authors: Lapice E Cocozza S Riccardi G et al.

Source: Diabetes Care. Jan2013, Vol. 36 Issue 1, pe18-e18. 1p.

Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex^®.

Authors: Carotenuto, A. Iodice, R. Petracca, M. et al.

Source: Acta Neurologica Scandinavica. Apr2017, Vol. 135 Issue 4, p442-448. 7p.

Role of type 2 diabetes mellitus in nonalcoholic fatty liver disease.

Authors: Bozzetto, L. Prinster, A. Cocozza, S. et al.

Source: European Journal of Clinical Investigation. Dec2011, Vol. 41 Issue 12, p1368-1368. 1p.

Identification of C12orf4 as a gene for autosomal recessive intellectual disability.

Authors: Philips, A.K. Pinelli, M. de Bie, C.I. et al.

Source: Clinical Genetics. Jan2017, Vol. 91 Issue 1, p100-105. 7p.

Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients.

Authors: Vaccaro O Lapice E Monticelli A et al.

Source: Diabetes Care. May2007, Vol. 30 Issue 5, p1156-1161. 6p.

URL: 25168077

Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers.

Authors: Pianese, L. Turano, M. Lo Casale, M. S. et al.

Source: Journal of Neurology, Neurosurgery & Psychiatry. Jul2004, Vol. 75 Issue 7, p1061-1063. 3p.

PO-0639: Feasibility of tract based dosimetric analysis in brain tumor patients.

Authors: Conson, M. Cella, L. D’Ippolito, E. et al.

Source: Radiotherapy & Oncology. May2017 Supplement 1, Vol. 123, pS334-S335. 1p.

Genetic abnormalities in Friedreich's ataxia.

Authors: Filla, Alessandro De Michele, Giuseppe Cocozza, Sergio et al.

Source: New England Journal of Medicine. 04/03/97, Vol. 336 Issue 14, p1021-1022. 2p.