Author

S. Di Donato

Observed names: S Di Donato, S di Donato, S. (d) Di Donato, St. Donato

Institution: Fondazione IRCCS Istituto Neurologico Carlo Besta

Observed institutions: University of Bern, University of Padua, Medical College of Wisconsin, Fondazione IRCCS Istituto Neurologico Carlo Besta

OpenAlex ID: A5111408159

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

2004 · C. Mariotti, C. Gellera, et al. · Neurological Sciences · 157

Glucose metabolism alterations in Friedreich's ataxia

1988 · G. Finocchiaro, G. Baio, et al. · Neurology · 99

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations

2001 · C. Gellera, B. Castellotti, et al. · Neuromuscular Disorders · 54

Prevalence of Inherited Ataxias in the Province of Padua, Italy

2004 · M. Zortea, M. Armani, et al. · Neuroepidemiology · 51

Systemic carnitine deficiency due to lack of electron transfer flavoprotein

1986 · S. Di Donato, F. E. Frerman, et al. · Neurology · 51

Pathogenic effect of an intermediate-size SCA-6 allele (CAG) 19 in a homozygous patient

2001 · C. Mariotti, C. Gellera, et al. · Neurology · 49

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

1995 · D Lorenzetti, D Pareyson, et al. · PubMed Central · 46

Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes,fibroblasts, and muscle mitochondria

1986 · G Finocchiaro, F Taroni, et al. · Neurology · 37

Sialidosis type I: pathological study in an adult.

1989 · A Allegranza, G Tredici, et al. · PubMed · 24

Cerebellar/spinocerebellar syndromes

2001 · C. Mariotti, S. Di Donato · Neurological Sciences · 18

Acid Maltase Deficiency in Adults

2008 · B. Bertagnolio, S. Di Donato, et al. · European Neurology · 16

Linkage Disequilibrium Analysis of Friedreich's Ataxia in 140 Caucasian Families: Positioning of the Disease Locus and Evaluation of Allelic Heterogeneity

1993 · G. (a) Sirugo, S. (b) Cocozza, et al. · European Journal of Human Genetics · 14

Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

1994 · The European Velnacrine Study Group, L. Harms, et al. · Journal of Neurology · 13

Computed tomography of olivopontocerebellar degeneration.

1983 · M Savoiardo, M Bracchi, et al. · PubMed Central · 13

The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxias

1998 · S. Di Donato · The Italian Journal of Neurological Sciences · 12

Friedreich's Ataxia in Northern Italy: I. Clinical, Neurophysiological and In Vivo Biochemical Studies

1980 · A. D’Angelo, S. Di Donato, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 11

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An Approach Using Lecithin Treatment for Olivopontocerebellar Atrophies

2008 · G. Finocchiaro, S. Di Donato, et al. · European Neurology · 5

Gene Transfer of Suicide Genes for the Treatment of Malignant Gliomas: Efficacy, Limitations, and Perspectives for a Combined Immunotherapy

1997 · S. Benedetti, F. Meco, et al. · Springer eBooks · 3

Author Index Vol. 23, 2004

2004 · Hei-Fen Hwang, Chih-Yi Chen, et al. · Neuroepidemiology · 1

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E25 Fmri Signal Changes In Frontal Cortex Correlates With Years-to-disease-onset In A Group Of Young Premanifest Huntington Disease Subjects

2014 · L. Nanetti, S. Ferraro, et al. · Journal of Neurology Neurosurgery & Psychiatry

F13 Progressive reduction of plasma 24S-hydroxycholestrol in prodromal HD subjects according with clinical and MRI features in the PREDICT-HD study

2012 · L Valerio, S Di Donato, et al. · Journal of Neurology Neurosurgery & Psychiatry

H03 Cerebral and extracerebral cholesterol biosynthesis is impaired in Huntington's disease patients

2010 · V Leoni, C Mariotti, et al. · Journal of Neurology Neurosurgery & Psychiatry

Sudden death from atypical Pneumonia in an adolescent.

2010 · S. Di Donato, Margherita Neri, et al.

Decrease of diffusivity in the caudate nucleus as potential biomarker in Huntington's Disease.

2009 · ML Mandelli, D Aquino, et al. · NeuroImage

AFG3L2 mutations cause autosomal dominant ataxia SCA28 and reveal an essential role for the mitochondrial m-AAA protease complex in the cerebellum

2009 · Daniela Di Bella, Federico Lazzaro, et al. · Journal of Neurology

Works count: 35

Citation count: 674

H-index: 13

I10-index: 16