Published in Ital J Neurol Sci on August 01, 1981
Lead poisoning from homemade wine: a case study. Environ Health Perspect (2001) 0.78
[Certification obligations of physicians]. Med Lav (2007) 2.36
Helicobacter pylori second-line rescue therapy with levofloxacin- and bismuth-containing quadruple therapy, after failure of standard triple or non-bismuth quadruple treatments. Aliment Pharmacol Ther (2015) 1.99
Evidence of early cortical atrophy in MS: relevance to white matter changes and disability. Neurology (2003) 1.94
Benign fibrous histiocytoma (BHF) of the cheek: CD 68-KP1 positivity. Oral Oncol (2001) 1.90
MECP2 mutation in male patients with non-specific X-linked mental retardation. FEBS Lett (2000) 1.82
Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutations in the CYP27A1 gene. Neurol Sci (2006) 1.75
Requests for electromyography from general practitioners and specialists: critical evaluation. Ital J Neurol Sci (1998) 1.59
Neuropsychological and MRI measures predict short-term evolution in benign multiple sclerosis. Neurology (2009) 1.59
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. Eur J Hum Genet (2002) 1.56
Cerebrotendinous xanthomatosis with predominant parkinsonian syndrome: further confirmation of the clinical heterogeneity. Mov Disord (2000) 1.53
Diagnosis of thoracic outlet syndrome. Relative value of electrophysiological studies. Acta Neurol Scand (1994) 1.47
CSF levels of beta-amyloid 1-42, tau and phosphorylated tau protein in CADASIL. Eur J Neurol (2008) 1.44
Late diagnosis in severe and mild intellectual disability in adulthood. J Intellect Disabil Res (2004) 1.43
Neocortical volume decrease in relapsing-remitting MS patients with mild cognitive impairment. Neurology (2004) 1.36
The age-related accumulation of protein carbonyl in rat liver correlates with the age-related decline in liver proteolytic activities. J Gerontol A Biol Sci Med Sci (1999) 1.30
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type. Neurology (2004) 1.26
Release of free, redox-active iron in the liver and DNA oxidative damage following phenylhydrazine intoxication. Biochem Pharmacol (1997) 1.25
Ataxia with vitamin E deficiency: update of molecular diagnosis. Neurol Sci (2010) 1.22
Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis. Brain (2001) 1.21
Correlates of MS disability assessed in vivo using aggregates of MR quantities. Neurology (2001) 1.20
The spectrum of Notch3 mutations in 28 Italian CADASIL families. J Neurol Neurosurg Psychiatry (2005) 1.19
Cognitive assessment and quantitative magnetic resonance metrics can help to identify benign multiple sclerosis. Neurology (2008) 1.19
Redox modulation of cell surface protein thiols in U937 lymphoma cells: the role of gamma-glutamyl transpeptidase-dependent H2O2 production and S-thiolation. Free Radic Biol Med (1999) 1.15
Nutritional state and energy balance in cirrhotic patients with or without hypermetabolism. Multicentre prospective study by the 'Nutritional Problems in Gastroenterology' Section of the Italian Society of Gastroenterology (SIGE). Dig Liver Dis (2005) 1.13
Hydrogen peroxide produced during gamma-glutamyl transpeptidase activity is involved in prevention of apoptosis and maintainance of proliferation in U937 cells. FASEB J (1999) 1.12
Cortical lesions in radiologically isolated syndrome. Neurology (2011) 1.12
Age-related changes in the regulation of autophagic proteolysis in rat isolated hepatocytes. J Gerontol A Biol Sci Med Sci (2001) 1.11
Gamma-glutamyl transpeptidase-dependent iron reduction and LDL oxidation--a potential mechanism in atherosclerosis. J Investig Med (1999) 1.10
Predictive role of positron emission tomography (PET) in the outcome of lymphoma patients. Br J Cancer (2004) 1.10
Age-related changes in the autophagic proteolysis of rat isolated liver cells: effects of antiaging dietary restrictions. J Gerontol A Biol Sci Med Sci (2001) 1.10
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1. Nat Genet (1997) 1.09
Measurement of lipid peroxidation in vivo: a comparison of different procedures. Lipids (1987) 1.07
18F-FDG PET/CT in the assessment of carcinoma of unknown primary origin. Radiol Med (2006) 1.06
Clinical and molecular findings in patients with giant axonal neuropathy (GAN). Neurology (2004) 1.06
Total parenteral nutrition-related gastroenterological complications. Dig Liver Dis (2006) 1.04
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts. Neurology (2003) 1.04
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates. Brain (1998) 1.03
Traumatic injuries: imaging of thoracic injuries. Eur Radiol (2002) 1.03
Drinking habits of subjects with hepatitis C virus-related chronic liver disease: prevalence and effect on clinical, virological and pathological aspects. Alcohol Alcohol (2000) 1.03
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients. Neurology (2010) 1.03
Restoration of nitric oxide availability after calcium antagonist treatment in essential hypertension. Hypertension (2001) 1.03
Non-invasive evaluation of central motor tract excitability changes following peripheral nerve stimulation in healthy humans. Electroencephalogr Clin Neurophysiol (1991) 1.02
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. Mov Disord (2000) 1.02
MR brain imaging of fucosidosis type I. AJNR Am J Neuroradiol (2001) 1.01
Wood dust and sino-nasal cancer: pooled reanalysis of twelve case-control studies. Am J Ind Med (1995) 1.00
Liver glutathione depletion induced by bromobenzene, iodobenzene, and diethylmaleate poisoning and its relation to lipid peroxidation and necrosis. Am J Pathol (1985) 1.00
A case-control study of cancer of the nose and paranasal sinuses and occupational exposures. Am J Ind Med (1992) 0.99
Cyclic treatment of chronic hepatic encephalopathy with rifaximin. Results of a double-blind clinical study. Minerva Gastroenterol Dietol (2003) 0.99
Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings. AJNR Am J Neuroradiol (1994) 0.99
Prognostic value of serum gamma-glutamyl transferase activity after myocardial infarction. Eur Heart J (2001) 0.98
A Rett syndrome MECP2 mutation that causes mental retardation in men. Neurology (2002) 0.98
Electrophysiologic evaluation of local steroid injection in carpal tunnel syndrome. Arch Phys Med Rehabil (1991) 0.98
Wernicke encephalopathy after gastrointestinal surgery for cancer: causes of diagnostic failure or delay. Int J Neurosci (2011) 0.97
Detection of 4-hydroxynonenal and other lipid peroxidation products in the liver of bromobenzene-poisoned mice. Biochim Biophys Acta (1986) 0.97
Enhancement of doxorubicin content by the antitumor drug lonidamine in resistant Ehrlich ascites tumor cells through modulation of energy metabolism. Biochem Pharmacol (1998) 0.97
gamma-Glutamyl transpeptidase-dependent lipid peroxidation in isolated hepatocytes and HepG2 hepatoma cells. Free Radic Biol Med (1997) 0.97
BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement. Acta Neurol Scand (1990) 0.97
Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study. J Neurol (2001) 0.97
Four novel CYP27A1 mutations in seven Italian patients with CTX. Eur J Neurol (2010) 0.96
An electromyographic evaluation of motor complications in thoracic herpes zoster. Electromyogr Clin Neurophysiol (1994) 0.96
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction. Neurology (2008) 0.96
Apoptotic response and cell cycle transition in ataxia telangiectasia cells exposed to oxidative stress. Life Sci (2000) 0.96
'Excitability changes of muscular responses to magnetic brain stimulation in patients with central motor disorders. Electroencephalogr Clin Neurophysiol (1991) 0.95
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene. Neuromuscul Disord (2003) 0.95
Membrane gamma-glutamyl transpeptidase activity of melanoma cells: effects on cellular H(2)O(2) production, cell surface protein thiol oxidation and NF-kappa B activation status. J Cell Sci (2000) 0.95
Cell response to oxidative stress induced apoptosis in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry (2004) 0.94
Trace elements and chronic liver diseases. J Trace Elem Med Biol (1997) 0.94
A case-referent study on nasal cancer and exposure to wood dust in the province of Siena, Italy. Scand J Work Environ Health (1983) 0.94
Cerebrotendinous xanthomatosis caused by two new mutations of the sterol-27-hydroxylase gene that disrupt mRNA splicing. J Lipid Res (1996) 0.94
Contrast enhanced MRI and ¹⁸F-FDG PET-CT in the assessment of multiple myeloma: a comparison of results in different phases of the disease. Eur J Radiol (2012) 0.93
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study. Brain Dev (1993) 0.92
Bronchiolitis obliterans with organizing pneumonia (BOOP), presenting as a ring-shaped opacity at HRCT (the atoll sign). A case report. Radiol Med (1999) 0.92
Altered cerebellar functional connectivity mediates potential adaptive plasticity in patients with multiple sclerosis. J Neurol Neurosurg Psychiatry (2004) 0.92
Clinical relevance and neurophysiological correlates of spasticity in cerebrotendinous xanthomatosis. J Neurol (2010) 0.92
Lipid peroxidation and cellular damage in extrahepatic tissues of bromobenzene-intoxicated mice. Am J Pathol (1986) 0.91
Tarlov cysts: clinical evaluation of an italian cohort of patients. Neurol Sci (2013) 0.91
Cerebrotendinous xanthomatosis: 11-year treatment with chenodeoxycholic acid in five patients. An electrophysiological study. J Neurol Sci (2001) 0.91
A case of hepatotoxicity caused by green tea. Free Radic Biol Med (2007) 0.91
Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form. J Neurol (1985) 0.91
Chronic progressive leptomeningitis associated with measles virus. Lancet (1997) 0.91
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome. Neurology (2001) 0.91
Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. J Neurol Neurosurg Psychiatry (2008) 0.90
Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren). Acta Neuropathol (1999) 0.90
Histochemical visualization of oxidant stress. Free Radic Biol Med (2000) 0.90
Endogenous oxidative stress induces distinct redox forms of tumor necrosis factor receptor-1 in melanoma cells. Ann N Y Acad Sci (2004) 0.90
Diagnostic specificity of sensory and motor nerve conduction variables in early detection of carpal tunnel syndrome. J Neurol (1989) 0.90
Retracted High-mobility group A1 protein inhibits p53-mediated intrinsic apoptosis by interacting with Bcl-2 at mitochondria. Cell Death Dis (2012) 0.89
Environmental household exposures to asbestos and occurrence of pleural mesothelioma. Am J Ind Med (1992) 0.89
Acute renal failure from inhalation of mycotoxins. Nephron (1993) 0.89
Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complex. Am J Hum Genet (1995) 0.89
Cerebrotendinous xanthomatosis: clinical and MRI study (a case report). J Neurol Neurosurg Psychiatry (1990) 0.88
Glucose 6-phosphate stimulation of MgATP-dependent Ca2+ uptake by rat kidney microsomes. Biochim Biophys Acta (1990) 0.88
Postnatal expression of glucose-6-phosphate dehydrogenase in different brain areas. Neurochem Res (1998) 0.88
Schnyder corneal crystalline dystrophy: description of a new family with evidence of abnormal lipid storage in skin fibroblasts. Am J Med Genet (1998) 0.87
Non-alcoholic fatty liver disease: a multicentre clinical study by the Italian Association for the Study of the Liver. Dig Liver Dis (2004) 0.87
Selective ipsilateral neuromuscular involvement in a case of facial and somatic hemiatrophy. Muscle Nerve (1997) 0.87
Heterogeneity in ataxia-telangiectasia: classical phenotype associated with intermediate cellular radiosensitivity. Am J Med Genet (1992) 0.87
Mortality due to asbestos-related causes among railway carriage construction and repair workers. Occup Med (Lond) (1999) 0.87
Alteration of haemostasis in non-metastatic gastric cancer. Dig Liver Dis (2001) 0.87