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A rare case of multiple sclerosis and McArdle disease

Neurological sciences, 2015-09, Vol.36 (9), p.1721-1723

2015

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Konjac-mannan (glucomannan) improves glycemia and other associated risk factors for coronary heart disease in type 2 diabetes. A randomized controlled metabolic trial

Diabetes care, 1999-06, Vol.22 (6), p.913-919

1999

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A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1

Neurology, 2000-11, Vol.55 (10), p.1467-1471

2000

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Effect on blood lipids of very high intakes of fiber in diets low in saturated fat and cholesterol

The New England journal of medicine, 1993-07, Vol.329 (1), p.21-26

1993

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A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation

Journal of neurology, 2008, Vol.255 (1), p.127-129

2008

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Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

Neurology, 1999-10, Vol.53 (7), p.1425

1999

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Dopamine D 2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

Neurology, 1999-10, Vol.53 (7), p.1425-1425

1999

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The role of VLA4 polymorphisms in multiple sclerosis: An association study

Journal of neuroimmunology, 2007-09, Vol.189 (1), p.125-128

2007

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CRYSTAL MEMORIES: CAPTURING OUR VOICES

The Gerontologist, 2008-10, Vol.48, p.237

Spadafora, P

2008

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Propionate inhibits incorporation of colonic [1,2-13C]acetate into plasma lipids in humans

The American journal of clinical nutrition, 1995-06, Vol.61 (6), p.1241-1247

1995

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NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy

Neuroscience letters, 2003-11, Vol.351 (2), p.75-78

2003

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Gene dosage influences the age at onset of SCA2 in a family from southern Italy

Clinical genetics, 2007-10, Vol.72 (4), p.381-383

2007

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LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease

Clinical genetics, 2007-04, Vol.71 (4), p.367-370

2007

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The parkin gene is not involved in late-onset Parkinson's disease

Neurology, 2001-07, Vol.57 (2), p.359-362

2001

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Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease

Neurology, 2002-03, Vol.58 (5), p.828-829

2002

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Use of amrinone and glucagon in a case of calcium channel blocker overdose

Annals of emergency medicine, 1993-07, Vol.22 (7), p.1225-1228

1993

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DNA multiallelic systems reveal gene/longevity associations not detected by diallelic systems. The APOB locus

Human genetics, 1997-03, Vol.99 (3), p.312-318

1997

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Accuracy of Reagent Strips in Detecting Hypoglycemia in the Emergency Department

Annals of emergency medicine, 1998-09, Vol.32 (3), p.305-309

1998

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LEVERAGING TECHNOLOGY TO PROMOTE ENGAGEMENT IN LEISURE ACTIVITIES IN SENIORS WITH COGNITIVE DECLINE

Innovation in aging, 2017-07, Vol.1 (suppl_1), p.61-61

2017

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Association of tau gene polymorphism with Parkinson's disease

Neurological sciences, 2003-10, Vol.24 (3), p.223-224

2003

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CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2) : early impairment of Wisconsin Card Sorting Test and saccade velocity

Journal of neurology, 1998-10, Vol.245 (10), p.647-652

1998

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Beneficial effects of viscous dietary fiber from Konjac-mannan in subjects with the insulin resistance syndrome: results of a controlled metabolic trial

Diabetes care, 2000-01, Vol.23 (1), p.9-14

2000

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Interaction between methane-producing status and diet on serum acetate concentration in humans

The Journal of nutrition, 1993-04, Vol.123 (4), p.681-688

1993

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Streptococcus bovis endocarditis and vertebral osteomyelitis

Heart & lung, 1996-03, Vol.25 (2), p.165-168

1996

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Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus

Epilepsia (Copenhagen), 2003-09, Vol.44 (9), p.1257-1258

2003

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A rare case of multiple sclerosis and McArdle disease

Konjac-mannan (glucomannan) improves glycemia and other associated risk factors for coronary heart disease in type 2 diabetes. A randomized controlled metabolic trial

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1

Effect on blood lipids of very high intakes of fiber in diets low in saturated fat and cholesterol

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation

Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

Dopamine D 2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

The role of VLA4 polymorphisms in multiple sclerosis: An association study

CRYSTAL MEMORIES: CAPTURING OUR VOICES

Propionate inhibits incorporation of colonic [1,2-13C]acetate into plasma lipids in humans

NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy

Gene dosage influences the age at onset of SCA2 in a family from southern Italy

LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease

The parkin gene is not involved in late-onset Parkinson's disease

Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease

Use of amrinone and glucagon in a case of calcium channel blocker overdose

DNA multiallelic systems reveal gene/longevity associations not detected by diallelic systems. The APOB locus

Accuracy of Reagent Strips in Detecting Hypoglycemia in the Emergency Department

LEVERAGING TECHNOLOGY TO PROMOTE ENGAGEMENT IN LEISURE ACTIVITIES IN SENIORS WITH COGNITIVE DECLINE

Association of tau gene polymorphism with Parkinson's disease

CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2) : early impairment of Wisconsin Card Sorting Test and saccade velocity

Beneficial effects of viscous dietary fiber from Konjac-mannan in subjects with the insulin resistance syndrome: results of a controlled metabolic trial

Interaction between methane-producing status and diet on serum acetate concentration in humans

Streptococcus bovis endocarditis and vertebral osteomyelitis

Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus

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