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Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

Neurology, 2004-01, Vol.62 (2), p.262-268

2004

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Abnormal head nociceptive withdrawal reaction to facial nociceptive stimuli in Parkinson's disease

Clinical neurophysiology, 2005-09, Vol.116 (9), p.2091-2098

2005

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High-efficiency endovascular gene delivery via therapeutic ultrasound

Journal of the American College of Cardiology, 2001-06, Vol.37 (7), p.1975-1980

2001

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Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation

Neurology, 2000-09, Vol.55 (5), p.702-705

2000

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Muscular cramps: proposals for a new classification

Acta neurologica Scandinavica, 2003-03, Vol.107 (3), p.176-186

2003

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Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

Neurology, 2001-03, Vol.56 (6), p.802-805

2001

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In-stent restenosis limitation with stent-based controlled-release nitric oxide: initial results in rabbits

Radiology, 2004-02, Vol.230 (2), p.377-382

2004

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l-dopa effects on preprogramming and control activity in a skilled motor act in Parkinson's disease

Clinical neurophysiology, 2002-02, Vol.113 (2), p.243-253

2002

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Growth retardation, developmental delay, distinctive face, multiple endocrine abnormalities, and adenylyl cyclase dysfunction: A new syndrome?

American journal of medical genetics, 2003-07, Vol.120A (3), p.389-394

2003

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Preprogramming and control activity of bimanual self-paced motor task in Parkinson's disease

Clinical neurophysiology, 2000-05, Vol.111 (5), p.873-883

2000

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SPG3A: An additional family carrying a new atlastin mutation

Neurology, 2002-12, Vol.59 (12), p.2002-2005

2002

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Multiple mtDNA deletions: Clinical and molecular correlations

Journal of inherited metabolic disease, 2000-03, Vol.23 (2), p.155-161

2000

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Afterdischarge activity in neuropathic patients with frequent muscle cramps

Acta neurologica Scandinavica, 2000-12, Vol.102 (6), p.359-362

2000

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Indobufen versus warfarin in the secondary prevention of major vascular events in nonrheumatic atrial fibrillation

Stroke (1970), 1997-05, Vol.28 (5), p.1015-1021

1997

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Indapamide Reduces Hypertensive Left Ventricular Hypertrophy: An International Multicenter Study

Journal of cardiovascular pharmacology, 1993, Vol.22 Suppl 6, p.106-106

1993

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RR interval variation, sympathetic skin reflex and QT dispersion in the assessment of autonomic function in peripheral neuropathy

Electromyography and clinical neurophysiology, 1999-12, Vol.39 (8), p.461

1999

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Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosis

Functional neurology, 2003-01, Vol.18 (1), p.29

2003

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P300 variations in parkinsonian patients before and during dopaminergic monotherapy: a suggested dopamine component in P300

Electroencephalography and clinical neurophysiology, 1991-09, Vol.80 (5), p.446-453

1991

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Electrophysiological (EEG, BAEP, VEP) study in patients with beta-thalassemia major

Acta neurologica Belgica, 1987-08, Vol.87 (4), p.181-190

1987

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Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas : rapid identification by fine needle aspiration biopsy

The journal of clinical endocrinology and metabolism, 1994-08, Vol.79 (2), p.657-661

1994

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Current insights into familial spastic paraparesis: new advances in an old disease

Functional neurology, 2003-01, Vol.18 (1), p.43

2003

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Evaluation of allergic etiology in perennial rhinitis

Annals of allergy, 1985-12, Vol.55 (6), p.854

1985

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Parkinson disease: Electrophysiological (CNV) analysis related to pharmacological treatment

Electroencephalography and clinical neurophysiology, 1986-12, Vol.64 (6), p.521-524

1986

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Predictive value of circulating endothelial microparticles for cardiovascular mortality in end-stage renal failure: a pilot study

Nephrology, dialysis, transplantation, 2012-05, Vol.27 (5), p.1873-1880

2012

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Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

Abnormal head nociceptive withdrawal reaction to facial nociceptive stimuli in Parkinson's disease

High-efficiency endovascular gene delivery via therapeutic ultrasound

Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation

Muscular cramps: proposals for a new classification

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

In-stent restenosis limitation with stent-based controlled-release nitric oxide: initial results in rabbits

l-dopa effects on preprogramming and control activity in a skilled motor act in Parkinson's disease

Growth retardation, developmental delay, distinctive face, multiple endocrine abnormalities, and adenylyl cyclase dysfunction: A new syndrome?

Preprogramming and control activity of bimanual self-paced motor task in Parkinson's disease

SPG3A: An additional family carrying a new atlastin mutation

Multiple mtDNA deletions: Clinical and molecular correlations

Afterdischarge activity in neuropathic patients with frequent muscle cramps

Indobufen versus warfarin in the secondary prevention of major vascular events in nonrheumatic atrial fibrillation

Indapamide Reduces Hypertensive Left Ventricular Hypertrophy: An International Multicenter Study

RR interval variation, sympathetic skin reflex and QT dispersion in the assessment of autonomic function in peripheral neuropathy

Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosis

P300 variations in parkinsonian patients before and during dopaminergic monotherapy: a suggested dopamine component in P300

Electrophysiological (EEG, BAEP, VEP) study in patients with beta-thalassemia major

Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas : rapid identification by fine needle aspiration biopsy

Current insights into familial spastic paraparesis: new advances in an old disease

Evaluation of allergic etiology in perennial rhinitis

Parkinson disease: Electrophysiological (CNV) analysis related to pharmacological treatment

Predictive value of circulating endothelial microparticles for cardiovascular mortality in end-stage renal failure: a pilot study

ABL Mutations in Late Chronic Phase Chronic Myeloid Leukemia Patients With Up-Front Cytogenetic Resistance to Imatinib Are Associated With a Greater Likelihood of Progression to Blast Crisis and Shorter Survival: A Study by the GIMEMA Working Party on Chronic Myeloid Leukemia

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