Search Results - "BONIFATI, M. D"
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SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy
Published in Neurology (18-01-2011)“…Duchenne muscular dystrophy (DMD) is the most common single-gene lethal disorder. Substantial patient-patient variability in disease onset and progression and…”
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Development and validation of the Myasthenia Gravis TeleScore (MGTS)
Published in Neurological sciences (01-07-2022)“…Objective The aim of our study was to validate the Myasthenia Gravis TeleScore (MGTS), a scale for the evaluation of MG patients in telemedicine. Introduction…”
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3
The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy
Published in Journal of neurology, neurosurgery and psychiatry (01-10-2006)“…Background: Steroid administration is beneficial in Duchenne muscular dystrophy (DMD), but the response, incidence, and the severity of side effects are…”
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4
A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy
Published in Muscle & nerve (01-09-2000)“…We randomized 18 Duchenne muscular dystrophy (DMD) boys whose age ranged from 5.2 to 14.6 years (mean, 7.3 years) for treatment with either deflazacort (0.9…”
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The quality of neurology residency programmes in Italy
Published in Lancet neurology (01-10-2003)Get more information
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6
Long-term cyclosporine treatment in a group of severe myasthenia gravis patients
Published in Journal of neurology (01-09-1997)“…We evaluated cyclosporine A (CsA) treatment in 9 patients (6 female and 3 male), 16-63 years old, with severe myasthenia gravis (MG) for a mean period of 2…”
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Quality of neurology residency programmes: an Italian survey
Published in European journal of neurology (01-05-2003)“…In recent years there has been a growing interest in medical and particularly neurological education and how this should be related to the needs for patient…”
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8
Structural and functional anatomy of the globular domain of complement protein C1q
Published in Immunology letters (01-09-2004)“…C1q is the first subcomponent of the classical pathway of the complement system and a major connecting link between innate and acquired immunity. As a…”
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9
New therapies in muscular dystrophies
Published in Neurological sciences (01-01-2000)“…Muscular dystrophies are a group of hereditary muscle disorders that often result in severe disability. Curative therapy is not yet available for muscular…”
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10
Steroids in muscular dystrophy: where do we stand?
Published in Neuromuscular disorders : NMD (01-08-1998)Get full text
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11
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents
Published in Cancer chemotherapy and pharmacology (2000)“…To evaluate the incidence and entity of muscle damage after hyperthermic limb perfusion (HLP) with doxorubicin or melphalan, two widely used chemotherapeutic…”
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Effect of sera from AChR-antibody negative myasthenia gravis patients on AChR and MuSK in cell cultures
Published in Journal of neuroimmunology (01-04-2007)“…Abstract A proportion of patients with myasthenia gravis (MG) do not have antibodies to the acetylcholine receptor (AChR). Some of these patients have…”
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13
Desmopressin Acetate in Percutaneous Ultrasound-Guided Kidney Biopsy: A Randomized Controlled Trial
Published in American journal of kidney diseases (01-06-2011)“…Background Bleeding complications occur in one-third of percutaneous kidney biopsies and increase costs of the hospital stay. The aim of the study was to…”
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14
Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study
Published in Lancet neurology (01-07-2008)“…Summary Background Mutations in LRRK2 , the gene that encodes leucine-rich repeat kinase 2, are a cause of Parkinson's disease (PD). The International LRRK2…”
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15
Neurology residency training in Europe: an Italian perspective
Published in Lancet neurology (01-04-2005)“…Education is the most important part of medical-science training. Assessment of training programmes and examination of trainees' skills are necessary to…”
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Lack of association between acetylcholine receptor ϵ polymorphisms and early-onset myasthenia gravis
Published in Muscle & nerve (01-03-2004)“…A patient with mutations in the acetylcholine receptor (AChR) ϵ subunit, who subsequently developed autoimmune myasthenia gravis (MG), led us to search for ϵ…”
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