Published in Angiology on February 26, 2002
Interventional occlusion of a thrombosed aortic conduit. Pediatr Cardiol (2006) 0.75
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. Lancet Neurol (2011) 2.44
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy. Neuromuscul Disord (2010) 2.14
miR-21 and 221 upregulation and miR-181b downregulation in human grade II-IV astrocytic tumors. J Neurooncol (2009) 1.68
Cerebral neoplastic enhancing lesions: multicenter, randomized, crossover intraindividual comparison between gadobutrol (1.0M) and gadoterate meglumine (0.5M) at 0.1 mmol Gd/kg body weight in a clinical setting. Eur J Radiol (2011) 1.52
Effectiveness of skeletal scintigraphy in transthyretin-related amyloidosis. Int J Cardiol (2013) 1.43
Nuclear factor kappa-B blockade reduces skeletal muscle degeneration and enhances muscle function in Mdx mice. Exp Neurol (2006) 1.39
Intra-arterial nimodipine for the treatment of symptomatic cerebral vasospasm after aneurysmal subarachnoid hemorrhage: preliminary results. AJNR Am J Neuroradiol (2004) 1.34
Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice. Am J Pathol (2006) 1.24
Temozolomide-induced shrinkage of a pituitary carcinoma causing Cushing's disease--report of a case and literature review. ScientificWorldJournal (2010) 1.21
Bulbar compression by an ectatic vertebral artery: a novel neurovascular construct relieved by microsurgical decompression. Neurosurgery (2005) 1.19
VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice. FASEB J (2007) 1.18
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology (2012) 1.17
Sleep disorders in children with Attention-Deficit/Hyperactivity Disorder (ADHD) recorded overnight by video-polysomnography. Sleep Med (2009) 1.13
Nuclear factor-kappaB activation and differential expression of survivin and Bcl-2 in human grade 2-4 astrocytomas. Cancer (2008) 1.13
MRI finding of simultaneous coexistence of growth hormone-secreting pituitary adenoma with intracranial meningioma and carotid artery aneurysms: report of a case. Pituitary (2007) 1.08
Motor function-muscle strength relationship in spinal muscular atrophy. Muscle Nerve (2004) 1.07
Drug-induced TINU syndrome and genetic characterization. Clin Nephrol (2012) 1.05
Flavocoxid counteracts muscle necrosis and improves functional properties in mdx mice: a comparison study with methylprednisolone. Exp Neurol (2009) 1.04
Muscle fat-fraction and mapping in Duchenne muscular dystrophy: evaluation of disease distribution and correlation with clinical assessments. Preliminary experience. Skeletal Radiol (2011) 1.02
Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data. Neuromuscul Disord (2004) 1.01
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol [EudraCT no.: 2006-000032-27]. Pharmacol Res (2006) 0.99
Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian study. J Child Neurol (2003) 0.98
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A. J Peripher Nerv Syst (2008) 0.97
Ictal and interictal EEG abnormalities in ADHD children recorded over night by video-polysomnography. Epilepsy Res (2007) 0.94
Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an association. Neuromuscul Disord (2002) 0.92
Oxidative stress in myotonic dystrophy type 1. Free Radic Res (2005) 0.92
Expression of the tumor necrosis factor receptor-associated factors 1 and 2 and regulation of the nuclear factor-kappaB antiapoptotic activity in human gliomas. J Neurosurg (2005) 0.90
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. Neuromuscul Disord (2002) 0.90
Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 gene. Neuromuscul Disord (2005) 0.90
Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings. Neurol Sci (2008) 0.89
Susceptibility of human melanoma cells to autologous natural killer (NK) cell killing: HLA-related effector mechanisms and role of unlicensed NK cells. PLoS One (2009) 0.89
Expression of telomeric repeat binding factor-1 in astroglial brain tumors. Neurosurgery (2005) 0.87
Auditory system involvement in late onset Pompe disease: a study of 20 Italian patients. Mol Genet Metab (2012) 0.87
Reduced adult neurogenesis and altered emotional behaviors in autoimmune-prone B-cell activating factor transgenic mice. Biol Psychiatry (2010) 0.87
Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset. J Peripher Nerv Syst (2012) 0.87
Sclerotherapy for cervical cystic lymphatic malformations in children. Our experience with computed tomography-guided 98% sterile ethanol insertion and a review of the literature. J Pediatr Surg (2010) 0.86
MRI of cardiac involvement in transthyretin familial amyloid polyneuropathy. AJR Am J Roentgenol (2010) 0.85
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy. Neurobiol Aging (2010) 0.84
The soy isoflavone genistein blunts nuclear factor kappa-B, MAPKs and TNF-α activation and ameliorates muscle function and morphology in mdx mice. Neuromuscul Disord (2011) 0.84
Expression of muscle-specific integrins in masseter muscle fibers during malocclusion disease. Int J Mol Med (2012) 0.83
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII). Neuromuscul Disord (2011) 0.83
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study. Eur J Hum Genet (2012) 0.83
Endocardial and epicardial deformations in cardiac amyloidosis and hypertrophic cardiomyopathy. Circ J (2011) 0.82
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy. J Neurol (2013) 0.82
Development of Hashimoto's thyroiditis after subacute thyroiditis: an unusual patient. Thyroid (2009) 0.82
A patient with stress-related onset and exacerbations of Graves disease. Nat Clin Pract Endocrinol Metab (2008) 0.81
A retrospective analysis of hospitalized patients with documented deep-venous thrombosis and their risk of pulmonary embolism. Angiology (2008) 0.81
Spontaneous recovery from isolated post-traumatic central hypogonadism in a woman. Hormones (Athens) (2010) 0.80
Immunohistochemical analysis of human skeletal muscle AMP deaminase deficiency. Evidence of a correlation between the muscle HPRG content and the level of the residual AMP deaminase activity. J Muscle Res Cell Motil (2006) 0.80
Immunohistochemical analysis of TGF-β1 and VEGF in gingival and periodontal tissues: a role of these biomarkers in the pathogenesis of scleroderma and periodontal disease. Int J Mol Med (2012) 0.80
Intraosseous mandibular artero-venous malformations: case report. J Craniomaxillofac Surg (2008) 0.80
Autonomic involvement in subacute and chronic immune-mediated neuropathies. Autoimmune Dis (2013) 0.80
Evidence of cardiovascular autonomic impairment in mitochondrial disorders. J Neurol (2007) 0.79
Intra-arterial nimodipine to treat symptomatic cerebral vasospasm following traumatic subarachnoid haemorrhage. Technical case report. Acta Neurochir (Wien) (2008) 0.79
Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy. Neuromuscul Disord (2008) 0.79
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two. Neuromuscul Disord (2009) 0.78
Integration of three-dimensional rotational angiography in radiosurgical treatment planning of cerebral arteriovenous malformations. Int J Radiat Oncol Biol Phys (2011) 0.78
Unusual features of central nervous system involvement in CMTX associated with a novel mutation of GJB1 gene. J Peripher Nerv Syst (2012) 0.78
Autonomic function in elderly uremics studied by spectral analysis of heart rate. Kidney Int (2005) 0.78
Immunolocalization and activation of transcription factor nuclear factor kappa B in dysimmune neuropathies and familial amyloidotic polyneuropathy. Arch Neurol (2004) 0.78
90th ENMC international workshop: European Spinal Muscular Atrophy Randomised Trial (EuroSMART) 9-10 February 2001, Naarden, The Netherlands. Neuromuscul Disord (2002) 0.77
Advanced virtual magnetic resonance imaging (MRI) techniques in neurovascular conflict: bidimensional image fusion and virtual cisternography. Radiol Med (2013) 0.77
Severe head trauma in patients with unexplained central hypothyroidism. Am J Med (2004) 0.77
Osteosclerotic myeloma with spinal leptomeningitis and severe polyneuropathy: A case report. J Comput Assist Tomogr (2006) 0.77
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency. Neuromuscul Disord (2007) 0.76
Left atrial function in cardiac amyloidosis. J Cardiovasc Med (Hagerstown) (2016) 0.76
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. Neurol Sci (2014) 0.76
Subacute inflammatory demyelinating polyneuropathy disclosed by massive nerve root enhancement in CMT1A. Muscle Nerve (2011) 0.76
Possible link between history of hypersensitivity to a specific non-steroidal anti-inflammatory drug (NSAID) and positive results following challenge test to alternative NSAIDS. Arzneimittelforschung (2009) 0.76
Does HLA Class II haplotype play a role in adult acute disseminated encephalomyelitis? Preliminary findings from a Southern Italy hospital-based study. Arch Ital Biol (2012) 0.75
[Management and development of the dangerous preparation archive]. Ann Ist Super Sanita (2006) 0.75
The unusual association of Graves' disease, chronic spontaneous urticaria, and premature ovarian failure: report of a case and HLA haplotype characterization. Arq Bras Endocrinol Metabol (2013) 0.75
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med (2015) 0.75
Brainstem ischemia, steno-occlusive pathology of the vertebral arteries, and alterations in the circadian blood pressure pattern: a case report. J Stroke Cerebrovasc Dis (2009) 0.75
Axial myopathy in myasthenia: a misleading cause of dropped head. Muscle Nerve (2004) 0.75
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med (2015) 0.75
Ulcerative colitis complicated by dural sina venous thrombosis. Int J Colorectal Dis (2002) 0.75
Long-term follow-up of ruptured intracranial aneurysms treated by microsurgical wrapping with autologous muscle. Neurosurg Rev (2012) 0.75
Cerebellar stroke in elderly patient with basilar artery agenesia: a case report. J Stroke Cerebrovasc Dis (2010) 0.75
Diffuse metabolic changes in the brain of patients with familial amyloid polyneuropathy. A proton MRSI study. J Neurol Sci (2006) 0.75
Apoptosis and apoptosis-related proteins in thyroid myopathies. Muscle Nerve (2002) 0.75
Calpain 3 deficiency in Quail Eater's disease. Ann Neurol (2004) 0.75
3 Tesla-Diffusion Tensor Imaging in Autosomal Dominant Polycystic Kidney Disease: The Nephrologist's Point of View. Nephron (2016) 0.75
Comparison of different techniques for detecting 17p12 duplication in CMT1A. Neuromuscul Disord (2005) 0.75
Pharyngeal enterogenous cyst associated with canalis basilaris medianus in a newborn. Pediatr Radiol (2012) 0.75
Pregnancy after azathioprine therapy for ulcerative colitis in a woman with autoimmune premature ovarian failure and Addison's disease: HLA haplotype characterization. Fertil Steril (2011) 0.75