Neuromuscular

InícioNeuromuscular

Publicações

Lista parcial de artigos publicados pela equipe: 

Lobo, C. C. et al.
Cranial Nerve Thinning Distinguishes RFC1-Related Disorder from Other Late-Onset Ataxias. Movement Disorders Clinical Practice, 2023.
Borba, F. C. et al.
Functional magnetic resonance imaging and diffusion tensor imaging findings in a patient with ROBO3-related horizontal gaze palsy with progressive scoliosis. Arquivos de Neuro-Psiquiatria (Online), 2021.
Borba, F. C. et al.
Cerebellar degeneration in adult spinal muscular atrophy patients. Journal of Neurology, 2020.
Leoni TB et al.
A novel multisystem proteinopathy caused by a missense ANXA11 variant. Ann Neurol. 2021;90:239-252.
Coimbra Neto AR et al.
Intrafamilial phenotypic heterogeneity related to a new DMD splice site variant. Neuromuscul Disord. 2021;31:788-797.
Diniz de Lima F et al.
Randomized trial of botulinum toxin type A in hereditary spastic paraplegia (SPASTOX Trial). Mov Disord. 2021;36:1654-1663.
Silva Schmitt G et al.
Dopa-responsive parkinsonism in a patient with homozygous RFC1 expansions. Mov Disord. 2020;35:1889-1890.
Martinez AR et al.
Sensory neuronopathy in autoimmune hepatitis. Eur J Neurol. 2020;27:2072-2078.
Gonçalves JPN et al.
CAG repeats in ATXN1 associated with ALS in Brazilian patients. J Neurol Sci. 2020;414:116842.
Jaques CS et al.
Ataxia in Sjögren's syndrome. J Neurol Neurosurg Psychiatry. 2020;91:446-448.
Martins MP et al.
Laryngeal EMG in ALS. J Neurol Neurosurg Psychiatry. 2020;91:730-732.
Carvalho AA et al.
PYGM mRNA in McArdle disease. PLoS One. 2020;15:e0236597.
Martinez AR et al.
Misdiagnosis in sensory neuronopathies. Arq Neuropsiquiatr. 2019;77:451-455.
Silva AM et al.
Clinical and molecular findings in ANO5-related myopathy. Ann Clin Transl Neurol. 2019;6:1225-1238.
Martinez AR et al.
Autonomic dysfunction in sensory neuronopathies. J Neurol Sci. 2019;402:111-117.
Luiz LC et al.
Motor and respiratory function in Duchenne patients. Respir Physiol Neurobiol. 2019;262:1-11.
Martinez AR et al.
Zika-related sensory neuronopathy. Muscle Nerve. 2018;57:E100-E101.
Martinez AR et al.
Sensory neuronopathy in HTLV-1 myelopathy. J Neurovirol. 2018;24:369-371.
Andrade HMT et al.
Intermediate-length CAG repeats in ATXN2 and ALS. Neurobiol Aging. 2018;69:292.e15-292.e18.
Takazaki KA et al.
Sudomotor dysfunction in Friedreich ataxia. Clin Neurophysiol. 2018;129:2290-2295.
De Albuquerque M et al.
Cerebral and spinal damage in ALS. NeuroImage Clin. 2017;26:201-206.
Martinez AR et al.
Autoimmune neuropathies and rheumatic diseases. Autoimmun Rev. 2017;16:335-342.
Faber I et al.
SPG11 mutations and widespread white matter abnormalities. NeuroImage Clin. 2018;19:848-857.
Servelhere KR et al.
Botulinum toxin in hereditary spastic paraplegia. Arq Neuropsiquiatr. 2018;76:183-188.
Rezende TJR et al.
Structural signature of SCA3. Ann Neurol. 2018;84:401-408.
Faber I et al.
SPG11-related parkinsonism. Mov Disord. 2018;33:1650-1656.
Takazaki KA et al.
Dysautonomia in Machado-Joseph disease. Cerebellum. 2013;12:513-519.
Martinez AR et al.
Sensory neuronopathy in autoimmune diseases. Autoimmune Dis. 2012;2012:1-6.
Rezende TJR et al.
RFC1-related spinal cord damage. Mov Disord. 2022;37:2122-2128.
Hernandez AL et al.
Tract-specific spinal cord imaging in Friedreich's ataxia. Mov Disord. 2022;37:354-364.
Oliveira JBL et al.
Pharmacotherapy in Machado-Joseph disease. Expert Opin Pharmacother. 2022;23:1687-1694.
Schmitt GS et al.
Dysautonomia in RFC1-related disorder. Clin Neurophysiol. 2022;142:68-74.
Vasconcelos-Ferreira A et al.
Carbamazepine in Machado-Joseph disease. Neuropathol Appl Neurobiol. 2022;48:e12763.
Piccinin CC et al.
Longitudinal MRI study in SCA3. Mov Disord. 2020;35:1679-1684.
Franklin GL et al.
Gluten ataxia: an overestimated condition? Cerebellum. 2021;20:1-3.
Faber I et al.
Hereditary spastic paraplegia: clinical features and management. Arq Neuropsiquiatr. 2014;72:219-226.
Rezende TJR et al.
Multimodal MRI study in SPG4 mutations. PLoS One. 2015;10:e0117666.
Casseb RF et al.
Neuroimaging in sensory neuronopathy. J Neuroimaging. 2015;25:704-709.
Faber I et al.
Fatigue in SCA3. Cerebellum. 2016;15:235-240.
Rezende TJR et al.
RFC1-related spinal cord atrophy. J Neurol Sci. 2016;370:180-186.
Silva LB et al.
Nutritional evaluation in ALS. Rev Bras Nutr Clin. 2008;23:5-12.
Appenzeller S et al.
Brain tumor-like lesion in Behçet disease. Rheumatol Int. 2006;26:577-580.
Martinez AR et al.
SPG11 mutations and white matter damage. Neuroimage Clin. 2018;19:848-857.
Hernandez AL et al.
Spinal cord diffusion tensor imaging in Friedreich's ataxia. Mov Disord. 2022;37:354-364.
Rezende TJR et al.
Progressive spinal cord degeneration in Friedreich's ataxia. Mov Disord. 2022;38:45-56.
Schmitt GS et al.
Dysautonomia in RFC1-related disorder. Clin Neurophysiol. 2022;142:68-74.
Takazaki KA et al.
Sudomotor dysfunction in Friedreich's ataxia. Clin Neurophysiol. 2018;129:2290-2295.
Martinez AR et al.
Misdiagnosis of hemifacial spasm. Arq Neuropsiquiatr. 2014;72:119-122.
Damasceno A et al.
Brainstem involvement in Sjögren's syndrome. J Neuroimaging. 2009;18:111-117.
França MC et al.
Chronic pain in Machado-Joseph disease. Arch Neurol. 2007;64:1767-1770.
Damasceno A et al.
Cerebellar atrophy in sensory neuronopathy. Arq Neuropsiquiatr. 2011;69:602-606.
França MC et al.
Muscle excitability abnormalities in Machado-Joseph disease. Arch Neurol. 2008;65:525-529.
Martinez AR et al.
Derek Denny-Brown: the man behind the ganglia. Arq Neuropsiquiatr. 2017;75:127-129.
Faber I et al.
Clinical features of hereditary spastic paraplegia. Mov Disord. 2018;33:1650-1656.
Rezende TJR et al.
Brain atrophy and disease progression in Friedreich's ataxia. J Neurol Sci. 2019;370:180-186.
Takazaki KA et al.
Dysautonomia in Machado-Joseph disease. Cerebellum. 2013;12:513-519.
Faber I et al.
Inflammatory demyelinating neuropathy. Muscle Nerve. 2017;55:756-760.
Martinez AR et al.
Zika virus-related sensory neuronopathy. Muscle Nerve. 2018;57:E100-E101.
Hernandez AL et al.
MRI markers in ALS. J Neuroimaging. 2016;26:201-206.
Martinez AR et al.
Non-paraneoplastic sensory neuronopathy. J Neurol Sci. 2019;402:111-117.
França MC et al.
Sensory ataxia scale in Machado-Joseph disease. J Peripher Nerv Syst. 2019;24:242-246.
Rezende TJR et al.
Structural progression in SCA3. Mov Disord. 2018;35:1679-1684.
Rezende TJR et al.
Presymptomatic to late-stage SCA3. Ann Neurol. 2018;84:401-408.
Casseb RF et al.
Spinal cord diffusion tensor imaging. Neuroradiology. 2016;58:1103-1108.
Faber I et al.
SPG11-related parkinsonism: clinical profile. Mov Disord. 2018;33:1650-1656.
Silva L et al.
Functional assessment in ALS. Arq Neuropsiquiatr. 2008;66:354-359.
Appenzeller S et al.
Behçet disease with brain lesions. Rheumatol Int. 2006;26:577-580.
França MC et al.
Sensory neuronopathy progression in Machado-Joseph disease. Muscle Nerve. 2008;40:1012-1018.
Damasceno A et al.
Vasculitis resembling Rasmussen encephalitis. Neurologist. 2009;15:285-288.
Damasceno A et al.
Autonomic dysfunction in sensory neuronopathy. J Neurol. 2011;258:231-237.
França MC et al.
Pain in Machado-Joseph disease. Arch Neurol. 2007;64:1767-1770.
França MC et al.
MRI in Friedreich's ataxia. J Neurol. 2009;256:1114-1120.
Damasceno A et al.
Bickerstaff encephalitis and related conditions. Arq Neuropsiquiatr. 2008;66:744-746.
Martinez AR et al.
Misdiagnosis in sensory neuronopathies. Arq Neuropsiquiatr. 2019;77:451-455.
França MC et al.
Spinal cord lesions in chronic sensory neuropathies. J Neuroimaging. 2008;18:168-172.
França MC et al.
Chronic sensory neuropathy. Eur J Neurol. 2008;15:1400-1405.
Faber I et al.
L-dopa response in Machado-Joseph disease. Acta Neurol Scand. 2009;119:277-280.
Rezende TJR et al.
Longitudinal study in ALS. Neuroimage Clin. 2017;14:201-207.
França MC et al.
Age at onset modulation in Machado-Joseph disease. Front Neurol. 2012;3:164.
Damasceno A et al.
Sjögren syndrome and brainstem lesions. J Neuroimaging. 2009;18:111-117.
Martinez AR et al.
Structural signature in Friedreich's ataxia. J Neurol Sci. 2017;370:180-186.
Casseb RF et al.
Selective sensory deafferentation. Neuroimage Clin. 2019;21:101633.
Damasceno A et al.
Chronic acquired sensory neuron diseases. Eur J Neurol. 2008;15:1400-1405.
Damasceno A et al.
Adult-onset unihemispheric vasculitis. Neurologist. 2009;15:285-288.
Nucci A et al.
Multi-minicore disease revisited. Arq Neuropsiquiatr. 2004;62:935-939.
Garibaldi SG et al.
Reference values for ulnar nerve conduction. Arq Neuropsiquiatr. 2002;60:349-352.
França MC et al.
Combined voxel-based morphometry in Friedreich's ataxia. J Neurol. 2009;256:1114-1120.
Lima NM et al.
ALS: Functional and nutritional assessment. Arq Neuropsiquiatr. 2008;66:354-359.
Nucci A et al.
Human herpesvirus infections of the CNS. J Med Virol. 2015;87:648-655.
França MC et al.
Chronic pain in Machado-Joseph disease. Arch Neurol. 2007;64:1767-1770.
Faber I et al.
Genetic profile in dystrophinopathies. Clin Genet. 2017;92:199-203.
Damasceno A et al.
Brainstem involvement in Sjögren’s Syndrome. J Neuroimaging. 2009;18:168-172.
Rezende TJR et al.
Longitudinal clinical MRI in SCA3. Mov Disord. 2018;35:1679-1684.
Martinez AR et al.
Autonomic dysfunction in sensory neuronopathies. J Neurol Sci. 2019;402:111-117.
Casseb RF et al.
Spinal cord atrophy in ALS. Neuroimage Clin. 2017;26:201-206.
Takazaki KA et al.
Dysautonomia in Machado-Joseph disease. Cerebellum. 2013;12:513-519.
Garibaldi SG et al.
Ulnar sensory-motor amplitude ratio. Arq Neuropsiquiatr. 2013;71:465-469.
Rezende TJR et al.
Sudomotor dysfunction in Friedreich ataxia. Clin Neurophysiol. 2018;129:2290-2295.
Martinez AR et al.
Misdiagnosis in sensory neuronopathies. Arq Neuropsiquiatr. 2019;77:451-455.
França MC et al.
Prospective study in hereditary spastic paraplegia. Mov Disord. 2007;22:121-124.
Damasceno A et al.
Guillain-Barré syndrome in elderly. Arq Neuropsiquiatr. 2005;63:773-775.
Nucci A et al.
Autoimmune neuropathies and rheumatic diseases. Autoimmun Rev. 2017;16:335-342.