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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 6, 2012
Electrophysiological characteristics in four patients from Brazil with stiff person syndromePaulo J Lorenzoni, Rosana H Scola, Cláudia S K Kay, et al.Journal of the Neurological Sciences|April 1, 2008
Cerebellar ataxia in non-paraneoplastic Lambert-Eaton myasthenic syndromePaulo J Lorenzoni, Rosana H Scola, Bethan Lang, et al.Arquivos De Neuro-Psiquiatria|September 19, 2007
Chronic inflammatory demyelinating polyradiculoneuropathy in chronic graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: case reportPaulo José Lorenzoni, Rosana Herminia Scola, Ana Lucila Moreira Carsten, et al.Annals of Clinical and Translational Neurology|February 8, 2017
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndromeXin-Ming Shen, Rosana H Scola, Paulo J Lorenzoni, et al.Archives of Neurology|April 11, 2007
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10Salmo Raskin, Tetsuo Ashizawa, Hélio A G Teive, et al.Arquivos De Neuro-Psiquiatria|February 6, 2004
Myopathy of distal lower limbs: the clinical variant of MiyoshiCristiane N Soares, Marcos R G de Freitas, Osvaldo J M Nascimento, et al.Arquivos De Neuro-Psiquiatria|June 18, 2002
Hemimasticatory spasm treated with botulinum toxin: case reportHélio A G Teive, Elcio J Piovesan, Francisco M B Germiniani, et al.Parkinsonism & Related Disorders|July 21, 2004
Parkinson's disease and thyroid dysfunctionRenato P Munhoz, Helio A G Teive, André R Troiano, et al.Arquivos De Neuro-Psiquiatria|April 11, 2007
Menkes' disease: case reportFabio Agertt, Ana C S Crippa, Paulo J Lorenzoni, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2007
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twinsRenato P Munhoz, Yosuke Wakutani, Connie Marras, et al.Pageof 6