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P. Lorenzoni · SciRah

Researcher profile · Semantic Scholar

P. Lorenzoni

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P. Lorenzoni — researcher profile on SciRah

h-index: 21
Works: 157
Citations: 1,440

Most-cited papers

When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?
P. Lorenzoni, L. Werneck, C. Kay, C. Silvado +1 more
2015Arquivos de Neuro-Psiquiatria62 citations Open access
Semantic Scholar
Clinical follow-up of pregnancy in myasthenia gravis patients.
R. D. Ducci, P. Lorenzoni, C. Kay, L. Werneck +1 more
2017Neuromuscular Disorders60 citations
Semantic Scholar
Salbutamol therapy in congenital myasthenic syndrome due to DOK7 mutation.
P. Lorenzoni, R. Scola, C. Kay, L. Filla +5 more
2013Journal of Neurological Sciences45 citations
Semantic Scholar
When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?
P. Lorenzoni, R. Scola, C. Kay, C. Silvado +1 more
2014Arquivos de Neuro-Psiquiatria42 citations Open access
Semantic Scholar
Novel synaptobrevin‐1 mutation causes fatal congenital myasthenic syndrome
Xin-Ming Shen, R. Scola, P. Lorenzoni, C. Kay +4 more
2017Annals of Clinical and Translational Neurology38 citations Open access
Semantic Scholar
Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literature.
I. C. Nettore, P. Mirra, A. M. Ferrara, Annarita Sibilio +12 more
2013Thyroid35 citations
Semantic Scholar
Duchenne muscular dystrophy: an historical treatment review.
L. Werneck, P. Lorenzoni, R. D. Ducci, O. Fustes +2 more
2019Arquivos de Neuro-Psiquiatria33 citations Open access
Semantic Scholar
Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness
D. Owen, A. Töpf, V. Preethish-Kumar, P. Lorenzoni +17 more
2018American Journal of Medical Genetics. Part A32 citations Open access
Semantic Scholar
Somatosensory evoked potentials in clinical practice: a review
O. Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +2 more
2020Arquivos de Neuro-Psiquiatria24 citations Open access
Semantic Scholar
Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort.
K. Polavarapu, Balaraju Sunitha, A. Töpf, V. Preethish-Kumar +22 more
2023Brain : a journal of neurology21 citations Open access
Semantic Scholar
Myasthenia gravis and azathioprine treatment: Adverse events related to thiopurine S-methyl-transferase (TPMT) polymorphisms.
P. Lorenzoni, C. Kay, Marcelo Farago Zanlorenzi, R. D. Ducci +2 more
2020Journal of Neurological Sciences17 citations
Semantic Scholar
Characterization of the amyotrophic lateral sclerosis-linked P56S mutation of the VAPB gene in Southern Brazil
Matheus Luis Castelan Trilico, P. Lorenzoni, C. Kay, Renata Dal Pra Ducci +3 more
2020Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration12 citations
Semantic Scholar
HLA-alleles class I and II associated with genetic susceptibility to neuromyelitis optica in Brazilian patients
C. Kay, R. Scola, R. Arndt, P. Lorenzoni +1 more
2018Arquivos de Neuro-Psiquiatria12 citations Open access
Semantic Scholar
Motor neuron disease in patients with HIV infection: Report of two cases and brief review of the literature.
P. Lorenzoni, R. D. Ducci, G. Dalledone, C. Kay +3 more
2018Clinical neurology and neurosurgery (Dutch-Flemish ed. Print)12 citations
Semantic Scholar
The immunogenetics of multiple sclerosis. The frequency of HLA-alleles class 1 and 2 is lower in Southern Brazil than in the European population
L. Werneck, P. Lorenzoni, R. Arndt, C. Kay +1 more
2016Arquivos de Neuro-Psiquiatria11 citations Open access
Semantic Scholar
Predictors of early left ventricular systolic dysfunction in duchenne muscular dystrophy patients
R. H. D. Cirino, R. Scola, R. D. Ducci, Ana Cristina Camarozano Wermelinger +5 more
2018Muscle and Nerve10 citations
Semantic Scholar
Multiple sclerosis: disease modifying therapy and the human leukocyte antigen.
L. Werneck, P. Lorenzoni, C. Kay, R. Scola
2018Arquivos de Neuro-Psiquiatria10 citations Open access
Semantic Scholar
Polymyositis without Beneficial Response to Steroid Therapy: Should Miyoshi Myopathy be a Differential Diagnosis?
R. Scalco, P. Lorenzoni, David S. Lynch, W. A. Martins +4 more
2017The American journal of case reports10 citations Open access
Semantic Scholar
Late-onset Pompe disease: what is the prevalence of limb-girdle muscular weakness presentation?
P. Lorenzoni, C. Kay, N. Higashi, V. D'Almeida +2 more
2017Arquivos de Neuro-Psiquiatria10 citations Open access
Semantic Scholar
Triple-seronegative myasthenia gravis: clinical and epidemiological characteristics
Paula Raquel do Vale Pascoal Rodrigues, C. Kay, R. D. Ducci, M. Utiumi +4 more
2023Arquivos de Neuro-Psiquiatria9 citations Open access
Semantic Scholar
Niemann-Pick disease type C: a case series of Brazilian patients.
P. Lorenzoni, Elaine H Cardoso, A. Crippa, C. Lourenço +9 more
2014Arquivos de Neuro-Psiquiatria9 citations Open access
Semantic Scholar
Horner syndrome: tribute to Professor Horner on his 190 th birthday
O. Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +2 more
2020Arquivos de Neuro-Psiquiatria8 citations Open access
Semantic Scholar
Treatment of epilepsy in patients with myasthenia gravis: Is really harder than it looks?
P. Lorenzoni, R. D. Ducci, Tallulah Spina Tensini, G. Dalledone +5 more
2017Journal of clinical neuroscience8 citations
Semantic Scholar
Congenital myasthenic syndrome in a cohort of patients with ‘double’ seronegative myasthenia gravis
P. Lorenzoni, R. D. Ducci, R. Arndt, N. M. C. Hrysay +6 more
2020Arquivos de Neuro-Psiquiatria7 citations Open access
Semantic Scholar
Celebrating the 70 years of pyridostigmine on therapy of Myasthenia Gravis: historical aspects of the preliminary trials
P. Lorenzoni, C. Kay, R. D. Ducci, O. Fustes +2 more
2019Arquivos de Neuro-Psiquiatria7 citations Open access
Semantic Scholar
Evaluation of Left-Sided Heart Chambers With Novel Echocardiographic Techniques in Men With Duchenne or Becker Muscular Dystrophy.
R. H. D. Cirino, R. Scola, R. D. Ducci, A. Camarozano +5 more
2019American Journal of Cardiology7 citations
Semantic Scholar
Is there a relationship between narcolepsy, multiple sclerosis and HLA-DQB1*06:02?
P. Lorenzoni, L. Werneck, Ana Christina de Souza Crippa, A. Zanatta +3 more
2016Arquivos de Neuro-Psiquiatria7 citations Open access
Semantic Scholar
Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review
P. Lorenzoni, C. Kay, R. D. Ducci, O. Fustes +5 more
2022Arquivos de Neuro-Psiquiatria6 citations Open access
Semantic Scholar
Pain-related nociceptive evoked potential and skin wrinkle test in small fiber neuropathy
O. H. Hernández Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +3 more
2021Arquivos de Neuro-Psiquiatria6 citations Open access
Semantic Scholar
Myasthenia gravis during pregnancy: what care should be taken?
R. D. Ducci, C. Kay, O. Fustes, L. Werneck +2 more
2020Arquivos de Neuro-Psiquiatria6 citations Open access
Semantic Scholar
How to Spot Congenital Myasthenic Syndromes Resembling the Lambert–Eaton Myasthenic Syndrome? A Brief Review of Clinical, Electrophysiological, and Genetics Features
P. Lorenzoni, R. Scola, C. Kay, L. Werneck +2 more
2018Neuromolecular medicine6 citations Open access
Semantic Scholar
Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromes
Y. Azuma, A. Töpf, T. Evangelista, P. Lorenzoni +5 more
2017Neurology: Genetics5 citations Open access
Semantic Scholar
Peripheral polyneuropathy from electrodiagnostic tests: a 10-year etiology and neurophysiology overview
R. D. Ducci, Camila Lorenzini Tessaro, C. Kay, O. Fustes +3 more
2021Arquivos de Neuro-Psiquiatria4 citations Open access
Semantic Scholar
Does oral salbutamol improve fatigue in multiple sclerosis? A pilot placebo-controlled study.
G. M. de Almeida, R. Scola, R. D. Ducci, R. H. D. Cirino +5 more
2020Multiple Sclerosis and Related Disorders4 citations
Semantic Scholar
Congenital myasthenic syndrome due to DOK7 mutation in a cohort of patients with 'unexplained' limb-girdle muscular weakness.
P. Lorenzoni, C. Kay, R. Arndt, N. M. C. Hrysay +6 more
2020Journal of clinical neuroscience4 citations
Semantic Scholar
Lambert-Eaton myasthenic syndrome: the 60th anniversary of Eaton and Lambert's pioneering article
P. Lorenzoni, C. Kay, L. Werneck, R. Scola
2017Arquivos de Neuro-Psiquiatria4 citations Open access
Semantic Scholar
Hereditary Neuropathy With Liability to Pressure Palsies: A Single-Center Experience in Southern Brazil
P. Lorenzoni, C. Kay, Cristiane Cavalet, R. Arndt +2 more
2016Neurology International4 citations Open access
Semantic Scholar
Myasthenia gravis and thymus: long-term follow-up screening of thymectomized and non-thymectomized patients.
P. Lorenzoni, L. Augusto, C. Kay, R. Scola +1 more
2013Arquivos de Neuro-Psiquiatria4 citations Open access
Semantic Scholar
Spectrum of SPTLC1-related disorders: a novel case of ‘Ser331 syndrome’ that expand the phenotype of hereditary sensory and autonomic neuropathy type 1A and motor neuron diseases
P. Lorenzoni, D. Bayer, R. D. Ducci, O. Fustes +4 more
2023Neurological Sciences3 citations
Semantic Scholar
Visual Evoked Potentials in Neuromyelitis Optica Spectrum Disorders
O. H. Hernández Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +2 more
2021Journal of Central Nervous System Disease3 citations Open access
Semantic Scholar
Somatosensory evoked potentials in Hirayama disease: A Brazilian study
O. Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +2 more
2020Surgical neurology international3 citations Open access
Semantic Scholar
Single-centre experience on genotypic and phenotypic features of southern Brazilian patients with McArdle disease
P. Lorenzoni, L. Werneck, C. Kay, R. Arndt +2 more
2018Acta Neurologica Belgica3 citations
Semantic Scholar
Immune-mediated rippling muscle disease in a patient with treated hypothyroidism.
R. D. Ducci, R. Scola, P. Lorenzoni, C. Kay +4 more
2017Journal of Neurological Sciences3 citations
Semantic Scholar
Myasthenia gravis and pregnancy: A brief review of 37 pregnancies
R. D. Ducci, P. Lorenzoni, C. Kay, L. C. Werneck +1 more
20153 citations
Semantic Scholar
Genetic screening for transthyretin familial amyloid polyneuropathy to avoid misdiagnosis in patients with polyneuropathy associated with high protein in the cerebrospinal fluid
P. Lorenzoni, Vinícius Riegel Giugno, R. D. Ducci, L. Werneck +2 more
2023Acta Neurologica Belgica2 citations
Semantic Scholar
Necrotizing myopathy: An uncommon initial manifestation of human immunodeficiency virus
R. D. Ducci, Francisco Beraldi de Magalhães, Daniel Collares, P. Lorenzoni +5 more
2016Muscle and Nerve2 citations
Semantic Scholar
Psychogenic movement disorders: an unusual presentation in childhood with improvement after placebo test.
R. Scola, P. Lorenzoni, C. Kay, H. Teive +2 more
2014Arquivos de Neuro-Psiquiatria2 citations Open access
Semantic Scholar
Somatosensory Evoked Potentials in Spinocerebellar Ataxia Type 3 and Type 10
L. Coutinho, O. Fustes, C. H. Camargo, Gabriel Abrahão Stoliar +8 more
2026Cerebellum1 citations Open access
Semantic Scholar
Paul Hoffmann and the cutaneous silent period test
O. Fustes, C. Kay, P. Lorenzoni, R. D. Ducci +2 more
2024Arquivos de Neuro-Psiquiatria1 citations Open access
Semantic Scholar
Clinical and genetic characterization of limb-girdle muscular dystrophy 2G/R7 in a large cohort of Brazilian patients
J. Saute, Eduardo B. U. Cavalcanti, P. Lorenzoni, P. D. de Souza +5 more
2024Arquivos de Neuro-Psiquiatria1 citations Open access
Semantic Scholar

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L. Werneck×38
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R. D. Ducci×27
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