Zobrazeno 1 - 10
of 190
pro vyhledávání: '"Paulo José, Lorenzoni"'
Autor:
Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci, Otto Jesus Hernandez Fustes, Paula Raquel do Vale Pascoal Rodrigues, Raquel Cristina Arndt, Rosana Herminia Scola, Lineu Cesar Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 02, Pp 001-004 (2024)
Carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive inherited disorder related to lipid metabolism affecting skeletal muscle. The first cases of CPT II deficiency causing myopathy were reported in 1973. In 1983, Werneck et
Externí odkaz:
https://doaj.org/article/ef0fa6c811994542ac3af4f780a87966
Autor:
Paula Raquel do Vale Pascoal Rodrigues, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci, Marco Antonio Takashi Utiumi, Otto Jesus Hernandez Fustes, Lineu Cesar Werneck, Paulo José Lorenzoni, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-007 (2024)
Background Myasthenia gravis (MG) is an autoimmune disease usually caused by antibodies against the acetylcholine receptor (AChR-Abs), muscle-specific tyrosine kinase (MuSK-Abs), or low-density lipoprotein receptor-related protein 4 (LRP4-Abs). Howev
Externí odkaz:
https://doaj.org/article/f1f761e852df46bfb0c8abb739988a34
Autor:
Renata Dal-Prá Ducci, Michelle Zonkowski Ribas, Enzo Oku Martinazzo, Otto Jesus Hernandez Fustes, Paulo José Lorenzoni, Claudia Suemi Kamoi Kay, Rosana Hermínia Scola
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 59, Iss 1, Pp 1-4 (2023)
Abstract Background Gaucher disease (GD) is an autosomal recessive disease characterized by an inborn metabolic error. Although pain attributed to skeletal involvement is one of the most frequent symptoms of this condition, some patients may have neu
Externí odkaz:
https://doaj.org/article/d842150c2ea2475a84cc398f47de3195
Autor:
Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci, Otto Jesus Hernandez Fustes, Paula Raquel do Vale Pascoal Rodrigues, Nyvia Milicio Coblinski Hrysay, Raquel Cristina Arndt, Lineu Cesar Werneck, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 10, Pp 922-933 (2023)
Limb-girdle muscular dystrophy (LGMD) is a group of myopathies that lead to progressive muscle weakness, predominantly involving the shoulder and pelvic girdles; it has a heterogeneous genetic etiology, with variation in the prevalence of subtypes ac
Externí odkaz:
https://doaj.org/article/7e132850852e459ca947b903ed74186b
Autor:
Otto Jesus Hernández Fustes, Cláudia Suemi Kamoi Kay, Paulo José Lorenzoni, Renata Dal-Prá Ducci, Lineu Cesar Werneck, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 9, Pp 824-831 (2021)
Abstract The authors present a review of the current use of somatosensory evoked potentials (SSEPs) in neurological practice as a non-invasive neurophysiological technique. For this purpose we have reviewed articles published in English or Portuguese
Externí odkaz:
https://doaj.org/article/fffb5c21139f4f0094fb5fd8fef0adf5
Autor:
Renata Dal-Prá Ducci, Cláudia Suemi Kamoi Kay, Otto Jesus Hernandez Fustes, Lineu Cesar Werneck, Paulo José Lorenzoni, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 7, Pp 624-629 (2021)
Abstract Myasthenia gravis (MG) is an autoimmune disease in which the peak incidence is among women of childbearing age. For this reason, there is an overlap between the occurrence of this disease and pregnancy. It is known that MG symptoms can worse
Externí odkaz:
https://doaj.org/article/b7840d85773740b38dce9632ae3714b0
Autor:
Otto Jesus Hernández Fustes, Cláudia Suemi Kamoi Kay, Paulo José Lorenzoni, Renata Dal-Prá Ducci, Lineu Cesar Werneck, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 7, Pp 647-649 (2021)
Abstract This paper reviews some aspects of the life and work of Professor Johann Friedrich Horner, on the occasion of the 190th anniversary of his birthday and 152 years after the publication of "Über eine Form von Ptosis". It also shows the import
Externí odkaz:
https://doaj.org/article/f617693a6fe343348895ca76ea77c2fe
Autor:
Otto Jesus Hernandez Fustes MD, PhD, Cláudia S K Kay MD, Paulo José Lorenzoni MD, PhD, Renata D-P Ducci MD, PhD, Lineu C Werneck MD, PhD, Rosana Herminia Scola MD, PhD
Publikováno v:
Journal of Central Nervous System Disease, Vol 13 (2021)
Background Neuromyelitis optica spectrum disorders (NMOSDs) are rare antibody-mediated disorders of the central nervous system, with a predilection for the spinal cord and optic nerves. The clinical utility of evoked potential recordings (EPs) has al
Externí odkaz:
https://doaj.org/article/55195241b8c046f397a1291ebd932c9c
Autor:
Paulo José Lorenzoni, Renata Dal-Pra Ducci, Raquel Cristina Arndt, Nyvia Milicio Coblinski Hrysay, Otto Jesus Hernandez Fustes, Ana Töpf, Hanns Lochmüller, Lineu Cesar Werneck, Cláudia Suemi Kamoi Kay, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria (2021)
ABSTRACT Background: Congenital myasthenic syndromes (CMS) have some phenotypic overlap with seronegative myasthenia gravis (SNMG). Objective: The aim of this single center study was to assess the minimum occurrence of CMS misdiagnosed as double SNMG
Externí odkaz:
https://doaj.org/article/03f56af0a51844f9b4f616620ab0fdbb
Autor:
Otto Jesus Hernández Fustes, Cláudia Suemi Kamoi Kay, Paulo José Lorenzoni, Renata Dal-Prá Ducci, Lineu Cesar Werneck, Rosana Herminia Scola
Publikováno v:
Arquivos de Neuro-Psiquiatria (2021)
ABSTRACT In 1951, the physiologist George Duncan Dawson presented his work with the averaging of the signal in the evoked potentials (EPs), opening a new stage in the development of clinical neurophysiology. The authors present aspects of Professor D
Externí odkaz:
https://doaj.org/article/12de31838c40498aac28cfbee8f75636