Lineu Cesar Werneck

19PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthMedical biochemistry - lipidsAllergyGene expression (incl. microarray and other genome-wide approaches)
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Publications (19)

|Jan 27, 2026
Somatosensory evoked potentials in neuromyelitis optica spectrum disorders.

Otto Jesus Hernandez Fustes, Cláudia Suemi Kamoi Kay, Paulo José Lorenzoni

|Oct 31, 2024
A TPM2 mutation causes congenital myopathy with fibre-type disproportion.

Paulo José Lorenzoni, Luciane Filla, Renata Dal-Prá Ducci

|Feb 23, 2024
Myopathy due to carnitine palmitoyltransferase II deficiency: updating genetic aspects of the first publication in Brazil.

Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci

|Feb 05, 2024
Triple-seronegative myasthenia gravis: clinical and epidemiological characteristics.

Paula Raquel do Vale Pascoal Rodrigues, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci

|Oct 18, 2023
Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review.

Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay, Renata Dal-Pra Ducci

|Mar 25, 2023
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.

Paulo José Lorenzoni, Dafne Luana Bayer, Renata Dal-Prá Ducci

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