Raquel Cristina Arndt

5PUBLICATIONS
11CO-AUTHORS
Infant and child healthMedical biochemistry - lipidsGene expression (incl. microarray and other genome-wide approaches)Soft condensed matterEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|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

|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

|Dec 21, 2021
Congenital myasthenic syndrome in a cohort of patients with 'double' seronegative myasthenia gravis.

Paulo José Lorenzoni, Renata Dal-Pra Ducci, Raquel Cristina Arndt

|May 16, 2019
HLA-alleles class I and II associated with genetic susceptibility to neuromyelitis optica in Brazilian patients.

Cláudia Suemi Kamoi Kay, Rosana Herminia Scola, Raquel Cristina Arndt

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Frequent Collaborators

5 joint publications

Cláudia Suemi Kamoi Kay

5 joint publications

Rosana Herminia Scola

5 joint publications

Paulo José Lorenzoni

5 joint publications

Lineu Cesar Werneck