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Dive into the research topics where Carmen Mendes is active.

Publication


Featured researches published by Carmen Mendes.


Journal of neuromuscular diseases | 2015

Effects of Aerobic Exercise Training in Late-Onset Pompe Disease Before and 1 Month after Enzyme Replacement Therapy

Rosângela Maria da Silva; Carmen Mendes; Carolina C. Aranda; Marco A. Curiati; Maret H. Rand; Sandra Obikawa Kyosen; Edna T. Sakata; Sueli Canossa; Beatriz Jurkiewicz Frangipani; Ana Maria Martins

Pompe disease is a progressive multisystem disease caused by a lysosomal acid α-glycosidase enzyme (GAA) defi ciency, resulting in lysosomal accumulation of glycogen. The late-onset form is characterized by progressive skeletal and respiratory muscle dysfunction leading to functional disability and impairment of quality of life. Enzyme replacement therapy (ERT) and treatments, such as protein-enriched diet and exercise training, have been proposed as possible countermeasures for muscle impairment in patients with late-onset Pompe disease (LOPD). However, there are no established guidelines on therapeutic exercise for individuals with LOPD, and evidence of a benefi cial effect of exercise training is relatively scarce in these patients, and is mainly before receiving ERT. This retrospective study reports the results of a home-based submaximal aerobic exercise on functional capacity and pulmonary function in a patient with LOPD with mild respiratory manifestation and moderate skeletal muscle disease, prior to ERT regimen and 1 month after receiving ERT.


Journal of neuromuscular diseases | 2015

Effects of Exercise Training on Functional Capacity and Quality of Life in a Patient with Late-Onset Pompe Disease Receiving Enzyme Replacement Therapy

Rosângela Maria da Silva; Carmen Mendes; Carolina C. Aranda; Marco A. Curiati; Maret H. Rand; Sandra Obikawa Kyosen; Edna T. Sakata; Sueli Canossa; Renata B. Oliveira; Ana Maria Martins

Pompe disease (PD) causes a progressive muscular weakness and impairment of patients’ mobility. Many patients develop intolerance to exercise due to reduced activity and consequent decline in muscle function. Exercise training prevents physical deconditioning and muscle wasting. Enzyme replacement therapy (ERT) was recently introduced, and has modifi ed the course of the disease. Other therapeutic interventions, such as exercise training, have been proposed as possible countermeasures for muscle impairment in patients with late-onset PD. We report the results of a 12-week home exercise training program on functional capacity and quality of life in a 20-year-old male patient with PD receiving ERT for 2 years.


The Journal of Allergy and Clinical Immunology: In Practice | 2016

Diagnosis and management of infusion-related hypersensitivity reactions to enzyme replacement therapy for lysosomal diseases: The role of desensitization.

Carolina Aranda; Luis Felipe Ensina; Inês Cristina Camelo Nunes; Marcia Carvalho Mallozi; Carmen Mendes; Ana Maria Martins; Dirceu Solé


Molecular Genetics and Metabolism | 2011

MRI Findings in Anderson- Fabry disease(AFD)

Carmen Mendes; Maria Lucia Borri; Patricia Feliciano; Sandra Obikawa Kyosen; Carolina Aranda; Maret H. Rand; Ana Maria Martins


Molecular Genetics and Metabolism | 2018

In silico and in vitro analysis of a novel GLA missense mutation in patients with severe renal involvement

Patricia Varela; Gianna Mastroianni Kirsztajn; Krissia Wallbach; Gustavo da Mata; Luiz Antonio Ribeiro de Moura; Silvia Moreira; Carmen Mendes; Marco A. Curiati; Vania D'Almeida; Ana Maria Martins; João Bosco Pesquero


Molecular Genetics and Metabolism | 2016

Infusion related hypersensitivity reaction to enzyme replacement therapy for lysosomal diseases

Carolina Aranda; Luis Felipe Ensina; Carmen Mendes; Inês Cristina Camelo-Nunes; Marco A. Curiati; Marcia Carvalho Mallozi; Dirceu Solé; Ana Maria Martins


Molecular Genetics and Metabolism | 2016

Agalsidase beta and infusion-related reactions: Findings in Brazilian patients

Marco A. Curiati; Carmen Mendes; Carolina Aranda; Murilo Maia; Luis Felipe Ensina; Dirceu Solé; Ana Maria Martins


Molecular Genetics and Metabolism | 2015

Immunology of mucopolysaccharidosis

Carolina Aranda; Dirceu Solé; Carmen Mendes; Maret H. Rand; Sandra Obikawa Kyosen; Patricia Feliciano; Marco A. Curiati; Mariana Asato; Marcia Carvalho Mallozi; Beatriz Tavares Costa-Carvalho; Vania D'Almeida; Ana Maria Martins


Molecular Genetics and Metabolism | 2015

Enzyme replacement therapy for mucopolysaccharidosis type II: Experience from a Brazilian reference center

Marco A. Curiati; Carmen Mendes; Maret H. Rand; Sueli Canossa; Cintia M. Goncalves; Rosangela Maria Silva; José Antonio Silva; Renata B. Oliveira; Sandra Obikawa Kyosen; Carolina Aranda; Ana Maria Martins


Molecular Genetics and Metabolism | 2015

Natural history of mucopolysaccharidosis in a referral center

Sandra Obikawa Kyosen; Camilla L. Patti; Carmen Mendes; Maret H. Rand; Carolina Aranda; Patricia Feliciano; João Bosco Pesquero; Vania D'Almeida; Ana Maria Martins

Collaboration


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Ana Maria Martins

Federal University of São Paulo

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Carolina Aranda

Federal University of São Paulo

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Marco A. Curiati

Federal University of São Paulo

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Sandra Obikawa Kyosen

Federal University of São Paulo

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Maret H. Rand

Federal University of São Paulo

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Dirceu Solé

Federal University of São Paulo

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Sueli Canossa

Federal University of São Paulo

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Luis Felipe Ensina

Federal University of São Paulo

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Marcia Carvalho Mallozi

Federal University of São Paulo

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Patricia Feliciano

Federal University of São Paulo

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