Sandra O. Kyosen

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 16 publications

Screening for Lysosomal Acid Lipase Deficiency in a Lipid Clinic.

Screening for Lysosomal Acid Lipase Deficiency in a Lipid Clinic.

Journal: Arquivos brasileiros de cardiologia

Published: December 10, 2024

Teaching and training of human resources for genetics and genomics in Brazil.

Teaching and training of human resources for genetics and genomics in Brazil.

Journal: Journal of community genetics

Published: February 28, 2024

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report.

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report.

Journal: Frontiers in genetics

Published: October 03, 2019

Short stature as a presenting symptom of attenuated Mucopolysaccharidosis type I: case report and clinical insights.

Short stature as a presenting symptom of attenuated Mucopolysaccharidosis type I: case report and clinical insights.

Journal: BMC endocrine disorders

Published: July 11, 2018

Endoscopic Findings in Lysosomal Acid Lipase Deficiency.

Endoscopic Findings in Lysosomal Acid Lipase Deficiency.

Journal: Journal of pediatric gastroenterology and nutrition

Published: May 16, 2018

CASE SERIES OF PATIENTS UNDER BIWEEKLY TREATMENT WITH LARONIDASE: A REPORT OF A SINGLE CENTER EXPERIENCE.

CASE SERIES OF PATIENTS UNDER BIWEEKLY TREATMENT WITH LARONIDASE: A REPORT OF A SINGLE CENTER EXPERIENCE.

Journal: Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo

Published: April 29, 2018

Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI.

Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI.

Journal: Genetics and molecular biology

Published: October 31, 2017

Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum.

Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum.

Journal: Case reports in pediatrics

Published: July 10, 2017

Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series.

Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series.

Journal: Orphanet journal of rare diseases

Published: October 13, 2015

Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships.

Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships.

Journal: Orphanet journal of rare diseases

Published: May 26, 2015

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

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

Journal: Journal of neuromuscular diseases

Published: January 01, 2015

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

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

Journal: Journal of neuromuscular diseases

Published: January 01, 2015

Showing 1-12 of 16

Last Updated: 09/26/2026