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Dévora Natalia Randon
Dévora Natalia Randon
Universidade Federal do Rio Grande do Sul
Medicine
Allele frequency
Loss of heterozygosity
Genotyping
unexpected death
3
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3
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0
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SARS-CoV-2 pandemic in the Brazilian community of rare diseases: A patient reported survey.
2021
American Journal of Medical Genetics Part C-seminars in Medical Genetics
Ida Vanessa Doederlein Schwartz
Dévora Natalia Randon
Natan Monsores
Carolina Fischinger Moura de Souza
Dafne Dain Gandelman Horovitz
Matheus Wilke
Decio Brunoni
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A decade of molecular diagnosis of Mucolipidosis II and III in Brazil: a pooled analysis of 32 patients
2021
Nataniel Floriano Ludwig
Fernanda Sperb-Ludwig
Dévora Natalia Randon
Pricila Bernardi
Liane de Rosso Giuliani
Carolina Araujo Moreno
Denise P. Cavalcanti
Luiz Cs da Silva
Ida Vanessa Doederlein Schwartz
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Prevalence of the most common pathogenic variants in three genes for inborn errors of metabolism associated with sudden unexpected death in infancy: a population-based study in south Brazil.
2020
Genetics and Molecular Biology
Dévora Natalia Randon
Fernanda Sperb-Ludwig
Fernanda Sales Luiz Vianna
Ana Paula Pizzio Becker
Carmen Regla-Vargas
Angela Sitta
Alexia Nedel SantAna
Ida Vanessa Doederlein Schwartz
Fernanda Hendges de Bitencourt
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