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Ana Kalise Böttcher

Showing results (1-10 of 12) with videos related to

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Cell Biochemistry and Function|September 12, 2024
What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 MicroduplicationRafaella Mergener, Lívia Polisseni Cotta Nascimento, Ana Kalise Böttcher, et al.
Cell Biochemistry and Function|April 28, 2026
Oxidative Stress and Inflammation in Methylmalonic and Propionic Acidemias: A ReviewBianca Gomes Dos Reis, Ana Kalise Böttcher, Franciele Fátima Lopes, et al.
Molecular Syndromology|October 9, 2025
Genetic Analysis Strategy for Diagnosing Congenital Heart DiseaseNatasha Malgarezi de Moraes, Bruna Lixinski Diniz, Ana Kalise Böttcher, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 2, 2025
Inflammation in maple syrup urine diseaseAna Kalise Böttcher, Luísa Tedesco, Bianca Gomes Dos Reis, et al.
Metabolic Brain Disease|September 26, 2025
Nitisinone treatment protect hereditary tyrosinemia type I patients against inflammation, DNA and protein oxidative damage by decreasing succinylacetone levelsRoberta Barbizan Mascarello, Jéssica Lamberty Faverzani, Franciele Fátima Lopes, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 22, 2025
First report of hypoplastic left heart syndrome in 3p- syndrome and review of candidate genesAna Kalise Böttcher, Monique Banik Siqueira, Natasha Malgarezi, et al.
Cell Biochemistry and Function|June 30, 2026
Toxicity of Organic Acids Leading to Renal Dysfunction in Glutaric Acidemia Type I: A Mini ReviewLuísa Tedesco, Gillian Guerreiro, Bianca Gomes Dos Reis, et al.
Genes|July 27, 2024
invdup(8)(8q24.13q24.3)-A Complex Alteration and Its Clinical ConsequencesRafaella Mergener, Marcela Rodrigues Nunes, Ana Kalise Böttcher, et al.
Molecular Syndromology|April 6, 2026
<i>HIRA</i>, <i>NKX2-5</i>, and <i>GATA4</i> Alterations versus Cardiac Malformations Related to 22q11.2 Deletion SyndromeBruna Lixinski Diniz, Desirée Deconte, Ana Kalise Böttcher, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|September 11, 2024
Turner syndrome and neuropsychological abnormalities: a review and case seriesBruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Cell Biochemistry and Function|September 12, 2024
What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 MicroduplicationRafaella Mergener, Lívia Polisseni Cotta Nascimento, Ana Kalise Böttcher, et al.
Cell Biochemistry and Function|April 28, 2026
Oxidative Stress and Inflammation in Methylmalonic and Propionic Acidemias: A ReviewBianca Gomes Dos Reis, Ana Kalise Böttcher, Franciele Fátima Lopes, et al.
Molecular Syndromology|October 9, 2025
Genetic Analysis Strategy for Diagnosing Congenital Heart DiseaseNatasha Malgarezi de Moraes, Bruna Lixinski Diniz, Ana Kalise Böttcher, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 2, 2025
Inflammation in maple syrup urine diseaseAna Kalise Böttcher, Luísa Tedesco, Bianca Gomes Dos Reis, et al.
Metabolic Brain Disease|September 26, 2025
Nitisinone treatment protect hereditary tyrosinemia type I patients against inflammation, DNA and protein oxidative damage by decreasing succinylacetone levelsRoberta Barbizan Mascarello, Jéssica Lamberty Faverzani, Franciele Fátima Lopes, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|January 22, 2025
First report of hypoplastic left heart syndrome in 3p- syndrome and review of candidate genesAna Kalise Böttcher, Monique Banik Siqueira, Natasha Malgarezi, et al.
Cell Biochemistry and Function|June 30, 2026
Toxicity of Organic Acids Leading to Renal Dysfunction in Glutaric Acidemia Type I: A Mini ReviewLuísa Tedesco, Gillian Guerreiro, Bianca Gomes Dos Reis, et al.
Genes|July 27, 2024
invdup(8)(8q24.13q24.3)-A Complex Alteration and Its Clinical ConsequencesRafaella Mergener, Marcela Rodrigues Nunes, Ana Kalise Böttcher, et al.
Molecular Syndromology|April 6, 2026
<i>HIRA</i>, <i>NKX2-5</i>, and <i>GATA4</i> Alterations versus Cardiac Malformations Related to 22q11.2 Deletion SyndromeBruna Lixinski Diniz, Desirée Deconte, Ana Kalise Böttcher, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|September 11, 2024
Turner syndrome and neuropsychological abnormalities: a review and case seriesBruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz, et al.
Pageof 2