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Cell Biochemistry and Function
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September 12, 2024
What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 Microduplication
Rafaella 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 Review
Bianca Gomes Dos Reis, Ana Kalise Böttcher, Franciele Fátima Lopes, et al.
Molecular Syndromology
|
October 9, 2025
Genetic Analysis Strategy for Diagnosing Congenital Heart Disease
Natasha 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 disease
Ana 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 levels
Roberta 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 genes
Ana 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 Review
Luísa Tedesco, Gillian Guerreiro, Bianca Gomes Dos Reis, et al.
Genes
|
July 27, 2024
invdup(8)(8q24.13q24.3)-A Complex Alteration and Its Clinical Consequences
Rafaella 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 Syndrome
Bruna 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 series
Bruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Cell Biochemistry and Function
|
September 12, 2024
What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 Microduplication
Rafaella 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 Review
Bianca Gomes Dos Reis, Ana Kalise Böttcher, Franciele Fátima Lopes, et al.
Molecular Syndromology
|
October 9, 2025
Genetic Analysis Strategy for Diagnosing Congenital Heart Disease
Natasha 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 disease
Ana 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 levels
Roberta 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 genes
Ana 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 Review
Luísa Tedesco, Gillian Guerreiro, Bianca Gomes Dos Reis, et al.
Genes
|
July 27, 2024
invdup(8)(8q24.13q24.3)-A Complex Alteration and Its Clinical Consequences
Rafaella 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 Syndrome
Bruna 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 series
Bruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz, et al.
Page
of 2