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Rodrigo R Arantes

Showing results (1-10 of 6) with videos related to

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American Journal of Medical Genetics. Part A|March 27, 2019
Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, BrazilNara O Carvalho, Dora M Del Castillo, José N Januário, et al.
Genetics and Molecular Biology|August 21, 2019
Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patientsThais R Villela, Bruna L Freire, Nathalia T P Braga, et al.
Microbiological Research|September 12, 2006
In vitro antifungal susceptibility of clinical isolates of Candida spp. obtained from patients with different predisposing factors to candidosisPatrícia M Pinto, Rita de Cássia Botelho Weikert-Oliveira, Juliana Pereira Lyon, et al.
Meta Gene|September 13, 2016
Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterizationNatália D Linhares, Eugênia R Valadares, Silvia S da Costa, et al.
Pediatric Nephrology (Berlin, Germany)|August 9, 2025
Risk factors for perinatal and neonatal mortality in cases with congenital anomalies of the kidney and urinary tract: a nested cohort studyRodrigo R Arantes, Marcos B Aguiar, Keyla C C M S Cunha, et al.
Orphanet Journal of Rare Diseases|September 2, 2022
Galactose epimerase deficiency: lessons from the GalNet registryBritt Derks, Didem Demirbas, Rodrigo R Arantes, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|March 27, 2019
Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, BrazilNara O Carvalho, Dora M Del Castillo, José N Januário, et al.
Genetics and Molecular Biology|August 21, 2019
Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patientsThais R Villela, Bruna L Freire, Nathalia T P Braga, et al.
Microbiological Research|September 12, 2006
In vitro antifungal susceptibility of clinical isolates of Candida spp. obtained from patients with different predisposing factors to candidosisPatrícia M Pinto, Rita de Cássia Botelho Weikert-Oliveira, Juliana Pereira Lyon, et al.
Meta Gene|September 13, 2016
Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterizationNatália D Linhares, Eugênia R Valadares, Silvia S da Costa, et al.
Pediatric Nephrology (Berlin, Germany)|August 9, 2025
Risk factors for perinatal and neonatal mortality in cases with congenital anomalies of the kidney and urinary tract: a nested cohort studyRodrigo R Arantes, Marcos B Aguiar, Keyla C C M S Cunha, et al.
Orphanet Journal of Rare Diseases|September 2, 2022
Galactose epimerase deficiency: lessons from the GalNet registryBritt Derks, Didem Demirbas, Rodrigo R Arantes, et al.
Pageof 1