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Têmis Maria Félix

Showing results (1-10 of 45) with videos related to

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Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|September 11, 2024
Evaluation of functioning and associated factors in children and adolescents with osteogenesis imperfectaArthur Cherem Netto Fernandes, Têmis Maria Félix
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2004
Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern BrazilTêmis Maria Félix, Sandra Leistner, Roberto Giugliani
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association|March 29, 2014
Muscle strength, joint range of motion, and gait in children and adolescents with osteogenesis imperfectaEvelise Brizola, Ana Lúcia Portella Staub, Têmis Maria Félix
Journal of Community Genetics|September 26, 2024
Building a National Policy for Rare Disease in BrazilTêmis Maria Félix, Bibiana Mello de Oliveira, Dafne Dain Gandelman Horovitz
American Journal of Medical Genetics. Part A|February 28, 2003
Satoyoshi syndrome in a Caucasian girl improved with glucocorticoids--a clinical reportCláudia Rafaela Cecchin, Têmis Maria Félix, Richard B Magalhães, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Parental origin of mutations in sporadic cases of Treacher Collins syndromeAlessandra Splendore, Ethylin Wang Jabs, Têmis Maria Félix, et al.
Genes|August 29, 2024
Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health PoliciesDafne Dain Gandelman Horovitz, Têmis Maria Félix, Victor Evangelista de Faria Ferraz
American Journal of Medical Genetics. Part A|August 28, 2010
Further characterization of microdeletion syndrome involving 2p15-p16.1Têmis Maria Félix, Aline Lourenço Petrin, Maria Teresa Vieira Sanseverino, et al.
American Journal of Medical Genetics. Part A|October 24, 2020
A new case of osteogenesis imperfecta type VIII and retinal detachmentLiliane Todeschini de Souza, Ricardo Rodrigues Nunes, Otavio de Azevedo Magalhães, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|October 5, 2017
CLINICAL FEATURES AND PATTERN OF FRACTURES AT THE TIME OF DIAGNOSIS OF OSTEOGENESIS IMPERFECTA IN CHILDRENEvelise Brizola, Marina Bauer Zambrano, Bruna de Souza Pinheiro, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|September 11, 2024
Evaluation of functioning and associated factors in children and adolescents with osteogenesis imperfectaArthur Cherem Netto Fernandes, Têmis Maria Félix
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2004
Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern BrazilTêmis Maria Félix, Sandra Leistner, Roberto Giugliani
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association|March 29, 2014
Muscle strength, joint range of motion, and gait in children and adolescents with osteogenesis imperfectaEvelise Brizola, Ana Lúcia Portella Staub, Têmis Maria Félix
Journal of Community Genetics|September 26, 2024
Building a National Policy for Rare Disease in BrazilTêmis Maria Félix, Bibiana Mello de Oliveira, Dafne Dain Gandelman Horovitz
American Journal of Medical Genetics. Part A|February 28, 2003
Satoyoshi syndrome in a Caucasian girl improved with glucocorticoids--a clinical reportCláudia Rafaela Cecchin, Têmis Maria Félix, Richard B Magalhães, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Parental origin of mutations in sporadic cases of Treacher Collins syndromeAlessandra Splendore, Ethylin Wang Jabs, Têmis Maria Félix, et al.
Genes|August 29, 2024
Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health PoliciesDafne Dain Gandelman Horovitz, Têmis Maria Félix, Victor Evangelista de Faria Ferraz
American Journal of Medical Genetics. Part A|August 28, 2010
Further characterization of microdeletion syndrome involving 2p15-p16.1Têmis Maria Félix, Aline Lourenço Petrin, Maria Teresa Vieira Sanseverino, et al.
American Journal of Medical Genetics. Part A|October 24, 2020
A new case of osteogenesis imperfecta type VIII and retinal detachmentLiliane Todeschini de Souza, Ricardo Rodrigues Nunes, Otavio de Azevedo Magalhães, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|October 5, 2017
CLINICAL FEATURES AND PATTERN OF FRACTURES AT THE TIME OF DIAGNOSIS OF OSTEOGENESIS IMPERFECTA IN CHILDRENEvelise Brizola, Marina Bauer Zambrano, Bruna de Souza Pinheiro, et al.
Pageof 5