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Showing results (401-410 of 744) with videos related to

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Revista Brasileira De Ortopedia|March 31, 2016
SURGICAL TREATMENT OF UNSTABLE PELVIC RING FRACTURE IN SKELETALLY IMMATURE PATIENTSJoao Antonio Matheus Guimarães, Ricardo de Souza Portes Meirelles, Luiz Augusto Peçanha Tavares Júnior, et al.
Headache|November 25, 2022
Burden of migraine in Brazil: A cross-sectional real-world studyMarcio Nattan Portes Souza, Joshua M Cohen, Tony Piha, et al.
Oral Health & Preventive Dentistry|May 9, 2018
Erosive Tooth Wear and Dietary Patterns: A Clinical StudyAlice Moreira Neves Pedrão, Leslie Andrews Portes, Everton Padilha Gomes, et al.
American Journal on Intellectual and Developmental Disabilities|February 22, 2023
The French Version of the DABS: Adaptation Process and Preliminary Field TestLorna von Rotz, Yannick Courbois, Vincent Des Portes, et al.
Molecular Biology Reports|June 21, 2024
The potential role of renin angiotensin system in acute leukemia: a narrative reviewKacio Roger Portes E Silva, Eugênia Maia Nogueira, André Luiz de Jesus Mendes, et al.
Journal of Visualized Experiments : Jove|July 10, 2023
AMEBaS: Automatic Midline Extraction and Background Subtraction of Ratiometric Fluorescence Time-Lapses of Polarized Single CellsRafael Badain, Daniel S C Damineli, Maria Teresa Portes, et al.
Journal of Biomedical Materials Research. Part A|January 22, 2011
Influence of polysaccharide composition on the biocompatibility of pullulan/dextran-based hydrogelsAicha Abed, Nabila Assoul, Maguette Ba, et al.
Neurology|April 21, 2017
Certainty of genuine treatment increases drug responses among intellectually disabled patientsKarin B Jensen, Irving Kirsch, Moa Pontén, et al.
Veterinary Parasitology|June 9, 2017
In vitro treatment of Toxoplasma gondii with copper(II) complexes induces apoptosis-like and cellular division alterationsJ A Portes, C S Motta, N F Azeredo, et al.
European Journal of Human Genetics : EJHG|January 5, 2017
Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsyMassimiliano Rossi, Nicolas Chatron, Audrey Labalme, et al.
Pageof 75

Showing results (401-410 of 744) with videos related to

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Pageof 75
Revista Brasileira De Ortopedia|March 31, 2016
SURGICAL TREATMENT OF UNSTABLE PELVIC RING FRACTURE IN SKELETALLY IMMATURE PATIENTSJoao Antonio Matheus Guimarães, Ricardo de Souza Portes Meirelles, Luiz Augusto Peçanha Tavares Júnior, et al.
Headache|November 25, 2022
Burden of migraine in Brazil: A cross-sectional real-world studyMarcio Nattan Portes Souza, Joshua M Cohen, Tony Piha, et al.
Oral Health & Preventive Dentistry|May 9, 2018
Erosive Tooth Wear and Dietary Patterns: A Clinical StudyAlice Moreira Neves Pedrão, Leslie Andrews Portes, Everton Padilha Gomes, et al.
American Journal on Intellectual and Developmental Disabilities|February 22, 2023
The French Version of the DABS: Adaptation Process and Preliminary Field TestLorna von Rotz, Yannick Courbois, Vincent Des Portes, et al.
Molecular Biology Reports|June 21, 2024
The potential role of renin angiotensin system in acute leukemia: a narrative reviewKacio Roger Portes E Silva, Eugênia Maia Nogueira, André Luiz de Jesus Mendes, et al.
Journal of Visualized Experiments : Jove|July 10, 2023
AMEBaS: Automatic Midline Extraction and Background Subtraction of Ratiometric Fluorescence Time-Lapses of Polarized Single CellsRafael Badain, Daniel S C Damineli, Maria Teresa Portes, et al.
Journal of Biomedical Materials Research. Part A|January 22, 2011
Influence of polysaccharide composition on the biocompatibility of pullulan/dextran-based hydrogelsAicha Abed, Nabila Assoul, Maguette Ba, et al.
Neurology|April 21, 2017
Certainty of genuine treatment increases drug responses among intellectually disabled patientsKarin B Jensen, Irving Kirsch, Moa Pontén, et al.
Veterinary Parasitology|June 9, 2017
In vitro treatment of Toxoplasma gondii with copper(II) complexes induces apoptosis-like and cellular division alterationsJ A Portes, C S Motta, N F Azeredo, et al.
European Journal of Human Genetics : EJHG|January 5, 2017
Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsyMassimiliano Rossi, Nicolas Chatron, Audrey Labalme, et al.
Pageof 75