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Shila Barati

Showing results (1-10 of 13) with videos related to

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Life (Basel, Switzerland)|December 19, 2020
Investigation of Genetic Variations of <i>IL6</i> and <i>IL6R</i> as Potential Prognostic and Pharmacogenetics Biomarkers: Implications for COVID-19 and Neuroinflammatory DisordersClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Diagnostics (Basel, Switzerland)|February 11, 2023
Longitudinal Structure-Function Evaluation in a Patient with <i>CDHR1</i>-Associated Retinal Dystrophy: Progressive Visual Function Loss with Retinal RemodelingAndrea Cusumano, Benedetto Falsini, Fabian D'Apolito, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic analysis of intellectual disability and autismPietro Chiurazzi, Aysha Karim Kiani, Jan Miertus, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
CardiomyopathiesVincenza Precone, Geraldo Krasi, Giulia Guerri, et al.
Genes|July 9, 2020
Analysis of <i>ACE2</i> Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological ComplicationsClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Non-syndromic monogenic male infertilityGiulia Guerri, Tiziana Maniscalchi, Shila Barati, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Syndromic infertilityGiulia Guerri, Tiziana Maniscalchi, Shila Barati, et al.
Molecular Genetics & Genomic Medicine|November 28, 2020
NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variantsSandro Michelini, Maurizio Ricci, Roberta Serrani, et al.
Lymphatic Research and Biology|September 22, 2020
Possible Role of the <i>RORC</i> Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative VariantsSandro Michelini, Maurizio Ricci, Roberta Serrani, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Life (Basel, Switzerland)|December 19, 2020
Investigation of Genetic Variations of <i>IL6</i> and <i>IL6R</i> as Potential Prognostic and Pharmacogenetics Biomarkers: Implications for COVID-19 and Neuroinflammatory DisordersClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Diagnostics (Basel, Switzerland)|February 11, 2023
Longitudinal Structure-Function Evaluation in a Patient with <i>CDHR1</i>-Associated Retinal Dystrophy: Progressive Visual Function Loss with Retinal RemodelingAndrea Cusumano, Benedetto Falsini, Fabian D'Apolito, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic analysis of intellectual disability and autismPietro Chiurazzi, Aysha Karim Kiani, Jan Miertus, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
CardiomyopathiesVincenza Precone, Geraldo Krasi, Giulia Guerri, et al.
Genes|July 9, 2020
Analysis of <i>ACE2</i> Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological ComplicationsClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Non-syndromic monogenic male infertilityGiulia Guerri, Tiziana Maniscalchi, Shila Barati, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Syndromic infertilityGiulia Guerri, Tiziana Maniscalchi, Shila Barati, et al.
Molecular Genetics & Genomic Medicine|November 28, 2020
NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variantsSandro Michelini, Maurizio Ricci, Roberta Serrani, et al.
Lymphatic Research and Biology|September 22, 2020
Possible Role of the <i>RORC</i> Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative VariantsSandro Michelini, Maurizio Ricci, Roberta Serrani, et al.
Pageof 2