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Showing results (31-40 of 44) with videos related to

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Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
Clinical Therapeutics|March 14, 2016
The Microbiome in Necrotizing Enterocolitis: A Case Report in Twins and MinireviewSuchitra K Hourigan, Allison Ta, Wendy S W Wong, et al.
Journal of Biomechanics|April 21, 2019
Ultrasound elastographic assessment of plantar fascia in runners using rearfoot strike and forefoot strikeTony Lin-Wei Chen, Cristine E Agresta, David B Lipps, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseasePatrizia Tarantino, I C Cirò Candiano, F Annesi, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseFrancesca Emanuela Rocca, F Annesi, I C Cirò Candiano, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseFerdinanda Annesi, E F Rocca, I C Cirò Candiano, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseInnocenza Claudia Cirò Candiano, F Annesi, E F Rocca, et al.
Lupus|April 11, 2017
Neuro-ophthalmologic manifestations in systemic lupus erythematosusF A de Andrade, G Guimarães Moreira Balbi, L G Bortoloti de Azevedo, et al.
Alimentary Pharmacology & Therapeutics|December 21, 2000
Multicentre randomized placebo-controlled trial of ursodeoxycholic acid with or without colchicine in symptomatic primary biliary cirrhosisP L Almasio, A Floreani, M Chiaramonte, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
Clinical Therapeutics|March 14, 2016
The Microbiome in Necrotizing Enterocolitis: A Case Report in Twins and MinireviewSuchitra K Hourigan, Allison Ta, Wendy S W Wong, et al.
Journal of Biomechanics|April 21, 2019
Ultrasound elastographic assessment of plantar fascia in runners using rearfoot strike and forefoot strikeTony Lin-Wei Chen, Cristine E Agresta, David B Lipps, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseasePatrizia Tarantino, I C Cirò Candiano, F Annesi, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseFrancesca Emanuela Rocca, F Annesi, I C Cirò Candiano, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseFerdinanda Annesi, E F Rocca, I C Cirò Candiano, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's diseaseInnocenza Claudia Cirò Candiano, F Annesi, E F Rocca, et al.
Lupus|April 11, 2017
Neuro-ophthalmologic manifestations in systemic lupus erythematosusF A de Andrade, G Guimarães Moreira Balbi, L G Bortoloti de Azevedo, et al.
Alimentary Pharmacology & Therapeutics|December 21, 2000
Multicentre randomized placebo-controlled trial of ursodeoxycholic acid with or without colchicine in symptomatic primary biliary cirrhosisP L Almasio, A Floreani, M Chiaramonte, et al.
Pageof 5