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Pagnamenta

Showing results (111-120 of 265) with videos related to

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AJNR. American Journal of Neuroradiology|July 21, 2022
ReplyE Prodi, L Danieli, C Manno, et al.
American Journal of Human Genetics|May 7, 2005
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletionOrly Elpeleg, Chaya Miller, Eli Hershkovitz, et al.
Plastic and Reconstructive Surgery. Global Open|May 21, 2025
Topical Application of Tranexamic Acid in Abdominoplasties Leads to Lower Drainage Volume and Earlier Drain RemovalIsabel Zucal, Laura De Pellegrin, Alberto Pagnamenta, et al.
Clinical Transplantation|May 1, 2018
Pulmonary hypertension is not a risk factor for grade 3 primary graft dysfunction after lung transplantationSilvia R Cottini, Giovanna Brandi, Alberto Pagnamenta, et al.
BMJ Open|May 29, 2019
Prevalence, clinical relevance and predictive factors of medication discrepancies revealed by medication reconciliation at hospital admission: prospective study in a Swiss internal medicine wardOlivier Giannini, Nicole Rizza, Michela Pironi, et al.
Molecular Biology and Evolution|March 27, 2001
Extreme length and length variation in the first ribosomal internal transcribed spacer of ladybird beetles (Coleoptera: Coccinellidae)J H von der Schulenburg, J M Hancock, A Pagnamenta, et al.
Clinical Case Reports|October 21, 2016
Activation of an exonic splice-donor site in exon 30 of <i>CDK5RAP2</i> in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, et al.
Cerebellum (London, England)|November 22, 2018
Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2G P D Argyropoulos, K E Watkins, E Belton-Pagnamenta, et al.
International Journal of Cardiology|August 9, 2022
Association among myocardial injury and mortality in Influenza: A prospective cohort studyLuigi Biasco, Amabile Valotta, Catherine Klersy, et al.
Human Mutation|March 25, 2018
A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephalyAlistair T Pagnamenta, Yoshiko Murakami, Consuelo Anzilotti, et al.
Pageof 27

Showing results (111-120 of 265) with videos related to

Sort By:
Pageof 27
AJNR. American Journal of Neuroradiology|July 21, 2022
ReplyE Prodi, L Danieli, C Manno, et al.
American Journal of Human Genetics|May 7, 2005
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletionOrly Elpeleg, Chaya Miller, Eli Hershkovitz, et al.
Plastic and Reconstructive Surgery. Global Open|May 21, 2025
Topical Application of Tranexamic Acid in Abdominoplasties Leads to Lower Drainage Volume and Earlier Drain RemovalIsabel Zucal, Laura De Pellegrin, Alberto Pagnamenta, et al.
Clinical Transplantation|May 1, 2018
Pulmonary hypertension is not a risk factor for grade 3 primary graft dysfunction after lung transplantationSilvia R Cottini, Giovanna Brandi, Alberto Pagnamenta, et al.
BMJ Open|May 29, 2019
Prevalence, clinical relevance and predictive factors of medication discrepancies revealed by medication reconciliation at hospital admission: prospective study in a Swiss internal medicine wardOlivier Giannini, Nicole Rizza, Michela Pironi, et al.
Molecular Biology and Evolution|March 27, 2001
Extreme length and length variation in the first ribosomal internal transcribed spacer of ladybird beetles (Coleoptera: Coccinellidae)J H von der Schulenburg, J M Hancock, A Pagnamenta, et al.
Clinical Case Reports|October 21, 2016
Activation of an exonic splice-donor site in exon 30 of <i>CDK5RAP2</i> in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, et al.
Cerebellum (London, England)|November 22, 2018
Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2G P D Argyropoulos, K E Watkins, E Belton-Pagnamenta, et al.
International Journal of Cardiology|August 9, 2022
Association among myocardial injury and mortality in Influenza: A prospective cohort studyLuigi Biasco, Amabile Valotta, Catherine Klersy, et al.
Human Mutation|March 25, 2018
A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephalyAlistair T Pagnamenta, Yoshiko Murakami, Consuelo Anzilotti, et al.
Pageof 27