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M Zuberi

Showing results (81-90 of 170) with videos related to

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Neurology|July 28, 2010
Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twinsT D Graves, S Rajakulendran, S M Zuberi, et al.
Epilepsy & Behavior : E&B|April 22, 2017
The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future researchMark P Jensen, Andreas Brunklaus, Liam Dorris, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2023
Single-step genome engineering in the bee gut symbiont <i>Snodgrassella alvi</i>Patrick J Lariviere, A H M Zuberi Ashraf, Sean P Leonard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Epilepsia|July 15, 2021
Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trialsJennifer Madan Cohen, Daniel Checketts, Eduardo Dunayevich, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|August 6, 2015
Erratum to: Expression of serum miR-200a, miR-200b and miR-200c as candidate biomarkers in epithelial ovarian cancer and their association with clinicopathological featuresM Zuberi, R Mir, J Das, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|June 12, 2015
Expression of serum miR-200a, miR-200b, and miR-200c as candidate biomarkers in epithelial ovarian cancer and their association with clinicopathological featuresM Zuberi, R Mir, J Das, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
Pregnancy Hypertension|November 19, 2021
Reduced urinary angiotensinogen excretion in preeclampsiaNatalie S Colόn, Ahmed F Pantho, Syeda H Afroze, et al.
Pageof 17

Showing results (81-90 of 170) with videos related to

Sort By:
Pageof 17
Neurology|July 28, 2010
Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twinsT D Graves, S Rajakulendran, S M Zuberi, et al.
Epilepsy & Behavior : E&B|April 22, 2017
The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future researchMark P Jensen, Andreas Brunklaus, Liam Dorris, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2023
Single-step genome engineering in the bee gut symbiont <i>Snodgrassella alvi</i>Patrick J Lariviere, A H M Zuberi Ashraf, Sean P Leonard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 16, 2010
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutationDaniella Nishri, Lubov Blumkin, Dorit Lev, et al.
Epilepsia|July 15, 2021
Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trialsJennifer Madan Cohen, Daniel Checketts, Eduardo Dunayevich, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|August 6, 2015
Erratum to: Expression of serum miR-200a, miR-200b and miR-200c as candidate biomarkers in epithelial ovarian cancer and their association with clinicopathological featuresM Zuberi, R Mir, J Das, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|June 12, 2015
Expression of serum miR-200a, miR-200b, and miR-200c as candidate biomarkers in epithelial ovarian cancer and their association with clinicopathological featuresM Zuberi, R Mir, J Das, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
Pregnancy Hypertension|November 19, 2021
Reduced urinary angiotensinogen excretion in preeclampsiaNatalie S Colόn, Ahmed F Pantho, Syeda H Afroze, et al.
Pageof 17