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Stojkovic

Showing results (411-420 of 1,167) with videos related to

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Neuromuscular Disorders : NMD|April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findingsMarc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Neuromuscular Disorders : NMD|June 26, 2024
Rapidly progressive myopathy: unveiling light chain amyloidosis as an initial manifestation of multiple myeloma: a case report and literature reviewP Kaminskiene, T Stojkovic, D Roos-Weil, et al.
Biomarkers in Medicine|February 8, 2013
Multiple sclerosis: individualized disease susceptibility and therapy responseVera Pravica, Milos Markovic, Maja Cupic, et al.
Behavioral Medicine (Washington, D.C.)|June 7, 2022
Preferences of COVID-19 Vaccines in the General Population in Belgrade, Serbia: A Qualitative StudyTatjana Gazibara, Smiljana Cvjetkovic, Marija Milic, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 2014
Apo-bacteriophytochromes modulate bacterial photosynthesis in response to low lightKathryn R Fixen, Anna W Baker, Emina A Stojkovic, et al.
Muscle & Nerve|December 6, 2017
Severe asymmetric muscle weakness revealing glycogenin-1 polyglucosan body myopathyTanya Stojkovic, Anaïs Chanut, Pascal Laforêt, et al.
Revue Neurologique|December 21, 2005
[Tonic pupils in Sjögren's syndrome]P Vermersch, S Dufourd-Delalande, S Defoort-Dhellemmes, et al.
Dementia and Geriatric Cognitive Disorders|September 25, 2015
Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset DementiaGorana Mandic-Stojmenovic, Elka Stefanova, Valerija Dobricic, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 9, 2014
T-wave variability for the prediction of fast ventricular arrhythmias – prospective, observer-blind studyStefan Stojkovic, Robin Ristl, Fabian T Moser, et al.
Mutation Research|December 2, 1996
Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD geneX Quilliet, O Chevallier-Lagente, E Eveno, et al.
Pageof 117

Showing results (411-420 of 1,167) with videos related to

Sort By:
Pageof 117
Neuromuscular Disorders : NMD|April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findingsMarc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Neuromuscular Disorders : NMD|June 26, 2024
Rapidly progressive myopathy: unveiling light chain amyloidosis as an initial manifestation of multiple myeloma: a case report and literature reviewP Kaminskiene, T Stojkovic, D Roos-Weil, et al.
Biomarkers in Medicine|February 8, 2013
Multiple sclerosis: individualized disease susceptibility and therapy responseVera Pravica, Milos Markovic, Maja Cupic, et al.
Behavioral Medicine (Washington, D.C.)|June 7, 2022
Preferences of COVID-19 Vaccines in the General Population in Belgrade, Serbia: A Qualitative StudyTatjana Gazibara, Smiljana Cvjetkovic, Marija Milic, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 2014
Apo-bacteriophytochromes modulate bacterial photosynthesis in response to low lightKathryn R Fixen, Anna W Baker, Emina A Stojkovic, et al.
Muscle & Nerve|December 6, 2017
Severe asymmetric muscle weakness revealing glycogenin-1 polyglucosan body myopathyTanya Stojkovic, Anaïs Chanut, Pascal Laforêt, et al.
Revue Neurologique|December 21, 2005
[Tonic pupils in Sjögren's syndrome]P Vermersch, S Dufourd-Delalande, S Defoort-Dhellemmes, et al.
Dementia and Geriatric Cognitive Disorders|September 25, 2015
Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset DementiaGorana Mandic-Stojmenovic, Elka Stefanova, Valerija Dobricic, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 9, 2014
T-wave variability for the prediction of fast ventricular arrhythmias – prospective, observer-blind studyStefan Stojkovic, Robin Ristl, Fabian T Moser, et al.
Mutation Research|December 2, 1996
Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD geneX Quilliet, O Chevallier-Lagente, E Eveno, et al.
Pageof 117