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Stojkovic

Showing results (361-370 of 1,167) with videos related to

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International Journal of Clinical Practice|July 20, 2022
Intestinal Ultrasonography as a Tool for Monitoring Disease Activity in Patients with Ulcerative ColitisMilica Stojkovic Lalosevic, Aleksandra Sokic Milutinovic, Vera Matovic Zaric, et al.
Journal of Neurology|July 5, 2001
Guillain-Barré syndrome resembling brainstem death in a patient with brain injuryT Stojkovic, M Verdin, J F Hurtevent, et al.
Journal of Neurology|October 31, 2003
Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosisC Monaca-Charley, T Stojkovic, A Duhamel, et al.
International Journal of Molecular Sciences|October 26, 2024
Circulatory Indicators of Lipid Peroxidation, the Driver of Ferroptosis, Reflect Differences between Relapsing-Remitting and Progressive Multiple SclerosisLjiljana Stojkovic, Ana Djordjevic, Milan Stefanovic, et al.
Neuromuscular Disorders : NMD|April 21, 2006
A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classificationD Ferriby, T Stojkovic, D Sternberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile formT Stojkovic, L Defebvre, X Quilliet, et al.
Genes & Nutrition|August 24, 2016
Erratum to: The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levelsIvana A Stojkovic, Ulrika Ericson, Gull Rukh, et al.
BMJ Open|January 22, 2020
Cross-cultural validation of the Retinopathy Treatment Satisfaction Questionnaire status version (RetTSQs) in Serbian community: a cross-sectional studyJelena Karadzic, Milenko Stojkovic, Dijana Risimic, et al.
Neurogenetics|February 4, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codonMarion Masingue, Jimmy Perrot, Robert-Yves Carlier, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|September 16, 2014
Modulation of γ2-MSH hepatoprotection by antisense peptides and melanocortin subtype 3 and 4 receptor antagonistsPetra Turcic, Nikola Stambuk, Pasko Konjevoda, et al.
Pageof 117

Showing results (361-370 of 1,167) with videos related to

Sort By:
Pageof 117
International Journal of Clinical Practice|July 20, 2022
Intestinal Ultrasonography as a Tool for Monitoring Disease Activity in Patients with Ulcerative ColitisMilica Stojkovic Lalosevic, Aleksandra Sokic Milutinovic, Vera Matovic Zaric, et al.
Journal of Neurology|July 5, 2001
Guillain-Barré syndrome resembling brainstem death in a patient with brain injuryT Stojkovic, M Verdin, J F Hurtevent, et al.
Journal of Neurology|October 31, 2003
Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosisC Monaca-Charley, T Stojkovic, A Duhamel, et al.
International Journal of Molecular Sciences|October 26, 2024
Circulatory Indicators of Lipid Peroxidation, the Driver of Ferroptosis, Reflect Differences between Relapsing-Remitting and Progressive Multiple SclerosisLjiljana Stojkovic, Ana Djordjevic, Milan Stefanovic, et al.
Neuromuscular Disorders : NMD|April 21, 2006
A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classificationD Ferriby, T Stojkovic, D Sternberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile formT Stojkovic, L Defebvre, X Quilliet, et al.
Genes & Nutrition|August 24, 2016
Erratum to: The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levelsIvana A Stojkovic, Ulrika Ericson, Gull Rukh, et al.
BMJ Open|January 22, 2020
Cross-cultural validation of the Retinopathy Treatment Satisfaction Questionnaire status version (RetTSQs) in Serbian community: a cross-sectional studyJelena Karadzic, Milenko Stojkovic, Dijana Risimic, et al.
Neurogenetics|February 4, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codonMarion Masingue, Jimmy Perrot, Robert-Yves Carlier, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|September 16, 2014
Modulation of γ2-MSH hepatoprotection by antisense peptides and melanocortin subtype 3 and 4 receptor antagonistsPetra Turcic, Nikola Stambuk, Pasko Konjevoda, et al.
Pageof 117