T. Stojkovic - Concepedia

Author

T. Stojkovic

Also Known As

Adeline Morisot, S. Leonard-Louis, Stojkovic, Tania, Stojkovic, Tanya, Stojkovic,, T, T Stojkovic, T. Stojkovic, Tania Stojkovic

Publications

992

Citations

H-Index

Concepts

All Affiliations

Sorbonne Université Pitié-Salpêtrière Hospital Assistance Publique – Hôpitaux de Paris Institut de Myologie Centre National de la Recherche Scientifique

About

T. Stojkovic is an author at Sorbonne Université specializing in medicine, pathology, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	678
2	Health Sciences	1	1	70
3	Public Health	1	1	157
4	Allergy	1	1	267
5	Anatomy	1	1	157

T. Stojkovic

Publications

893

Citations

H-Index

Page 1

	Year	Citations
Anti-HMGCR Autoantibodies in European Patients With Autoimmune Necrotizing Myopathies Yves Allenbach, Laurent Drouot, Aude Rigolet, Medicine ImmunohematologyImmunodeficienciesImmunologyPathologyRheumatoid Disorder	2014	267
Follow-Up of Patients with History of Cervical Artery Dissection Didier Leys, Thierry Moulin, T. Stojkovic, Cerebrovascular Diseases Cerebrovascular DiseaseRecurrent DissectionSurgeryAnatomyNeurovascular Disease	1995	157
Long-term follow-up of neurosarcoidosis D. Ferriby, J. de Sèze, T. Stojkovic, Neurology	2001	119
Dermatomyositis With or Without Anti-Melanoma Differentiation-Associated Gene 5 Antibodies Yves Allenbach, Gaëlle Leroux, Xavier Suárez‐Calvet, American Journal Of Pathology Autoimmune DiseaseHistopathologyClinical DermatologyAutoimmunityDermatology	2016	97
Cardiac assessment of limb–girdle muscular dystrophy 2I patients: An echography, Holter ECG and magnetic resonance imaging study Karim Wahbi, Christophe Meune, El Hadi Hamouda, Neuromuscular Disorders Cardiac AssessmentCardiomyopathyKinesiologyHealth SciencesElectrophysiological Evaluation	2008	70
Antibodies to clustered acetylcholine receptor: expanding the phenotype Perrine Devic, P. Petiot, Thomas Simonet, European Journal of Neurology	2013	60
The first European family with tibial muscular dystrophy outside the Finnish population J. de Sèze, Bjarne Udd, Henna Haravuori, Neurology Family MedicineFinnish AncestorsMendelian DisorderGenetic DisorderGenetics	1998	44
Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene Xavier Quilliet, Odile Chevallier-Lagente, Éric Eveno, Mutation Research/DNA Repair Xpd GeneGene TherapiesGenome InstabilityRetroviral TransductionImmunology	1996	30
Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort Alzira Alves de Siqueira Carvalho, Emmanuele Lacene, Guy Brochier, Genetic Testing and Molecular Biomarkers	2018	23
Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family Agnès Jacquin, Olivier Rouaud, P Soichot, Case Reports in Neurology	2013	13

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