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Astrid Rasmussen

Showing results (61-70 of 125) with videos related to

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Human Molecular Genetics|May 23, 2002
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotypeSubramaniam Ganesh, Antonio V Delgado-Escueta, Toshimitsu Suzuki, et al.
Annals of the Rheumatic Diseases|May 4, 2025
A cross-sectional observational study of patients with sicca with salivary autoantibodies defines a potential new phenotype of Sjögren's diseaseMartha Tsaliki, Joshua Cavett, Biji T Kurien, et al.
Rheumatology (Oxford, England)|March 22, 2016
Previous diagnosis of Sjögren's Syndrome as rheumatoid arthritis or systemic lupus erythematosusAstrid Rasmussen, Lida Radfar, David Lewis, et al.
Lupus Science & Medicine|April 15, 2017
Use of SLICC criteria in a large, diverse lupus registry enables SLE classification of a subset of ACR-designated subjects with incomplete lupusTeresa Aberle, Rebecka L Bourn, Hua Chen, et al.
RMD Open|December 15, 2021
Genetic variants at the <i>RTP4/MASP1</i> locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndromeKatrine Brække Norheim, Juliana Imgenberg-Kreuz, Andrei Alexsson, et al.
Clinical and Experimental Rheumatology|November 18, 2017
Minor salivary gland fibrosis in Sjögren's syndrome is elevated, associated with focus score and not solely a consequence of agingKerry M Leehan, Nathan P Pezant, Astrid Rasmussen, et al.
Neuroscience Letters|August 1, 2006
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Maria E Alonso, et al.
Epilepsia|December 3, 2003
Recent developments in the quest for myoclonic epilepsy genesAntonio V Delgado-Escueta, Katerina B Perez-Gosiengfiao, Dongsheng Bai, et al.
Annals of the Rheumatic Diseases|April 24, 2015
Interaction between innate immunity and Ro52-induced antibody causes Sjögren's syndrome-like disorder in miceBarbara M Szczerba, Paulina Kaplonek, Nina Wolska, et al.
Epilepsy Research|August 30, 2002
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5Toshimitsu Suzuki, Ryoji Morita, Yoshihisa Sugimoto, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|May 23, 2002
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotypeSubramaniam Ganesh, Antonio V Delgado-Escueta, Toshimitsu Suzuki, et al.
Annals of the Rheumatic Diseases|May 4, 2025
A cross-sectional observational study of patients with sicca with salivary autoantibodies defines a potential new phenotype of Sjögren's diseaseMartha Tsaliki, Joshua Cavett, Biji T Kurien, et al.
Rheumatology (Oxford, England)|March 22, 2016
Previous diagnosis of Sjögren's Syndrome as rheumatoid arthritis or systemic lupus erythematosusAstrid Rasmussen, Lida Radfar, David Lewis, et al.
Lupus Science & Medicine|April 15, 2017
Use of SLICC criteria in a large, diverse lupus registry enables SLE classification of a subset of ACR-designated subjects with incomplete lupusTeresa Aberle, Rebecka L Bourn, Hua Chen, et al.
RMD Open|December 15, 2021
Genetic variants at the <i>RTP4/MASP1</i> locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndromeKatrine Brække Norheim, Juliana Imgenberg-Kreuz, Andrei Alexsson, et al.
Clinical and Experimental Rheumatology|November 18, 2017
Minor salivary gland fibrosis in Sjögren's syndrome is elevated, associated with focus score and not solely a consequence of agingKerry M Leehan, Nathan P Pezant, Astrid Rasmussen, et al.
Neuroscience Letters|August 1, 2006
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Maria E Alonso, et al.
Epilepsia|December 3, 2003
Recent developments in the quest for myoclonic epilepsy genesAntonio V Delgado-Escueta, Katerina B Perez-Gosiengfiao, Dongsheng Bai, et al.
Annals of the Rheumatic Diseases|April 24, 2015
Interaction between innate immunity and Ro52-induced antibody causes Sjögren's syndrome-like disorder in miceBarbara M Szczerba, Paulina Kaplonek, Nina Wolska, et al.
Epilepsy Research|August 30, 2002
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5Toshimitsu Suzuki, Ryoji Morita, Yoshihisa Sugimoto, et al.
Pageof 13