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G Larsen

Showing results (451-460 of 463) with videos related to

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Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the <i>MTOR</i> gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.
Transplantation Proceedings|December 21, 2010
Outstanding survival and regeneration process by the use of intelligent acellular dermal matrices and mesenchymal stem cells in a burn pig modelE Mansilla, R Spretz, G Larsen, et al.
Diabetes Care|November 15, 2012
Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-upSusanne E Boonen, Deborah J G Mackay, Johanne M D Hahnemann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2018
Iterative near-term ecological forecasting: Needs, opportunities, and challengesMichael C Dietze, Andrew Fox, Lindsay M Beck-Johnson, et al.
Tumori|April 13, 2012
Prospective Registry On Mesothelioma Peritonei Treatment (PROMPT): study design and rationaleChristopher Cao, Tristan D Yan, David L Morris, et al.
Acta Oncologica (Stockholm, Sweden)|May 1, 2015
Nationwide improvement of rectal cancer treatment outcomes in Norway, 1993-2010Marianne G Guren, Hartwig Kørner, Frank Pfeffer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 13, 2019
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristicsAllan Bayat, Alexej Knaus, Annika Wollenberg Juul, et al.
Annals of Neurology|December 18, 2015
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutationElena Gardella, Felicitas Becker, Rikke S Møller, et al.
Epilepsia|July 1, 2015
Mutations in KCNT1 cause a spectrum of focal epilepsiesRikke S Møller, Sarah E Heron, Line H G Larsen, et al.
Molecular Syndromology|October 27, 2016
Gene Panel Testing in Epileptic Encephalopathies and Familial EpilepsiesRikke S Møller, Line H G Larsen, Katrine M Johannesen, et al.
Pageof 47

Showing results (451-460 of 463) with videos related to

Sort By:
Pageof 47
Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the <i>MTOR</i> gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.
Transplantation Proceedings|December 21, 2010
Outstanding survival and regeneration process by the use of intelligent acellular dermal matrices and mesenchymal stem cells in a burn pig modelE Mansilla, R Spretz, G Larsen, et al.
Diabetes Care|November 15, 2012
Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-upSusanne E Boonen, Deborah J G Mackay, Johanne M D Hahnemann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2018
Iterative near-term ecological forecasting: Needs, opportunities, and challengesMichael C Dietze, Andrew Fox, Lindsay M Beck-Johnson, et al.
Tumori|April 13, 2012
Prospective Registry On Mesothelioma Peritonei Treatment (PROMPT): study design and rationaleChristopher Cao, Tristan D Yan, David L Morris, et al.
Acta Oncologica (Stockholm, Sweden)|May 1, 2015
Nationwide improvement of rectal cancer treatment outcomes in Norway, 1993-2010Marianne G Guren, Hartwig Kørner, Frank Pfeffer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 13, 2019
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristicsAllan Bayat, Alexej Knaus, Annika Wollenberg Juul, et al.
Annals of Neurology|December 18, 2015
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutationElena Gardella, Felicitas Becker, Rikke S Møller, et al.
Epilepsia|July 1, 2015
Mutations in KCNT1 cause a spectrum of focal epilepsiesRikke S Møller, Sarah E Heron, Line H G Larsen, et al.
Molecular Syndromology|October 27, 2016
Gene Panel Testing in Epileptic Encephalopathies and Familial EpilepsiesRikke S Møller, Line H G Larsen, Katrine M Johannesen, et al.
Pageof 47