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Line Borgwardt

Showing results (1-10 of 26) with videos related to

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Ugeskrift for Laeger|October 1, 2008
[Autoimmune polyglandular syndrome in a 13-year old girl]Line Borgwardt, Pernille Pedersen, Birgit Peitersen
Pediatric Endocrinology Reviews : PER|October 28, 2014
Alpha-mannosidosis - a review of genetic, clinical findings and options of treatmentLine Borgwardt, Allan Meldgaard Lund, Christine I Dali
Journal of Medical Case Reports|September 24, 2021
Concomitant familial hypocalciuric hypercalcemia and single parathyroid adenoma: a case reportSimone Diedrichsen Marstrand, Charlotte Landbo Tofteng, Anne Jarløv, et al.
Hormones (Athens, Greece)|February 19, 2022
Severe weight loss in a hypothyroid patient as an acute presentation of autoimmune polyglandular syndrome type IIElvira Silajdzija, Sofie Bliddal, Line Borgwardt, et al.
Journal of Gastrointestinal Oncology|November 18, 2024
Rare germline chromosome 1 duplication identified in young male with colon cancer: a case report investigating causalityAnna Byrjalsen, Sara L Garcia, Line Borgwardt, et al.
Endocrine Connections|July 21, 2020
Genotype-phenotype associations in PPGLs in 59 patients with variants in SDHX genesAilsa Maria Main, Maria Rossing, Line Borgwardt, et al.
BMC Medical Genomics|January 29, 2024
Whole genome sequencing in clinical practiceFrederik Otzen Bagger, Line Borgwardt, Andreas Sand Jespersen, et al.
Clinical Physiology and Functional Imaging|March 11, 2010
Estimating GFR in children with 99mTc-DTPA renography: a comparison with single-sample 51Cr-EDTA clearanceHenrik Gutte, Michael L Møller, Andreas K Pfeifer, et al.
Journal of Inherited Metabolic Disease|October 9, 2024
Extended long-term efficacy and safety of velmanase alfa treatment up to 12 years in patients with alpha-mannosidosisNathalie Guffon, Line Borgwardt, Anna Tylki-Szymańska, et al.
Frontiers in Immunology|October 5, 2020
Case Report: Hyper IgM Syndrome Identified by Whole Genome Sequencing in a Young Syrian Man Presenting With Atypical, Severe and Recurrent Mucosal LeishmaniasisCamilla Heldbjerg Drabe, Rasmus L Marvig, Line Borgwardt, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Ugeskrift for Laeger|October 1, 2008
[Autoimmune polyglandular syndrome in a 13-year old girl]Line Borgwardt, Pernille Pedersen, Birgit Peitersen
Pediatric Endocrinology Reviews : PER|October 28, 2014
Alpha-mannosidosis - a review of genetic, clinical findings and options of treatmentLine Borgwardt, Allan Meldgaard Lund, Christine I Dali
Journal of Medical Case Reports|September 24, 2021
Concomitant familial hypocalciuric hypercalcemia and single parathyroid adenoma: a case reportSimone Diedrichsen Marstrand, Charlotte Landbo Tofteng, Anne Jarløv, et al.
Hormones (Athens, Greece)|February 19, 2022
Severe weight loss in a hypothyroid patient as an acute presentation of autoimmune polyglandular syndrome type IIElvira Silajdzija, Sofie Bliddal, Line Borgwardt, et al.
Journal of Gastrointestinal Oncology|November 18, 2024
Rare germline chromosome 1 duplication identified in young male with colon cancer: a case report investigating causalityAnna Byrjalsen, Sara L Garcia, Line Borgwardt, et al.
Endocrine Connections|July 21, 2020
Genotype-phenotype associations in PPGLs in 59 patients with variants in SDHX genesAilsa Maria Main, Maria Rossing, Line Borgwardt, et al.
BMC Medical Genomics|January 29, 2024
Whole genome sequencing in clinical practiceFrederik Otzen Bagger, Line Borgwardt, Andreas Sand Jespersen, et al.
Clinical Physiology and Functional Imaging|March 11, 2010
Estimating GFR in children with 99mTc-DTPA renography: a comparison with single-sample 51Cr-EDTA clearanceHenrik Gutte, Michael L Møller, Andreas K Pfeifer, et al.
Journal of Inherited Metabolic Disease|October 9, 2024
Extended long-term efficacy and safety of velmanase alfa treatment up to 12 years in patients with alpha-mannosidosisNathalie Guffon, Line Borgwardt, Anna Tylki-Szymańska, et al.
Frontiers in Immunology|October 5, 2020
Case Report: Hyper IgM Syndrome Identified by Whole Genome Sequencing in a Young Syrian Man Presenting With Atypical, Severe and Recurrent Mucosal LeishmaniasisCamilla Heldbjerg Drabe, Rasmus L Marvig, Line Borgwardt, et al.
Pageof 3