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Ugeskrift for Laeger
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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 treatment
Line 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 report
Simone 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 II
Elvira 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 causality
Anna 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 genes
Ailsa Maria Main, Maria Rossing, Line Borgwardt, et al.
BMC Medical Genomics
|
January 29, 2024
Whole genome sequencing in clinical practice
Frederik 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 clearance
Henrik 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-mannosidosis
Nathalie 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 Leishmaniasis
Camilla Heldbjerg Drabe, Rasmus L Marvig, Line Borgwardt, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 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 treatment
Line 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 report
Simone 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 II
Elvira 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 causality
Anna 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 genes
Ailsa Maria Main, Maria Rossing, Line Borgwardt, et al.
BMC Medical Genomics
|
January 29, 2024
Whole genome sequencing in clinical practice
Frederik 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 clearance
Henrik 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-mannosidosis
Nathalie 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 Leishmaniasis
Camilla Heldbjerg Drabe, Rasmus L Marvig, Line Borgwardt, et al.
Page
of 3