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1. A core outcome set for efficacy of acute treatment of hereditary angioedema

2. Meta-analysis of ACE inhibitor–induced angioedema identifies novel risk locus

5. The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

6. Consensus on treatment goals in hereditary angioedema: A global Delphi initiative

7. Long-term safety and efficacy of subcutaneous C1-inhibitor in older patients with hereditary angioedema

10. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

12. Gene Editing–Mediated Disruption of Epidermolytic Ichthyosis–Associated KRT10 Alleles Restores Filament Stability in Keratinocytes

15. Oral Plasma Kallikrein Inhibitor BCX7353 is Safe and Effective as an On-Demand Treatment of Angioedema Attacks in Hereditary Angioedema (HAE) Patients: Results of the ZENITH-1 Trial

19. Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome

20. Safety and Usage of C1-Inhibitor in Hereditary Angioedema: Berinert Registry Data

22. Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL

27. Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura

29. Health-Related Quality Of Life (HRQoL) In Adult Patients With Hereditary Angioedema Due To C1 Inhibitor Deficiency (HAE-C1-INH) Assessed By SF-36v2

30. IHAE-Qol: Specific Health-Related Quality Of Life (HRQoL) Questionnaire In Hereditary Angioedema Due To C1 Inhibitor Deficiency (HAE-C1INH)

31. Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease

35. Clinical Expression and New SPINK5 Splicing Defects in Netherton Syndrome: Unmasking a Frequent Founder Synonymous Mutation and Unconventional Intronic Mutations

36. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency

40. Disease expression in women with hereditary angioedema

41. Functional C1-Inhibitor diagnostics in hereditary angioedema: Assay evaluation and recommendations

43. A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3

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