Lars Magin-Steinmuller
Singen, TH, Germany
Last Updated: 09/26/2026
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Found 9 publications
Cardiac transthyretin/leukocyte chemotactic factor (LECT) 2 double amyloidosis in a patient suffering from heart failure.
Journal: Clinical research in cardiology : official journal of the German Cardiac Society
Published: January 26, 2022
Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.
Journal: The Journal of allergy and clinical immunology
Published: September 17, 2020
Prevalence of hereditary transthyretin amyloid polyneuropathy in idiopathic progressive neuropathy in conurban areas.
Journal: Neurological research and practice
Published: May 15, 2019
Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case-control study.
Journal: The British journal of dermatology
Published: November 23, 2018
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema.
Journal: Allergy
Published: July 17, 2018
Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema.
Journal: Clinical and translational allergy
Published: July 04, 2018
Hereditary angioedema with a mutation in the plasminogen gene.
Journal: Allergy
Published: August 06, 2017
Mixed leukocyte cell-derived chemotaxin 2 and amyloid A renal amyloidosis in a Kazakh-German patient.
Journal: Clinical kidney journal
Published: October 27, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026