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Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes

Thrombocytosis in children and adolescents—classification, diagnostic approach, and clinical management

2021 . Stockklausner, Clemens | Duffert, C. M. | Cario, H. | Knöfler, R. | Streif, W. | Kulozik, A. E.

Effects of tranexamic acid on human nasal ciliary beat frequency

2021 . Behr, W. | Horschke, F. | Nastev, A. | Mueller, C. E. | Sommer, J. U. | Folz, B. | Li, H. | Geisthoff, U. W. | Stuck, B. A. | Birk, R.

Factor VII activating protease (FSAP) is not essential in the pathophysiology of angioedema in patients with C1 inhibitor deficiency

2021 . Gramstad, Olav Rogde | Kandanur, Sai Priya Sarma | Etscheid, Michael | Nielsen, Erik Waage | Kanse, Sandip

Sulthiame impairs mitochondrial function in vitro and may trigger onset of visual loss in Leber hereditary optic neuropathy

2021 . Reinert, Marie-Christine | Pacheu-Grau, David | Catarino, Claudia B. | Klopstock, Thomas | Ohlenbusch, Andreas | Schittkowski, Michael | Wilichowski, Ekkehard | Rehling, Peter | Brockmann, Knut

Evaluating the interreader agreement and intrareader reproducibility of Visual Field Defects in Thyroid Eye Disease– Compressive Optic Neuropathy

2021 . Garip Kuebler, Aylin | Halfter, Kathrin | Reznicek, Lukas | Klingenstein, Annemarie | Priglinger, Siegfried | Hintschich, Christoph

Magnetic Resonance Neurography: Improved Diagnosis of Peripheral Neuropathies

2021 . Hayes, Jennifer | Bendszus, Martin

Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report

2021 . Bork, Konrad | Anderson, John T. | Caballero, Teresa | Craig, Timothy | Johnston, Douglas T. | Li, H. Henry | Longhurst, Hilary J. | Radojicic, Cristine | Riedl, Marc A.

Risk factors in bee and Vespula venom allergy: state of the art

2021 . Stoevesandt, Johanna | Trautmann, Axel

Smoking and alcohol, health-related quality of life and psychiatric comorbidities in Leber’s Hereditary Optic Neuropathy mutation carriers: a prospective cohort study

2021 . , Andrea | Catarino, Claudia B. | Rampeltshammer, Verena | Schindler, David | Gallenmüller, Constanze | Priglinger, Claudia | Pogarell, Oliver | Rüther, Tobias | Klopstock, Thomas

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