Robin Lochbaum
Overview
Explore the profile of Robin Lochbaum including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
133
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lochbaum R, Hoffmann T, Greve J, Hahn J
Orphanet J Rare Dis
. 2025 Feb;
20(1):47.
PMID: 39893484
Background: Patients with hereditary angioedema (HAE) experience recurrent, unpredictable episodes of edema. These swellings are often preceded by prodromal symptoms. HAE management includes acute treatment, long-term prophylaxis (LTP), and short-term...
2.
Johnson F, Burian N, Santer M, Strasser V, Steinbichler T, Hofauer B, et al.
J Clin Med
. 2024 Nov;
13(22).
PMID: 39598044
Salivary gland tumor operations are associated with complications including facial nerve dysfunction (FND) and salivary fistula. The objective of this study was to investigate the effect of extracapsular dissection (ECD)...
3.
Greve J, Lochbaum R, Trainotti S, Ebert E, Buttgereit T, Scherer A, et al.
Allergol Select
. 2024 Nov;
8:346-357.
PMID: 39564138
Background And Objectives: Patients with rare diseases like hereditary angioedema (HAE) are usually referred to an angioedema center to ensure guideline-compliant and experience-based therapy. Even though there are established guidelines...
4.
Wang Y, Hofmann L, Huber D, Lochbaum R, Ludwig S, Brunner C, et al.
J Clin Med
. 2024 Sep;
13(18).
PMID: 39336917
: Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic disorder leading to frequent bleeding in several organs. As HHT diagnosis is demanding and depends on clinical criteria, liquid biopsy would be...
5.
Muller H, Hahn J, Gierke A, Stark R, Brunner C, Hoffmann T, et al.
Pflugers Arch
. 2024 Mar;
476(6):993-1005.
PMID: 38438679
Increase in transendothelial water permeability is an essential etiological factor in a variety of diseases like edema and shock. Despite the high clinical relevance, there has been no precise method...
6.
Lochbaum R, Trainotti S, Hoffmann T, Greve J, Hahn J
J Dermatolog Treat
. 2023 Dec;
35(1):2290362.
PMID: 38086754
Background: Hereditary angioedema with normal C1-inhibitor (HAE-nC1-INH) is a rare genetic disease. The symptoms can resemble other forms of hereditary angioedema (HAE), but the specific laboratory values are inconspicuous. The...
7.
Lochbaum R, Hoffmann T, Greve J, Hahn J
J Dtsch Dermatol Ges
. 2023 Nov;
21(11):1283-1290.
PMID: 37946655
No abstract available.
8.
Johnson F, Stenzl A, Hofauer B, Heppt H, Ebert E, Wollenberg B, et al.
Clin Rev Allergy Immunol
. 2023 Nov;
65(3):354-364.
PMID: 37914894
Hereditary angioedema (HAE) and acquired C1-inhibitor deficiency (AAE-C1-INH) are orphan diseases. Berotralstat is a recently licensed long-term prophylaxis (LTP) and the first oral therapy for HAE patients. No approved therapies...
9.
Trainotti S, Johnson F, Hahn J, Hofauer B, Greve J, Wollenberg B, et al.
J Allergy Clin Immunol Pract
. 2023 Sep;
11(12):3772-3779.
PMID: 37716525
Background: Acquired angioedema with C1-inhibitor deficiency (AAE-C1-INH) is a rare condition resembling hereditary angioedema (HAE), but with late onset and low C1-inhibitor (C1-INH) due to consumption potentially caused by autoimmune...
10.
Lochbaum R, Hoffmann T, Greve J, Hahn J
J Dtsch Dermatol Ges
. 2023 Jul;
21(11):1283-1289.
PMID: 37483139
Bradykinin-mediated angioedema is a rare, non-allergic, potentially life-threatening disease. ACE inhibitor-induced angioedema and hereditary angioedema (HAE) are the two most common presentations. Therapeutic options, pathophysiology and diagnosis continue to be...