Peter H Hoeger
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Explore the profile of Peter H Hoeger including associated specialties, affiliations and a list of published articles.
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29
Citations
494
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Recent Articles
1.
Wahjudi T, Nitsch A, Sperhake J, Hoeger P
Eur J Clin Microbiol Infect Dis
. 2025 Feb;
PMID: 39961949
Lack of immune stimulation ("immune debt") in the wake of the COVID-19 pandemic has led to a resurgence of many paediatric infectious diseases, recently including parvovirus B19 (PVB19). We observed...
2.
Schmid F, Kerl-French K, Meier-Schiesser B, Lehmberg K, Hoeger P
J Allergy Clin Immunol Glob
. 2024 Apr;
3(2):100233.
PMID: 38560722
Background: Leukocyte adhesion deficiency type 1 (LAD-1) is a congenital immunodeficiency leading to impaired trafficking of neutrophils to inflammation sites. Solitary or multiple pyoderma gangrenosum (PG)-like skin ulcers (PGLUs) have...
3.
Hoeger P
Pediatr Dermatol
. 2024 Jan;
41(1):180-181.
PMID: 38284784
The purported antiviral effect of dupilumab may be considered a positive side effect. Its mechanism, however, points to an underlying immunomodulation with potentially far-reaching consequences.
4.
Cesarato N, Schwieger-Briel A, Gossmann Y, Henne S, Hillmann K, Frommherz L, et al.
Br J Dermatol
. 2023 Sep;
189(6):741-749.
PMID: 37671665
Background: Short anagen hair (SAH) is a rare paediatric hair disorder characterized by a short anagen phase, an inability to grow long scalp hair and a negative psychological impact. The...
5.
Li D, Technau-Hafsi K, Giehl K, Hoeger P, Has C
Br J Dermatol
. 2023 Jul;
189(5):630-631.
PMID: 37406221
No abstract available.
6.
Braun T, Wehner M, Teichler A, Betz R, Hoeger P
Pediatr Dermatol
. 2023 Apr;
40(3):466-467.
PMID: 37012647
Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant hair loss disorder characterized by coarse, wiry, and twisted hair developing during early childhood, and followed by progressive hair loss...
7.
Has C, Hess M, Anemuller W, Blume-Peytavi U, Emmert S, Folster-Holst R, et al.
J Eur Acad Dermatol Venereol
. 2022 Oct;
37(2):402-410.
PMID: 36196047
Background: Epidermolysis bullosa (EB) is a rare genetic disorder manifesting with skin and mucosal membrane blistering in different degrees of severity. Objective: Epidemiological data from different countries have been published,...
8.
Hoeger P, Koehler L, Reipschlaeger M, Mercier S
Pediatr Dermatol
. 2022 Sep;
40(1):182-187.
PMID: 36102338
Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) is a genodermatosis with autosomal dominant inheritance caused by mutations in FAM111B. We report another case with a new...
9.
Schmid F, Hoeger P
J Am Acad Dermatol
. 2021 Nov;
87(2):490-491.
PMID: 34752824
No abstract available.
10.
Wahjudi T, Kutzner H, Bleeke M, Hoeger P
Pediatr Dermatol
. 2021 May;
38(4):875-878.
PMID: 33931899
We report the case of a 4-year-old boy, post-human stem cell transplantation for severe combined immunodeficiency (SCID) due to adenosine deaminase deficiency (ADA), who developed multiple dermatofibrosarcoma protuberans (DFSP). We...