Rainer Ganschow
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Explore the profile of Rainer Ganschow including associated specialties, affiliations and a list of published articles.
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Articles
69
Citations
492
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Recent Articles
1.
Ganschow R, Maucksch C, Rauschkolb P, Schneider M
Front Pediatr
. 2025 Feb;
12:1443338.
PMID: 39917088
Liver-related abnormalities are commonly observed in patients with congenital heart disease, and these may lead to secondary manifestations such as pruritus. Odevixibat is an ileal bile acid transporter inhibitor under...
2.
Lemke J, Weigert A, Bagci S, Born M, Ganschow R, Katzer D
Children (Basel)
. 2024 Jun;
11(6).
PMID: 38929273
Objectives: This study aimed to analyse the clinical course of 45 children with severe alpha-1-antitrypsin deficiency (AATD) registered in our clinic to detect possible predictors of poor outcomes. Methods: The...
3.
Ganschow R, Maucksch C
JPGN Rep
. 2023 May;
4(2):e301.
PMID: 37200711
A male pediatric patient with elevated liver enzyme and bile acid levels, bile duct hypoplasia, mild liver fibrosis, and pruritus was initially diagnosed with progressive familial intrahepatic cholestasis. The patient...
4.
Guckert L, Reutter H, Saleh N, Ganschow R, Muller A, Ebach F
Int J Pediatr
. 2022 Mar;
2022:7580546.
PMID: 35242194
Background: Nonurgent visits in pediatric Emergency Departments are a growing burden. In order to find predictors for those nonurgent visits, we performed a retrospective analysis of unscheduled visits at the...
5.
Bogs T, Saleh N, Yavuz S, Fazeli W, Ganschow R, Schreiner F
Vaccines (Basel)
. 2022 Feb;
10(2).
PMID: 35214783
We report a 15-year-old boy who developed aseptic meningitis 10 days after administration of the second dose of the COVID-19 vaccine BNT162b2. Although accompanying aphthous mouth ulcers resembling herpetic stomatitis...
6.
Reinsberg M, Siebert S, Dreher C, Bogs T, Ganschow R, Yavuz S
Int Arch Allergy Immunol
. 2021 Dec;
183(5):517-525.
PMID: 34903689
Background: Asthma diagnosis may be challenging particularly in patients with mild symptoms without an obstructive pattern in spirometry. Detection of airway hyperresponsiveness (AHR) by a positive methacholine challenge (MCC) is...
7.
Splittstoesser V, Vollbach H, Plamper M, Garbe W, De Franco E, Houghton J, et al.
Front Endocrinol (Lausanne)
. 2021 May;
12:665336.
PMID: 33935973
Background: Neonatal diabetes with congenital hypothyroidism (NDH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the GLI-similar 3 coding gene . Almost 20 patients have...
8.
Yavuz S, Bagci S, Bolat A, Akin O, Ganschow R
Pediatr Allergy Immunol
. 2020 Dec;
32(5):937-944.
PMID: 33378119
Background: The aim of this study was to investigate the association of serum periostin levels with clinical features in children with asthma. Methods: Children with physician-diagnosed asthma who attended regularly...
9.
Himmelreich N, Dimitrov B, Geiger V, Zielonka M, Hutter A, Beedgen L, et al.
Hum Mutat
. 2019 May;
40(7):938-951.
PMID: 31067009
ALG3-CDG is one of the very rare types of congenital disorder of glycosylation (CDG) caused by variants in the ER-mannosyltransferase ALG3. Here, we summarize the clinical, biochemical, and genetic data...
10.
Franke I, Aydin M, Kurylowicz L, Lopez C, Ganschow R, Lentze M, et al.
BMC Nephrol
. 2019 Feb;
20(1):45.
PMID: 30732569
Background: Nephrotic syndrome (NS) is one of the most frequent occurring chronic kidney diseases in childhood, despite its rarely occurrence in the general population. Detailed information about clinical data of...