Markus Ries
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Explore the profile of Markus Ries including associated specialties, affiliations and a list of published articles.
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90
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1304
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Recent Articles
1.
von der Forst M, Dietrich M, Schmitt F, Popp E, Ries M
Sci Rep
. 2025 Jan;
15(1):620.
PMID: 39753701
The goal of this analysis is to describe seasonal disaster patterns in Central Europe in order to raise awareness and improve hospital disaster planning and resilience, particularly during peak events....
2.
Urban O, Driedger J, Garbade S, Hoffmann G, Kolker S, Ries M, et al.
Orphanet J Rare Dis
. 2024 Dec;
19(1):457.
PMID: 39633384
Purpose: Aicardi syndrome is a rare epileptic encephalopathy, almost exclusively affecting girls. It was first described as a triad of infantile spasms, chorioretinal defects and agenesis of the corpus callosum....
3.
Katzenschlager S, Mohr S, Kaltschmidt N, Peterstorfer F, Weilbacher F, Gunther P, et al.
Eur J Emerg Med
. 2024 Sep;
32(2):123-130.
PMID: 39264430
Background: In hypoxemic children with difficult airway, or for minor elective procedures, the use of a supraglottic airway device may be preferred to endotracheal intubation, whether with a laryngeal mask...
4.
Kalm T, Schob C, Voller H, Gardeitchik T, Gilissen C, Pfundt R, et al.
Am J Hum Genet
. 2024 May;
111(6):1206-1221.
PMID: 38772379
Utilizing trio whole-exome sequencing and a gene matching approach, we identified a cohort of 18 male individuals from 17 families with hemizygous variants in KCND1, including two de novo missense...
5.
Adami T, Ries M
PLoS One
. 2023 Nov;
18(11):e0289193.
PMID: 38033112
Background: Early stages of catastrophes like COVID-19 are often led by chaos and panic. To characterize the initial chaos phase of clinical research in such situations, we analyzed the first...
6.
Thalwitzer K, Driedger J, Xian J, Saffari A, Zacher P, Bolsterli B, et al.
Neurology
. 2023 Jul;
101(9):e879-e891.
PMID: 37407264
Background And Objectives: Pathogenic variants in are among the major genetic causes of neurodevelopmental disorders. Despite the increasing number of individuals diagnosed without a history of epilepsy, little is known...
7.
Ries M, Mendoza G, Arash-Kaps L, Amraoui Y, Quack F, Hardt B, et al.
Genet Med
. 2022 Oct;
24(12):2434-2443.
PMID: 36194207
Purpose: Gangliosidoses are a group of inherited neurogenetic autosomal recessive lysosomal storage disorders usually presenting with progressive macrocephaly, developmental delay, and regression, leading to significant morbidity and premature death. A...
8.
Ries M
Front Public Health
. 2022 Oct;
10:975667.
PMID: 36187698
Background: In the context of a holistic and comprehensive disaster response effort to the COVID-19 pandemic, many countries across the globe mobilized their military forces in order to cope with...
9.
Trudzinski F, Presotto M, Buck E, Herth F, Ries M
Sci Rep
. 2022 Sep;
12(1):15497.
PMID: 36109566
Alpha-1 antitrypsin deficiency (AATD, OMIM #613490) is a rare metabolic disorder affecting lungs and liver. The purpose of this study is to assess the impact of the US orphan drug...
10.
Patry C, Fichtner A, Hocker B, Ries M, Peter Schmitt C, Tonshoff B
Pediatr Nephrol
. 2022 Apr;
38(1):227-236.
PMID: 35460394
Background: Decision-making in the field of pediatric dialysis requires evidence from clinical trials, but, similar to other fields of pediatric medicine, might be affected by a low trial publication rate....