H Jungbluth
Overview
Explore the profile of H Jungbluth 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
94
Citations
954
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.
Kruijt N, van den Bersselaar L, Hopman M, Snoeck M, van Rijswick M, Wiggers T, et al.
Sports Med Open
. 2023 May;
9(1):33.
PMID: 37204519
Introduction: Exertional heat stroke (EHS) is a medical emergency, occurring when the body generates more heat than it can dissipate, and frequently associated with exertional rhabdomyolysis (ERM). In the present...
2.
van den Bersselaar L, Gubbels M, Jungbluth H, Schouten M, van der Kooi A, Quinlivan R, et al.
J Neuromuscul Dis
. 2022 Sep;
9(6):765-775.
PMID: 36120788
Background: Patients with neuromuscular disorders are at increased risk of suffering perioperative complications. Current knowledge concerning this topic is based on small retrospective studies and expert opinion. Therefore, an individualized...
3.
van den Bersselaar L, Riazi S, Snoeck M, Jungbluth H, Voermans N
Neuromuscul Disord
. 2021 Dec;
32(1):86-97.
PMID: 34916120
No abstract available.
4.
van den Bersselaar L, Greven T, Bulger T, Voermans N, van Petegem F, Schiemann A, et al.
Br J Anaesth
. 2021 Jun;
127(2):e63-e65.
PMID: 34127251
No abstract available.
5.
Kruijt N, van den Bersselaar L, Wijma J, Verbeeck W, Coenen M, Neville J, et al.
Neuromuscul Disord
. 2020 Nov;
30(12):949-958.
PMID: 33250373
Neuroleptic malignant syndrome and serotonin syndrome are two syndromes whose molecular bases remain poorly understood. The phenotypes of both syndromes overlap with other syndromes that have a clear genetic background,...
6.
Kruijt N, van den Bersselaar L, Kamsteeg E, Verbeeck W, Snoeck M, Everaerd D, et al.
Eur J Neurol
. 2020 Sep;
28(2):647-659.
PMID: 32978841
Background And Purpose: Rhabdomyolysis is a medical emergency characterized by acute skeletal muscle breakdown with a sudden rise and subsequent fall of serum creatine kinase (CK) levels. Rhabdomyolysis events are...
7.
Knuiman G, Kusters B, Eshuis L, Snoeck M, Lammens M, Heytens L, et al.
J Neurol
. 2019 Feb;
266(4):876-887.
PMID: 30788618
Objective: The histopathological features of malignant hyperthermia (MH) and non-anaesthetic (mostly exertional) rhabdomyolysis (RM) due to RYR1 mutations have only been reported in a few cases. Methods: We performed a...
8.
van Ruitenbeek E, Custers J, Verhaak C, Snoeck M, Erasmus C, Kamsteeg E, et al.
Neuromuscul Disord
. 2018 Dec;
29(1):30-38.
PMID: 30578099
Mutations in RYR1 are a common genetic cause of non-dystrophic neuromuscular disorders. To obtain baseline data concerning the prevalence of fatigue, the psychological disease burden and quality of life associated...
9.
Marks S, van Ruitenbeek E, Fallon P, Johns P, Phadke R, Mein R, et al.
Neuromuscul Disord
. 2018 Mar;
28(5):422-426.
PMID: 29576327
Myopathies due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene are amongst the most common non-dystrophic neuromuscular disorders and have been associated with both dominant and recessive inheritance....
10.
Piano Mortari E, Folgiero V, Marcellini V, Romania P, Bellacchio E, DAlicandro V, et al.
Autophagy
. 2017 Nov;
14(1):22-37.
PMID: 29130391
Vici syndrome is a human inherited multi-system disorder caused by recessive mutations in EPG5, encoding the EPG5 protein that mediates the fusion of autophagosomes with lysosomes. Immunodeficiency characterized by lack...