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M Snoeck

Showing results (21-30 of 27) with videos related to

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Biochemistry and Biophysics Reports|April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody diseaseJ P Molenaar, M M Snoeck, S Treves, et al.
Neuromuscular Disorders : NMD|December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire studyE van Ruitenbeek, J A E Custers, C Verhaak, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Acta Anaesthesiologica Scandinavica|October 6, 1997
In vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: results of testing patients surviving fulminant MH and unrelated low-risk subjects. The European Malignant Hyperthermia GroupH Ording, V Brancadoro, S Cozzolino, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Brain : a Journal of Neurology|February 11, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patientsJoery P Molenaar, Jamie I Verhoeven, Richard J Rodenburg, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Biochemistry and Biophysics Reports|April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody diseaseJ P Molenaar, M M Snoeck, S Treves, et al.
Neuromuscular Disorders : NMD|December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire studyE van Ruitenbeek, J A E Custers, C Verhaak, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Acta Anaesthesiologica Scandinavica|October 6, 1997
In vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: results of testing patients surviving fulminant MH and unrelated low-risk subjects. The European Malignant Hyperthermia GroupH Ording, V Brancadoro, S Cozzolino, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Brain : a Journal of Neurology|February 11, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patientsJoery P Molenaar, Jamie I Verhoeven, Richard J Rodenburg, et al.
Pageof 3