Mirian C. H. Janssen - Department of Pediatrics, Amalia Children's Hospital

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论文共 206 篇作者统计合作学者相似作者

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VACCINE SAFETY IN CHILDREN WITH GENETICALLY CONFIRMED MITOCHONDRIAL DISEASE

Annemarie de Vreugd, Franz A. Zimmermann, Katja Steinbrücker,Maaike C. de Vries,Lonneke de Boer,Mirian CH Janssen,Martina Huemer,Saskia B. Wortmann

Immunology letters (2024): 106946-106946

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Feasibility, Safety, and Efficacy of a Ketogenic Diet in Patients with Mitochondrial Myopathy

Heidi Zweers-van Essen, Gijsje Beerink, Elke Buit, Karlijn Gerrits, Astrid Dorhout, Sophie Kroesen, Annemiek van Wegberg,Mirian Janssen, Saskia Wortmann,Silvie Timmers,Christiaan Saris

crossref（2024）

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Impact of Theta Transcranial Alternating Current Stimulation on Language Production in Adult Classic Galactosemia Patients

Britt Derks, Varsha Shashi Kumar, Sai Yadnik,Bianca Panis,Annet M. Bosch,David Cassiman,Mirian C. H. Janssen,Teresa Schuhmann,M. Estela Rubio-Gozalbo,Bernadette M. Jansma

JOURNAL OF INHERITED METABOLIC DISEASE（2024）

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Whole-body Ndufs4 Knockout Mice with Isolated Complex I Deficiency Engage a Futile Adaptive Brain Response

Melissa A. E. van de Wal,Cenna Doornbos, Janne Bibbe,Judith R. Homberg,Clara van Karnebeek, Martijn Huijnen,Jaap Keijer,Evert M. van Schothorst,Peter A. C. ' T Hoen,Mirian C. H. Janssen,Merel J. W. Adjobo-Hermans,Mariusz R. Wieckowski,Werner J. H. Koopman

Biochimica et biophysica acta Proteins and proteomics（2024）

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Social Cognition, Emotion Regulation and Social Competence in Classical Galactosemia Patients Without Intellectual Disability

Merel E. Hermans,Gert J. Geurtsen,Carla E. M. Hollak,Mirian C. H. Janssen,Janneke G. Langendonk, Valerie L. V. Merckelbach,Esmee Oussoren,Kim J. Oostrom,Annet M. Bosch

ACTA NEUROPSYCHIATRICA（2024）

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Dysarthria and Dysphagia in Patients with Mitochondrial Diseases

R. E. M. Kuin,J. T. Groothuis, P. Buit,M. C. H. Janssen,S. Knuijt

Molecular Genetics and Metabolism（2024）

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Bone Quality in LAMA2-related Muscular Dystrophy and SELENON-related Congenital Myopathy, a One-Year Prospective Natural History Study

Karlijn Bouman,Anne T. M. Dittrich,Jan T. Groothuis,Baziel G. M. van Engelen,Heidi Zweers-van Essen, Anja de Baaij-Daalmeyer,Mirian C. H. Janssen,Corrie E. Erasmus,Jos M. T. Draaisma,Nicol C. Voermans

NEUROMUSCULAR DISORDERS (2024): 105-113

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Newborn Screening for Primary Carnitine Deficiency: Who Will Benefit? - a Retrospective Cohort Study

Loek Crefcoeur,Sacha Ferdinandusse,Saskia N. van der Crabben,Eugenie Dekkers,Sabine A. Fuchs,Hidde Huidekoper,Mirian Janssen,Janneke Langendonk,Rose Maase, Monique de Sain, Estela Rubio,Francjan J. van Spronsen,Frederic Maxime Vaz, Rendelien Verschoof,Maaike de Vries,Frits Wijburg,Gepke Visser,Mirjam Langeveld

Journal of Medical Geneticsno. 12 (2023): 1177-1185

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