Michael Champion - Concepedia

Author

Michael Champion

Evelina London Children's Healthcare ORCID

Also Known As

M Champion, M. Champion, MP Champion, Michael Champion, Michael W. Champion, Michael W. Champion (book author)

123

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Evelina London Children's Healthcare Guy's and St Thomas' NHS Foundation Trust Wellcome Centre for Mitochondrial Research Newcastle University Arizona State University

About

Michael Champion is an author at Evelina London Children's Healthcare specializing in medicine, education, and technology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	4	4	71
2	Arts	2	2	208
3	Engineering	2	2	27
4	Business	1	1	27
5	Health Sciences	1	1	13

Michael Champion

Publications

Citations

H-Index

Page 1

	Year	Citations
Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease Yoav H. Messinger, Nancy J. Mendelsohn, William J. Rhead, Genetics in Medicine Primary ImmunodeficiencyMaternal ImmunizationAutoimmune DiseaseAllergyImmunodeficiencies	2012	209
Video Games as a Means to Reduce Age-Related Cognitive Decline: Attitudes, Compliance, and Effectiveness Walter R. Boot, Michael Champion, Daniel P. Blakely, Frontiers in Psychology AgingOnline GamingCognitionVideo GamesCognitive Abilities	2013	181
Genetic dysfunction of <i>MT-ATP6</i> causes axonal Charcot-Marie-Tooth disease Robert D. S. Pitceathly, Sinéad M. Murphy, Ellen Cottenie, Neurology	2012	110
Response of 33 UK patients with infantile‐onset Pompe disease to enzyme replacement therapy Alexander Broomfield, Joan Fletcher, James Davison, Journal of Inherited Metabolic Disease	2015	70
Defective mitochondrial protease LonP1 can cause classical mitochondrial disease Bradley Peter, Christie Louisa Waddington, Monika Oláhová, Human Molecular Genetics GeneticsPathologyMolecular GeneticsDisease Gene IdentificationClinical Genetics	2018	65
Genotypes and phenotypes of patients in the UK with carbohydrate‐deficient glycoprotein syndrome type 1 Faiqa Imtiaz, Viki Worthington, Michael Champion, Journal of Inherited Metabolic Disease	2000	64
Clinical presentation and proteomic signature of patients with <i>TANGO2</i> mutations Nadja Mingirulli, Angela Pyle, Denisa Hathazi, Journal of Inherited Metabolic Disease	2019	55
Auxiliary Liver Transplantation for Propionic Acidemia: A 10‐Year Follow‐Up Mohamed Rela, Narendra Battula, Mansoor Madanur, American Journal of Transplantation	2007	45
The genotypic and phenotypic spectrum of MTO1 deficiency James J. O’Byrne, Maja Tarailo‐Graovac, Aisha Ghani, Molecular Genetics and Metabolism	2017	35
Pathogenic variants in <i>HTRA2</i> cause an early‐onset mitochondrial syndrome associated with 3‐methylglutaconic aciduria Monika Oláhová, Kyle Thompson, Steven Hardy, Journal of Inherited Metabolic Disease	2016	29

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