P.Y. Jeannet - Concepedia

Author

P.Y. Jeannet

University Hospital of Lausanne

Also Known As

P. -Y. Jeannet, P.-Y. Jeannet, P.Y. Jeannet, Pierre-Yves Jeannet

Publications

Citations

H-Index

Concepts

All Affiliations

University Hospital of Lausanne Government of Western Australia Department of Health Hospital de Sant Pau Medical University of Warsaw University Medical Center Freiburg

About

P.Y. Jeannet is an author at University Hospital of Lausanne specializing in medicine, rehabilitation, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	937
2	Health Sciences	2	2	78
3	Public Health	2	2	155
4	Engineering	1	1	717
5	Applied Physiology	1	1	66

P.Y. Jeannet

Publications

Citations

H-Index

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	Year	Citations
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations Catherine L. Bladen, David Salgado, Soledad Monges, Human Mutation Dmd MutationsTrial PlanningEngineeringMendelian DisorderGenetic Disorder	2015	717
Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe Catherine L. Bladen, Rachel Thompson, J. Jackson, Journal of Neurology Spine CarePrimary CareHealth PolicyMedicineInternational Health	2013	102
Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients P.Y. Jeannet, Kamiar Aminian, Clemens Bloetzer, European Journal of Paediatric Neurology Physical ActivityKinesiologyMultiple ParametersContinuous MonitoringDaily Physical Activity	2010	66
Local variability in respiratory syncytial virus disease severity A.H. Brandenburg, P.Y. Jeannet, H A van Steensel-Moll, Archives of Disease in Childhood Local VariabilityPediatric EpidemiologyRespiratory DiseasesMedicineClinical Epidemiology	1997	53
Morphological, clinical and genetic aspects in a family with a novel LAMP-2 gene mutation (Danon disease) Johannes Alexander Lobrinus, Daniel F. Schorderet, M Payot, Neuromuscular Disorders Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2005	37
Autosomal dominant nemaline myopathy: A new phenotype unlinked to previously known genetic loci P.Y. Jeannet, L. Mittaz, M. Dunand, Neuromuscular Disorders Rare DiseasesNew PhenotypeAutoimmune DiseaseMendelian DisorderGenetic Disorder	2006	16
Hirayama disease associated with a severe rhythmic movement disorder involving neck flexions P.Y. Jeannet, Thierry Küntzer, T Deonna, Neurology Motor DysfunctionDynamic Cord CompressionNeck DisorderYogaCervical Myelopathy	2005	12

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