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Spieren voor Spieren | Researchclopedia

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Spieren voor Spieren

Amsterdam, North Hollandnonprofit

11

Works

793

Citations

14

h-index

Top Research Topics

Metabolism and Genetic Disorders Neurogenetic and Muscular Disorders Research Mitochondrial Function and Pathology

Top Researchers

W. Ludo van der Pol Utrecht University

202 works6,376 citationsh-index: 45

Recent Research

What is on the agenda? About the importance of a collaborative research agenda set by Dutch neuromuscular patients, their families and the neuromuscular field

C. van Esch,A. Horemans,et al.

20260 citations

Muscle metabolism and nutrition

Hyperglycemia and glycemic control in critically ill and hospitalized patients

Congenital Anomalies and Fetal Surgery

Genetic Neurodegenerative Diseases

Cerebral Palsy and Movement Disorders

Diabetes and associated disorders

RNA modifications and cancer

Occupational Therapy Practice and Research

Muscle and Compartmental Disorders

W. Ludo van der Pol University Medical Center Utrecht

72 works3,666 citationsh-index: 33

Renske I. Wadman Utrecht University

73 works2,477 citationsh-index: 30

Inge Cuppen Utrecht University

69 works1,883 citationsh-index: 22

Marja Schoenmakers Noordwest Ziekenhuisgroep

40 works1,688 citationsh-index: 23

Camiel A. Wijngaarde University Medical Center Utrecht

37 works1,662 citationsh-index: 23

Natural History of Mandibular Function in Spinal Muscular Atrophy Types 2 and 3

H. Willemijn van Bruggen,Camiel A. Wijngaarde,et al.

20246 citations

Development of an International SMA Bulbar Assessment for Inter-professional Administration

Sally Dunaway Young,Katlyn McGrattan,et al.

202311 citations

Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

Marise van der Heul,Inge Cuppen,et al.

202060 citations

Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

Jeannette C. Bleeker,Gepke Visser,et al.

202039 citations

Impact of newborn screening for very‐long‐chain acyl‐CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes

Jeannette C. Bleeker,Irene L. Kok,et al.

201952 citations