Ference J. Loupatty - Concepedia

Author

Ference J. Loupatty

University of Amsterdam

Also Known As

Ference J Loupatty, Ference J. Loupatty, Ference Loupatty

Publications

519

Citations

H-Index

Concepts

All Affiliations

University of Amsterdam Amsterdam UMC Location University of Amsterdam Emma Kinderziekenhuis OLVG

About

Ference J. Loupatty is an author at University of Amsterdam specializing in medicine, urology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	352
2	Natural Sciences	1	1	91
3	Biochemistry	1	1	91
4	Clinical Nutrition	1	1	79
5	Metabolism	1	1	91

Ference J. Loupatty

Publications

516

Citations

H-Index

Page 1

	Year	Citations
Enzymology of the branched‐chain amino acid oxidation disorders: the valine pathway Ronald J. A. Wanders, Marinus Durán, Ference J. Loupatty Journal of Inherited Metabolic Disease BiosynthesisCellular EnzymologyBiochemistryMitochondrial FunctionNatural Sciences	2010	91
Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration Ference J. Loupatty, Peter T. Clayton, Jos P.N. Ruiter, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsProgressive Infantile Neurodegeneration	2006	84
Multicenter comparison study of current methods to measure 25-hydroxyvitamin D in serum Marcel J.W. Janssen, Jos P.M. Wielders, Corinne C. Bekker, Steroids MedicineBioanalysisClinical Nutrition25-Hydroxyvitamin DClinical Chemistry	2012	79
3-Methylglutaconic Aciduria Type I Is Caused by Mutations in AUH Lodewijk IJlst, Ference J. Loupatty, Jos P.N. Ruiter, The American Journal of Human Genetics UrologySomatic VariantAutoimmune DiseaseMendelian DisorderGenetic Disorder	2002	73
Can serum L-lactate, D-lactate, creatine kinase and I-FABP be used as diagnostic markers in critically ill patients suspected for bowel ischemia Peter HJ van der Voort, Berit Westra, J. P. J. Wester, BMC Anesthesiology	2014	63
NMR spectroscopic studies on the late onset form of 3‐methylglutaconic aciduria type I and other defects in leucine metabolism Udo F. H. Engelke, Berry Kremer, Leo A. J. Kluijtmans, NMR in Biomedicine	2006	60
Hypertrophic cardiomyopathy, cataract, developmental delay, lactic acidosis: A novel subtype of 3‐methylglutaconic aciduria Gabriella Di Rosa, Federica Deodato, Ference J. Loupatty, Journal of Inherited Metabolic Disease	2006	31
Clinical, biochemical, and molecular findings in three patients with 3-hydroxyisobutyric aciduria Ference J. Loupatty, Annemarie van der Steen, Lodewijk IJlst, Molecular Genetics and Metabolism 3-Hydroxyisobutyric AciduriaElectrolyte DisorderUrologyMolecular FindingsRenal Function	2006	25
Direct Nonisotopic Assay of 3-Methylglutaconyl-CoA Hydratase in Cultured Human Skin Fibroblasts to Specifically Identify Patients with 3-Methylglutaconic Aciduria Type I Ference J. Loupatty, Jos P.N. Ruiter, Lodewijk IJlst, Clinical Chemistry	2004	10

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