Loek L Crefcoeur (Loek Crefcoeur)

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 5

Top Topics

Peritoneal Dialysis

Randomized Controlled Trial

Low Birth Weight

Top Venues

Journal of inherited metabolic disease

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Loek L Crefcoeur, Sacha Ferdinandusse, Saskia N van der Crabben, Eugènie Dekkers, Sabine A Fuchs, Hidde Huidekoper, Mirian Ch Janssen, Janneke Langendonk, Rose Maase, Monique de Sain, Estela Rubio, Francjan J van Spronsen, Frédéric Maxime Vaz, Rendelien Verschoof, Maaike de Vries, Frits Wijburg, Gepke Visser, Mirjam Langeveld
Newborn screening for primary carnitine deficiency: who will benefit? - a retrospective cohort study. Journal of medical genetics (2023)
Loek L Crefcoeur, Mireille C Melles, Tobias A Bruning, Rob Rodrigues Pereira, Janneke G Langendonk
Primary carnitine deficiency is a life-long disease. JIMD reports 63 (6) (2022)
Loek L Crefcoeur, Margaretha Rebecca Heiner-Fokkema, Rose E Maase, Gepke Visser, Monique G M de Sain-van der Velden
Assessment of carnitine excretion and its ratio to plasma free carnitine as a biomarker for primary carnitine deficiency in newborns. JIMD reports 64 (1) (2022)
Loek L Crefcoeur, Gepke Visser, Sacha Ferdinandusse, Frits A Wijburg, Mirjam Langeveld, Barbara Sjouke
Clinical characteristics of primary carnitine deficiency: A structured review using a case-by-case approach. Journal of inherited metabolic disease 45 (3) (2022)
Loek L Crefcoeur, Margaretha Rebecca Heiner-Fokkema, Rose E Maase, Gepke Visser, Monique G M de Sain-van der Velden
Assessment of carnitine excretion and its ratio to plasma free carnitine as a biomarker for primary carnitine deficiency in newborns. JIMD reports 64 (1) (2022)