Jaak Jaeken

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 5

Top Topics

Dna Methylation

Replacement Therapy

Extracellular Matrix

Top Venues

Journal of mother and child

Cellular and molecular life sciences : CMLS

Journal of inherited metabolic disease

Orphanet journal of rare diseases

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

Publications

Laura Di Patria, Giosuè Annibalini, Amelia Morrone, Lorenzo Ferri, Roberta Saltarelli, Luca Galluzzi, Aurora Diotallevi, Matteo Bocconcelli, Maria Alice Donati, Rita Barone, Renzo Guerrini, Jaak Jaeken, Vilberto Stocchi, Elena Barbieri
Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation. Cellular and molecular life sciences : CMLS 79 (3) (2022)
Kristl G Claeys, Luc Breysem, Eric Legius, Hilde Brems, David Cassiman, Matthieu Moisse, Pieter Vermeersch, Levtchenko Elena, Jaak Jaeken
A Patient with neonatal cholestasis. Journal of mother and child 24 (4) (2021)
Jaak Jaeken
Congenital disorders of glycosylation: A multi-genetic disease family with multiple subcellular locations. Journal of mother and child 24 (2) (2020)
Marie-Anne Morren, Jaak Jaeken, Gepke Visser, Isabelle Salles, Chris Van Geet, null null, Ilenia Simeoni, Ernest Turro, Kathleen Freson
PIGO deficiency: palmoplantar keratoderma and novel mutations. Orphanet journal of rare diseases 12 (1) (2017)
Jaak Jaeken, Romain Péanne
What is new in CDG? Journal of inherited metabolic disease 40 (4) (2017)