G. Roende

Low bone turnover phenotype in Rett syndrome: results of biochemical bone marker analysis

K. Brøndum‐Nielsen, K. Ravn, J. Jensen, 2014, Pediatric Research.

Bone Markers in Rett Syndrome

J. Jensen, G. Roende, 2016 .

Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations

Z. Tümer, M. Duno, O. Skjeldal, 2011, Orphanet journal of rare diseases.

DXA measurements in rett syndrome reveal small bones with low bone mass

K. Brøndum‐Nielsen, K. Ravn, J. Jensen, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Patients With Rett Syndrome Sustain Low-Energy Fractures

K. Brøndum‐Nielsen, K. Ravn, J. Jensen, 2011, Pediatric Research.

Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants.

H. J. Schelhaas, S. Naidu, E. Gardella, 2024, Epilepsia.