Publications 2025

Böker T, Kirkhus E, Pripp AH, Rand-Hendriksen S, Paus B, Smith HJ, Lundby R (2025)
The natural history of protrusio acetabuli in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up CT study
Orphanet J Rare Dis, 20 (1), 118
DOI 10.1186/s13023-025-03628-0, PubMed 40075421

Skattebøl L, Lundby R, Øverås MH, Sowa P, Celius EG, Harbo HF, Nordhøy W, Høgestøl EA, Nygaard GO (2025)
Quantitative susceptibility mapping of paramagnetic rim lesions in early multiple sclerosis: A cross-sectional study of brain age and disability
Neuroimage Rep, 5 (3), 100277
DOI 10.1016/j.ynirp.2025.100277, PubMed 41050950

Publications 2019

Böker T, Vanem TT, Pripp AH, Rand-Hendriksen S, Paus B, Smith HJ, Lundby R (2019)
Dural ectasia in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up study
Spine J, 19 (8), 1412-1421
DOI 10.1016/j.spinee.2019.04.010, PubMed 30998996

Vanem TT, Böker T, Sandvik GF, Kirkhus E, Smith HJ, Andersen K, Drolsum L, Lundby R, Røe C, Krohg-Sørensen K, Geiran OR, Paus B, Rand-Hendriksen S (2019)
Marfan syndrome: Evolving organ manifestations-A 10-year follow-up study
Am J Med Genet A, 182 (2), 397-408
DOI 10.1002/ajmg.a.61441, PubMed 31825148

Publications 2018

Riise N, Lindberg BR, Kulseth MA, Fredwall SO, Lundby R, Estensen ME, Drolsum L, Merckoll E, Krohg-Sørensen K, Paus B (2018)
Clinical diagnosis of Larsen syndrome, Stickler syndrome and Loeys-Dietz syndrome in a 19-year old male: a case report
BMC Med Genet, 19 (1), 155
DOI 10.1186/s12881-018-0671-0, PubMed 30170566

Publications 2012

Lundby R, Rand-Hendriksen S, Hald JK, Pripp AH, Smith HJ (2012)
The pulmonary artery in patients with Marfan syndrome: a cross-sectional study
Genet Med, 14 (11), 922-7
DOI 10.1038/gim.2012.82, PubMed 22791209

Publications 2011

Lundby R, Kirkhus E, Rand-Hendriksen S, Hald J, Pripp AH, Smith HJ (2011)
CT of the hips in the investigation of protrusio acetabuli in Marfan syndrome. A case control study
Eur Radiol, 21 (7), 1485-91
DOI 10.1007/s00330-011-2073-y, PubMed 21318473

Publications 2009

Lundby R, Rand-Hendriksen S, Hald JK, Lilleås FG, Pripp AH, Skaar S, Paus B, Geiran O, Smith HJ (2009)
Dural ectasia in Marfan syndrome: a case control study
AJNR Am J Neuroradiol, 30 (8), 1534-40
DOI 10.3174/ajnr.A1620, PubMed 19461064

Rand-Hendriksen S, Lundby R, Tjeldhorn L, Andersen K, Offstad J, Semb SO, Smith HJ, Paus B, Geiran O (2009)
Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome
Eur J Hum Genet, 17 (10), 1222-30
DOI 10.1038/ejhg.2009.30, PubMed 19293838

Publications 2007

Rand-Hendriksen S, Tjeldhorn L, Lundby R, Semb SO, Offstad J, Andersen K, Geiran O, Paus B (2007)
Search for correlations between FBN1 genotype and complete Ghent phenotype in 44 unrelated Norwegian patients with Marfan syndrome
Am J Med Genet A, 143A (17), 1968-77
DOI 10.1002/ajmg.a.31759, PubMed 17663468

Publications 2004

Akre B, Rasmussen M, Lundby R (2004)
[Pyridoxine-dependent seizures]
Tidsskr Nor Laegeforen, 124 (2), 162-4
PubMed 14743226