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