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A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features.
Kirchhoff M, Bisgaard AM, Duno M, Hansen FJ, Schwartz M. Kirchhoff M, et al. Among authors: hansen fj. Eur J Med Genet. 2007 Jul-Aug;50(4):256-63. doi: 10.1016/j.ejmg.2007.05.001. Epub 2007 May 18. Eur J Med Genet. 2007. PMID: 17576104
Cerebral folate deficiency: life-changing supplementation with folinic acid.
Hansen FJ, Blau N. Hansen FJ, et al. Mol Genet Metab. 2005 Apr;84(4):371-3. doi: 10.1016/j.ymgme.2004.12.001. Epub 2005 Jan 22. Mol Genet Metab. 2005. PMID: 15781200
Hypertrichosis in patients with SURF1 mutations.
Ostergaard E, Bradinova I, Ravn SH, Hansen FJ, Simeonov E, Christensen E, Wibrand F, Schwartz M. Ostergaard E, et al. Among authors: hansen fj. Am J Med Genet A. 2005 Nov 1;138(4):384-8. doi: 10.1002/ajmg.a.30972. Am J Med Genet A. 2005. PMID: 16222681
Gait disturbance interpreted as cerebellar ataxia after MMR vaccination at 15 months of age: a follow-up study.
Plesner AM, Hansen FJ, Taudorf K, Nielsen LH, Larsen CB, Pedersen E. Plesner AM, et al. Among authors: hansen fj. Acta Paediatr. 2000 Jan;89(1):58-63. doi: 10.1080/080352500750029077. Acta Paediatr. 2000. PMID: 10677059
A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy.
Riisager M, Duno M, Hansen FJ, Krag TO, Vissing CR, Vissing J. Riisager M, et al. Among authors: hansen fj. Neuromuscul Disord. 2013 Jul;23(7):562-7. doi: 10.1016/j.nmd.2013.04.006. Epub 2013 Jun 6. Neuromuscul Disord. 2013. PMID: 23746544
Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.
Ostergaard E, Hansen FJ, Sorensen N, Duno M, Vissing J, Larsen PL, Faeroe O, Thorgrimsson S, Wibrand F, Christensen E, Schwartz M. Ostergaard E, et al. Among authors: hansen fj. Brain. 2007 Mar;130(Pt 3):853-61. doi: 10.1093/brain/awl383. Epub 2007 Feb 7. Brain. 2007. PMID: 17287286
A novel RNASEH2B splice site mutation responsible for Aicardi-Goutieres syndrome in the Faroe Islands.
Ostergaard E, Joensen F, Sundberg K, Duno M, Hansen FJ, Batbayli M, Sørensen N, Born AP. Ostergaard E, et al. Among authors: hansen fj. Acta Paediatr. 2012 Nov;101(11):e509-13. doi: 10.1111/j.1651-2227.2012.02807.x. Epub 2012 Sep 5. Acta Paediatr. 2012. PMID: 22882256
Cerebellar hypoplasia in children with the carbohydrate-deficient glycoprotein syndrome.
Jensen PR, Hansen FJ, Skovby F. Jensen PR, et al. Among authors: hansen fj. Neuroradiology. 1995 May;37(4):328-30. doi: 10.1007/BF00588349. Neuroradiology. 1995. PMID: 7666974
Threshold electrical stimulation (TES) in ambulant children with CP: a randomized double-blind placebo-controlled clinical trial.
Dali Cí, Hansen FJ, Pedersen SA, Skov L, Hilden J, Bjørnskov I, Strandberg C, Christensen J, Haugsted U, Herbst G, Lyskjaer U. Dali Cí, et al. Among authors: hansen fj. Dev Med Child Neurol. 2002 Jun;44(6):364-9. doi: 10.1017/s0012162201002237. Dev Med Child Neurol. 2002. PMID: 12088304 Free article. Clinical Trial.
Pigment variant of neuronal ceroid-lipofuscinosis.
Goebel HH, Gullotta F, Bajanowski T, Hansen FJ, Braak H. Goebel HH, et al. Among authors: hansen fj. Am J Med Genet. 1995 Jun 5;57(2):155-9. doi: 10.1002/ajmg.1320570209. Am J Med Genet. 1995. PMID: 7668321
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