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88 results
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Rett variants: a suggested model for inclusion criteria.
Hagberg BA, Skjeldal OH. Hagberg BA, et al. Among authors: skjeldal oh. Pediatr Neurol. 1994 Jul;11(1):5-11. doi: 10.1016/0887-8994(94)90082-5. Pediatr Neurol. 1994. PMID: 7986294
De novo mutations in SCN1A are associated with classic Rett syndrome: a case report.
Henriksen MW, Ravn K, Paus B, von Tetzchner S, Skjeldal OH. Henriksen MW, et al. Among authors: skjeldal oh. BMC Med Genet. 2018 Oct 11;19(1):184. doi: 10.1186/s12881-018-0700-z. BMC Med Genet. 2018. PMID: 30305042 Free PMC article.
Epilepsy in classic Rett syndrome: Course and characteristics in adult age.
Henriksen MW, Breck H, von Tetzchner S, Paus B, Skjeldal OH, Brodtkorb E. Henriksen MW, et al. Among authors: skjeldal oh. Epilepsy Res. 2018 Sep;145:134-139. doi: 10.1016/j.eplepsyres.2018.06.012. Epub 2018 Jun 23. Epilepsy Res. 2018. PMID: 29966812
Spinal deformity and disability in patients with Rett syndrome.
Riise R, Brox JI, Sorensen R, Skjeldal OH. Riise R, et al. Among authors: skjeldal oh. Dev Med Child Neurol. 2011 Jul;53(7):653-7. doi: 10.1111/j.1469-8749.2011.03935.x. Epub 2011 Apr 18. Dev Med Child Neurol. 2011. PMID: 21501153
Rett syndrome: geographic variation in prevalence in Norway.
Skjeldal OH, von Tetzchner S, Aspelund F, Herder GA, Lofterłd B. Skjeldal OH, et al. Brain Dev. 1997 Jun;19(4):258-61. doi: 10.1016/s0387-7604(97)00572-x. Brain Dev. 1997. PMID: 9187475
Vision, cognition and developmental characteristics of girls and women with Rett syndrome.
von Tetzchner S, Jacobsen KH, Smith L, Skjeldal OH, Heiberg A, Fagan JF. von Tetzchner S, et al. Among authors: skjeldal oh. Dev Med Child Neurol. 1996 Mar;38(3):212-25. doi: 10.1111/j.1469-8749.1996.tb15083.x. Dev Med Child Neurol. 1996. PMID: 8631518
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations.
Kyllerman M, Skjeldal OH, Lundberg M, Holme I, Jellum E, von Döbeln U, Fossen A, Carlsson G. Kyllerman M, et al. Among authors: skjeldal oh. Mov Disord. 1994 Jan;9(1):22-30. doi: 10.1002/mds.870090105. Mov Disord. 1994. PMID: 8139602
Medium chain acyl-CoA dehydrogenase deficiency and fatal valproate toxicity.
Njølstad PR, Skjeldal OH, Agsteribbe E, Huckriede A, Wannag E, Søvik O, Waaler PE. Njølstad PR, et al. Among authors: skjeldal oh. Pediatr Neurol. 1997 Feb;16(2):160-2. doi: 10.1016/s0887-8994(96)00318-9. Pediatr Neurol. 1997. PMID: 9090694
Childhood autism: the need for physical investigations.
Skjeldal OH, Sponheim E, Ganes T, Jellum E, Bakke S. Skjeldal OH, et al. Brain Dev. 1998 Jun;20(4):227-33. doi: 10.1016/s0387-7604(98)00031-x. Brain Dev. 1998. PMID: 9661967
Rett syndrome--distribution of phenotypes with special attention to the preserved speech variant.
Skjeldal OH, von Tetzchner S, Jacobsen K, Smith L, Heiberg A. Skjeldal OH, et al. Neuropediatrics. 1995 Apr;26(2):87. doi: 10.1055/s-2007-979732. Neuropediatrics. 1995. PMID: 7566462 No abstract available.
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