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Publications (original articles or review articles) published in 2016 from OUS - Department of Clinical Neurosciences for Children

20 publications found

Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P (2016)
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
Hum Mutat, 37 (4), 359-63
DOI 10.1002/humu.22960, PubMed 26820108

Fletcher-Watson S, Apicella F, Auyeung B, Beranova S, Bonnet-Brilhault F, Canal-Bedia R, Charman T, Chericoni N, Conceição IC, Davies K, Farroni T, Gomot M, Jones E, Kaale A, Kapica K, Kawa R, Kylliäinen A, Larsen K, Lefort-Besnard J, Malvy J, Manso de Dios S, Markovska-Simoska S, Millo I, Miranda N, Pasco G et al. (2016)
Attitudes of the autism community to early autism research
Autism, 21 (1), 61-74
DOI 10.1177/1362361315626577, PubMed 26975669

Gardsjord ES, Romm KL, Friis S, Barder HE, Evensen J, Haahr U, ten Velden Hegelstad W, Joa I, Johannessen JO, Langeveld J, Larsen TK, Opjordsmoen S, Rund BR, Simonsen E, Vaglum P, McGlashan T, Melle I, Røssberg JI (2016)
Subjective quality of life in first-episode psychosis. A ten year follow-up study
Schizophr Res, 172 (1-3), 23-8
DOI 10.1016/j.schres.2016.02.034, PubMed 26947210

Gravdal Kvarme L, Albertini-Früh E, Brekke I, Gardsjord R, Halvorsrud L, Liden H (2016)
On duty all the time: health and quality of life among immigrant parents caring for a child with complex health needs
J Clin Nurs, 25 (3-4), 362-71
DOI 10.1111/jocn.13056, PubMed 26818363

Hegelstad WT, Bronnick KS, Barder HE, Evensen JH, Haahr U, Joa I, Johannessen JO, Langeveld J, Larsen TK, Melle I, Opjordsmoen S, Rund BR, Rossberg JI, Simonsen E, Vaglum PW, McGlashan TH, Friis S (2016)
Preventing Poor Vocational Functioning in Psychosis Through Early Intervention
Psychiatr Serv, 68 (1), 100-103
DOI 10.1176/appi.ps.201500451, PubMed 27582238

Heuser K, Nakken KO, Sandvig I, Taubøll E (2016)
[What causes febrile convulsions?]
Tidsskr Nor Laegeforen, 136 (1), 36-8
DOI 10.4045/tidsskr.14.1503, PubMed 26757658

Hope S, Johannessen CH, Aanonsen NO, Strømme P (2016)
The investigation of inborn errors of metabolism as an underlying cause of idiopathic intellectual disability in adults in Norway
Eur J Neurol, 23 Suppl 1, 36-44
DOI 10.1111/ene.12884, PubMed 26563096

Lemke JR, Geider K, Helbig KL, Heyne HO, Schütz H, Hentschel J, Courage C, Depienne C, Nava C, Heron D, Møller RS, Hjalgrim H, Lal D, Neubauer BA, Nürnberg P, Thiele H, Kurlemann G, Arnold GL, Bhambhani V, Bartholdi D, Pedurupillay CR, Misceo D, Frengen E, Strømme P, Dlugos DJ et al. (2016)
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
Neurology, 86 (23), 2171-8
DOI 10.1212/WNL.0000000000002740, PubMed 27164704

Lundman E, Gaup HJ, Bakkeheim E, Olafsdottir EJ, Rootwelt T, Storrøsten OT, Pettersen RD (2016)
Implementation of newborn screening for cystic fibrosis in Norway. Results from the first three years
J Cyst Fibros, 15 (3), 318-24
DOI 10.1016/j.jcf.2015.12.017, PubMed 26795017

Mikkelsen R, Rødevand LN, Wiig US, Zahl SM, Berntsen T, Skarbø AB, Egge A, Helseth E, Andersson S, Wester K (2016)
Neurocognitive and psychosocial function in children with benign external hydrocephalus (BEH)-a long-term follow-up study
Childs Nerv Syst, 33 (1), 91-99
DOI 10.1007/s00381-016-3267-z, PubMed 27848005

Nyquist A, Moser T, Jahnsen R (2016)
Fitness, Fun and Friends through Participation in Preferred Physical Activities: Achievable for Children with Disabilities?
Int. J. Disabil. Dev. Educ., 63 (3), 334-356
DOI 10.1080/1034912X.2015.1122176

Pedurupillay CR, Amundsen SS, Barøy T, Rasmussen M, Blomhoff A, Stadheim BF, Ørstavik K, Holmgren A, Iqbal T, Frengen E, Misceo D, Strømme P (2016)
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2
Neuromuscul Disord, 26 (9), 570-5
DOI 10.1016/j.nmd.2016.06.457, PubMed 27450922

Pedurupillay CR, Landsend EC, Vigeland MD, Ansar M, Frengen E, Misceo D, Strømme P (2016)
Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
Genes (Basel), 7 (8)
DOI 10.3390/genes7080041, PubMed 27472364

Popperud TH, Boldingh MI, Brunborg C, Faiz KW, Heldal AT, Maniaol AH, Müller KI, Rasmussen M, Øymar K, Kerty E (2016)
Juvenile myasthenia gravis in Norway: A nationwide epidemiological study
Eur J Paediatr Neurol, 21 (2), 312-317
DOI 10.1016/j.ejpn.2016.09.001, PubMed 27666466

Ramstad K, Jahnsen R, Diseth TH (2016)
Associations between recurrent musculoskeletal pain and visits to the family doctor (GP) and specialist multi-professional team in 74 Norwegian youth with cerebral palsy
Child Care Health Dev, 42 (5), 735-41
DOI 10.1111/cch.12366, PubMed 27283955

Ramstad K, Terjesen T (2016)
Hip pain is more frequent in severe hip displacement: a population-based study of 77 children with cerebral palsy
J Pediatr Orthop B, 25 (3), 217-21
DOI 10.1097/BPB.0000000000000282, PubMed 26895291

Rolfsjord LB, Skjerven HO, Carlsen KH, Mowinckel P, Bains KE, Bakkeheim E, Lødrup Carlsen KC (2016)
The severity of acute bronchiolitis in infants was associated with quality of life nine months later
Acta Paediatr, 105 (7), 834-41
DOI 10.1111/apa.13396, PubMed 26970427

Skauli N, Wallace S, Chiang SC, Barøy T, Holmgren A, Stray-Pedersen A, Bryceson YT, Strømme P, Frengen E, Misceo D (2016)
Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype
Genes (Basel), 7 (12)
DOI 10.3390/genes7120108, PubMed 27916860

Stadskleiv K, Jahnsen R, von Tetzchner S (2016)
Structure of Executive Functioning in Children with Cerebral Palsy: an Investigation of Anderson's Developmental Model
J. Dev. Phys. Disabil., 28 (5), 665-684
DOI 10.1007/s10882-016-9500-6

Strand EB, Lillestol K, Jason LA, Tveito K, Diep LM, Valla SS, Sunnquist M, Helland IB, Herder I, Dammen T (2016)
Comparing the DePaul Symptom Questionnaire with physician assessments: a preliminary study
FATIGUE, 4 (1), 52-62
DOI 10.1080/21641846.2015.1126026