FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Petter Strømme

Research Profile

Disorders

Living Beings

Geographic Areas

Norway

Concepts & Ideas

Anatomy

Brain

Physiology

Procedures

Co-author Network

Publications

TOP 3
Tuva Barøy; Anne Blomhoff; Madeleine Fannemel; JR Helle; Asbjørn Holmgren; Doriana Misceo; Olaug Kristin Rødningen; Alice Stormyr; Asbjørg Stray-Pedersen; Petter Strømme; Bjørn Tvedt; Eirik Frengen
Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.
Imer Önder Slettedal; Hilde Margrete Dahl; Josep Dalmau; Inger Sandvig; Petter Strømme
Young girl with psychosis, cognitive failure and seizures.
Petter Strømme; Nafeeza F Ali; Cristin Davidson; Kostantin Dobrenis; Linda Ellevog; Maria Gulinello; Arne Klungland; Matthew C Micsenyi; Roy Sillitoe; Gloria Stephney; Steven U Walkley
X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Petter Strømme (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Tuva Barøy; Anne Blomhoff; Madeleine Fannemel; JR Helle; Asbjørn Holmgren; Doriana Misceo; Olaug Kristin Rødningen; Alice Stormyr; Asbjørg Stray-Pedersen; Petter Strømme; Bjørn Tvedt; Eirik Frengen
Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.
Orphanet journal of rare diseases 2013;8():3.
2012: Imer Önder Slettedal; Hilde Margrete Dahl; Josep Dalmau; Inger Sandvig; Petter Strømme
Young girl with psychosis, cognitive failure and seizures.
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 2012;132(18):2073-6.
2011: Petter Strømme; Nafeeza F Ali; Cristin Davidson; Kostantin Dobrenis; Linda Ellevog; Maria Gulinello; Arne Klungland; Matthew C Micsenyi; Roy Sillitoe; Gloria Stephney; Steven U Walkley
X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction.
Brain : a journal of neurology 2011;134(Pt 11):3369-83.
2011: Doriana Misceo; O K Rødningen; T Barøy; H Sorte; J R Mellembakken; Petter Strømme; M Fannemel; Eirik Frengen
A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.
American journal of medical genetics. Part A 2011;155A(2):403-8.
2010: Tuva Barøy; Doriana Misceo; Oivind Braaten; JR Helle; Madeleine Fannemel; Petter Strømme; Eirik Frengen
A de novo 15q13.2q13.3 deletion in a boy with an Angelman syndrome like phenotype.
European journal of medical genetics 2010;53(4):221-4.
2010: Petter Strømme; P Suren; O J Kanavin; T Rootwelt; Berit Woldseth; Michael Abdelnoor; Per Magnus
Parental consanguinity is associated with a seven-fold increased risk of progressive encephalopathy: a cohort study from Oslo, Norway.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2010;14(2):138-45.
2009: Doriana Misceo; M Fannemel; T Barøy; R Roberto; B Tvedt; T Jaeger; V Bryn; Petter Strømme; Eirik Frengen
SCA27 caused by a chromosome translocation: further delineation of the phenotype.
Neurogenetics 2009;10(4):371-4.
2008: Petter Strømme
[Artistic creativeness and Huntington disease].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 2008;128(19):2226.
2008: Petter Strømme
[Mental retardation].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 2008;128(7):841; author reply 841.
2008: Gregor Gilfillan; Kaja K Selmer; Ingrid Roxrud; Raffaella Smith; Mårten Kyllerman; Kristin Louise Eiklid; Mette Kroken; Morten Mattingsdal; Thore Egeland; Harald Stenmark; Hans Sjøholm; Andres Server; Lena Samuelsson; Arnold Christianson; Patrick Tarpey; Annabel Whibley; Michael R Stratton; P Andrew Futreal; Jon Teague; Sarah Edkins; Jozef Gecz; Gillian Turner; F Lucy Raymond; Charles Schwartz; Roger E Stevenson; DAG UNDLIEN; Petter Strømme
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
American journal of human genetics 2008;82(4):1003-10.
2008: Petter Strømme; Per Magnus; Øivind Juris Kanavin; Terje Rootwelt; Berit Woldseth; Michael Abdelnoor
Mortality in childhood progressive encephalopathy from 1985 to 2004 in Oslo, Norway: a population-based study.
Acta paediatrica (Oslo, Norway : 1992) 2008;97(1):35-40.
2007: Karen Helene Ørstavik; G P S Knudsen; Hilde Nordgarden; Eli Ormerod; Petter Strømme; Lazarous P Lazarou; Lyndon G Rosser; Trine E Prescott; Gunnar Houge
Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene.
American journal of medical genetics. Part A 2007;143A(13):1510-3.
2007: L Kleppa; Ø J Kanavin; Arne Klungland; Petter Strømme
A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome.
Neuroscience 2007;145(4):1397-406.
2006: Øivind J Kanavin; Monika Haakonsen; Andrès Server; Tariq J Bajwa; Marjo S van der Knaap; Petter Strømme
Microphthalmia and brain atrophy: a novel neurodegenerative disease.
Annals of neurology 2006;59(4):719-23.
2005: Petter Strømme; Carl Birger van der Hagen; Monika Haakonsen; Knut Risberg; Raoul Hennekam
Follow-up of a girl with cleft lip and palate and multiple malformations: trisomy 20 mosaicism.
Scandinavian journal of plastic and reconstructive surgery and hand surgery / Nordisk plastikkirurgisk forening [and] Nordisk klubb for handkirurgi 2005;39(3):178-9.
2004: Arpad Matlary; Trine E Prescott; Bjørn Tvedt; Knut Lindberg; Andres Server; Jean Aicardi; Petter Strømme
Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEG.
Clinical dysmorphology 2004;13(4):257-60.
2003: Gunnar Houge; Thomas Liehr; Jacqueline Schoumans; Gro Oddveig Ness; Kjetil Solland; Heike Starke; Uwe Claussen; Petter Strømme; Bjug Akre; Stefan Vermeulen
Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR.
American journal of medical genetics. Part A 2003;118A(3):235-40.
2000: Petter Strømme
Aetiology in severe and mild mental retardation: a population-based study of Norwegian children.
Developmental medicine and child neurology 2000;42(2):76-86.
1999: Petter Strømme; Kjetil Sundet; Cato Mørk; J J Cassiman; J P Fryns; S Claes
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11.
Journal of medical genetics 1999;36(5):374-8.
1998: Petter Strømme; K Valvatne
Mental retardation in Norway: prevalence and sub-classification in a cohort of 30037 children born between 1980 and 1985.
Acta paediatrica (Oslo, Norway : 1992) 1998;87(3):291-6.
1997: K H Orstavik; Petter Strømme; J Ek; A Torvik; O H Skjeldal
Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?
Journal of medical genetics 1997;34(10):849-51.
1996: Petter Strømme; F Sandboe
Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).
Acta ophthalmologica Scandinavica 1996;74(1):45-7.
1995: Petter Strømme; Oddvar Stokke; Egil Jellum; O H Skjeldal; R Baumgartner
Atypical methylmalonic aciduria with progressive encephalopathy, microcephaly and cataract in two siblings--a new recessive syndrome?
Clinical genetics 1995;48(1):1-5.
1995: W J Orderud; O H Skjeldal; Petter Strømme
[Neuronal migration disorders. Radiological and clinical aspects].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 1995;115(16):1952-6.
1994: O H Skjeldal; Petter Strømme; E Christensen
[Adrenoleukodystrophy--clinical, biochemical and therapeutic aspects].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 1994;114(28):3321-3.
1993: Erik Strom; Petter Strømme; J Westvik; S J Pedersen
Renal cysts in the carbohydrate-deficient glycoprotein syndrome.
Pediatric nephrology (Berlin, Germany) 1993;7(3):253-5.
1993: Petter Strømme; J Knudtzon; J Westvik; L Traaholt; P Brandt-Hansen
Cleft lip and palate, scoliosis, skeletal and cardiac malformations and other dysmorphic features in a child. Case report.
Scandinavian journal of plastic and reconstructive surgery and hand surgery / Nordisk plastikkirurgisk forening [and] Nordisk klubb for handkirurgi 1993;27(1):71-4.
1992: Petter Strømme; O H Skjeldal; J Knudtzon
[Mental retardation in children. Prevalence and etiology].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 1992;112(6):749-51.
1991: J K Hald; P Hj Nakstad; O H Skjeldal; Petter Strømme
Bilateral arachnoid cysts of the temporal fossa in four children with glutaric aciduria type I.
AJNR. American journal of neuroradiology 1991;12(3):407-9.
1991: Petter Strømme; Jan Maehlen; Erik Strom; A Torvik
[The carbohydrate deficient glycoprotein syndrome].
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 1991;111(10):1236-7.
1991: Petter Strømme
The diagnosis of syndromes by use of a dysmorphology database.
Acta paediatrica Scandinavica 1991;80(1):106-9.