Staffan Lundberg

Oromotor, word retrieval, and dichotic listening performance in young adults with previous Rolandic epilepsy

Törnhage, Maria; Sandberg, Eva Nordahl; Lundberg, Staffan

Part of European journal of paediatric neurology, p. 139-144, 2020

• DOI for Oromotor, word retrieval, and dichotic listening performance in young adults with previous Rolandic epilepsy

A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin crease

Stattin, Eva-Lena; Johansson, Josefin; Gudmundsson, Sanna; Ameur, Adam et al.

Part of American Journal of Medical Genetics. Part A, p. 1405-1410, 2018

• DOI for A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin crease

Oxidative proteome alterations during skeletal muscle ageing

Lourenço Dos Santos, Sofia; Baraibar, Martin A; Lundberg, Staffan; Eeg-Olofsson, Orvar et al.

Part of Redox Biology, p. 267-274, 2015

• DOI for Oxidative proteome alterations during skeletal muscle ageing
• Download full text (pdf) of Oxidative proteome alterations during skeletal muscle ageing

Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus

Livingston, John H; Mayer, Josephine; Jenkinson, Emma; Kasher, Paul et al.

Part of Neuropediatrics, p. 175-182, 2014

• DOI for Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Anderson, Beverley H.; Kasher, Paul R.; Mayer, Josephine; Szynkiewicz, Marcin et al.

Part of Nature Genetics, p. 338-342, 2012

• DOI for Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Oromotor, word retrieval, and dichotic listening performance in young adults with previous Rolandic epilepsy

Törnhage, Maria; Sandberg, Eva Nordahl; Lundberg, Staffan

Part of European journal of paediatric neurology, p. 139-144, 2020

• DOI for Oromotor, word retrieval, and dichotic listening performance in young adults with previous Rolandic epilepsy

A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin crease

Stattin, Eva-Lena; Johansson, Josefin; Gudmundsson, Sanna; Ameur, Adam et al.

Part of American Journal of Medical Genetics. Part A, p. 1405-1410, 2018

• DOI for A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin crease

Oxidative proteome alterations during skeletal muscle ageing

Lourenço Dos Santos, Sofia; Baraibar, Martin A; Lundberg, Staffan; Eeg-Olofsson, Orvar et al.

Part of Redox Biology, p. 267-274, 2015

• DOI for Oxidative proteome alterations during skeletal muscle ageing
• Download full text (pdf) of Oxidative proteome alterations during skeletal muscle ageing

Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus

Livingston, John H; Mayer, Josephine; Jenkinson, Emma; Kasher, Paul et al.

Part of Neuropediatrics, p. 175-182, 2014

• DOI for Leukoencephalopathy with Calcifications and Cysts: A Purely Neurological Disorder Distinct from Coats Plus

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Anderson, Beverley H.; Kasher, Paul R.; Mayer, Josephine; Szynkiewicz, Marcin et al.

Part of Nature Genetics, p. 338-342, 2012

• DOI for Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Incomplete hippocampal inversion-is there a relation to epilepsy?

Bajic, Dragan; Kumlien, Eva; Mattsson, Peter; Lundberg, Staffan et al.

Part of European Radiology, p. 2544-2550, 2009

• DOI for Incomplete hippocampal inversion-is there a relation to epilepsy?

Incomplete inversion of the hippocampus: a common developmental anomaly

Bajic, Dragan; Wang, Cheng; Kumlien, Eva; Mattsson, Peter et al.

Part of European Radiology, p. 138-142, 2008

• DOI for Incomplete inversion of the hippocampus: a common developmental anomaly

Children with rolandic epilepsy have abnormalities of oromotor and dichotic listening performance

Lundberg, Staffan; Frylmark, Astrid; Eeg-Olofsson, Orvar

Part of Developmental Medicine & Child Neurology, p. 603-608, 2005

• DOI for Children with rolandic epilepsy have abnormalities of oromotor and dichotic listening performance

Children with rolandic epilepsy have abnormalities of oromotor and dichotic listening performance

Lundberg, S; Frylmark, A; Eeg-Olofsson, O

Part of Developmental Medicine & Child Neurology, p. 603-608, 2005

• DOI for Children with rolandic epilepsy have abnormalities of oromotor and dichotic listening performance

Development of cognitive functions in children with rolandic epilepsy

Lindgren, Åsa; Kihlgren, Margareta; Melin, Lennart; Croona, Cecilia et al.

Part of Epilepsy & Behavior, p. 903-910, 2004