Staffan Lundberg

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

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

Ingår i European journal of paediatric neurology, s. 139-144, 2020

• DOI för 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.

Ingår i American Journal of Medical Genetics. Part A, s. 1405-1410, 2018

• DOI för 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.

Ingår i Redox Biology, s. 267-274, 2015

• DOI för Oxidative proteome alterations during skeletal muscle ageing
• Ladda ner fulltext (pdf) av 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.

Ingår i Neuropediatrics, s. 175-182, 2014

• DOI för 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.

Ingår i Nature Genetics, s. 338-342, 2012

• DOI för 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

Ingår i European journal of paediatric neurology, s. 139-144, 2020

• DOI för 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.

Ingår i American Journal of Medical Genetics. Part A, s. 1405-1410, 2018

• DOI för 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.

Ingår i Redox Biology, s. 267-274, 2015

• DOI för Oxidative proteome alterations during skeletal muscle ageing
• Ladda ner fulltext (pdf) av 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.

Ingår i Neuropediatrics, s. 175-182, 2014

• DOI för 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.

Ingår i Nature Genetics, s. 338-342, 2012

• DOI för 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.

Ingår i European Radiology, s. 2544-2550, 2009

• DOI för 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.

Ingår i European Radiology, s. 138-142, 2008

• DOI för 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

Ingår i Developmental Medicine & Child Neurology, s. 603-608, 2005

• DOI för 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

Ingår i Developmental Medicine & Child Neurology, s. 603-608, 2005

• DOI för 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.

Ingår i Epilepsy & Behavior, s. 903-910, 2004