M Andersson Grönlund

Summary

Country: Sweden

Publications

  1. doi request reprint Ophthalmological findings in children and adolescents with Silver-Russell syndrome
    M Andersson Grönlund
    Institute of Neuroscience and Physiology Ophthalmology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden
    Br J Ophthalmol 95:637-41. 2011
  2. doi request reprint Ophthalmological findings in children and young adults with genetically verified mitochondrial disease
    M A Grönlund
    Department of Paediatric Ophthalmology, The Queen Silvia Children s Hospital, Sahlgrenska University Hospital Ostra, SE 416 85 Gothenburg, Sweden
    Br J Ophthalmol 94:121-7. 2010
  3. doi request reprint Relationships between ophthalmological and neuropaediatric findings in children adopted from Eastern Europe
    Marita Andersson Grönlund
    Institute of Neuroscience and Physiology Ophthalmology, Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden
    Acta Ophthalmol 88:227-34. 2010
  4. ncbi request reprint Visual function and ocular features in children and adolescents with attention deficit hyperactivity disorder, with and without treatment with stimulants
    M A Grönlund
    Section of Ophthalmology, Institute of Clinical Neuroscience, The Sahlgrenska Academy at Goteborg University, Goteborg, Sweden
    Eye (Lond) 21:494-502. 2007
  5. ncbi request reprint The effects of endurance training in persons with a hereditary myosin myopathy
    K S Sunnerhagen
    Department of Clinical Neuroscience Rehabilitation Medicine, Sahlgrenska Academy, Goteborg University, Goteborg, Sweden
    Acta Neurol Scand 110:80-6. 2004
  6. ncbi request reprint New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7
    N Darin
    Department of Pediatrics, Sahlgrenska University Hospital, Goteborg, Sweden
    Neurology 68:2041-2. 2007
  7. ncbi request reprint Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency
    N Darin
    Department of Pediatrics, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 34:311-7. 2003
  8. ncbi request reprint Myopathies associated with myosin heavy chain mutations
    A Oldfors
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Acta Myol 23:90-6. 2004
  9. ncbi request reprint Two new mutations in the MTATP6 gene associated with Leigh syndrome
    A R Moslemi
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 36:314-8. 2005
  10. doi request reprint Progressive encephalopathy and complex I deficiency associated with mutations in MTND1
    A R Moslemi
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 39:24-8. 2008

Detail Information

Publications12

  1. doi request reprint Ophthalmological findings in children and adolescents with Silver-Russell syndrome
    M Andersson Grönlund
    Institute of Neuroscience and Physiology Ophthalmology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden
    Br J Ophthalmol 95:637-41. 2011
    ..To evaluate ophthalmological findings in children with Silver-Russell syndrome (SRS)...
  2. doi request reprint Ophthalmological findings in children and young adults with genetically verified mitochondrial disease
    M A Grönlund
    Department of Paediatric Ophthalmology, The Queen Silvia Children s Hospital, Sahlgrenska University Hospital Ostra, SE 416 85 Gothenburg, Sweden
    Br J Ophthalmol 94:121-7. 2010
    ..To describe ophthalmological phenotypes in patients with mitochondrial disease and known genotypes...
  3. doi request reprint Relationships between ophthalmological and neuropaediatric findings in children adopted from Eastern Europe
    Marita Andersson Grönlund
    Institute of Neuroscience and Physiology Ophthalmology, Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden
    Acta Ophthalmol 88:227-34. 2010
    ..This study aimed to evaluate and relate visual function, ocular dimensions and neuropaediatric findings in adoptees from Eastern Europe...
  4. ncbi request reprint Visual function and ocular features in children and adolescents with attention deficit hyperactivity disorder, with and without treatment with stimulants
    M A Grönlund
    Section of Ophthalmology, Institute of Clinical Neuroscience, The Sahlgrenska Academy at Goteborg University, Goteborg, Sweden
    Eye (Lond) 21:494-502. 2007
    ..To investigate visual function and ocular features in children with attention deficit hyperactivity disorder (AD/HD) and establish whether treatment with stimulants is reflected in functioning of the visual system...
  5. ncbi request reprint The effects of endurance training in persons with a hereditary myosin myopathy
    K S Sunnerhagen
    Department of Clinical Neuroscience Rehabilitation Medicine, Sahlgrenska Academy, Goteborg University, Goteborg, Sweden
    Acta Neurol Scand 110:80-6. 2004
    ..To evaluate muscle performance and its consequences in eight individuals with a hereditary myopathy and the effects of an 8-week endurance training program...
  6. ncbi request reprint New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7
    N Darin
    Department of Pediatrics, Sahlgrenska University Hospital, Goteborg, Sweden
    Neurology 68:2041-2. 2007
  7. ncbi request reprint Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency
    N Darin
    Department of Pediatrics, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 34:311-7. 2003
    ....
  8. ncbi request reprint Myopathies associated with myosin heavy chain mutations
    A Oldfors
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Acta Myol 23:90-6. 2004
    ..These patients showed slowly progressive muscle weakness but no overt cardiomyopathy. These two muscle diseases, which are caused by mutations in MyHC, form the basis of a novel entity: "Myosin myopathies"...
  9. ncbi request reprint Two new mutations in the MTATP6 gene associated with Leigh syndrome
    A R Moslemi
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 36:314-8. 2005
    ..This mutation was absent in the patient's parents and sister suggesting that the mutation was de novo. Our findings expand the spectrum of mutations causing LS and emphasize the role of MTATP6 gene mutations in pathogenesis of LS...
  10. doi request reprint Progressive encephalopathy and complex I deficiency associated with mutations in MTND1
    A R Moslemi
    Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
    Neuropediatrics 39:24-8. 2008
    ..The findings in this patient as well as in patient 2 demonstrate new clinical expressions of mutations in MTND1. The findings in patient 2 also illustrates that MTND mutations may be pathogenic even at a low percentage...
  11. ncbi request reprint Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
    H Tajsharghi
    Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden
    Neurology 58:780-6. 2002
    ..The current study was undertaken to investigate the relation between expression of the mutant MyHC IIa and pathologic changes in muscle...
  12. ncbi request reprint Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles
    N Darin
    Department of Pediatrics, Sahlgrenska University Hospital, Goteborg, Sweden
    Ann Neurol 44:242-8. 1998
    ..These findings suggests that this new disease should be classified as a variant of hereditary inclusion body myopathy...