G Malm

Summary

Affiliation: Karolinska University Hospital
Country: Sweden

Publications

  1. ncbi Congenital cytomegalovirus infections
    Gunilla Malm
    Department of Pediatrics, Karolinska University Hospital, Huddinge, S 14186 Stockholm, Sweden
    Semin Fetal Neonatal Med 12:154-9. 2007
  2. ncbi Effect of maternal herpes simplex virus (HSV) serostatus and HSV type on risk of neonatal herpes
    Elizabeth L Brown
    Department of Epidemiology, University of Washington, Seattle, WA 98122, USA, and Department of Pediatrics, Karolinska University Hospital, Stockholm, Sweden
    Acta Obstet Gynecol Scand 86:523-9. 2007
  3. ncbi Outcome in six children with mucopolysaccharidosis type IH, Hurler syndrome, after haematopoietic stem cell transplantation (HSCT)
    Gunilla Malm
    Department of Clinical Science, Intervention and Technology, Division of Paediatrics, Karolinska Institutet, Huddinge, Sweden
    Acta Paediatr 97:1108-12. 2008
  4. ncbi Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year period
    G Malm
    Division of Paediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Huddinge, Sweden
    Acta Paediatr 99:1253-7. 2010
  5. ncbi Neonatal herpes simplex virus infection
    Gunilla Malm
    Department of Clinical Science, Intervention and Technology, Division of Pediatrics, Karolinska University Hospital, Huddinge, Stockholm, Sweden
    Semin Fetal Neonatal Med 14:204-8. 2009
  6. ncbi Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence
    Gunilla Malm
    Division of Paediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institute, Karolinska University Hospital, Huddinge, Sweden
    Acta Paediatr 97:1577-81. 2008
  7. ncbi Ophthalmological findings in children with congenital toxoplasmosis. Report from a Swedish prospective screening study of congenital toxoplasmosis with two years of follow-up
    K T Fahnehjelm
    Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, Sweden
    Acta Ophthalmol Scand 78:569-75. 2000
  8. ncbi Congenital cytomegalovirus infection: the impact of cerebral cortical malformations
    M L Engman
    Department of Clinical Science, Intervention and Technology, Division of Pediatrics, Karolinska Institutet and Karolinska University Hospital, Huddinge, Stockholm, Sweden
    Acta Paediatr 99:1344-9. 2010
  9. ncbi A child with muscle-eye-brain disease. Ophthalmological and neurological characteristics
    K T Fahnehjelm
    Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, Sweden
    Acta Ophthalmol Scand 79:72-5. 2001
  10. ncbi Low incidence of toxoplasma infection during pregnancy and in newborns in Sweden
    B Evengard
    Dept Immunology, Microbiology and Pathology, Karolinska Institute at Huddinge University Hospital, Stockholm, Sweden
    Epidemiol Infect 127:121-7. 2001

Collaborators

Detail Information

Publications17

  1. ncbi Congenital cytomegalovirus infections
    Gunilla Malm
    Department of Pediatrics, Karolinska University Hospital, Huddinge, S 14186 Stockholm, Sweden
    Semin Fetal Neonatal Med 12:154-9. 2007
    ..Until vaccines and non-toxic antiviral agents are available, hygienic measures are important as prophylaxis. Treatment with antiviral agents may have a place in children with central nervous system involvement during the neonatal period...
  2. ncbi Effect of maternal herpes simplex virus (HSV) serostatus and HSV type on risk of neonatal herpes
    Elizabeth L Brown
    Department of Epidemiology, University of Washington, Seattle, WA 98122, USA, and Department of Pediatrics, Karolinska University Hospital, Stockholm, Sweden
    Acta Obstet Gynecol Scand 86:523-9. 2007
    ..We have conducted pooled analyses of data from 3 cohorts to evaluate the effects of maternal HSV serostatus and HSV type on risk of neonatal HSV acquisition and severity...
  3. ncbi Outcome in six children with mucopolysaccharidosis type IH, Hurler syndrome, after haematopoietic stem cell transplantation (HSCT)
    Gunilla Malm
    Department of Clinical Science, Intervention and Technology, Division of Paediatrics, Karolinska Institutet, Huddinge, Sweden
    Acta Paediatr 97:1108-12. 2008
    ..To follow-up six children with severe mucopolysaccharidosis type IH, Hurler syndrome, who were treated before 24 months of age with haematopoietic stem cell transplantation...
  4. ncbi Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year period
    G Malm
    Division of Paediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Huddinge, Sweden
    Acta Paediatr 99:1253-7. 2010
    ..The aim of this study was to present the natural clinical course in children and adolescents with MPS III diagnosed during a 30-year period in Sweden...
  5. ncbi Neonatal herpes simplex virus infection
    Gunilla Malm
    Department of Clinical Science, Intervention and Technology, Division of Pediatrics, Karolinska University Hospital, Huddinge, Stockholm, Sweden
    Semin Fetal Neonatal Med 14:204-8. 2009
    ..Neurological follow-up and training programs to minimize the consequences of a disability are important clinical aspects...
  6. ncbi Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence
    Gunilla Malm
    Division of Paediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institute, Karolinska University Hospital, Huddinge, Sweden
    Acta Paediatr 97:1577-81. 2008
    ..The aim of this study was to estimate the incidence and prevalence of mucopolysaccharidoses (MPS disorders) in Scandinavia...
  7. ncbi Ophthalmological findings in children with congenital toxoplasmosis. Report from a Swedish prospective screening study of congenital toxoplasmosis with two years of follow-up
    K T Fahnehjelm
    Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, Sweden
    Acta Ophthalmol Scand 78:569-75. 2000
    ..Congenital toxoplasmosis may lead to severe visual impairment or neurological sequelae in the child...
  8. ncbi Congenital cytomegalovirus infection: the impact of cerebral cortical malformations
    M L Engman
    Department of Clinical Science, Intervention and Technology, Division of Pediatrics, Karolinska Institutet and Karolinska University Hospital, Huddinge, Stockholm, Sweden
    Acta Paediatr 99:1344-9. 2010
    ..The aim of this study was to investigate the prevalence of congenital cytomegalovirus infections in a cohort of children with neurological disability and cerebral cortical malformations recognized by neuroimaging...
  9. ncbi A child with muscle-eye-brain disease. Ophthalmological and neurological characteristics
    K T Fahnehjelm
    Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, Sweden
    Acta Ophthalmol Scand 79:72-5. 2001
    ..To describe a child with Muscle-Eye-Brain disease (MEB), one of three types of congenital muscular dystrophy associated with ocular abnormalities...
  10. ncbi Low incidence of toxoplasma infection during pregnancy and in newborns in Sweden
    B Evengard
    Dept Immunology, Microbiology and Pathology, Karolinska Institute at Huddinge University Hospital, Stockholm, Sweden
    Epidemiol Infect 127:121-7. 2001
    ..7% and in the Stockholm area 14.0%. The incidence of infection during pregnancy was low, as the birth prevalence of congenital toxoplasmosis. Neonatal screening warrants consideration in view of the low cost and feasibility...
  11. ncbi Ocular findings in four children with mucopolysaccharidosis I-Hurler (MPS I-H) treated early with haematopoietic stem cell transplantation
    Kristina Teär Fahnehjelm
    Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
    Acta Ophthalmol Scand 84:781-5. 2006
    ..To present visual functions and ocular findings in four children with mucopolysaccharidosis I-Hurler (MPS I-H) treated early with stem cell transplantation (SCT)...
  12. ncbi [Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis]
    Gunilla Malm
    Barnens sjukhus, Huddinge Universitetssjukhus
    Lakartidningen 99:1804-9. 2002
    ....
  13. ncbi Neuropsychologic outcomes in children with neonatal herpes encephalitis
    Mona Lisa Engman
    Division of Pediatrics, Department of Clinical Science, Intervention, and Technology, Karolinska University Hospital, Huddinge, Sweden
    Pediatr Neurol 38:398-405. 2008
    ..Neuropsychologic assessment is essential in the habilitation of the child, and a prerequisite for the evaluation of new treatments and for the assessment of deterioration of cerebral function related to relapses...
  14. ncbi Detection of herpes simplex virus DNA in dried blood spots making a retrospective diagnosis possible
    Ilona Lewensohn-Fuchs
    Department of Immunology, Microbiology and Pathology, Division of Clinical Virology, Karolinska Institutet, F 68 Huddinge University Hospital, 14186 Stockholm, Sweden
    J Clin Virol 26:39-48. 2003
    ....
  15. ncbi 1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family
    Karen M Lower
    Eur J Hum Genet 12:787-9. 2004
  16. ncbi Allogeneic hematopoietic stem cell transplantation for inherited disorders: experience in a single center
    Olle Ringden
    Center for Allogeneic Stem Cell Transplantation, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden
    Transplantation 81:718-25. 2006
    ..Allogeneic hematopoietic stem cell transplantation (ASCT) is a possible cure for many inherited disorders...
  17. ncbi Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
    Jacqueline Schoumans
    Department of Molecular Medicine and Surgery, Karolinska Institute, Karolinska University Hospital Solna, Stockholm, Sweden
    Eur J Hum Genet 15:143-9. 2007
    ..However, in a considerable proportion of individuals demonstrating the CdLS phenotype, mutations in any of these two genes are not found and other potential loci harboring additional CdLS-causing genes should be considered...