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Search: WFRF:(Samuelsson Lena) > (2005-2009)

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  • Andersson-Roswall, Lena, 1965, et al. (author)
  • Verbal cognition and attention deficits do not explain the verbal memory decline associated with pharmacoresistant partial epilepsy
  • 2007
  • In: Epilepsy & Behavior. - : Elsevier BV. - 1525-5050. ; 11:3, s. 413-420
  • Journal article (peer-reviewed)abstract
    • The aim of this study was to explore whether change in verbal memory with time in patients with epilepsy is influenced by performance on tasks assessing verbal cognition or attention/processing speed. Thirty-six patients and twenty-five healthy controls were tested twice with median retest intervals of 4.8 and 3.1 years, respectively. Aspects of verbal memory, verbal cognition, and attention/processing speed were assessed. Decline in one verbal memory variable (Cronholm–Molander Memory Test Paired Associates—Delayed Recall) was the strongest correlate of epilepsy. The second strongest correlate was a decrease in one attention/processing speed variable (Digit Symbol). The relationship between decline in verbal memory and epilepsy was not influenced by the decline in attention/processing speed, and the results did not support the notion that limited mental reserves as reflected in impaired verbal cognition or attention/processing speed can explain the relationship between verbal memory and epilepsy.
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  • Dellve, Lotta, 1965, et al. (author)
  • Stress and well-being among parents of children with rare diseases: a prospective intervention study
  • 2006
  • In: Journal of Advanced Nursing. - Oxford : Wiley. - 0309-2402 .- 1365-2648. ; 53:4, s. 392-402
  • Journal article (peer-reviewed)abstract
    • AIM: This paper reports a study to assess stress, well-being and supportive resources experienced by mothers and fathers of children with rare disabilities, and how these variables were affected by an intensive family competence intervention. BACKGROUND: Despite diagnosis-specific studies, little overall knowledge exists about life-consequences for families of children with rare disorders. METHOD: We used a prospective design with baseline data and two follow-ups (at 6 and 12 months) after an intervention. The intervention aimed at empowering parents in managing their child's disability. Parents from all parts of Sweden visiting a national centre for families of children with rare disabilities were consecutively selected (n = 136 mothers, 108 fathers). Instruments of parental stress, social support, self-rated health, optimism and life satisfaction and perceived physical or psychological strain were used. Stratified analyses were carried out for mothers and fathers, and related to parental demands: single mothers, full-time employment, participation in a parent association, child's age and type of disability. RESULTS: We found high parental stress, physical and emotional strain among mothers, especially among single mothers. Fathers showed high stress related to incompetence, which decreased after the intervention. Decreased strain was found among full-time working mothers and fathers after the intervention. Parents' perceived knowledge and active coping and mothers' perceived social support were increased at follow-up. Factors related to parents' overall life satisfaction (57-70% explained variance) changed after the intervention, from being more related to internal demands (perceived strain, incompetence and social isolation) to other conditions, such as problems related to spouse, paid work and social network. CONCLUSION: Parents, especially fathers and full-time working parents, may benefit from an intensive family competence programme.
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  • Ekström, Anne-Berit, 1960, et al. (author)
  • Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms
  • 2008
  • In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. - : Wiley. - 1552-4841 .- 1552-485X. ; 147B:6, s. 918-926
  • Journal article (peer-reviewed)abstract
    • Myotonic dystrophy type 1 (DM1) is an autosomal dominant disorder, caused by an expansion of a CTG triplet repeat in the DMPK gene. The aims of the present study were to classify a cohort of children with DM1, to describe their neuropsychiatric problems and cognitive level, to estimate the size of the CTG expansion, and to correlate the molecular findings with the neuropsychiatric problems. Fifty-seven children and adolescents (26 females; 31 males) with DM1 (CTG repeats > 40) were included in the study. The following instruments were used: Autism Diagnostic Interview-Revised (ADI-R), 5-15, Griffiths Mental Development Scales, and the Wechsler Scales. Based on age at onset and presenting symptoms, the children were divided into four DM1 groups; severe congenital (n = 19), mild congenital (n = 18), childhood (n = 18), and classical DM1 (n = 2). Forty-nine percent had an autism spectrum disorder (ASD) and autistic disorder was the most common diagnosis present in 35% of the subjects. Eighty-six percent of the individuals with DM1 had mental retardation (MR), most of them moderate or severe MR. ASD was significantly correlated with the DM1 form; the more severe the form of DM1, the higher the frequency of ASD. The frequency of ASD increased with increasing CTG repeat expansions. ASD and/or other neuropsychiatric disorders such as attention deficit hyperactivity disorder, and Tourette's disorder were found in 54% of the total DM1. group. In conclusion, awareness of ASD comorbidity in DM1. is essential. Further studies are warranted to elucidate the molecular etiology causing neurodevelopmental symptoms such as ASD and MR in DM1. (c) 2008 Wiley-Liss, Inc.
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  • Engman, Elisabeth, 1942, et al. (author)
  • Serial cognitive change patterns across time after temporal lobe resection for epilepsy
  • 2006
  • In: Epilepsy Behav. - : Elsevier BV. - 1525-5050. ; 8:4, s. 765-72
  • Journal article (peer-reviewed)abstract
    • Longitudinal cognitive outcome with respect to general cognitive status and memory at the group and individual levels was studied 10 years after temporal lobe resection for epilepsy. Twenty-five patients who had undergone a medium-term follow-up (T2, median = 2.7 years) also underwent a long-term follow-up (T3, median = 9.8 years). At the group level, there was a significant increment across time, partly due to practice, in IQ (P value from 0.049 to <0.0001) but not in memory variables. On the basis of the normative interval of reassessed matched controls, the analysis at the individual level of change from baseline to T2 disclosed decrements in 12-29% of the patients and increments in 8-21%. These proportions diminished at T3 (0-12 and 0-16%) and the dominating pattern of Performance IQ and verbal memory was a return toward baseline. These findings make the interpretation of an initial (T2) postoperative increment or decrement more problematic and underline the need for a comprehensive evaluation across time, including both at the group and individual levels.
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  • Eriksson-Gustavsson, Anna-Lena, 1949-, et al. (author)
  • Didaktiska samtal i specialpedagogiska kontexter : En studie av undervisning i grundläggande svenska och matematik
  • 2007
  • Reports (other academic/artistic)abstract
    • Larmrapporter om hur  svenska  elever  presterar  har  under  senare tid avlöst varandra. I de senaste nationella och också internationellt järnförande  studierna   av  elevers  skriftspråkliga  och  rnatematiska förmåga, har det visat sig att svenska  elever presterar  sämre såväl inom  "matematikens  som  svenskans   områden"   (NU  2003, PISA, Tirnss). Den internationella  OECD-studien PISA visar t.ex. att 17% av svenska elever i skolår 9 presterar  på den lägsta nivån i matema­ tik. Vad gäller läsförståelsen så presterar 13 % av svenska elever på den lägsta nivån. Det är ingen orimlig tanke att dessa elever har va­ rit föremål för specialundervisning. Specialundervisningen och den specialpedagogiska  verksamheten   i  maternatik  och  svenska  lyfts implicit upp på agendan.Specialpedagogisk verksamhet, specialundervisning och special­ pedagogik,  har  under  senare  tid varit föremål  för studier,  diskus­ sioner och debatt i olika sammanhang (Börjesson, 1997; Haug, 1998, Persson, 1998; Nilholm, 2003; Brodin &  Lindstrand,  2004). Analys och  problematisering av  begreppen  norrnalitet  och avvikelse  har varit  centralt,  likaväl  som  bearbetning  av ideologiska  och teoretiska perspektiv  på  kunskapsområdet specialpedagogik I en  del studier har centrala  begrepp  analyserats  och problematiserats  för att bidra till utvecklingen  av en teoretisk  ram eftersom specialpedagogiken hittills ansetts  vara  ett kunskapsområde med en svag  teoriförank­ ring (Skrtic, 1988; Helldin, 1997). Andra studier med specialpedago­ gisk  inriktning   har  foku1 rat  organisatoriska  perspektiv  vad  gäller specialpedagogisk verksamhet.  Dessa studier  har berört specialun­ dervisningens  omfattning,  t.ex. antal elever som åtnjutit specialpe­ dagogiska  insatser  samt  orsaker  till dessa insatser  (Persson, 1998). De två ovan  beskrivna  perspektiven visar  på  den  tudelning som specialpedagogiken och  den  specialpedagogiska  kunskapen  idag kännetecknas  av. Det är  å ena sidan  den  politiska och norrnativa ideologiska diskursen  där norrnalitet och avvikelse problematiseras utifrån  det svenska  samhällets  krav  på likvärdighet,  jämställdhet, deltagande och demokrati. Å andra sidan finns den handlingsorien­ terade  diskursen  med fokus  på organisering,  resurser  och kompe­ tens. Den senare  praxisinriktade  forskningen  skiljer oftast inte på begreppen specialpedagogik  och specialundervisning och det är företrädesvis denna inriktning  som debatterats i press och media un­ der 90-talet och som vi senare ska visa behöver studeras  vad gäller undervisningen i företrädesvis ämnena matematik och svenska.
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  • Result 1-10 of 30
Type of publication
journal article (20)
reports (4)
book chapter (3)
conference paper (2)
licentiate thesis (1)
Type of content
peer-reviewed (20)
other academic/artistic (10)
Author/Editor
Samuelsson, Lena, 19 ... (6)
Hellström, Anna-Lena ... (2)
Bergbom, Ingegerd, 1 ... (2)
Fischer, J. (1)
Minthon, Lennart (1)
Theliander, Hans, 19 ... (1)
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Kere, J (1)
Sánchez, F. (1)
Abecasis, G (1)
Allen, M (1)
Barker, JNWN (1)
Burden, D (1)
Capon, F (1)
Christophers, E (1)
Elder, JT (1)
Gudjonsson, JE (1)
Huffmeier, U (1)
Jenisch, S (1)
Karason, A (1)
Nair, RP (1)
Novelli, G (1)
Prud'homme, JF (1)
Qin, ZHS (1)
Saarialho-Kere, U (1)
Stahle, M (1)
Stuart, P (1)
Tillman, D (1)
Traupe, H (1)
Trembath, R (1)
Valdimarsson, H (1)
Veal, C (1)
Voorhees, JJ (1)
Weichenthal, M (1)
Cluster 17 Collabora ... (1)
Nilsson, Staffan, 19 ... (1)
Knutsson, Susanne, 1 ... (1)
Hallberg, Lillemor R ... (1)
Strömberg, Dan, 1959 (1)
Kere, Juha (1)
Larsson, Christer (1)
Woxenius, Johan, 196 ... (1)
Lindblad, Bengt (1)
Wahlström, Jan, 1939 (1)
Dave, Göran, 1945 (1)
Asberg, Marie (1)
Karlsson, Björn (1)
Erhardt, Sophie (1)
Nilsson, Staffan (1)
Hagell, Peter (1)
Hansson, Oskar (1)
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University
University of Gothenburg (15)
Linköping University (12)
Lund University (4)
Karolinska Institutet (4)
Royal Institute of Technology (2)
Mid Sweden University (2)
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Chalmers University of Technology (2)
Linnaeus University (2)
University of Borås (2)
Kristianstad University College (1)
Uppsala University (1)
Luleå University of Technology (1)
Halmstad University (1)
Örebro University (1)
Jönköping University (1)
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Language
English (22)
Swedish (7)
Danish (1)
Research subject (UKÄ/SCB)
Medical and Health Sciences (11)
Social Sciences (7)
Natural sciences (3)
Engineering and Technology (3)

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