7 results on '"Gyato K"'
Search Results
2. Evaluation of a social-skills training group intervention with children treated for brain tumors: a pilot study.
- Author
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Barakat, L.P., Hetzke, J.D., Foley, B., Carey, M.E., Gyato, K., Phillips, P.C., Barakat, Lamia P, Hetzke, Jennifer D, Foley, Bernadette, Carey, Marissa E, Gyato, Kunsang, and Phillips, Peter C
- Subjects
CHILDREN ,SOCIAL skills ,BRAIN tumors - Abstract
Objective: To evaluate the effectiveness of a manual-based, social-skills training, group intervention to improve social skills and social functioning of children treated for brain tumors, and to assess the impact of cognitive functioning on the effectiveness of the intervention.Methods: Three social-skills training group interventions, each comprised of 5 to 7 children ages 8 to 14 years, were conducted. A parent component was included. In total, 13 children and their parents and teachers completed standard measures prior to and 9 months after the intervention. Children participated in a neuropsychological test battery at baseline.Results: Social skills and social functioning variables changed in the direction of improved functioning, with several scores showing significant improvement from baseline to the follow-up assessment. Small to medium effect sizes were documented. Higher verbal and nonverbal functioning were associated with greater improvement.Conclusions: Findings are suggestive of the potential effectiveness of social-skills training in groups for children with brain tumors. Multisite, randomized, controlled studies are recommended as the next step. [ABSTRACT FROM AUTHOR]- Published
- 2003
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3. Reduced frontal white matter integrity in early-onset schizophrenia: a preliminary study.
- Author
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Kumra S, Ashtari M, McMeniman M, Vogel J, Augustin R, Becker DE, Nakayama E, Gyato K, Kane JM, Lim K, and Szeszko P
- Subjects
- Adolescent, Age of Onset, Anisotropy, Child, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Mental Processes, Pilot Projects, Psychiatric Status Rating Scales, Schizophrenic Psychology, Brain pathology, Schizophrenia pathology
- Abstract
Background: Research suggests that brain frontal white matter (WM) might be qualitatively altered in adolescents with early onset schizophrenia (EOS). Diffusion tensor imaging provides a relatively new approach for quantifying possible connectivity of WM in vivo., Methods: Diffusion tensor imaging was used to examine the WM integrity of frontal regions at seven levels from 25 mm above to 5 mm below the anterior commissure-posterior commissure (AC-PC) plane. Three other regions were examined: the occipital region at the AC-PC plane and the genu and splenium of the corpus callosum. Fractional anisotropy was compared between 12 adolescents (nine male, 3 female) with EOS (onset of psychotic symptoms by age 18 years) and nine age-similar healthy comparison subjects (six male, 3 female)., Results: Adolescents with EOS had significantly reduced fractional anisotropy in the frontal WM at the AC-PC plane in both hemispheres and in the occipital WM at the AC-PC plane in the right hemisphere., Conclusions: These preliminary data support a hypothesis that alterations in brain WM integrity occur in adolescents with EOS. Abnormalities found in this study were similar to those reported in adults with chronic schizophrenia. Additional studies are needed to assess whether there is progression of WM abnormalities in schizophrenia., (Copyright 2004 Society of Biological Psychiatry)
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- 2004
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4. A critical review of the clinical effects of therapeutic irradiation damage to the brain: the roots of controversy.
- Author
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Armstrong CL, Gyato K, Awadalla AW, Lustig R, and Tochner ZA
- Subjects
- Adult, Brain surgery, Brain Neoplasms drug therapy, Brain Neoplasms surgery, Child, Cognition Disorders etiology, Humans, Radiation Dosage, Radiosurgery, Stroke drug therapy, Stroke surgery, Time Factors, Brain radiation effects, Brain Neoplasms radiotherapy, Radiotherapy adverse effects, Stroke radiotherapy
- Abstract
We critically examined the damaging affects of therapeutic irradiation by comparing results from cross-disciplinary studies of early- and late-delayed radiotherapy effects. Focus is attained by concentrating on clinical treatment issues (volume of brain, dose, timing of effects, age, modality types, and stereotactic treatment techniques), rather than on methodological means or problems, which is necessary to understand the mechanisms and characteristics of radiotherapy-induced behavioral dysfunction including cognition. We make observations and hypotheses about the actual risks from radiotherapy that could be informative in the treatment decision process, and which may lessen the concerns of some patients and their families about the risks they take when receiving radiation. Conditions that predispose to radiation injury are reviewed: (1) higher doses even to part of the brain versus lower doses to the whole brain, (2) combined treatment modalities, (3) malignancy itself, (4) radiation early during postnatal brain development, and (5) late-delayed effects (more than 3 years posttreatment). Current neurocognitive frameworks for understanding cognitive change over time in children and adults are summarized, along with the literature on effects of brain tumors and treatment on depression. No studies have as yet identified candidate brain regions that are more sensitive to radiotherapy. Two studies have provided early, preliminary evidence for a specific vulnerability of visual attention/memory to the early stage of late radiation damage. Furthermore, radiation effects appear severe only in a minority of patients. Risk is related to direct and indirect effects of cancer type, concurrent clinical factors, and premorbid risk factors.
- Published
- 2004
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5. Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency.
- Author
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Gyato K, Wray J, Huang ZJ, Yudkoff M, and Batshaw ML
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- Adult, Age of Onset, Amino Acid Metabolism, Inborn Errors genetics, Biomarkers, Female, Humans, Middle Aged, Mutation, Neuropsychological Tests, Ornithine Carbamoyltransferase genetics, Polymorphism, Single-Stranded Conformational, Urea metabolism, Amino Acid Metabolism, Inborn Errors physiopathology, Cognition physiology, Heterozygote, Ornithine Carbamoyltransferase Deficiency Disease, Phenotype
- Abstract
We compared neurocognitive indices with clinical status, mutation analysis, and urea synthetic capacity in 19 women heterozygous for ornithine transcarbamylase deficiency. Although as a group, these women had average IQ scores, they displayed a specific neuropsychological phenotype with significant strengths in verbal intelligence, verbal learning, verbal memory, and reading, and significant weaknesses in fine motor dexterity/speed and nonsignificant weaknesses in nonverbal intelligence, visual memory, attention/executive skills, and math. This suggests selective vulnerability of white matter and better preservation of gray matter. When the group was divided into symptomatic and asymptomatic subgroups, based on either clinical history or residual urea synthetic capacity, the asymptomatic subgroup outperformed the symptomatic subgroup on all tested domains of neuropsychological functioning. Furthermore, the amount of residual urea synthetic capacity was predictive of several end point cognitive measures. There was no correlation between neonatal versus late-onset mutation or between normal or abnormal allopurinol challenge and neuropsychological outcome. In sum, we identified a specific metabolic and neurocognitive phenotype in women heterozygous for ornithine transcarbamylase deficiency. The findings support the importance of maintaining meticulous metabolic control in children with urea cycle disorders, because even mildly symptomatic subjects demonstrate cognitive deficits.
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- 2004
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6. Neuropsychological functioning and social functioning of survivors of pediatric brain tumors: evidence of nonverbal learning disability.
- Author
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Carey ME, Barakat LP, Foley B, Gyato K, and Phillips PC
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- Brain Damage, Chronic psychology, Child, Female, Humans, Learning Disabilities psychology, Male, Postoperative Complications psychology, Psychometrics statistics & numerical data, Reference Values, Verbal Learning, Brain Damage, Chronic diagnosis, Brain Neoplasms surgery, Learning Disabilities diagnosis, Neuropsychological Tests statistics & numerical data, Postoperative Complications diagnosis, Social Adjustment, Survivors psychology
- Abstract
The purpose of the study was to examine if survivors of pediatric brain tumors exhibit a pattern of performance consistent with nonverbal learning disability (NVLD) and to explore the relationship between neuropsychological and social functioning in these children. A comprehensive neuropsychological battery and objective measures of psychosocial function designed to assess NVLD were administered to 15 survivors of brain tumors, ages 8-12 years. Despite the small sample size, a trend for better verbal skills compared to nonverbal skills was found using composite scores. Parents reported significant social deficits and a tendency for greater internalizing behavior problems as expected in NVLD. Additionally, there was a trend for a positive association between nonverbal scores and social function. Further research is needed to determine if the NVLD pattern observed is attributable to white matter damage of the right hemisphere. Routine neuropsychological and psychosocial assessment and intervention are indicated.
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- 2001
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7. Metachromatic leukodystrophy and nonverbal learning disability: neuropsychological and neuroradiological findings in heterozygous carriers.
- Author
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Weber Byars AM, McKellop JM, Gyato K, Sullivan T, and Franz DN
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- Adolescent, Adult, Child, Child, Preschool, Female, Genotype, Heterozygote, Humans, Learning Disabilities diagnosis, Learning Disabilities enzymology, Leukodystrophy, Metachromatic genetics, Leukodystrophy, Metachromatic pathology, Magnetic Resonance Imaging, Male, Phenotype, Syndrome, Brain pathology, Cerebroside-Sulfatase deficiency, Family psychology, Learning Disabilities genetics, Leukodystrophy, Metachromatic psychology, Neuropsychological Tests
- Abstract
Metachromatic leukodystrophy (MLD) is an autosomal recessive neurodegenerative disorder due to deficiency of the enzyme arylsulfatase A that leads to progressive, diffuse demyelination. The syndrome of nonverbal learning disability has been attributed to white matter abnormality and has been reported in children with this disorder and in some healthy family member carriers of gene. We examined the neuropsychologic profiles and MRIs of eight members of the family of a 7-year-old girl with this disease, all of whom were heterozygous carriers of the mutation and five of whom were also carriers of the MLD pseudodeficiency gene. All had low normal levels of arylsulfatase A, and seven of the eight had average or better profiles across all assessed neuropsychological domains. The patient's younger sister had a profile with features of the syndrome of nonverbal learning disability despite a normal MRI, whereas two members with minor white matter findings did not. This family does not provide evidence for the syndrome of nonverbal learning disability in heterozygous carriers of the gene for MLD, even when associated with the MLD pseudodeficiency gene.
- Published
- 2001
- Full Text
- View/download PDF
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