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How do group workers respond to suicidal behavior? Experiences and perceptions of suicidal female adolescents residing in secure residential youth care in the Netherlands

PloS one, 2023-03, Vol.18 (3), p.e0283744-e0283744

2023

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Adolescent Loneliness and Social Skills: Agreement and Discrepancies Between Self-, Meta-, and Peer-Evaluations

Journal of youth and adolescence, 2016-12, Vol.45 (12), p.2406-2416

2016

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Mindfulness-based stress reduction intervention for elementary school teachers: a mixed method study

Trials, 2021-11, Vol.22 (1), p.826-10, Article 826

2021

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Interaction between dopamine D2 receptor genotype and parental rule-setting in adolescent alcohol use: evidence for a gene-parenting interaction

Molecular psychiatry, 2010-07, Vol.15 (7), p.727-735

2010

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Positive parenting and its mediating role in the relationship between parental resilience and quality of life in children with developmental disabilities in Java Island, Indonesia

Research in developmental disabilities, 2021-05, Vol.112, p.103911-103911, Article 103911

2021

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Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Journal of medical genetics, 2010-08, Vol.47 (8), p.507-512

2010

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Prospective associations between loneliness and emotional intelligence

Journal of adolescence (London, England.), 2015-02, Vol.39 (1), p.40-48

2015

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Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

American journal of human genetics, 1999-02, Vol.64 (2), p.479-494

1999

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Measuring safety perceptions of students with behavioural problems in special education: A validation study of the safe at school questionnaire

British journal of special education, 2024-03, Vol.51 (1), p.60-70

2024

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Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation

Molecular human reproduction, 2005-03, Vol.11 (3), p.223-228

2005

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Efficacy of carnitine in the treatment of children with attention-deficit hyperactivity disorder

Prostaglandins, leukotrienes and essential fatty acids, 2002-07, Vol.67 (1), p.33-38

2002

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Residential Youth Care Combined with Systemic Interventions: Exploring Relationships between Family-Centered Care and Outcomes

Residential treatment for children & youth, 2022-01, Vol.39 (1), p.34-56

2022

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A simplified and reliable assay for complex I in human blood lymphocytes

Journal of immunological methods, 2007-09, Vol.326 (1), p.76-82

2007

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Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

American journal of human genetics, 1996-04, Vol.58 (4), p.703-711

1996

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Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset

Annals of neurology, 1998-04, Vol.43 (4), p.540-544

1998

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Adolescent Personality Factors in Self-Ratings and Peer Nominations and Their Prediction of Peer Acceptance and Peer Rejection

Journal of personality assessment, 1997-12, Vol.69 (3), p.534-554

1997

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Pearson syndrome and the role of deletion dimers and duplications in the mtDNA

Journal of inherited metabolic disease, 2004-01, Vol.27 (1), p.47-55

2004

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Parental Resilience and Quality of Life in Children with Developmental Disabilities in Indonesia: The Role of Protective Factors

Journal of developmental and physical disabilities, 2023-10, Vol.35 (5), p.743-758

2023

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Parental Resilience and the Quality of Life of Children with Developmental Disabilities in Indonesia

International journal of disability, development, and education, 2022-11, Vol.69 (6), p.1946-1962

2022

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Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia

The Journal of pediatrics, 1996-05, Vol.128 (5), p.679-683

1996

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X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts

Journal of inherited metabolic disease, 1996-01, Vol.19 (2), p.157-160

1996

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Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

Human genetics, 1999-07, Vol.105 (1-2), p.157-161

1999

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Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

Pediatrics (Evanston), 2000-09, Vol.106 (3), p.596-600

2000

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Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

The Journal of pediatrics, 1996-05, Vol.128 (5), p.683-687

1996

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Mitochondrial injury : Lessons from the fialuridine trial

Drug safety, 1997-07, Vol.17 (1), p.1-7

1997

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How do group workers respond to suicidal behavior? Experiences and perceptions of suicidal female adolescents residing in secure residential youth care in the Netherlands

Adolescent Loneliness and Social Skills: Agreement and Discrepancies Between Self-, Meta-, and Peer-Evaluations

Mindfulness-based stress reduction intervention for elementary school teachers: a mixed method study

Interaction between dopamine D2 receptor genotype and parental rule-setting in adolescent alcohol use: evidence for a gene-parenting interaction

Positive parenting and its mediating role in the relationship between parental resilience and quality of life in children with developmental disabilities in Java Island, Indonesia

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Prospective associations between loneliness and emotional intelligence

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Measuring safety perceptions of students with behavioural problems in special education: A validation study of the safe at school questionnaire

Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation

Efficacy of carnitine in the treatment of children with attention-deficit hyperactivity disorder

Residential Youth Care Combined with Systemic Interventions: Exploring Relationships between Family-Centered Care and Outcomes

A simplified and reliable assay for complex I in human blood lymphocytes

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset

Adolescent Personality Factors in Self-Ratings and Peer Nominations and Their Prediction of Peer Acceptance and Peer Rejection

Pearson syndrome and the role of deletion dimers and duplications in the mtDNA

Parental Resilience and Quality of Life in Children with Developmental Disabilities in Indonesia: The Role of Protective Factors

Parental Resilience and the Quality of Life of Children with Developmental Disabilities in Indonesia

Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia

X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts

Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

Mitochondrial injury : Lessons from the fialuridine trial

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