Family Health Concept

subject area of

• ?-thalassemia in association with a new ?-chain hemoglobin variant [?116(g18)Arg?Leu]: Implications for carrier screening and prenatal diagnosis  Academic Article
• A Conceptual Model of the Factors Affecting the Recreation and Leisure Participation of Children with Disabilities  Academic Article
• A Family-based Intervention to Promote Healthy Lifestyles in an Aboriginal Community in Canada  Academic Article
• A Novel Type 2A von Willebrand Factor Mutation (V1499E) Associated With Variable Clinical Expression  Academic Article
• A case series of 72 neonates with renal vein thrombosis  Academic Article
• A comparison of risk factors associated with community-associated methicillin-resistant and -susceptibleStaphylococcus aureusinfections in remote communities  Academic Article
• A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic?  Academic Article
• A modified Delphi process to identify clinical and research priorities in patient and family centred critical care  Academic Article
• A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome  Academic Article
• Absence of germline p16INK4a alterations in p53 wild type Li-Fraumeni syndrome families  Academic Article
• Amoxicillin oral provocation challenge in a primary care clinic: a descriptive analysis  Academic Article
• An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13  Academic Article
• Are neonatal clinical practice guidelines truly evidence‐based? A case for incorporating family values and preferences  Academic Article
• Assessment of family needs in children with physical disabilities: development of a family needs inventory  Academic Article
• Associations and costs of parental symptoms of psychiatric distress in a multi-diagnosis group of children with special needs  Academic Article
• Asymptomatic thrombophilia—a family affair  Academic Article
• Beyond stereotypes of cerebral palsy: Exploring the lived experiences of young Canadians  Academic Article
• Bleeding disorders in neonates  Academic Article
• Blepharophimosis, minor facial anomalies, genital anomalies, and mental retardation: Report of two sibs with a unique syndrome  Academic Article
• Bringing the Family's Voice to Research  Academic Article
• CK8/18 expression, the basal phenotype, and family history in identifying BRCA1-associated breast cancer in the Ontario site of the Breast Cancer Family Registry  Academic Article
• Cancer diagnosis: An opportune time to help patients and their families stop smoking?  Academic Article
• Care recipients’ physical frailty is independently associated with subjective burden in informal caregivers in the community setting: a cross-sectional study  Academic Article
• Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency  Academic Article
• Chronicity of mental comorbidity in children with new‐onset physical illness  Academic Article
• Clinical features of facioscapulohumeral muscular dystrophy 2  Academic Article
• Clustering of motor and nonmotor traits in leucine-rich repeat kinase 2 G2019S Parkinson's disease nonparkinsonian relatives: A multicenter family study  Academic Article
• Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening  Academic Article
• Comparing the experiences of rural and urban family caregivers of the terminally ill  Academic Article
• Comparison of direct and indirect methods of estimating health state utilities for resource allocation: review and empirical analysis  Academic Article
• Connecting Families to Their Health Record and Care Team: The Use, Utility, and Impact of a Client/Family Health Portal at a Children’s Rehabilitation Hospital  Academic Article
• Coping with Dravet syndrome: parental experiences with a catastrophic epilepsy  Academic Article
• Cost comparison of genetic and clinical screening in families with hereditary hemorrhagic telangiectasia  Academic Article
• Creating “therapeutic landscapes” at home: The experiences of families of children with autism  Academic Article
• Deaths from asthma in New Zealand.  Academic Article
• Depressive symptoms among mothers of children with epilepsy: A review of prevalence, associated factors, and impact on children  Academic Article
• Determinants of participation in family and recreational activities of young children with cerebral palsy  Academic Article
• Development of a Parent-Proxy Quality-of-Life Chronic Cough-Specific Questionnaire  Academic Article
• Development of daily activities in school-age children with cerebral palsy  Academic Article
• Does Experience Influence Judgements of Pain Behaviour? Evidence from Relatives of Pain Patients and Therapists  Academic Article
• Early brain development in infants at high risk for autism spectrum disorder  Academic Article
• Early detection and intervention for obsessive-compulsive disorder in childhood and adolescence  Academic Article
• Effect of sibling number in the household and birth order on prevalence of Helicobacter pylori: a cross-sectional study  Academic Article
• Ethical Challenges in the Provision of Mental Health Services for Children and Families During Disasters  Academic Article
• Experiences of a low-intensity anticoagulation regimen for extended secondary prevention of venous thromboembolism  Academic Article
• Extending knowledge on inherited platelet disorders associated with thrombocytopenia  Academic Article
• Factors Influencing Family Participation in a Longitutdinal Study: Comparison of Pediatric and Healthy Samples  Academic Article
• Factors affecting the delivery of family-centered care in pediatric oncology  Academic Article
• Familial Aggregation of Psychiatric Disorders in a Community Sample of Adolescents  Academic Article
• Familial Amyotrophic Lateral Sclerosis  Academic Article
• Familial Factors Influence Level of Functioning in Pervasive Developmental Disorder  Academic Article
• Family History of Problem Drinking Is Associated With Less Sensitivity of Alcohol Demand to a Next-Day Responsibility  Academic Article
• Family needs of parents of children and youth with cerebral palsy  Academic Article
• Family-Centered Service for Children With Cerebral Palsy and Their Families: A Review of the Literature  Academic Article
• Family-centred services in the Netherlands: validating a self-report measure for paediatric service providers  Academic Article
• Family-oriented services in pediatric rehabilitation: a scoping review and framework to promote parent and family wellness  Academic Article
• For Which Glaucoma Suspects Is It Appropriate to Initiate Treatment?  Academic Article
• Gender differences in the effects of family adversity on the risk of onset of DSM-III-R social phobia  Academic Article
• Generalized epilepsy with febrile seizures plus: Further heterogeneity in a large family  Academic Article
• Genetic association of the GDNF alpha-receptor genes with schizophrenia and clozapine response  Academic Article
• Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24  Academic Article
• Group Interprofessional Chronic Pain Management in the Primary Care Setting: A Pilot Study of Feasibility and Effectiveness in a Family Health Team in Ontario  Academic Article
• Guelph Family Health Study: pilot study of a home-based obesity prevention intervention  Academic Article
• Guelph Family Health Study’s Home-Based Obesity Prevention Intervention Increases Fibre and Fruit Intake in Preschool-Aged Children  Academic Article
• Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family  Academic Article
• Hb Castilla [β32(B14)Leu → Arg] Caused by a De Novo Mutation  Academic Article
• Health status and health-related quality of life in survivors of cancer in childhood in Latin America: A MISPHO feasibility study  Academic Article
• Helping Families Cope with the Severe Stress of Dravet Syndrome  Academic Article
• Helping families cope with the devastation of Dravet syndrome  Academic Article
• Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia–Parkinsonism kindred  Academic Article
• High Hb A₂β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia  Academic Article
• High Urinary Calcium Excretion and Genetic Susceptibility to Hypertension and Kidney Stone Disease  Conference Paper
• Hospital and home chemotherapy for children with leukemia: A randomized cross-over study  Academic Article
• How diet modification challenges are magnified in vulnerable or marginalized people with diabetes and heart disease: a systematic review and qualitative meta-synthesis.  Academic Article
• Human milk composition differs in healthy mothers and mothers with celiac disease  Academic Article
• IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE  Academic Article
• Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids  Academic Article
• Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients  Academic Article
• Identification of the first mutation in a BRE motif of the β-globin gene and its inheritance with two other α-globin gene mutations in a Lebanese family.  Academic Article
• Impacts of an environmental disaster on psychosocial health and well-being in Karakalpakstan  Academic Article
• Indicators of distress in families of children with cerebral palsy  Academic Article
• Influence of Parental and Family Adjustment on the Later Psychological Adjustment of Children Treated for Cancer  Academic Article
• Integrating Mental Health Services Within Primary Care Settings  Academic Article
• Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder  Academic Article
• Is Uterine Papillary Serous Adenocarcinoma a Manifestation of the Hereditary Breast–Ovarian Cancer Syndrome?  Academic Article
• Key references: Protein C, protein S, and antithrombin deficiencies.  Academic Article
• Legitimising and rationalising in talk about satisfaction with formal healthcare among bereaved family members  Academic Article
• Maternal Obesity and Developmental Programming of Metabolic Disorders in Offspring: Evidence from Animal Models  Academic Article
• Maturity Onset Diabetes in the Young (MODY) type 3.  Academic Article
• Measuring family-centred practices of professionals in early intervention services in Taiwan  Academic Article
• Models of partnership within family-centred care in the acute paediatric setting: a discussion paper  Academic Article
• Molecular Characterization of a Novel 55.1 kb^Gγ(^Aγδβ)⁰-thalassemia Deletion in Two Canadian Families  Academic Article
• Motivational interviewing with families in the home environment  Academic Article
• Muscle Phosphofructokinase Deficiency With Neonatal Seizures and Nonprogressive Course  Academic Article
• Natural killer T cells in families of patients with systemic lupus erythematosus: Their possible role in regulation of IGG production  Academic Article
• Neurobehavioral side effects of corticosteroids during active treatment for acute lymphoblastic leukemia in children are age-dependent: Report from Dana-Farber Cancer Institute ALL Consortium Protocol 00-01  Academic Article
• Neuropathological findings in chorea-acanthocytosis: new insights into mechanisms underlying parkinsonism and seizures  Academic Article
• Nurse Practitioner Activities in Ontario Family Health Teams Comparing Three Different Data Sources  Academic Article
• Parent participation in paediatric rehabilitation treatment centres in the Netherlands: a parents' viewpoint  Academic Article
• Parents of children with spinal muscular atrophy are not obligate carriers: Carrier testing is important for reproductive decision-making  Academic Article
• Partial deletion of an antithrombin III allele in a kindred with a type 1 deficiency  Academic Article
• Paternal transmission of the congenital form of myotonic dystrophy type 1: A new case and review of the literature  Academic Article
• Perceptions of family participation among parents of children with cerebral palsy followed from infancy to toddler hood  Academic Article
• Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer  Academic Article
• Pharmacists Managing People with Diabetes in Primary Care: 10 Years of Experience at the Hamilton Family Health Team  Academic Article
• Physical activity as medicine among family health teams: an environmental scan of physical activity services in an interdisciplinary primary care setting  Academic Article
• Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders  Academic Article
• Predictive genetic testing for coronary artery disease  Academic Article
• Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders  Academic Article
• Predictors of Low-Acuity Emergency Department Use by Patients Enrolled in a Family Health Team  Academic Article
• Predictors of caregiver burden across the home-based palliative care trajectory in Ontario, Canada  Academic Article
• Predictors of mammographic density among women with a strong family history of breast cancer  Academic Article
• Predictors of needs for families of children with cerebral palsy  Academic Article
• Presenting the model of risk, disability and hard-to-reach families to inform early intervention services  Academic Article
• Prevalência de transtornos mentais em indivíduos de uma unidade de referência para Programa Saúde da Família em Santa Cruz do Sul, Rio Grande do Sul, Brasil  Academic Article
• Prothrombin 20210A and familial thrombophilia  Academic Article
• Recurrence Risk for Autism Spectrum Disorders: A Baby Siblings Research Consortium Study  Academic Article
• Relation between body mass index and depression: a structural equation modeling approach  Academic Article
• Relationship of nutritional status to health and societal participation in children with cerebral palsy  Academic Article
• Resettlement, mental health, and coping: a mixed methods survey with recently resettled refugee parents in Canada  Academic Article
• Risk factors for developmental dysplasia of the hip: a meta-analysis  Academic Article
• Service Needs of Families where one Parent has an Affective Illness: Implications for Service, Education, and Policy  Academic Article
• Single Nucleotide Polymorphisms in Taste Receptor Genes Are Associated with Snacking Patterns of Preschool-Aged Children in the Guelph Family Health Study: A Pilot Study  Academic Article
• Systematic review: family history in risk assessment for common diseases.  Academic Article
• The Development of an Off-Therapy Needs Questionnaire and Protocol for Survivors of Childhood Cancer  Academic Article
• The Emerging Role of Social Work in Primary Health Care: A Survey of Social Workers in Ontario Family Health Teams.  Academic Article
• The Health and Well-Being of Caregivers of Children With Cerebral Palsy  Academic Article
• The Relationship Between E. coli Indicator Bacteria in Well-water and Gastrointestinal Illnesses in Rural Families  Academic Article
• The implementation and validation of the NoMAD during a complex primary care intervention  Academic Article
• The relationship between parental psychiatric disorder and child physical and sexual abuse: findings from the Ontario health supplement  Academic Article
• The relevance of family-centred medicine and the implications for doctor education  Academic Article
• Therapy behaviours in paediatric rehabilitation: essential attributes for intervention with children with physical disabilities  Academic Article
• To screen or not to screen? Exploring the value of parent mental health screening in children’s rehabilitation services  Academic Article
• Transtornos mentais em comunidade atendida pelo Programa Saúde da Família  Academic Article
• Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia  Academic Article
• Understanding academic clinicians’ varying attitudes toward the treatment of childhood obesity in Canada: A descriptive qualitative approach  Conference Paper
• Understanding paediatric rehabilitation therapists' lack of use of outcome measures  Academic Article
• Understanding participation of children with cerebral palsy in family and recreational activities  Academic Article
• Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong  Academic Article
• What Makes Family Caregivers Happy During the First 2 Years Post Stroke?  Academic Article
• β-thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion  Academic Article
• β‐thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (‐CTTT) β ⁰ ‐thalassemia mutation  Academic Article
• “Living with dying”: The evolution of family membersʼ experience of mechanical ventilation  Academic Article
• “Primary care is primary care”: Use of Normalization Process Theory to explore the implementation of primary care services for transgender individuals in Ontario  Academic Article