Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Developmental Disabilities"" wg kryterium: Temat

  Lista filtrów

Ogranicz do:

Wyrównaj
Wyświetlanie 1-20 z 44364
Tytuł:
The Impact of Emergency Pandemic HCBS Funding on the Continuity and Security of People with Intellectual and Developmental Disabilities.
Autorzy:
Friedman C; CQL | The Council on Quality and Leadership, 100 West Road, Suite 300, Towson, MD, 21204, USA. .
Pokaż więcej
Źródło:
Journal of autism and developmental disorders [J Autism Dev Disord] 2024 Mar; Vol. 54 (3), pp. 1068-1077. Date of Electronic Publication: 2022 Dec 09.
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*
Autism Spectrum Disorder*
Humans ; Child ; Pandemics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Pivotal Role of Oxytocin's Mechanism of Thermoregulation in Prader-Willi Syndrome, Schaaf-Yang Syndrome, and Autism Spectrum Disorder.
Autorzy:
Camerino C; Department of Precision and Regenerative Medicine, School of Medicine, University of Bari Aldo Moro, P.za G. Cesare 11, 70100 Bari, Italy.; Department of Physiology and Pharmacology 'V. Erspamer', Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome, Italy.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Feb 08; Vol. 25 (4). Date of Electronic Publication: 2024 Feb 08.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Autism Spectrum Disorder*/genetics
Autism Spectrum Disorder*/metabolism
Body Temperature Regulation*
Chromosome Disorders*
Developmental Disabilities*/genetics
Developmental Disabilities*/metabolism
Facies*
Hypopituitarism*
Imprinting Disorders*
Oxytocin*
Prader-Willi Syndrome*/genetics
Prader-Willi Syndrome*/metabolism
Humans ; Infant ; Muscle Hypotonia
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Perceived barriers and facilitators to infection prevention and control in Dutch residential care facilities for people with intellectual and developmental disabilities: a cross-sectional study.
Autorzy:
Houben F; Department of Social Medicine, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, 6200 MD, Maastricht, P.O. box 616, The Netherlands. .; Department of Sexual Health, Infectious Diseases and Environmental Health, Living Lab Public Health Mosa, South Limburg Public Health Service, 6400 AA, Heerlen, P.O. box 33, The Netherlands. .
den Heijer CD; Department of Social Medicine, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, 6200 MD, Maastricht, P.O. box 616, The Netherlands.; Department of Sexual Health, Infectious Diseases and Environmental Health, Living Lab Public Health Mosa, South Limburg Public Health Service, 6400 AA, Heerlen, P.O. box 33, The Netherlands.; Department of Medical Microbiology, Infectious Diseases and Infection Prevention, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University Medical Centre (MUMC+), 6202 AZ, Maastricht, P.O. box 5800, The Netherlands.
Dukers-Muijrers NH; Department of Sexual Health, Infectious Diseases and Environmental Health, Living Lab Public Health Mosa, South Limburg Public Health Service, 6400 AA, Heerlen, P.O. box 33, The Netherlands.; Department of Health Promotion, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, 6200 MD, Maastricht, P.O. box 616, The Netherlands.
Smeets-Peels C; Stichting Pergamijn, Mercator 2, 6135 KW, Sittard, The Netherlands.
Hoebe CJ; Department of Social Medicine, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, 6200 MD, Maastricht, P.O. box 616, The Netherlands.; Department of Sexual Health, Infectious Diseases and Environmental Health, Living Lab Public Health Mosa, South Limburg Public Health Service, 6400 AA, Heerlen, P.O. box 33, The Netherlands.; Department of Medical Microbiology, Infectious Diseases and Infection Prevention, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University Medical Centre (MUMC+), 6202 AZ, Maastricht, P.O. box 5800, The Netherlands.
Pokaż więcej
Źródło:
BMC public health [BMC Public Health] 2024 Mar 05; Vol. 24 (1), pp. 704. Date of Electronic Publication: 2024 Mar 05.
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*/prevention & control
Ethnicity*
Humans ; Child ; Cross-Sectional Studies ; Dietary Supplements ; Hygiene
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Short-term neonatal and long-term neurodevelopmental outcome of children born term low birth weight.
Autorzy:
Kim HY; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea.
Cho GJ; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea. .
Ahn KH; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea.
Hong SC; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea.
Oh MJ; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea.
Kim HJ; Department of Obstetrics and Gynecology, Korea University College of Medicine, 148 Gurodong-Ro, Guro-Gu, Seoul, 08308, Republic of Korea.
Pokaż więcej
Źródło:
Scientific reports [Sci Rep] 2024 Jan 27; Vol. 14 (1), pp. 2274. Date of Electronic Publication: 2024 Jan 27.
Typ publikacji:
Journal Article
MeSH Terms:
Infant, Low Birth Weight*
Developmental Disabilities*/epidemiology
Developmental Disabilities*/etiology
Infant, Newborn ; Infant ; Child ; Humans ; Female ; Child, Preschool ; Male ; Cohort Studies ; Birth Weight ; Gestational Age
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Conceptualising the empowerment of caregivers raising children with developmental disabilities in Ethiopia: a qualitative study.
Autorzy:
Szlamka Z; Department of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK. .; Care Policy and Evaluation Centre, London School of Economics and Political Science, Houghton Street, London, WC2A 2AE, UK. .
Ahmed I; Department of Psychiatry, School of Medicine, WHO Collaborating Centre for Mental Health Research and Capacity-Building, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Genovesi E; Department of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Kinfe M; Department of Psychiatry, School of Medicine, WHO Collaborating Centre for Mental Health Research and Capacity-Building, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Hoekstra RA; Department of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Hanlon C; Department of Health Service and Population Research, Institute of Psychiatry, Centre for Global Mental Health, Psychology & Neuroscience, King's College London, London, UK.; Department of Psychiatry, School of Medicine, WHO Collaborating Centre for Mental Health Research and Capacity-Building, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.; Centre for Innovative Drug Development and Therapeutic Trials for Africa, Addis Ababa University, Addis Ababa, Ethiopia.
Pokaż więcej
Źródło:
BMC health services research [BMC Health Serv Res] 2023 Dec 15; Vol. 23 (1), pp. 1420. Date of Electronic Publication: 2023 Dec 15.
Typ publikacji:
Journal Article
MeSH Terms:
Caregivers*/education
Developmental Disabilities*
Child ; Humans ; Ethiopia ; Qualitative Research ; Self-Help Groups
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Young adults with intellectual and developmental disabilities who participate in Special Olympics are less likely to be diagnosed with depression.
Autorzy:
Lloyd M; Faculty of Health Sciences, Ontario Tech University, 2000 Simcoe St N., Oshawa, ON, L1G 0C5, Canada. .
Temple VA; School of Exercise Science, Physical & Health Education, University of Victoria, Victoria, BC, Canada.
Foley JT; Department of Physical Education, SUNY Cortland, Cortland, NY, USA.
Yeatman S; Faculty of Health Sciences, Ontario Tech University, 2000 Simcoe St N., Oshawa, ON, L1G 0C5, Canada.
Lunsky Y; Azrieli Adult Neurodevelopmental Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.; ICES, Toronto, ON, Canada.
Huang A; ICES, Toronto, ON, Canada.
Balogh R; Faculty of Health Sciences, Ontario Tech University, 2000 Simcoe St N., Oshawa, ON, L1G 0C5, Canada.; ICES, Toronto, ON, Canada.
Pokaż więcej
Źródło:
Social psychiatry and psychiatric epidemiology [Soc Psychiatry Psychiatr Epidemiol] 2023 Nov; Vol. 58 (11), pp. 1699-1708. Date of Electronic Publication: 2022 Dec 22.
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*/diagnosis
Developmental Disabilities*/epidemiology
Intellectual Disability*/diagnosis
Intellectual Disability*/epidemiology
Child ; Humans ; Young Adult ; Retrospective Studies ; Depression/diagnosis ; Depression/epidemiology ; Ontario/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
STAG2: Computational Analysis of Missense Variants Involved in Disease.
Autorzy:
Ros-Pardo D; Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), C/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Gómez-Puertas P; Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), C/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Marcos-Alcalde Í; Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), C/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Jan 20; Vol. 25 (2). Date of Electronic Publication: 2024 Jan 20.
Typ publikacji:
Journal Article
MeSH Terms:
Cohesins*/genetics
Developmental Disabilities*/genetics
Humans ; CCCTC-Binding Factor/genetics ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; De Lange Syndrome/genetics ; DNA ; Mutation ; Mutation, Missense
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel IARS1 variants cause syndromic developmental disorder with epilepsy in a Chinese patient and the literature review.
Autorzy:
Jiang J; Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Feng Y; Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Tang Q; Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Zhao C; Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Guo M; Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Wu J; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Guo R; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Lu H; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Sun X; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Gao J; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Xue H; Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2326. Date of Electronic Publication: 2023 Nov 28.
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*/genetics
Epilepsy*/genetics
Child ; Humans ; Female ; Infant ; Phenotype ; Seizures ; China
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems.
Autorzy:
Mir A; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Song Y; Division of Medical Genetics, 3Billion Inc, Seoul, South Korea.
Lee H; Division of Medical Genetics, 3Billion Inc, Seoul, South Korea.
Nadeali Z; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.; GenTArget Corp (GTAC), Deputy of Research and Technology, Isfahan University of Medical Sciences, Isfahan, Iran.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2305. Date of Electronic Publication: 2023 Oct 25.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Developmental Disabilities*/genetics
Speech*
Adolescent ; Humans ; Male ; DNA-Binding Proteins/genetics ; Mutation ; Seizures
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identification of a de novo variant in the ASXL2 gene related to Shashi-Pena syndrome.
Autorzy:
Zheng Y; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Yang L; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Niu M; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Zhao S; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Liang L; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Wu Y; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Li T; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Yang F; Cipher Gene LLC, Beijing, China.
Yang Z; Cipher Gene LLC, Beijing, China.
Wang Y; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Wang D; Department of Neurology, Xi'an Children's Hospital, Xi'an, China.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Nov; Vol. 11 (11), pp. e2251. Date of Electronic Publication: 2023 Jul 26.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Developmental Disabilities*/genetics
Intellectual Disability*/genetics
Female ; Humans ; Infant ; Epigenesis, Genetic ; Muscle Hypotonia/genetics ; Repressor Proteins/genetics ; Transcription Factors/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Expanding the mutational spectrum of ZTTK syndrome: A de novo variant with global developmental delay and malnutrition in a Chinese patient.
Autorzy:
Tang S; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
You J; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Liu L; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Ouyang H; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Jiang N; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Duan J; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Li C; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Luo Y; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Zhang W; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Zhan M; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Liu C; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Lyu GZ; AmCare Genomics Lab, Guangzhou, Guangdong, China.
Zhang VW; AmCare Genomics Lab, Guangzhou, Guangdong, China.
Zhao H; Department of Digestive System Diseases, Hunan Children's Hospital, Changsha, China.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2188. Date of Electronic Publication: 2023 Jul 24.
Typ publikacji:
Case Reports; Journal Article; Review; Research Support, Non-U.S. Gov't
MeSH Terms:
Developmental Disabilities*/genetics
Developmental Disabilities*/pathology
Eye Diseases*
Intellectual Disability*/genetics
Intellectual Disability*/pathology
Malnutrition*
Child ; Female ; Humans ; Infant ; East Asian People ; Mutation ; Syndrome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Effects of Syntactic, Semantic, and Pragmatic Prominence on Pronoun Interpretation in Adults With Intellectual and Developmental Disabilities.
Autorzy:
Hawthorne K; Department of Hearing, Speech, and Language Sciences, Sorenson Language and Communication Center, Gallaudet University, Washington, DC.
Loveall SJ; Department of Special Education and Communication Disorders, University of Nebraska-Lincoln.
Pokaż więcej
Źródło:
Journal of speech, language, and hearing research : JSLHR [J Speech Lang Hear Res] 2023 Sep 13; Vol. 66 (9), pp. 3606-3621. Date of Electronic Publication: 2023 Aug 10.
Typ publikacji:
Journal Article
MeSH Terms:
Semantics*
Developmental Disabilities*
Humans ; Adult ; Female ; Child ; Language ; Fixation, Ocular ; Communication
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A novel variant in the QRICH1 gene was identified in a patient with severe developmental delay.
Autorzy:
Wang D; Department of Oral and Maxillofacial Surgery, affiliated Dongguan Hospital, Southern Medical University (Dongguan people's Hospital), Dongguan, China.
Wu J; Department of Pediatric Endocrinology and Metabolism, Key Laboratory of Birth Defects and Related Diseases of Women and Children, West China Second Hospital of Sichuan University, Chengdu, China.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2227. Date of Electronic Publication: 2023 Jun 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Developmental Disabilities*/genetics
DNA-Binding Proteins*/genetics
Transcription Factors*/genetics
Child ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Profile of children assisted in a teaching outpatient clinic of developmental disabilities in São Paulo, Brazil.
Autorzy:
da Frota MA; Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Resegue RM; Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Colucci A; Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Micheletti C; Universidade Federal de São Paulo, São Paulo, SP, Brasil.
Pokaż więcej
Źródło:
Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo [Rev Paul Pediatr] 2023 May 29; Vol. 41, pp. e2022005. Date of Electronic Publication: 2023 May 29 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*/diagnosis
Developmental Disabilities*/epidemiology
Parents*
Female ; Humans ; Child ; Aged ; Brazil/epidemiology ; Retrospective Studies ; Mothers
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Learning science alongside peers with intellectual and developmental disabilities.
Autorzy:
Rubenzer KN; Department of Neuroscience, The Center for Learning and Memory, Waggoner Center for Alcohol and Addiction Research, Institute of Neuroscience, University of Texas at Austin, Austin, Texas, United States of America.
Pierce JT; Department of Neuroscience, The Center for Learning and Memory, Waggoner Center for Alcohol and Addiction Research, Institute of Neuroscience, University of Texas at Austin, Austin, Texas, United States of America.
Pokaż więcej
Źródło:
PLoS biology [PLoS Biol] 2023 Jun 13; Vol. 21 (6), pp. e3002147. Date of Electronic Publication: 2023 Jun 13 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Developmental Disabilities*
Learning*
Adult ; Child ; Humans ; Students
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The association between parental risks and childhood development: findings from a community-based survey in East China.
Autorzy:
Zheng S; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Fang J; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Bai G; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
He X; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Hua M; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Zhu B; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Chen W; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Dong W; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Wang L; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China.
Huang X; Section of Child Health and Development, the United Nations Children's Fund, UNICEF Office for China, Beijing, China.
Wang H; Department of Children Health, National Center for Maternal and Children Health, Chinese Center for Disease Control and Prevention, Beijing, China.
Shao J; Department of Child Health Care, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, 57 Zhu-Gan Road, Gongshu District, 310003, Hangzhou, China. .
Pokaż więcej
Źródło:
BMC public health [BMC Public Health] 2023 May 12; Vol. 23 (1), pp. 878. Date of Electronic Publication: 2023 May 12.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Developmental Disabilities*/epidemiology
Child Development*
Humans ; Child, Preschool ; Child ; Infant ; Cross-Sectional Studies ; China/epidemiology ; Surveys and Questionnaires
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Strategies for addressing the needs of children with or at risk of developmental disabilities in early childhood by 2030: a systematic umbrella review.
Autorzy:
Smythe T; International Centre for Evidence in Disability, London School of Hygiene & Tropical Medicine, London, UK. .; Department of Health and Rehabilitation Sciences, Division of Physiotherapy, Stellenbosch University, Cape Town, South Africa. .
Scherer N; International Centre for Evidence in Disability, London School of Hygiene & Tropical Medicine, London, UK.
Nanyunja C; Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.; Department of Infectious Disease On Epidemiology & International Health, School of Hygiene & Tropical Medicine, London, UK.
Tann CJ; Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.; Department of Infectious Disease On Epidemiology & International Health, School of Hygiene & Tropical Medicine, London, UK.; Neonatal Medicine, University College London NHS Trust, London, UK.
Olusanya BO; Centre for Healthy Start Initiative, Lagos, Nigeria.
Pokaż więcej
Źródło:
BMC medicine [BMC Med] 2024 Feb 02; Vol. 22 (1), pp. 51. Date of Electronic Publication: 2024 Feb 02.
Typ publikacji:
Systematic Review; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Attention Deficit Disorder with Hyperactivity*
Autism Spectrum Disorder*
Child ; Child, Preschool ; Humans ; Developmental Disabilities/epidemiology ; Family ; Meta-Analysis as Topic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 44364

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies