Suchergebnisse - "Developmental Disabilities complications"

Rôle du médecin traitant dans le suivi des patients avec déficience intellectuelle et développementale

Autoren: Graindorge, Clément Bochatay, Alexandre Chung, Christopher et al.

Quelle: Revue médicale suisse, Vol. 16, No 708 (2020) pp. 1811-1816

Schlagwörter: Hospitalization, Developmental Disabilities/complications, 03 medical and health sciences, 0302 clinical medicine, Caregivers, General Practitioners, Communication, Humans, Physician's Role, Intellectual Disability/complications, ddc:613

Dateibeschreibung: application/pdf

Zugangs-URL: https://archive-ouverte.unige.ch/unige:145051/ATTACHMENT01
https://archive-ouverte.unige.ch/unige:145051

Using realist methods for intervention development to fill a methodological gap: A case study showing the development of an oral hygiene intervention for people with intellectual developmental disabilities

Autoren: Mac Giolla Phadraig, Caoimhin Asimakopoulou, Koula Faulks, Denise et al.

Weitere Verfasser: Mac Giolla Phadraig, Caoimhin Asimakopoulou, Koula Faulks, Denise et al.

Quelle: ISSN: 0301-5661.

Schlagwörter: behavioral science, dental health education, oral health, oral hygiene, MESH: Developmental Disabilities / complications, MESH: Developmental Disabilities / therapy, MESH: Health Promotion, MESH: Intellectual Disability / complications, MESH: Oral Health, MESH: Oral Hygiene, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/36759914; PUBMED: 36759914

Verfügbarkeit: https://uca.hal.science/hal-04323742
https://uca.hal.science/hal-04323742v1/document
https://uca.hal.science/hal-04323742v1/file/Mac%20Giolla%20Phadraig%20et%20al%20Comm%20Dent%20Oral%20Epid%202023%20Using%20realist%20methods%20for%20intervention%20development%20to%20fill%20a.pdf
https://doi.org/10.1111/cdoe.12844

Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous KDM5B Variants.

Autoren: Lebon, S. Quinodoz, M. Peter, V.G. et al.

Schlagwörter: Abortion, Eugenic, Agenesis of Corpus Callosum/complications, Agenesis of Corpus Callosum/diagnosis, Agenesis of Corpus Callosum/genetics, Child, Preschool, Developmental Disabilities/complications, Developmental Disabilities/genetics, Facial Asymmetry/complications, Facial Asymmetry/genetics, Family, Female, Fetal Diseases/diagnosis, Fetal Diseases/genetics, Heterozygote, Humans, Intellectual Disability/complications, Intellectual Disability/diagnosis, Intellectual Disability/genetics, Jumonji Domain-Containing Histone Demethylases/genetics, Mutation, Missense, Nuclear Proteins/genetics, Pedigree, Pregnancy, Repressor Proteins/genetics, Siblings, Switzerland, KDM5B

Dateibeschreibung: application/pdf

Relation: Genes; https://iris.unil.ch/handle/iris/82387; serval:BIB_14ADEBC9C07B; 000699848500001

Verfügbarkeit: https://iris.unil.ch/handle/iris/82387
https://doi.org/10.3390/genes12091397

Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Autoren: Tripathy, R. Leca, I. van Dijk, T. et al.

Schlagwörter: Agenesis of Corpus Callosum/complications, Agenesis of Corpus Callosum/diagnostic imaging, Agenesis of Corpus Callosum/genetics, Agenesis of Corpus Callosum/pathology, Animals, Newborn, Apoptosis/genetics, Brain/metabolism, Brain/pathology, Cells, Cultured, Cerebellum/abnormalities, Cerebellum/diagnostic imaging, Child, Developmental Disabilities/complications, Developmental Disabilities/diagnostic imaging, Developmental Disabilities/genetics, Disease Models, Animal, Embryo, Mammalian, Female, Gene Expression Regulation, Developmental/genetics, Humans, Male, Malformations of Cortical Development/complications, Malformations of Cortical Development/diagnostic imaging, Malformations of Cortical Development/genetics, Mice

Relation: Neuron; https://iris.unil.ch/handle/iris/150790; serval:BIB_769F69929167; 000453922000012

Verfügbarkeit: https://iris.unil.ch/handle/iris/150790
https://doi.org/10.1016/j.neuron.2018.10.044

Early motor developmental milestones and schizophrenia: A systematic review and meta-analysis

Autoren: Svetlana Filatova Kristiina Moilanen Tuula Hurtig et al.

Weitere Verfasser: Svetlana Filatova Kristiina Moilanen Tuula Hurtig et al.

Quelle: Schizophrenia Research. 188:13-20

Schlagwörter: Adolescent, motor milestones, delay, Developmental Disabilities, Early development, Developmental Disabilities/complications, 03 medical and health sciences, Child Development, 0302 clinical medicine, Humans, psychosis, Preschool, Child, Biological Psychiatry, childhood, Delay, Infant, Newborn, Infant, Newborn, Psychosis, Childhood, Motor milestones, early development, 3. Good health, Psychiatry and Mental health, Motor Skills, Child, Preschool, Schizophrenia, Schizophrenia/complications

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/28131598
https://www.sciencedirect.com/science/article/abs/pii/S0920996417300427
http://jultika.oulu.fi/Record/nbnfi-fe201803276201
https://www.schres-journal.com/article/S0920-9964(17)30042-7/abstract
https://pubmed.ncbi.nlm.nih.gov/28131598/
https://research-information.bris.ac.uk/en/publications/early-motor-developmental-milestones-and-schizophrenia-a-systemat
https://www.repository.cam.ac.uk/handle/1810/263467
http://urn.fi/urn:nbn:fi-fe201803276201
https://epub.ub.uni-muenchen.de/36683/

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats

Autoren: Jerome L. Gorski Michael J. Noetzel Jacqueline M. Hoover et al.

Quelle: Human Mutation, vol. 33, no. 1, pp. 165-179

Schlagwörter: Chromosome Aberrations, Male, 0301 basic medicine, 0303 health sciences, DNA Copy Number Variations, Chromosomes, Human, Pair 10, Developmental Disabilities, Chromosome Mapping, Genetic Variation, Infant, Penetrance, Abnormalities, Multiple/genetics, Child, Child, Preschool, Developmental Disabilities/complications, Developmental Disabilities/genetics, Female, Homologous Recombination, Humans, In Situ Hybridization, Fluorescence, Intellectual Disability/complications, Intellectual Disability/genetics, Nerve Growth Factors/genetics, Oligonucleotide Array Sequence Analysis, Segmental Duplications, Genomic/genetics, Sequence Deletion, Vesicular Acetylcholine Transport Proteins/genetics, 03 medical and health sciences, Segmental Duplications, Genomic, Intellectual Disability, Abnormalities, Multiple, Nerve Growth Factors

Dateibeschreibung: application/pdf

Zugangs-URL: https://serval.unil.ch/resource/serval:BIB_821E7FE324C6.P001/REF.pdf
https://pubmed.ncbi.nlm.nih.gov/21948486
https://europepmc.org/article/MED/21948486
https://serval.unil.ch/notice/serval:BIB_821E7FE324C6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655525
https://serval.unil.ch/resource/serval:BIB_821E7FE324C6.P001/REF.pdf
https://onlinelibrary.wiley.com/doi/10.1002/humu.21614
https://serval.unil.ch/resource/serval:BIB_821E7FE324C6.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_821E7FE324C61
https://serval.unil.ch/notice/serval:BIB_821E7FE324C6

Video‐fluoroscopic study of swallowing in children with neurodevelopmental disorders

Autoren: To, R Fung, CW Wong, V et al.

Quelle: Pediatrics International. 46:26-30

Schlagwörter: Male, Hematoma, Subdural - complications - rehabilitation, Adolescent, Developmental Disabilities, Developmental Disabilities - complications - rehabilitation, Video Recording, Down Syndrome - complications - rehabilitation, Fluoroscopy - methods, Pilot Projects, 03 medical and health sciences, 0302 clinical medicine, Chinese children, Central Nervous System Diseases, Humans, Cerebral Palsy - complications - rehabilitation, Subdural - complications - rehabilitation, Central Nervous System Diseases - complications - rehabilitation, Hematoma, Cerebral Palsy, Neurodevelopmental disorders, Video-fluoroscopic study of swallowing, Deglutition Disorders - etiology - radiography - rehabilitation, Infant, 3. Good health, Hematoma, Subdural, Olivopontocerebellar Atrophies - complications - rehabilitation, Fluoroscopy, Olivopontocerebellar Atrophies, Hong Kong, Female, Down Syndrome, Deglutition Disorders

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/15043660
https://pubmed.ncbi.nlm.nih.gov/15043660/
http://doi.wiley.com/10.1111/j.1442-200X.2004.t01-1-.x
https://ci.nii.ac.jp/naid/10017673663
https://www.ncbi.nlm.nih.gov/pubmed/15043660
http://onlinelibrary.wiley.com/doi/10.1111/j.1442-200X.2004.t01-1-.x/abstract
https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1442-200X.2004.t01-1-.x
http://hdl.handle.net/10722/72367

Minor anomalije u djece sa smetnjama u razvoju

Autoren: Goršeta, Kristina Škrinjarić, Ilija Jukić, Jelka et al.

Quelle: Paediatria Croatica. 46:115

Schlagwörter: anomalije - epidemiologija, razvojni poremećaji - komplikacije, abnormalities - epidemiology, developmental disabilities - complications

Zugangs-URL: https://www.bib.irb.hr/112541

Traditional chinese medicine (tongue acupuncture) in children with drooling problems

Autoren: Wong, V Wong, W Sun, JG

Quelle: Pediatric Neurology. 25:47-54

Schlagwörter: Male, Medicine, Adolescent, Sialorrhea/etiology/*therapy, Developmental Disabilities, Acupuncture Therapy, Severity of Illness Index, 03 medical and health sciences, 0302 clinical medicine, Tongue, Acupuncture Therapy/*methods, Humans, Single-Blind Method, Medicine, Chinese Traditional, Preschool, Child, Cross-Over Studies, Developmental Disabilities/*complications, Chinese Traditional, Sialorrhea, 3. Good health, Treatment Outcome, Child, Preschool, Female

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/11483396
https://www.pedneur.com/article/S0887-8994(01)00292-2/fulltext
http://hub.hku.hk/handle/10722/143567
http://www.sciencedirect.com/science/article/pii/S0887899401002922
https://www.sciencedirect.com/science/article/abs/pii/S0887899401002922
http://europepmc.org/abstract/MED/11483396
https://pubmed.ncbi.nlm.nih.gov/11483396/
http://hdl.handle.net/10722/143567

Separation and Comorbidity of Hyperactivity and Conduct Disturbance in Chinese Schoolboys

Autoren: Luk, SL Leung, PWL BaconShone, J et al.

Quelle: Journal of Child Psychology and Psychiatry. 37:841-853

Schlagwörter: Cross-Cultural Comparison, Male, Developmental Disabilities, Developmental Disabilities - Complications, Child Behavior Disorders, Comorbidity, Hyperkinesis, Stress, Stress, Psychological - Complications, 03 medical and health sciences, Cognition Disorders - Complications, 0302 clinical medicine, Analysis Of Variance, Humans, 0501 psychology and cognitive sciences, Child, Hyperkinesis - Diagnosis - Epidemiology, Family Health, Analysis of Variance, Psychological Tests, 05 social sciences, Psychological - Complications, Reproducibility of Results, Achievement, Hong Kong - Epidemiology, Child Behavior Disorders - Diagnosis - Epidemiology, Hong Kong, Regression Analysis, Reproducibility Of Results, Cognition Disorders, Stress, Psychological

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/8923227
https://www.ncbi.nlm.nih.gov/pubmed/8923227
http://hub.hku.hk/handle/10722/178105
https://acamh.onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-7610.1996.tb01480.x
https://core.ac.uk/display/38011641
http://hdl.handle.net/10722/178105

Melatonin treatment of a blind child with serious sleep disorders / Melatoninbehandling av et blindt barn med store sövnforstyrrelser

Autoren: Ramstad, K Loge, J H

Quelle: Tidsskrift for Den Norske Laegeforening. 122(10):1005

A Comparison of Receptive-Expressive Language Profiles between Toddlers with Autism Spectrum Disorder and Developmental Language Delay

Weitere Verfasser: Kyeong In Seol Seung Ha Song Ka Lim Kim et al.

Quelle: T201404054.pdf

Schlagwörter: Child Development Disorders, Pervasive/complications, Child, Preschool, Developmental Disabilities/complications, Early Diagnosis, Female, Humans, Infant, Language, Language Development, Language Development Disorders/complications, Language Development Disorders/diagnosis, Language Tests, Male, Republic of Korea, Autism spectrum disorder, expressive language, receptive language, toddlers

Dateibeschreibung: 1721~1728

Relation: YONSEI MEDICAL JOURNAL; J02813; https://ir.ymlib.yonsei.ac.kr/handle/22282913/100314; T201404054; 57583

Verfügbarkeit: https://ir.ymlib.yonsei.ac.kr/handle/22282913/100314
https://doi.org/10.3349/ymj.2014.55.6.1721

Idiopathic desquamative interstitial pneumonia in a child: a case report.

Autoren: Bressieux-Degueldre, S. Rotman, S. Hafen, G. et al.

Quelle: BMC research notes, vol. 7, pp. 383

Schlagwörter: Child, Preschool, Developmental Disabilities/complications, Female, Humans, Kidney Diseases/complications, Lung/pathology, Lung Diseases, Interstitial/diagnosis, Interstitial/etiology, Skin Diseases/complications

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/24954625; info:eu-repo/semantics/altIdentifier/eissn/1756-0500; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_5760D867EA432; https://serval.unil.ch/notice/serval:BIB_5760D867EA43; https://serval.unil.ch/resource/serval:BIB_5760D867EA43.P001/REF.pdf

Verfügbarkeit: https://serval.unil.ch/notice/serval:BIB_5760D867EA43
https://doi.org/10.1186/1756-0500-7-383
https://serval.unil.ch/resource/serval:BIB_5760D867EA43.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_5760D867EA432

Read and write difficulties within Swedish for Immigrants (Sfi), disability and/or circumstances? / Läs och skrivsvårigheter inom Sfi, funktionshinder och/eller omständighet?

Autoren: Larsson, Annelie

Quelle: Socialmedicinsk Tidskrift. 86(5):464

Sleep disorders in healthy children follows often a "learnt" behavioral pattern. Diurnal rhytm disturbances are dominating among children with functional disabilities / Sömnstörningar hos friska barn är ofta ett "inlärt" beteende. Hos barn med funktionshinder dominerar rubbningar i dygnsrytmen

Autoren: Palm, L Hellsten, H

Quelle: Läkartidningen. 96(47):5200

Early mental disturbances are underlying causes of severe juvenile delinquency - increased research is necessary / Tidig psykisk störning ligger bakom allvarlig ungdomsbrottslighet - ökad forsknig krävs

Autoren: Adler, H Frisk, M Lidberg, L

Quelle: Läkartidningen. 89(14):1174

From Shortage to Surge: A Developmental Switch in Hippocampal-Prefrontal Coupling in a Gene-Environment Model of Neuropsychiatric Disorders.

Autoren: Hartung, Henrike Cichon, Nicole De Feo, Vito et al.

Quelle: Cerebral cortex 26(11), 4265-4281 (2016). doi:10.1093/cercor/bhw274

Schlagwörter: info:eu-repo/classification/ddc/610, Animals, Newborn, Cognition Disorders: genetics, Cognition Disorders: pathology, Cognition Disorders: physiopathology, Developmental Disabilities: chemically induced, Developmental Disabilities: complications, Developmental Disabilities: genetics, Disease Models, Animal, Evoked Potentials: drug effects, Evoked Potentials: genetics, Female, Gene-Environment Interaction, Hippocampus: drug effects, Hippocampus: physiology, Interferon Inducers: toxicity, Mice, Inbred C57BL, Transgenic, Mutation: genetics, Nerve Tissue Proteins: genetics, Nerve Tissue Proteins: metabolism, Neural Pathways: drug effects, Neural Pathways: physiology, Poly I-C: toxicity, Prefrontal Cortex: drug effects, Prefrontal Cortex: pathology, Prefrontal Cortex: physiopathology

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/1047-3211; info:eu-repo/semantics/altIdentifier/issn/1460-2199; info:eu-repo/semantics/altIdentifier/pmid/pmid:27613435; https://pub.dzne.de/record/138888

Verfügbarkeit: https://pub.dzne.de/record/138888
https://pub.dzne.de/search?p=id:%22DZNE-2020-05210%22

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

Autoren: Chakraborty, Pranesh K Schmitz-Abe, Klaus Kennedy, Erin K et al.

Quelle: Chakraborty, P K, Schmitz-Abe, K, Kennedy, E K, Mamady, H, Naas, T, Durie, D, Campagna, D R, Lau, A, Sendamarai, A K, Wiseman, D H, May, A, Jolles, S, Connor, P, Powell, C, Heeney, M M, Giardina, P-J, Klaassen, R J, Kannengiesser, C, Thuret, I, Thompson, A A, Marques, L, Hughes, S, Bonney, D K, Bottomley, S S, Wynn, R F, Laxer, R M, Minniti, C P, Moppett, J, Bordon, V, Geraghty, M, Joyce, P B M, Markianos, K, Rudner, A D, Holcik, M & Fleming, M D 2014, 'Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, ....

Schlagwörter: Alleles, Anemia, Sideroblastic/complications, Developmental Disabilities/complications, Fever/complications, Genetic Diseases, X-Linked/complications, HEK293 Cells, Humans, Immunologic Deficiency Syndromes/complications, Mutation/genetics, RNA Nucleotidyltransferases/genetics

Verfügbarkeit: https://research.manchester.ac.uk/en/publications/83ec7ce9-fa19-4afa-9d41-fa388055c2e1
https://doi.org/10.1182/blood-2014-08-591370

Preventive Management of Children with Congenital Anomalies and Syndromes

Autoren: Golder N. Wilson W. Carl Cooley

Resource Type: eBook.

Schlagworte: Genetic disorders in children--Complications--Prevention, Developmental disabilities--Complications--Prevention

Categories: HEALTH & FITNESS / Children & Adolescents, MEDICAL / Pediatrics