المؤلفون: Somsri Kotchawat, Anuson Siwarin, Cua Ngoc Le, Sarunya Maneerattanasak, Youwarat Nuprasert, Chumpron Ponprasert, Chumponut Talunkphet, Poungpen Srimoung, Charuai Suwanbamrung, Ponlapat Satian, Orratai Nontapet

المصدر: One Health
One Health, Vol 10, Iss, Pp 100168-(2020)

مصطلحات موضوعية: ER2, Guideline of DPCG at emergency room for admission to in patient department, EC for DRAS, Excellent Centre for Dengue Research and Academic Service, HCT, Hematocrit, DHF, Dengue haemorrhagic fever, OPD, Outpatient department, Lansaka model, the larval indices surveillance system for a sustainable solution to the dengue problem in southern Thailand, WBC, White blood count (Dengue infection WBC ≤ 5000 cells/mm3.), NSS, Normal saline solution, Care provision, Tertiary hospital, the province hospital that mean tertiary care level of health care system in Thailand, 0302 clinical medicine, DLR, Dextrose lactate ringer, ER3, Guideline of DPCG at emergency room for serious dengue to province hospital, ER1, Guideline of DPCG at emergency room for hospital discharge for observing at home, OPD3, DPCG at outpatient department for serious dengue case and send to province hospital, Health care, SRRT, Surveillance and Rapid Response Team, Dengue patient care guideline, 030212 general & internal medicine, Household, Primary care unit, DALY, Disability adjusted life year, WHO 1997, Guideline for classification dengue DF/DHF/DSS by WHO regional publication, SEARO No. 29, lcsh:R5-920, CBC, Complete blood count, HGT/DTX, Haemogluco test/Dextrostix, ER, Emergency room, CPAR, Community participatory action, PCU1, DPCG at primary care unit for dengue case with fever>48 h and send to district hospital, Vital signs, BT (Body temperature), PR (Pulse), RR (Respiratory rate), and BP (Blood pressure), Infectious Diseases, KAP, Preparedness, OPD2, DPCG at outpatient department for admission to inpatient department, district hospital, IPD, Inpatient department, DEN, Dengue virus, Thematic analysis, lcsh:Medicine (General), Secondary hospital, the district hospital that mean secondary care level of health care system in Thailand, Research Paper, medicine.medical_specialty, NSAIDs, Non-steroidal anti-inflammatory drugs, 030231 tropical medicine, CVI, Content validity index, Participatory action research, WHO 2009, Guideline for classification dengue, dengue with or without signs (WS) and severe dengue (D, D ± WS, SD), Qualitative property, DSS, Dengue shock syndrome, OPD1, DPCG at outpatient department for continuous observation at home, WHO, World health organization, IPD2, DPCG at inpatient department for severe dengue and send to province hospital Iowa model: The Model was developed at the University of Iowa Hospitals and Clinics in 1990s to serve as a guide for nurses to use research findings to help improve patient care, Hospital, 03 medical and health sciences, PCU2, DPCG at primary care unit for dengue case with fever<48 h for observation at home/community, medicine, DAR, Dextrose acetate ringer, PCUs, Primary care units (PCUs), IPD1, DPCG at inpatient department for dengue patient grade I and II, business.industry, Public health, Public Health, Environmental and Occupational Health, Guideline, DF, Dengue fever, DPCG, Dengue patient care guideline, Family medicine, business, WA, Warning signs

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1da877ad259d6c4ee7a80093a65d51ae
https://doi.org/10.1016/j.onehlt.2020.100168

المؤلفون: Naudion, S., Moutton, S., Coupry, I., Sole, G., Deforges, J., Guerineau, E., Hubert, Cédric, Deves, S., Pilliod, J., Rooryck, C., Abel, C., Le Breton, F., Collardeau-Frachon, S., Cordier, M. P., Delezoide, A. L., Goldenberg, A., Loget, P., Melki, J., Odent, S., Patrier, S., Verloes, A., Viot, G., Blesson, S., Bessières, B., Lacombe, D., Arveiler, B., Goizet, C., Fergelot, P.

المساهمون: CHU Bordeaux [Bordeaux], Neurogénétique moléculaire, Université d'Évry-Val-d'Essonne (UEVE) - Institut National de la Santé et de la Recherche Médicale (INSERM), Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes 1 (UR1) - Centre National de la Recherche Scientifique (CNRS) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Unité fonctionnelle de génétique clinique, Assistance publique - Hôpitaux de Paris (AP-HP) - Hôpital Robert Debré - Université Paris Diderot - Paris 7 (UPD7), AP-HP Hôpital Necker - Enfants Malades [Paris], Laboratoire de Génétique Humaine, Développement et Cancer, Université Bordeaux Segalen - Bordeaux 2, Service de génétique médicale, Université de Bordeaux (UB) - CHU Bordeaux [Bordeaux] - Groupe hospitalier Pellegrin, Université d'Évry-Val-d'Essonne (UEVE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Université Paris Diderot - Paris 7 (UPD7)-Hôpital Robert Debré-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-Hôpital Robert Debré-Université Paris Diderot - Paris 7 (UPD7), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré-Université Paris Diderot - Paris 7 (UPD7)

المصدر: Clinical Genetics
Clinical Genetics, Wiley, 2016, 89 (3), pp.371-377 <10.1111/cge.12679>
Clinical Genetics, Wiley, 2016, 89 (3), pp.371-377. ⟨10.1111/cge.12679⟩
Clinical Genetics, 2016, 89 (3), pp.371-377. ⟨10.1111/cge.12679⟩

مصطلحات موضوعية: Male, [SDV]Life Sciences [q-bio], Filamins, DNA Mutational Analysis, Infant, Newborn, Melnick-Needles, Otopalatodigital, frontometaphyseal dysplasia, Osteochondrodysplasias, MNS, OPD2, Pedigree, FMD, FLNA, Craniofacial Abnormalities, [SDV] Life Sciences [q-bio], Fetus, Phenotype, Mutation, Humans, filamin A, Female, Hand Deformities, Congenital

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::eed258db637b9aa8fddf0faa4abcd363
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01214017

المؤلفون: Suwanbamrung C; School of Public Health, Walailak University, Nakhon Si Thammarat Province, Thailand.; Excellent Center for Dengue Research and Academic Service (EC for DRAS), Walailak University, Thailand., Le CN; School of Public Health, Walailak University, Nakhon Si Thammarat Province, Thailand.; Excellent Center for Dengue Research and Academic Service (EC for DRAS), Walailak University, Thailand., Maneerattanasak S; School of Public Health, Walailak University, Nakhon Si Thammarat Province, Thailand.; Excellent Center for Dengue Research and Academic Service (EC for DRAS), Walailak University, Thailand., Satian P; Lansaka Hospital, Nakhon Si Thammarat Province, Thailand., Talunkphet C; Lansaka Hospital, Nakhon Si Thammarat Province, Thailand., Nuprasert Y; Lansaka Hospital, Nakhon Si Thammarat Province, Thailand., Siwarin A; Lansaka Hospital, Nakhon Si Thammarat Province, Thailand., Kotchawat S; Maharaj Nakhon Si Thammarat Hospital, Nakhon Si Thammarat Province, Thailand., Srimoung P; Maharaj Nakhon Si Thammarat Hospital, Nakhon Si Thammarat Province, Thailand., Ponprasert C; Public Health Official of Lansaka District, Nakhon Si Thammarat Province, Thailand.; Excellent Center for Dengue Research and Academic Service (EC for DRAS), Walailak University, Thailand., Nontapet O; School of Nursing, Walailak University, Nakhon Si Thammarat Province, Thailand.; Excellent Center for Dengue Research and Academic Service (EC for DRAS), Walailak University, Thailand.

المصدر: One health (Amsterdam, Netherlands) [One Health] 2020 Sep 17; Vol. 10, pp. 100168. Date of Electronic Publication: 2020 Sep 17 (Print Publication: 2020).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 101660501 Publication Model: eCollection Cited Medium: Print ISSN: 2352-7714 (Print) Linking ISSN: 23527714 NLM ISO Abbreviation: One Health Subsets: PubMed not MEDLINE

المؤلفون: Naudion S; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France., Moutton S; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Coupry I; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Sole G; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France.; CHU Bordeaux, Fédération des Neurosciences Cliniques, Bordeaux, France., Deforges J; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France., Guerineau E; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Hubert C; Plateforme Génome Transcriptome, Centre de Génomique Fonctionnelle de Bordeaux, Université de Bordeaux, Bordeaux, France., Deves S; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France., Pilliod J; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Rooryck C; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Abel C; CHU Lyon, Service de Génétique, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France., Le Breton F; CHU Lyon, Service de Pathologie du Nord, Hôpital de la Croix-Rousse, Lyon, France., Collardeau-Frachon S; CHU de Lyon, Centre de Pathologie Est, Hospices Civils de Lyon, Lyon, France., Cordier MP; CHU Lyon, Service de Génétique Médicale, Hôpital Mère Enfant, Lyon, France., Delezoide AL; APHP, Service de Biologie du Développement, Hôpital Robert Debré, Paris, France., Goldenberg A; CHU Rouen, Service de Génétique Médicale, Rouen, France., Loget P; CHU Rennes, Service d'Anatomie Cytologie Pathologique, Rennes, France., Melki J; INSERM U78, Laboratoire de Neurogénétique Moléculaire, Université de Paris XI, Paris, France., Odent S; CHU de Rennes, Service de Génétique Clinique, Centre de Référence Anomalies du Développement CLAD-Ouest, Hôpital Sud, Rennes, France., Patrier S; CHU Rouen, Service d'Anatomie Pathologique, Rouen, France., Verloes A; Département de Génétique, APHP-Hôpital universitaire Robert Debré, Université Sorbonne Paris-Cité, Faculté de Médecine Denis Diderot-Paris 7, and INSERM UMR 1141, Paris, France., Viot G; APHP, Service de Génétique Médicale, Maternité Port-Royal, Paris, France., Blesson S; CHRU Tours, Service de Génétique, Hôpital Bretonneau, Tours, France., Bessières B; APHP, Service Histo-Embryologie et Cytogénétique, Hôpital Necker, Paris, France., Lacombe D; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Arveiler B; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Goizet C; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France., Fergelot P; CHU Bordeaux, Centre de Référence des Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Bordeaux, France.; University Bordeaux, Laboratoire Maladies Rares, Génétique et Métabolisme (MRGM), Bordeaux, France.; Plateforme Génome Transcriptome, Centre de Génomique Fonctionnelle de Bordeaux, Université de Bordeaux, Bordeaux, France.

المصدر: Clinical genetics [Clin Genet] 2016 Mar; Vol. 89 (3), pp. 371-7. Date of Electronic Publication: 2015 Oct 29.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

مواضيع طبية MeSH: Fetus* , Mutation* , Phenotype*, Craniofacial Abnormalities/*genetics , Filamins/*genetics , Hand Deformities, Congenital/*genetics , Osteochondrodysplasias/*genetics, Craniofacial Abnormalities/diagnosis ; Craniofacial Abnormalities/metabolism ; DNA Mutational Analysis ; Female ; Hand Deformities, Congenital/diagnosis ; Hand Deformities, Congenital/metabolism ; Humans ; Infant, Newborn ; Male ; Osteochondrodysplasias/diagnosis ; Osteochondrodysplasias/metabolism ; Pedigree

SCR Disease Name: Otopalatodigital Spectrum Disorder

المؤلفون: Robertson S; Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand

المصدر: 1993.

المصدر: In: GeneReviews ^® Adam MP; Ardinger HH; Pagon RA; Wallace SE; Bean LJH; Mirzaa G; Amemiya A

نوع المنشور: Review

بيانات الدورية: Publisher: University of Washington, Seattle Cited Medium: Internet