المؤلفون: Anastasia K Ketko, Chinhong Lin, Bethany B Moore, Ann Marie LeVine

المصدر: PLoS ONE, Vol 8, Iss 12, p e82680 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3846784?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/69fd8fd02db54f17aa4a971febf7a940

المؤلفون: Chunhong Lin, Ann Marie LeVine, Anastasia K. Ketko

المصدر: Critical Care Medicine. 40:1-328

مصطلحات موضوعية: biology, business.industry, medicine, biology.protein, Inflammasome, Critical Care and Intensive Care Medicine, business, Flagellin, medicine.drug, Cell biology, Surfactant protein A

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::227b5ced5ac70102bc2acea4e1346418
https://doi.org/10.1097/01.ccm.0000424402.04656.63

المؤلفون: Fatih Süheyl Ezgü, Kaustuv Bhattacharya, Raymond Y. Wang, Roberto Giugliani, Max Holtz, Brett H. Graham, Mahmut Çoker, Rena E. Falk, José Francisco da Silva Franco, Robert D. Steiner, Alfons Macaya, Robert M. Greenstein, William S. Sly, Grant A. Mitchell, Ngu Lock-Hock, Gregory M. Pastores, Mercedes Pineda, Loreta Cimbalistiene, Laila Arash, Klane K. White, Antonio González-Meneses, Anastasia K. Ketko, Michael Beck, Marina Szlago, Adriana M. Montaño, Dennis Bartholomew, Akemi Tanaka, Mark S. Sands

المساهمون: Ege Üniversitesi

المصدر: JOURNAL OF MEDICAL GENETICS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Journal of medical genetics, London : BMJ Publishing group, 2016, vol. 53, iss. 6, p. 403-418
Journal of medical genetics, vol 53, iss 6
Journal of Medical Genetics

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Adolescent, Mucopolysaccharidosis, Sly syndrome, Hepatosplenomegaly, Metabolic disorders, Mucopolysaccharidosis VII, Medical and Health Sciences, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Hydrops fetalis, Surveys and Questionnaires, medicine, Genetics, Humans, Medical history, Clinical genetics, Family history, Preschool, Child, Genetics (clinical), Glucuronidase, Genetics & Heredity, business.industry, Genotype-Phenotype Correlations, Infant, Enzyme replacement therapy, Biological Sciences, medicine.disease, Lysosomal Storage Diseases, 030104 developmental biology, Phenotype, Clinical genetics, Genetics, Metabolic disorders, Child, Preschool, Female, medicine.symptom, business, 030217 neurology & neurosurgery, MPS, lysosomal storage disease, β-glucuronidase

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b94c3aaa5f62e908319f0f9188207a
https://hdl.handle.net/10668/9860

المؤلفون: Michelle Nemshak, Anastasia K. Ketko, Matthew Niedner, Rebecca Vartanian, Craig M. Martin

المصدر: Pediatrics. 136(2)

مصطلحات موضوعية: business.industry, Infant, Newborn, Hyperoxia, medicine.disease, Patient care, Oxygen Saturation Measurement, Patient safety, ALARM, Clinical Alarms, Intensive Care Units, Neonatal, Pediatrics, Perinatology and Child Health, Health care, Alarm management, Medicine, Humans, Equipment Failure, Medical emergency, business, Oxygen saturation (medicine)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e1b612d38df987943e669ed382d72c0
https://pubmed.ncbi.nlm.nih.gov/26148949