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Showing results 921 to 940 of 2038

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Issue DateTitleJournal Title
2011Matrix metalloproteinases and bullae in pediatric Henoch Schönlein purpuraPEDIATRIC DERMATOLOGY
2015Mean platelet volume in young children with urinary tract infection SCIENTIFIC REPORTS
2020Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019 LANCET
2014Mechanistic links between COPD and lung cancer: a role of microRNA let-7?NATURE REVIEWS CANCER
2015Medical Litigation and the Care of Newborns Neonatal Medicine
2019Medical staff tend to underestimate the quality of life in children and adolescents with inflammatory bowel diseaseACTA PAEDIATRICA
2009MedRefSNP: a database of medically investigated SNPsHUMAN MUTATION
2019Mental health and psychosocial adjustment in pediatric chronic kidney disease derived from the KNOW-Ped CKD studyPEDIATRIC NEPHROLOGY
2019Mesenteric venous thrombosis as a complication of appendicitis in an adolescent: A case report and literature review MEDICINE
2007Methylprednisolone and cyclosporin therapy in a patient with nephrotic proteinuria [3]INDIAN JOURNAL OF PEDIATRICS
2006Methylprednisolone pulse therapy by the Tune–Mendoza protocol in a child with severe Henoch–Schönlein nephritisSCANDINAVIAN JOURNAL OF RHEUMATOLOGY
2019Micronutrients Are Not Deficient in Children with Nonorganic Failure to Thrive PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION
2013miR-122, IL28B genotype and the response to interferon in chronic hepatitis C virus infection.NATURE REVIEWS IMMUNOLOGY
2008Mite and cockroach allergens activate protease-activated receptor 2 and delay epidermal permeability barrier recovery JOURNAL OF INVESTIGATIVE DERMATOLOGY
2012Mitochondria DNA polymorphisms are associated with susceptibility to endometriosis.DNA AND CELL BIOLOGY
2020Mitochondrial and Nuclear Mitochondrial Variants in Allergic Diseases ALLERGY ASTHMA & IMMUNOLOGY RESEARCH
2020Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndromeEUROPEAN JOURNAL OF ENDOCRINOLOGY
2013Mitochondrial disease and epilepsyBRAIN & DEVELOPMENT
2018Mitochondrial Mutations in Cholestatic Liver Disease with Biliary Atresia SCIENTIFIC REPORTS
2008Mitochondrial respiratory chain defects: underlying etiology in various epileptic conditionsEPILEPSIA

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