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Isla Ogilvie

Explore the profile of Isla Ogilvie including associated specialties, affiliations and a list of published articles. Areas
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Articles 7
Citations 426
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Recent Articles
1.
Ogilvie I, Khoury H, Goetghebeur M, El Khoury A, Giaquinto C
BMC Infect Dis . 2012 Mar; 12:62. PMID: 22429601
Background: Rotavirus affects 95% of children worldwide by age 5 years and is the leading cause of severe dehydrating diarrhea. The objective of this review was to estimate the burden...
2.
Cameron J, Janer A, Levandovskiy V, MacKay N, Rouault T, Tong W, et al.
Am J Hum Genet . 2011 Sep; 89(4):486-95. PMID: 21944046
Severe combined deficiency of the 2-oxoacid dehydrogenases, associated with a defect in lipoate synthesis and accompanied by defects in complexes I, II, and III of the mitochondrial respiratory chain, is...
3.
Ogilvie I, Khoury H, El Khoury A, Goetghebeur M
Hum Vaccin . 2011 Mar; 7(5):523-33. PMID: 21422818
Background: Rotaviral gastroenteritis (RVGE) is the leading cause of severe diarrhea in children under five years of age worldwide. This comprehensive review aims to estimate the burden of RVGE among...
4.
Khoury H, Ogilvie I, El Khoury A, Duan Y, Goetghebeur M
BMC Infect Dis . 2011 Jan; 11:9. PMID: 21214934
Background: Rotavirus gastroenteritis (RVGE) is the most common cause of severe childhood diarrhea worldwide. Objectives were to estimate the burden of RVGE among children less than five years old in...
5.
Ogilvie I, Khoury A, Cui Y, Dasbach E, Grabenstein J, Goetghebeur M
Vaccine . 2009 Jun; 27(36):4891-904. PMID: 19520205
Streptococcus pneumoniae infections in adults are associated with substantial morbidity, mortality, and costs. A literature review was conducted to identify strengths and limitations of the cost-effectiveness of pneumococcal polysaccharide vaccine...
6.
Ogilvie I, Kennaway N, Shoubridge E
J Clin Invest . 2005 Oct; 115(10):2784-92. PMID: 16200211
NADH:ubiquinone oxidoreductase (complex I) deficiency is a common cause of mitochondrial oxidative phosphorylation disease. It is associated with a wide range of clinical phenotypes in infants, including Leigh syndrome, cardiomyopathy,...
7.
Antonicka H, Ogilvie I, Taivassalo T, Anitori R, Haller R, Vissing J, et al.
J Biol Chem . 2003 Aug; 278(44):43081-8. PMID: 12941961
Deficiencies in the activity of complex I (NADH: ubiquinone oxidoreductase) are an important cause of human mitochondrial disease. Complex I is composed of at least 46 structural subunits that are...