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Duodecim; Laaketieteellinen Aikakauskirja
|
February 7, 2006
[Diabetic with hallucination]
Carola Saloranta, Tiinamaija Tuomi
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Efficacy and safety of nateglinide in type 2 diabetic patients with modest fasting hyperglycemia
Carola Saloranta, Kenneth Hershon, Michele Ball, et al.
The American Journal of Clinical Nutrition
|
June 7, 2003
Dietary intakes and plasma concentrations of carotenoids and tocopherols in relation to glucose metabolism in subjects at high risk of type 2 diabetes: the Botnia Dietary Study
Katriina Ylönen, Georg Alfthan, Leif Groop, et al.
European Journal of Pediatrics
|
June 14, 2015
Fetal left ventricular noncompaction cardiomyopathy and fatal outcome due to complete deficiency of mitochondrial trifunctional protein
Tiina Ojala, Irmeli Nupponen, Carola Saloranta, et al.
Diabetes Care
|
July 2, 2003
Associations of dietary fiber with glucose metabolism in nondiabetic relatives of subjects with type 2 diabetes: the Botnia Dietary Study
Katriina Ylönen, Carola Saloranta, Carina Kronberg-Kippilä, et al.
Diabetes Care
|
November 28, 2002
Nateglinide improves early insulin secretion and controls postprandial glucose excursions in a prediabetic population
Carola Saloranta, Christiane Guitard, Eckhard Pecher, et al.
Plos Medicine
|
June 16, 2007
Genetic prediction of future type 2 diabetes
Valeriya Lyssenko, Peter Almgren, Dragi Anevski, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2019
SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy
Anna H Hakonen, Anne Polvi, Carola Saloranta, et al.
The New England Journal of Medicine
|
October 22, 2010
Mutant CHUK and severe fetal encasement malformation
Jenni Lahtela, Heidi O Nousiainen, Vedran Stefanovic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 13, 2007
Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions
Pia Vuorela, Sirpa Ala-Mello, Carola Saloranta, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Duodecim; Laaketieteellinen Aikakauskirja
|
February 7, 2006
[Diabetic with hallucination]
Carola Saloranta, Tiinamaija Tuomi
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Efficacy and safety of nateglinide in type 2 diabetic patients with modest fasting hyperglycemia
Carola Saloranta, Kenneth Hershon, Michele Ball, et al.
The American Journal of Clinical Nutrition
|
June 7, 2003
Dietary intakes and plasma concentrations of carotenoids and tocopherols in relation to glucose metabolism in subjects at high risk of type 2 diabetes: the Botnia Dietary Study
Katriina Ylönen, Georg Alfthan, Leif Groop, et al.
European Journal of Pediatrics
|
June 14, 2015
Fetal left ventricular noncompaction cardiomyopathy and fatal outcome due to complete deficiency of mitochondrial trifunctional protein
Tiina Ojala, Irmeli Nupponen, Carola Saloranta, et al.
Diabetes Care
|
July 2, 2003
Associations of dietary fiber with glucose metabolism in nondiabetic relatives of subjects with type 2 diabetes: the Botnia Dietary Study
Katriina Ylönen, Carola Saloranta, Carina Kronberg-Kippilä, et al.
Diabetes Care
|
November 28, 2002
Nateglinide improves early insulin secretion and controls postprandial glucose excursions in a prediabetic population
Carola Saloranta, Christiane Guitard, Eckhard Pecher, et al.
Plos Medicine
|
June 16, 2007
Genetic prediction of future type 2 diabetes
Valeriya Lyssenko, Peter Almgren, Dragi Anevski, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2019
SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy
Anna H Hakonen, Anne Polvi, Carola Saloranta, et al.
The New England Journal of Medicine
|
October 22, 2010
Mutant CHUK and severe fetal encasement malformation
Jenni Lahtela, Heidi O Nousiainen, Vedran Stefanovic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 13, 2007
Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions
Pia Vuorela, Sirpa Ala-Mello, Carola Saloranta, et al.
Page
of 2