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Diabetologia
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June 25, 2005
Heritability of model-derived parameters of beta cell secretion during intravenous and oral glucose tolerance tests: a study of twins
M Lehtovirta, J Kaprio, L Groop, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 5, 1998
Major decrease in the volume of the entorhinal cortex in patients with Alzheimer's disease carrying the apolipoprotein E epsilon4 allele
K Juottonen, M Lehtovirta, S Helisalmi, et al.
Neuroscience Letters
|
February 16, 1996
Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease
S Helisalmi, A Mannermaa, M Lehtovirta, et al.
Diabetologia
|
November 7, 1999
Heritability of albumin excretion rate in families of patients with Type II diabetes
C M Forsblom, T Kanninen, M Lehtovirta, et al.
Neuroreport
|
December 15, 1995
Increased acetylcholinesterase activity in the CSF of Alzheimer patients carrying apolipoprotein epsilon4 allele
H Soininen, M Lehtovirta, S Helisalmi, et al.
Biological Psychiatry
|
March 15, 2000
Hippocampus in Alzheimer's disease: a 3-year follow-up MRI study
M P Laakso, M Lehtovirta, K Partanen, et al.
Annals of Biomedical Engineering
|
October 21, 1998
Estimation of blood flow heterogeneity in human skeletal muscle using intravascular tracer data: importance for modeling transcapillary exchange
P Vicini, R C Bonadonna, M Lehtovirta, et al.
Neuroscience Letters
|
August 1, 1997
No association between alpha1-antichymotrypsin polymorphism, apolipoprotein E and patients with late-onset Alzheimer's disease
S Helisalmi, A Mannermaa, M Lehtovirta, et al.
Diabetologia
|
April 18, 2000
Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins
M Lehtovirta, J Kaprio, C Forsblom, et al.
Human Molecular Genetics
|
January 4, 2001
Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL)
M Lehtovirta, A Kyttälä, E L Eskelinen, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 68) with videos related to
Sort By:
Page
of 7
Diabetologia
|
June 25, 2005
Heritability of model-derived parameters of beta cell secretion during intravenous and oral glucose tolerance tests: a study of twins
M Lehtovirta, J Kaprio, L Groop, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 5, 1998
Major decrease in the volume of the entorhinal cortex in patients with Alzheimer's disease carrying the apolipoprotein E epsilon4 allele
K Juottonen, M Lehtovirta, S Helisalmi, et al.
Neuroscience Letters
|
February 16, 1996
Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease
S Helisalmi, A Mannermaa, M Lehtovirta, et al.
Diabetologia
|
November 7, 1999
Heritability of albumin excretion rate in families of patients with Type II diabetes
C M Forsblom, T Kanninen, M Lehtovirta, et al.
Neuroreport
|
December 15, 1995
Increased acetylcholinesterase activity in the CSF of Alzheimer patients carrying apolipoprotein epsilon4 allele
H Soininen, M Lehtovirta, S Helisalmi, et al.
Biological Psychiatry
|
March 15, 2000
Hippocampus in Alzheimer's disease: a 3-year follow-up MRI study
M P Laakso, M Lehtovirta, K Partanen, et al.
Annals of Biomedical Engineering
|
October 21, 1998
Estimation of blood flow heterogeneity in human skeletal muscle using intravascular tracer data: importance for modeling transcapillary exchange
P Vicini, R C Bonadonna, M Lehtovirta, et al.
Neuroscience Letters
|
August 1, 1997
No association between alpha1-antichymotrypsin polymorphism, apolipoprotein E and patients with late-onset Alzheimer's disease
S Helisalmi, A Mannermaa, M Lehtovirta, et al.
Diabetologia
|
April 18, 2000
Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins
M Lehtovirta, J Kaprio, C Forsblom, et al.
Human Molecular Genetics
|
January 4, 2001
Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL)
M Lehtovirta, A Kyttälä, E L Eskelinen, et al.
Page
of 7