Zobrazeno 1 - 10
of 30
pro vyhledávání: '"C, Nounopoulos"'
Publikováno v:
Diabetic Medicine. 13:434-440
NIDDM appears to be an inherited condition. Our aim was to identify early metabolic abnormalities in non-diabetic offspring with one NIDDM parent and with a strongly positive (n = 58, age 27.8 +/- 7.0 years) or a negative family history (n = 38, age
Publikováno v:
The Journal of sports medicine and physical fitness. 48(1)
Recent investigations have suggested the occurrence of transient cardiac dysfunction and reversible myocardial injury in healthy individuals after heavy exercise. Our purpose was to examine if the release of N-terminal pro-brain natriuretic peptide (
Publikováno v:
Minerva medica. 97(3)
Bisalbuminemia is a rare inherent or acquired abnormality characterized by the occurrence of 2 distinct albumin bands or a single widened albumin band, after electrophoretic screening of blood proteins. Despite the fact that the presence of 2 albumin
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 13(5)
NIDDM appears to be an inherited condition. Our aim was to identify early metabolic abnormalities in non-diabetic offspring with one NIDDM parent and with a strongly positive (n = 58, age 27.8 +/- 7.0 years) or a negative family history (n = 38, age
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 12(9)
Since a number of animal studies have shown that insulin-like growth I (IGF-I) stimulates nerve regeneration, the aim of our study was to evaluate the possible relationship between IGF-I and IGF-I receptors in diabetic patients with peripheral neurop
Autor:
T. Theodoridis, D. Angelidou, A. Terzi, V. Kokkinou, A. Kalofoutis, K. Triantafyllou, Sokratis Pastromas, Antonis S. Manolis, A. Papapanagiotou, M. El-Ali, C. Nounopoulos, Dimitrios Sakellariou, S. Koulouris
Publikováno v:
Atherosclerosis Supplements. 9:241
Publikováno v:
Acta paediatrica Scandinavica. 79(10)
Although total, free and esterified carnitine blood levels were found to be low (p less than 0.001) in phenylketonuric patients under dietary treatment compared to controls, no clinical signs of carnitine deficiency were noticed. Exclusion from the P
Autor:
Chryssanthi Dasopoulou, C. Nounopoulos, D. Aggelidou, P. Symeonides, S. Koulouris, K. Triantafyllou, A. Kalofoutis, M. El Ali, A. Papapanagiotou, T. Theodoridis
Publikováno v:
Atherosclerosis Supplements. 8:88
Autor:
C. Dasopoulou, C. Nounopoulos, I. Michaelides, Ilias Karabinos, P. Symeonides, Antonis S. Manolis, K. Triantafyllou, A. Kalofoutis, A. Papapanagiotou, S. Koulouris
Publikováno v:
Atherosclerosis Supplements. 7:67
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