Zobrazeno 1 - 10
of 18
pro vyhledávání: '"K. Topaloglu"'
Publikováno v:
The West Indian medical journal. 65(1)
To reveal the possible role of glucagon-like peptide-1 (GLP-1) in newly diagnosed Type 1 diabetic children.Twenty-five newly diagnosed children and 22 healthy children were included in the study.In oral glucose tolerance tests, no correlation was obs
Akademický článek
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Autor:
Junaid Shabbeer, Kenneth H. Astrin, Robert J. Desnick, Ali K. Topaloglu, Bingzheng Tong, Grace A. Ashley, Christine M. Eng
Publikováno v:
Molecular Medicine. 5:806-811
Fabry disease, an X-linked inborn error of glycosphingolipid catabolism, results from the deficient activity of the lysosomal exoglycohydrolase α-galactosidase A (EC 3.2.1.22; α-Gal A). The nature of the molecular lesions in the α-Gal A gene in 30
Autor:
Ilpo Huhtaniemi, Anthony P. Coll, Emily L. Thompson, Zorica Jovanovic, Waljit S. Dhillo, Benjamin G. Challis, Stephen O'Rahilly, Y. C. Loraine Tung, Giles S.H. Yeo, A. K. Topaloglu, Debra Rimmington, Robert K. Semple, Marcus P. Corander, Kevin Murphy
Publikováno v:
Journal of Neuroendocrinology
Journal of Neuroendocrinology; Vol 22
Journal of Neuroendocrinology; Vol 22
PubMedID: 20041982 Growing evidence suggests the tachykinin neurokinin B (NKB) may modulate gonadotrophin secretion and play a role in sex-steroid feedback within the reproductive axis. NKB signalling has recently been identified as being necessary f
Autor:
Ali K, Topaloglu
Publikováno v:
Pediatric endocrinology reviews : PER. 3
Congenital hypothyroidism (CH) is most commonly caused by defects in thyroid development leading to thyroid dysgenesis (80-90%), which consists of thyroid agenesis, ectopy or hypoplasia. Thyroid dysgenesis occurs mostly as a sporadic disease. However
Publikováno v:
European Urology Supplements. 13:e1484
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 43(1)
Fibronectin (FN) is known to have important roles in host defense against infection. The risk for neonatal sepsis increases with the degree of immaturity of the host. Conflicting results have been reported on the relationship between plasma FN levels
Conference
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Publikováno v:
Molecular medicine (Cambridge, Mass.). 5(12)
BACKGROUND: Fabry disease, an X-linked inborn error of glycosphingolipid catabolism, results from the deficient activity of the lysosomal exoglycohydrolase alpha-galactosidase A (EC 3.2.1.22; alpha-Gal A). The nature of the molecular lesions in the a
Publikováno v:
Journal of inherited metabolic disease. 22(1)