Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Hulthén, U L"'
Autor:
Fava, Cristiano, Montagnana, Martina, Rosberg, L., Burri, P., Jönsson, A., Wanby, P., Wahrenberg, H., Hulthén, U. L., Aurell, M., Guidi, Giancesare, Melander, O.
Publikováno v:
DNA sequence : the journal of DNA sequencing and mapping. 18(5)
Gitelman's syndrome (GS) is an inherited autosomal recessive disorder due to loss of function mutations in the SLC12A3 gene encoding the Na-Cl co-transporter (NCCT), the target of thiazide diuretics. The defective function of the NCCT, which normally
Autor:
Anwaar, I., Rendell, M., Gottsäter, A., Lindgärde, F., Hulthén, U. L., Mattiasson, I., Gottsäter, A, Lindgärde, F, Hulthén, U L
Publikováno v:
Journal of Internal Medicine; Apr2000, Vol. 247 Issue 4, p463-470, 8p
Publikováno v:
Journal of Internal Medicine; Nov99, Vol. 246 Issue 5, p477-488, 12p
Publikováno v:
Journal of Internal Medicine; Feb98, Vol. 243 Issue 2, p141-147, 7p, 3 Charts
Publikováno v:
Journal of Human Hypertension; Nov2001, Vol. 15 Issue 11, p781, 5p
Publikováno v:
Journal of Internal Medicine; Mar2001, Vol. 249 Issue 3, p237-246, 10p
Autor:
Berglund, A. Scott, Hulthen, U.L., Manheim, P., Thorsson, O., Wollmer, P., Tornquist, C., Berglund, A S, Hulthén, U L, Manhem, P, Törnquist, C
Publikováno v:
Journal of Internal Medicine; Mar2001, Vol. 249 Issue 3, p247-251, 5p, 1 Chart
Publikováno v:
Journal of Human Hypertension; Dec2000, Vol. 14 Issue 12, p819, 5p
Autor:
Melander, O, Bengtsson, K, Orho-Melander, M, Lindblad, U, Forsblom, C, Råstam, L, Groop, L, Hulthén, U L
Publikováno v:
Journal of Human Hypertension; Jan2000, Vol. 14 Issue 1, p43, 4p
Autor:
Melander O, Mattiasson I, Marsál K, Groop L, Hulthén UL, Melander, O, Mattiasson, I, Marsál, K, Groop, L, Hulthén, U L
Publikováno v:
Journal of Hypertension; 1999 Nov, Vol. 17 Issue 11, p1557-1561, 5p