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L Károlyi

Showing results (1-10 of 5) with videos related to

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Herzschrittmachertherapie & Elektrophysiologie|June 5, 2009
[Not Available]S G Spitzer, L Károlyi, H H Ebert
Journal of Molecular Medicine (Berlin, Germany)|May 20, 1998
The molecular genetic approach to "Bartter's syndrome"L Károlyi, M C Koch, K H Grzeschik, et al.
Biochemical and Biophysical Research Communications|January 23, 1997
Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel functionC Derst, M Konrad, A Köckerling, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1996
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndromeL Károlyi, A Ziegler, M Pollak, et al.
Kidney International|September 12, 1998
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domainH H Lemmink, N V Knoers, L Károlyi, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Herzschrittmachertherapie & Elektrophysiologie|June 5, 2009
[Not Available]S G Spitzer, L Károlyi, H H Ebert
Journal of Molecular Medicine (Berlin, Germany)|May 20, 1998
The molecular genetic approach to "Bartter's syndrome"L Károlyi, M C Koch, K H Grzeschik, et al.
Biochemical and Biophysical Research Communications|January 23, 1997
Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel functionC Derst, M Konrad, A Köckerling, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1996
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndromeL Károlyi, A Ziegler, M Pollak, et al.
Kidney International|September 12, 1998
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domainH H Lemmink, N V Knoers, L Károlyi, et al.
Pageof 1