Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Stephan C. Reinalter"'
Publikováno v:
Pediatric Research. 55:261-266
In hyperprostaglandin E syndrome (HPGES) and classic Bartter syndrome (cBS), tubular salt and water losses stimulate renin secretion, which is dependent on enhanced cyclooxygenase-2 (COX-2) enzymatic activity. In contrast to other renal COX metabolit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a05a13c1a472b11879406956eff33ac
https://doi.org/10.1203/01.pdr.0000101747.09626.6b
https://doi.org/10.1203/01.pdr.0000101747.09626.6b
Autor:
Melanie Peters, G.ünter Klaus, Stephan C. Reinalter, Burkhard Tönshoff, Nikola Jeck, Andreas Leonhardt, Hannsjörg W. Seyberth, Martin Konrad
Publikováno v:
The American Journal of Medicine. 112:183-190
Purpose Hypokalemic salt-losing tubulopathies (Bartter-like syndromes) comprise a set of clinically and genetically distinct inherited renal disorders. Mutations in four renal membrane proteins involved in electrolyte reabsorption have been identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ab5be5a84fc5a610b202c7904cc0bc
https://doi.org/10.1016/s0002-9343(01)01086-5
https://doi.org/10.1016/s0002-9343(01)01086-5
Publikováno v:
Prostaglandins, Leukotrienes and Essential Fatty Acids (PLEFA). 62:175-181
20-Hydroxy-arachidonic acid (20-HETE) was determined in urine by an isotope dilution assay using gas chromatography/mass spectrometry (GC/MS). After addition of 18O2-internal standard, 20-HETE was extracted from urine with hexane either directly or a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8db31d42eefee247b450a7d2dcd75ae1
https://doi.org/10.1054/plef.2000.0138
https://doi.org/10.1054/plef.2000.0138
Publikováno v:
The Journal of Pediatrics. 129:519-528
In hyperprostaglandin E syndrome (HPS) renal wasting of electrolytes and water is consistently associated with enhanced synthesis of prostaglandin E2. In contrast to Bartter or Gitelman syndrome (BS/GS), HPS is characterized by its severe prenatal ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690dd13fe820fe917328e3c6c96a02f1
https://doi.org/10.1016/s0022-3476(96)70116-6
https://doi.org/10.1016/s0022-3476(96)70116-6
Autor:
Hannsjörg W. Seyberth, Stephan C. Reinalter, Ulla Pechmann, Jolanta Heinzinger, Nikola Jeck, Petra Waldegger, Siegfried Waldegger, Martin Konrad, Rolf Beetz, Carsten A. Pressler
Publikováno v:
Journal of the American Society of Nephrology : JASN. 17(8)
Genetic defects of the Na+-K+-2Cl- (NKCC2) sodium potassium chloride co-transporter result in severe, prenatal-onset renal salt wasting accompanied by polyhydramnios, prematurity, and life-threatening hypovolemia of the neonate (antenatal Bartter syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb6482e05e47be6bd0f9050cd582fafe
https://pubmed.ncbi.nlm.nih.gov/16807401
https://pubmed.ncbi.nlm.nih.gov/16807401
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 21(7)
To analyse whether congenital furosemide- or thiazide-like renal salt loss protects against the potential prohypertensive effects of two cyclooxygenase (COX) inhibitors: rofecoxib, a COX-2 selective inhibitor, and indomethacin, an unselective COX-inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1463c450889d19ea837a91f7dad4e45
https://pubmed.ncbi.nlm.nih.gov/16554326
https://pubmed.ncbi.nlm.nih.gov/16554326
Autor:
Melanie Peters, Karl P. Schlingmann, Stephan C. Reinalter, Martin Kömhoff, Nikola Jeck, Siegfried Waldegger, Hannsjörg W. Seyberth
Publikováno v:
American journal of physiology. Regulatory, integrative and comparative physiology. 288(4)
The molecular basis of inherited salt-losing tubular disorders with secondary hypokalemia has become much clearer in the past two decades. Two distinct segments along the nephron turned out to be affected, the thick ascending limb of Henle's loop and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f74963765f3398d7be946fdadcd97d3a
https://pubmed.ncbi.nlm.nih.gov/15793031
https://pubmed.ncbi.nlm.nih.gov/15793031
Publikováno v:
Acta physiologica Scandinavica. 181(4)
UNLABELLED Long standing confusion exists in the terminology of hypokalaemic salt-losing tubulopathies (SLTs). SLTs are autosomal recessively transmitted and characterized by normotensive secondary hyperreninism/hyperaldosteronism with hypokalaemic m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d79cafcdc390e4d2c59e9a4a918c5b
https://pubmed.ncbi.nlm.nih.gov/15283765
https://pubmed.ncbi.nlm.nih.gov/15283765
Autor:
Stephan C. Reinalter, Nikola Jeck, Siegfried Waldegger, Hannsjörg W. Seyberth, Martin Konrad, Martin Holder, Petra Waldegger, Karl P. Schlingmann
Publikováno v:
The New England journal of medicine. 350(13)
Mutations in genes encoding chloride transporters cause Bartter's syndrome. An antenatal form associated with salt wasting and deafness has been observed in persons with mutations in BSND, the gene...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5bc22b5436438486ab4b57d1d98a2af
https://pubmed.ncbi.nlm.nih.gov/15044637
https://pubmed.ncbi.nlm.nih.gov/15044637
Autor:
Hermann Josef Gröne, Martin Konrad, Hannsjörg W. Seyberth, Günter Klaus, Stephan C. Reinalter
Publikováno v:
The Journal of pediatrics. 139(3)
Evaluation of the benefit/risk ratio of long-term treatment with indomethacin in salt-losing tubulopathies with special attention to renal function.Twelve patients (median age, 14.9 years) had received indomethacin for a median of 13 years (median cu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3d66f26cdb9ef59693a3447eb1b1f1c
https://pubmed.ncbi.nlm.nih.gov/11562620
https://pubmed.ncbi.nlm.nih.gov/11562620