Zobrazeno 1 - 10
of 75
pro vyhledávání: '"H W, Seyberth"'
Autor:
H. W. Seyberth, M. Schwab
Publikováno v:
Pädiatrie ISBN: 9783642546716
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2cb2d160b2ae5ca1323f95433d2c6f0
https://doi.org/10.1007/978-3-642-54671-6_136-1
https://doi.org/10.1007/978-3-642-54671-6_136-1
Autor:
P. Ronco, Sebastian Bachmann, Franziska Theilig, N. Bouby, Hermann Pavenstädt, Rolf M. Nüsing, H. W. Seyberth, B. Nafz, H. Debiec
Publikováno v:
American Journal of Physiology-Renal Physiology. 291:F987-F994
Renal volume regulation is modulated by the action of cyclooxygenases (COX) and the resulting generation of prostanoids. Epithelial expression of COX isoforms in the cortex directs COX-1 to the distal convolutions and cortical collecting duct, and CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb566f028b61e811fb31f2e28cdf89f5
https://doi.org/10.1152/ajprenal.00099.2006
https://doi.org/10.1152/ajprenal.00099.2006
Autor:
S. C. Reinalter, Nives Radošević, Goran Palčevski, Vera Vlahović-Palčevski, A. Vogt, H. W. Seyberth, M. Ufer, Igor Francetić
Publikováno v:
Pharmacoepidemiology and Drug Safety. 14:735-739
Purpose To compare the utilisation of systemic antimicrobials at the paediatric units of the university hospitals in Marburg (Germany) and Rijeka (Croatia). Methods A prospective, observational analysis of hospital records from 300 incident users of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a389368a0c69413bcaca9f10ebdbca
https://doi.org/10.1002/pds.1108
https://doi.org/10.1002/pds.1108
Autor:
Lars Hellmeyer, Rolf F. Maier, S. Marek, H. W. Seyberth, M. Kömhoff, Stephan Schmidt, I. Tekesin
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 208:232-235
INTRODUCTION A polyhydramnion is diagnosed in 0.4 to 3.3 % of all pregnancies. The most common causes of increased amniotic fluid include maternal diabetes mellitus, fetal malformations and chromosomal aberrations, twin-to-twin transfusion syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b0eb882f118528ad3cfaabf7add6cf
https://doi.org/10.1055/s-2004-835870
https://doi.org/10.1055/s-2004-835870
Autor:
R. M. Nusing, H. W. Seyberth
Publikováno v:
Acta Physiologica Scandinavica. 181:523-528
Hyperprostaglandin E syndrome/antenatal Bartter syndrome is characterized by NaCl wasting and volume depletion, juxtaglomerula hypertrophy, hyperreninism and secondary hyperaldosteronism. Primary causes are mutations in the gene for Na-K-2Cl-cotransp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5e0ff4b474384b228468ac5b7b5ee8
https://doi.org/10.1111/j.1365-201x.2004.01326.x
https://doi.org/10.1111/j.1365-201x.2004.01326.x
Publikováno v:
Monatsschrift Kinderheilkunde. 149:1066-1069
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::871bef0fe912f3163bda18f16ed7f9d9
https://doi.org/10.1007/s001120170069
https://doi.org/10.1007/s001120170069
Publikováno v:
Zeitschrift f�r Rheumatologie. 59:365-369
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adea95069ef15546630b723e37bb4e7b
https://doi.org/10.1007/s003930070043
https://doi.org/10.1007/s003930070043
Autor:
C. Brautigam, H. W. Seyberth, A.B.P. van Kuilenburg, Birgit Assmann, Ron A. Wevers, Georg F. Hoffmann, Marinus Duran, L. Wagner, A. H. van Gennip
Publikováno v:
Journal of Inherited Metabolic Disease, 20, 681-688
Journal of inherited metabolic disease, 20(5), 681-688. Springer Netherlands
Journal of inherited metabolic disease, 20, 681-688. Springer Netherlands
Journal of Inherited Metabolic Disease, 20, pp. 681-688
Journal of inherited metabolic disease, 20(5), 681-688. Springer Netherlands
Journal of inherited metabolic disease, 20, 681-688. Springer Netherlands
Journal of Inherited Metabolic Disease, 20, pp. 681-688
We describe a boy of consanguineous parents who suffered from intractable diarrhoea due to congenital microvillous atrophy, a recessively inherited autosomal disorder. He developed severe cholestatis starting at 2 weeks of age and leading to liver ci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a1992d5ac495837b28c81c621350052
https://hdl.handle.net/11245/1.137787
https://hdl.handle.net/11245/1.137787
Publikováno v:
Journal of Inherited Metabolic Disease. 19:687-694
Hyperprostaglandin E syndrome is a rare disease usually presenting with renal symptoms such as polyuria, polyhydramnios, hypercalciuria, hypokalaemia, and recurrent episodes of extreme fever, diarrhoea, and convulsions. We report a severe variant of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f678237f41ce4f31cb6a8a1dfa9d1ab4
https://doi.org/10.1007/bf01799846
https://doi.org/10.1007/bf01799846