H. W. Seyberth

发表

Primary gene structure and expression studies of rodent paracellin-1.

K. Grzeschik, S. Nielsen, H. Gröne, 2001, Journal of the American Society of Nephrology : JASN.

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies.

H. Gröne, M. Konrad, H. W. Seyberth, 2001, The Journal of pediatrics.

Improved sample preparation for the quantitative mass spectrometric determination of prostaglandins in biological samples.

H. W. Seyberth, R. Mrongovius, H. Müller, 1981, Journal of chromatography.

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.

S. Rahman, M. Konrad, S. Waldegger, 2005, Journal of the American Society of Nephrology : JASN.

Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.

M. Konrad, S. Waldegger, C. Derst, 2003, Kidney international.

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

M. Konrad, K. Pasel, H. Seyberth, 2001, Pediatrics.

Prostaglandin E production and hypercalcaemia in rats bearing the Walker carcinosarcoma

K. Strein, H. Minne, H. W. Seyberth, 1980, British Journal of Cancer.

Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes.

M. Konrad, M. Peters, H. W. Seyberth, 2001, Contributions to nephrology.

CYCLIC ADENOSINE MONOPHOSPHATE IN PHAGOCYTIZING GRANULOCYTES AND ALVEOLAR MACROPHAGES

K. Jakobs, H. W. Seyberth, E. Hackenthal, 1973, The Journal of cell biology.

Effect of hydroxyeicosatetraenoic acids on furosemide-sensitive chloride secretion in rat distal colon.

H. W. Seyberth, S. Weber, M. Wegmann, 2000, The Journal of pharmacology and experimental therapeutics.

Effect of prostaglandin endoperoxides and metabolites on bone resorption in vitro

J. Oates, W. Hubbard, H. W. Seyberth, 1977, Nature.

Mass spectrometric determination of urinary prostaglandins in preterm infants

H. W. Seyberth, R. Mrongovius, H. Müller, 1980, European Journal of Clinical Pharmacology.

Combined capillary column gas chromatography-mass spectrometric method for the quantitative analysis of urinary prostaglandins.

H. W. Seyberth, H. Müller, T. Erlenmaier, 1979, Journal of chromatography.

Prothrombin Marburg--a dysfunctional coagulation protein.

V. Kretschmer, H. W. Seyberth, M. Kraus, 1997, Thrombosis research.

Toxicity, clearance and distribution of endotoxin in mice as influenced by actinomycin D, cycloheximide, -amanitin and lead acetate.

H. W. Seyberth, E. Hackenthal, H. Schmidt‐Gayk, 1972, Toxicon : official journal of the International Society on Toxinology.

Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

V. Tasic, T. Seeman, M. Konrad, 2001, Journal of the American Society of Nephrology : JASN.

Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?

M. Durán, A. V. van Kuilenburg, R. Wevers, 1997, Journal of Inherited Metabolic Disease.

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

M. Konrad, E. Kuwertz-Broeking, A. Reis, 2000, European Journal of Human Genetics.

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

A. Karschin, M. Konrad, E. Wischmeyer, 2001, Kidney international.

Hereditary hypokalemic salt-losing tubulopathies

M. Konrad, H. W. Seyberth, N. Jeck, 2000 .

Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function.

A. Karschin, M. Konrad, G. Deschênes, 1997, Biochemical and biophysical research communications.

In Vivo residual activities of the phenylalanine hydroxylating system in phenylketonuria and variants

P. Lutz, F. Trefz, H. W. Seyberth, 1981, Journal of Inherited Metabolic Disease.

Pharmacotyping of hypokalaemic salt-losing tubular disorders.

M. Peters, H. W. Seyberth, N. Jeck, 2004, Acta physiologica Scandinavica.

Prostaglandins and renin release studies in the isolated perfused rat kidney.

H. W. Seyberth, E. Hackenthal, U. Schwertschlag, 1980, Progress in biochemical pharmacology.

Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia

M. Beer, O. Hiort, P. Schneider, 2006, Orphanet journal of rare diseases.

Urinary excretion rate of 6-keto-prostaglandin F1 alpha as an index of circulating prostacyclin.

H. W. Seyberth, E. Hackenthal, H. Müller, 1983, Advances in prostaglandin, thromboxane, and leukotriene research.