Hannsjörg W. Seyberth

Author

Also Known As

H Seyberth, H W Seyberth, H. Seyberth, H. W. SEYBERTH, H. W. Seyberth, H.W Seyberth, H.W. Seyberth, HANNSJÖRG W. SEYBERTH, Hannsjorg Seyberth, Hannsjorg W Seyberth

168

Publications

7.9K

Citations

H-Index

113

Concepts

All Affiliations

Philipps University of Marburg Heidelberg University Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology University Hospital Heidelberg Universitätskinderklinik

About

Hannsjörg W. Seyberth is an author at Philipps University of Marburg specializing in medicine, physiology, and urology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	54	5K
2	Biochemistry	15	16	841
3	Health Sciences	7	7	376
4	Natural Sciences	7	7	1K
5	Engineering	1	1	25

Hannsjörg W. Seyberth

Publications

6.9K

Citations

H-Index

Page 1

	Year	Citations
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family Karl P. Schlingmann, Stefanie Weber, Melanie Peters, Nature Genetics Trpm Gene FamilyNatural SciencesGeneticsGenetic DisorderMolecular Biology	2002	775
Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, Proceedings of the National Academy of Sciences	2004	369
Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function Martin Kömhoff, H.-J. Gröne, Thomas Klein, American Journal of Physiology-Renal Physiology Renal PathologyRenal InflammationPathologyCox IsoformsCellular Physiology	1997	362
Bartter's syndrome: A disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis John R. Gill, Jurgen C. Fro ̈lich, Robert E. Bowden, The American Journal of Medicine Adrenal GlandUrologyProstaglandin SynthesisPhysiologyBenign Prostatic Hyperplasia	1976	324
Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels Karl P. Schlingmann, Martin Konrad, Nikola Jeck, New England Journal of Medicine BiologyChloride TransportersDeafness ResultingAntenatal FormGenetic Disorder	2004	280
Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Stefanie Weber, Linda Schneider, Melanie Peters, Journal of the American Society of Nephrology	2001	269
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies Melanie Peters, Nikola Jeck, Stephan C. Reinalter, The American Journal of Medicine Electrolyte DisorderUrologySodium HomeostasisMedicinePhysiology	2002	261
Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype Nikola Jeck, Martin Konrad, Melanie Peters, Pediatric Research BiologyMixed Bartter-gitelman PhenotypeChloride Channel GeneGeneticsMolecular Genetics	2000	194
Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650] Lothar Károlyi, Martin Konrad, Arnold Köckerling, Human Molecular Genetics Electrolyte DisorderGeneticsRenal PathologyPathologyBartter-like Syndromes	1997	190
Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang, New England Journal of Medicine	2016	181

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