Search filters

List of works by Hannsjörg W. Seyberth

A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity

scientific article (publication date: 2004)

A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies

scientific article published in January 2004

Activating mutation of the renal epithelial chloride channel ClC-Kb, predisposing to hypertension

scientific article

An improved terminology and classification of Bartter-like syndromes

scientific article

Bartter's and Gitelman's syndrome.

scientific article published on 30 November 2016

Barttin increases surface expression and changes current properties of ClC-K channels

scientific journal article

Basics and dynamics of neonatal and pediatric pharmacology

scientific article published on January 2011

CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease

scientific article published on 06 April 2005

Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies

scientific article published in February 2002

Determination of misoprostol free acid in human breast milk and serum by gas chromatography/negative ion chemical ionization tandem mass spectrometry

scientific article published in September 2002

Developing a European framework for research on children's medicines: an examination of the proposed EU regulation on medicinal products for paediatric use.

scientific article published on 16 September 2005

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

scientific article

Dominant role of prostaglandin E2 EP4 receptor in furosemide-induced salt-losing tubulopathy: a model for hyperprostaglandin E syndrome/antenatal Bartter syndrome

scientific article published on 23 June 2005

Effects of celecoxib and diclofenac on blood pressure, renal function, and vasoactive prostanoids in young and elderly subjects

scientific article

Expression of prostanoid receptors in human ductus arteriosus

scientific article

Expression of the potassium channel ROMK in adult and fetal human kidney

scientific article

Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalization

scientific article published on 14 May 2005

Genetics of hereditary disorders of magnesium homeostasis

scientific article published on 22 November 2003

Hereditary Hypokalemic Salt-losing Tubular Disorders.

scientific article published on July 2003

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus

scientific article

Historical development of pediatric pharmacology.

scientific article published in January 2011

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

scientific article (publication date: June 2002)

Increased systolic blood pressure with rofecoxib in congenital furosemide-like salt loss.

scientific article published on 22 March 2006

Induction of microsomal prostaglandin E2 synthase in the macula densa in children with hypokalemic salt-losing tubulopathies

scientific article published on 19 November 2003

Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter

scientific article published on 28 June 2006

Loop disorders: insights derived from defined genotypes

scientific article published on 11 November 2010

Low-dose aspirin in pregnancy: maternal and neonatal aspirin concentrations and neonatal prostanoid formation

scientific article (publication date: 2003)

Osteoarthritis of the knee--clinical assessments and inflammatory markers

scientific article published on 01 June 2004

Paediatric clinical pharmacology in Europe

scholarly article by Maurizio Bonati et al published 1 November 2006 in CrossRef Listing of Deleted DOIs

Pathophysiology and clinical presentations of salt-losing tubulopathies

scientific article published on 16 July 2015

Perinatal management of a preterm neonate affected by hyperprostaglandin E2 syndrome (HPS).

scientific article

Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations

scientific journal article

Problems of prescription drug use in children

scientific article published on 16 January 2009

Regulation of CLC-Ka/barttin by the ubiquitin ligase Nedd4-2 and the serum- and glucocorticoid-dependent kinases

scientific article

Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome

scientific article published in July 2002

Salt handling in the distal nephron: lessons learned from inherited human disorders.

scientific article

Salt wasting and deafness resulting from mutations in two chloride channels

scientific article

[Drug therapy in childhood and adolescence. A challenge between patient protection and therapy safety]

scientific article published on 01 January 2003

pH dependence of extracellular calcium sensing receptor activity determined by a novel technique

scientific article published in January 2005

Paulina is supported by:

About Paulina

Help