Arnold Köckerling

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 et al. · Human Molecular Genetics · 1997 · 190 citations · Full text

Electrolyte Disorder, Genetics, Renal Pathology +19

Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function

Christian Derst, Martin Konrad, Arnold Köckerling et al. · Biochemical and Biophysical Research Communications · 1997 · 99 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +9

Origin of cAMP-dependent Cl- secretion from both crypts and surface epithelia of rat intestine

Arnold Köckerling, Michael Fromm · American Journal of Physiology-Cell Physiology · 1993 · 92 citations

Protein Secretion, Cl- Secretion, Digestive Tract +18

Impaired response to furosemide in hyperprostaglandin E syndrome: Evidence for a tubular defect in the loop of Henle

Arnold Köckerling, Stephan C. Reinalter, H. W. Seyberth · The Journal of Pediatrics · 1996 · 74 citations

Clinical Disorders, Hyperprostaglandin E Syndrome, Physiology +7

Electrogenic Na+ absorption of rat distal colon is confined to surface epithelium: a voltage-scanning study

Arnold Köckerling, Detlef Sorgenfrei, Michael Fromm · American Journal of Physiology-Cell Physiology · 1993 · 67 citations

Sodium Homeostasis, Nm Aldosterone, Membrane Transport +15