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KAI SCHLINGMANN, D.O.
D.O.
Emergency Medicine Physician
NPI: 1699189068Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
20A16507(CA)
Research & Publications (18)
Autosomal dominant hypoparathyroidism with severe hypomagnesemia and hypocalcemia, successfully treated with recombinant PTH and continuous subcutaneous magnesium infusion.
PMID 18556971·J Pediatr Endocrinol Metab·2008
5-case
TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism.
PMID 17481860·Biochim Biophys Acta·2007
6-review
Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.
PMID 17197439·J Biol Chem·2007
7-preclinical
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.
PMID 17033971·Am J Hum Genet·2006
7-preclinical
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.
PMID 16107578·J Am Soc Nephrol·2005
8-other
Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis.
PMID 16075242·Pflugers Arch·2005
6-review
Characterization of an A-kinase anchor protein in equine spermatozoa and examination of the effect of semen cooling and cryopreservation on the binding of that protein to the regulatory subunit of protein kinase-A.
PMID 16008231·Am J Vet Res·2005
4-observational
Gene locus ambiguity in posterior urethral valves/prune-belly syndrome.
PMID 15912376·Pediatr Nephrol·2005
8-other
A critical role of TRPM channel-kinase for human magnesium transport.
PMID 15845589·J Physiol·2005
6-review
Salt handling in the distal nephron: lessons learned from inherited human disorders.
PMID 15793031·Am J Physiol Regul Integr Comp Physiol·2005
5-case
Salt wasting and deafness resulting from mutations in two chloride channels.
PMID 15044642·N Engl J Med·2004
5-case
Insights into the molecular nature of magnesium homeostasis.
PMID 15001450·Am J Physiol Renal Physiol·2004
6-review
Genetics of hereditary disorders of magnesium homeostasis.
PMID 14634861·Pediatr Nephrol·2004
6-review
Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.
PMID 12911542·Kidney Int·2003
7-preclinical
Induction of endogenous genes by peroxisome proliferator activated receptor alpha ligands in a human kidney cell line and in vivo.
PMID 12798359·J Steroid Biochem Mol Biol·2003
7-preclinical
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
PMID 12032568·Nat Genet·2002
8-other
Primary gene structure and expression studies of rodent paracellin-1.
PMID 11729235·J Am Soc Nephrol·2001
4-observational
Inhibition of neointima formation by a nonpeptide alpha(v)beta(3) integrin receptor antagonist in a rabbit cuff model.
PMID 10723088·J Cell Biochem·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 13651 WILLARD STREET
PANORAMA CITY, CA 91402 - Phone
- (818) 314-2900
Quick Facts
- NPI
- 1699189068
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 18
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