- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Severe rhabdomyolysis in homozygote carnitine palmitoyltransferase II deficiency ; Vol. 19 2020
EXCLI journal ; Vol. 19 2020
- Classification
-
Medizin, Gesundheit
- Creator
-
Schnedl, Wolfgang J.
Schenk, Michael
Enko, Dietmar
Mangge, Harald
- Handle
-
2003/39927
- URN
-
urn:nbn:de:101:1-2020122502460542809187
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:28 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Schnedl, Wolfgang J.
- Schenk, Michael
- Enko, Dietmar
- Mangge, Harald
Other Objects (12)
Clinical aspects of human carnitine deficiency
Abcc6 deficiency prevents rhabdomyolysis-induced acute kidney injury
Carnitine palmitoyltransferase 2 deficiency, malignant hyperthermia and anesthesia
Furosemide-induced severe hypokalemia with rhabdomyolysis without cardiac arrest
Reversible Severe Rhabdomyolysis Associated with Thyrotoxic Hypokalemic Periodic Paralysis
Clinical, biochemical and genetic characterization of muscle carnitine palmitoyltransferase II (CPT II) deficiency
Carnitine deficiency is associated with decreased exercise activity in hemodialysis patients
Primary carnitine deficiency – diagnosis after heart transplantation: better late than never!
Rhabdomyolysis presenting with severe hypokalemia in hypertensive patients: a case series
Palbociclib in combination with simvastatin induce severe rhabdomyolysis: a case report
Risk factors for severe acute kidney injury among patients with rhabdomyolysis
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features
Clinical aspects of human carnitine deficiency
Abcc6 deficiency prevents rhabdomyolysis-induced acute kidney injury
Carnitine palmitoyltransferase 2 deficiency, malignant hyperthermia and anesthesia
Furosemide-induced severe hypokalemia with rhabdomyolysis without cardiac arrest
Reversible Severe Rhabdomyolysis Associated with Thyrotoxic Hypokalemic Periodic Paralysis
Clinical, biochemical and genetic characterization of muscle carnitine palmitoyltransferase II (CPT II) deficiency
Carnitine deficiency is associated with decreased exercise activity in hemodialysis patients
Primary carnitine deficiency – diagnosis after heart transplantation: better late than never!
Rhabdomyolysis presenting with severe hypokalemia in hypertensive patients: a case series
Palbociclib in combination with simvastatin induce severe rhabdomyolysis: a case report
Risk factors for severe acute kidney injury among patients with rhabdomyolysis
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features
Clinical aspects of human carnitine deficiency
Abcc6 deficiency prevents rhabdomyolysis-induced acute kidney injury
Carnitine palmitoyltransferase 2 deficiency, malignant hyperthermia and anesthesia
Furosemide-induced severe hypokalemia with rhabdomyolysis without cardiac arrest
Reversible Severe Rhabdomyolysis Associated with Thyrotoxic Hypokalemic Periodic Paralysis
Clinical, biochemical and genetic characterization of muscle carnitine palmitoyltransferase II (CPT II) deficiency
Carnitine deficiency is associated with decreased exercise activity in hemodialysis patients
Primary carnitine deficiency – diagnosis after heart transplantation: better late than never!
Rhabdomyolysis presenting with severe hypokalemia in hypertensive patients: a case series
Palbociclib in combination with simvastatin induce severe rhabdomyolysis: a case report
Risk factors for severe acute kidney injury among patients with rhabdomyolysis