Malignant Hyperthermia
By Beverley Mcneil. Springer US, 2005
1,061 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/aa6675d8aff7f105df24bf007a119f37a0373690
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- A. Huerta-Alardin
- J. Varon
- S. Hamilton
- P. Marik
- Dimitra K. Georgiou
- J. Lanner
- A. Joshi
- Aniruddh Raghu
Citations in the corpus
- Bench-to-bedside review: Rhabdomyolysis – an overview for clinicians (2004, background): “Malignant hyperthermia is an autosomal dominant genetic disorder in 50% of cases and an autosomal recessive genetic disorder in 20% of cases that affects males more frequently than females [35].”
- Ryanodine receptors: structure, expression, molecular details, and function in calcium release. (2010, background): “The incidence of MH is 1 in 15,000 anesthetized children and 1 in 50,000 to 100,000 anesthetized adults (MacLennan 1992; Strazis and Fox 1993; Rosenberg et al. 2007).”