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Malignant Hyperthermia.
Kaur H, Katyal N, Yelam A, Kumar K, Srivastava H, Govindarajan R. Kaur H, et al. Mo Med. 2019 Mar-Apr;116(2):154-159. Mo Med. 2019. PMID: 31040503 Free PMC article. Review.
This review also aims to highlight the genetics and pathology of MH, along with its association with various inherited myopathy syndromes like central core disease, multi-mini core disease, Native-American myopathy, and King-Denborough syndrome....
This review also aims to highlight the genetics and pathology of MH, along with its association with various inherited myopathy syndromes li …
Ryanodine Receptor 1-Related Myopathies: Diagnostic and Therapeutic Approaches.
Lawal TA, Todd JJ, Meilleur KG. Lawal TA, et al. Neurotherapeutics. 2018 Oct;15(4):885-899. doi: 10.1007/s13311-018-00677-1. Neurotherapeutics. 2018. PMID: 30406384 Free PMC article. Review.
A range of RYR1-RM clinical phenotypes has also emerged more recently and includes King Denborough syndrome, RYR1 rhabdomyolysis-myalgia syndrome, atypical periodic paralysis, congenital neuromuscular disease with uniform type 1 fibers, and late-onset …
A range of RYR1-RM clinical phenotypes has also emerged more recently and includes King Denborough syndrome, RYR1 rhabd …
King-Denborough syndrome: contracture testing and literature review.
Heiman-Patterson TD, Rosenberg HR, Binning CP, Tahmoush AJ. Heiman-Patterson TD, et al. Pediatr Neurol. 1986 May-Jun;2(3):175-7. doi: 10.1016/0887-8994(86)90013-5. Pediatr Neurol. 1986. PMID: 2907859 Review.
The King-Denborough syndrome (KDS) is characterized by dysmorphic features, myopathy, and malignant hyperthermia (MH). ...
The King-Denborough syndrome (KDS) is characterized by dysmorphic features, myopathy, and malignant hyperthermia (MH). …
Ryanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature.
Lawal TA, Todd JJ, Witherspoon JW, Bönnemann CG, Dowling JJ, Hamilton SL, Meilleur KG, Dirksen RT. Lawal TA, et al. Skelet Muscle. 2020 Nov 16;10(1):32. doi: 10.1186/s13395-020-00243-4. Skelet Muscle. 2020. PMID: 33190635 Free PMC article. Review.
As additional phenotypes were associated with RYR1 variations (including King-Denborough syndrome, exercise-induced rhabdomyolysis, lethal multiple pterygium syndrome, adult-onset distal myopathy, atypical periodic paralysis with or without myalgia, mi …
As additional phenotypes were associated with RYR1 variations (including King-Denborough syndrome, exercise-induced rha …
[Anesthetic management of the King-Denborough syndrome].
Iwatsubo T, Yoshikawa M, Karashima Y, Kurita N, Shimoda T, Takahashi H, Horiuchi T, Kitaguchi K, Furuya H. Iwatsubo T, et al. Masui. 2001 Apr;50(4):390-3. Masui. 2001. PMID: 11345752 Review. Japanese.
The King-Denborough syndrome (KDS) is a congenital myopathy with musculoskeletal abnormalities, and definitely associated with susceptibility to malignant hyperthermia (MH). ...It is rare that a diagnosis of KDS is made preoperatively since the MH-induction i …
The King-Denborough syndrome (KDS) is a congenital myopathy with musculoskeletal abnormalities, and definitely associat …
Malignant hyperthermia and neuromuscular disease.
Wedel DJ. Wedel DJ. Neuromuscul Disord. 1992;2(3):157-64. doi: 10.1016/0960-8966(92)90001-m. Neuromuscul Disord. 1992. PMID: 1483040 Review.
Malignant hyperthermia (MH) is a rare clinical syndrome characterized by hypermetabolism and triggered by specific anesthetic agents. ...A variety of other diseases have been implicated and can be classified as possibly associated (King-Denborough syndrome …
Malignant hyperthermia (MH) is a rare clinical syndrome characterized by hypermetabolism and triggered by specific anesthetic agents. …