Lynch PJ - Search Results

1

Ryanodine receptor mutations in malignant hyperthermia and central core disease.

McCarthy TV, Quane KA, Lynch PJ. McCarthy TV, et al. Among authors: lynch pj. Hum Mutat. 2000;15(5):410-7. doi: 10.1002/(SICI)1098-1004(200005)15:5<410::AID-HUMU2>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10790202 Review.

2

A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree.

Brown RL, Pollock AN, Couchman KG, Hodges M, Hutchinson DO, Waaka R, Lynch P, McCarthy TV, Stowell KM. Brown RL, et al. Hum Mol Genet. 2000 Jun 12;9(10):1515-24. doi: 10.1093/hmg/9.10.1515. Hum Mol Genet. 2000. PMID: 10888602

3

Detection of a novel mutation in the ryanodine receptor gene in an Irish malignant hyperthermia pedigree: correlation of the IVCT response with the affected and unaffected haplotypes.

Keating KE, Giblin L, Lynch PJ, Quane KA, Lehane M, Heffron JJ, McCarthy TV. Keating KE, et al. Among authors: lynch pj. J Med Genet. 1997 Apr;34(4):291-6. doi: 10.1136/jmg.34.4.291. J Med Genet. 1997. PMID: 9138151 Free PMC article.

4

Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia.

Manning BM, Quane KA, Lynch PJ, Urwyler A, Tegazzin V, Krivosic-Horber R, Censier K, Comi G, Adnet P, Wolz W, Lunardi J, Muller CR, McCarthy TV. Manning BM, et al. Among authors: lynch pj. Hum Mutat. 1998;11(1):45-50. doi: 10.1002/(SICI)1098-1004(1998)11:1<45::AID-HUMU7>3.0.CO;2-K. Hum Mutat. 1998. PMID: 9450902 No abstract available.

5

Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation.

Manning BM, Quane KA, Ording H, Urwyler A, Tegazzin V, Lehane M, O'Halloran J, Hartung E, Giblin LM, Lynch PJ, Vaughan P, Censier K, Bendixen D, Comi G, Heytens L, Monsieurs K, Fagerlund T, Wolz W, Heffron JJ, Muller CR, McCarthy TV. Manning BM, et al. Among authors: lynch pj. Am J Hum Genet. 1998 Mar;62(3):599-609. doi: 10.1086/301748. Am J Hum Genet. 1998. PMID: 9497245 Free PMC article.

6

A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.

Lynch PJ, Tong J, Lehane M, Mallet A, Giblin L, Heffron JJ, Vaughan P, Zafra G, MacLennan DH, McCarthy TV. Lynch PJ, et al. Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):4164-9. doi: 10.1073/pnas.96.7.4164. Proc Natl Acad Sci U S A. 1999. PMID: 10097181 Free PMC article.

7

Mutation screening of dihydropyridine receptor gamma subunit cDNA from malignant hyperthermia susceptible patients.

Lynch PJ, Couch FJ, Gregg RG, Powers PA, Hogan K, McCarthy TV. Lynch PJ, et al. Biochem Soc Trans. 1995 May;23(2):352S. doi: 10.1042/bst023352s. Biochem Soc Trans. 1995. PMID: 7672382 No abstract available.

8

Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindred.

Lynch PJ, Krivosic-Horber R, Reyford H, Monnier N, Quane K, Adnet P, Haudecoeur G, Krivosic I, McCarthy T, Lunardi J. Lynch PJ, et al. Anesthesiology. 1997 Mar;86(3):620-6. doi: 10.1097/00000542-199703000-00014. Anesthesiology. 1997. PMID: 9066328 Free article.

9

Mid-Infrared Electrochromics Enabled by Intraband Modulation in Carbon Nanotube Networks.

Lynch PJ, Tripathi M, Amorim Graf A, Ogilvie SP, Large MJ, Salvage J, Dalton AB. Lynch PJ, et al. ACS Appl Mater Interfaces. 2023 Mar 1;15(8):11225-11233. doi: 10.1021/acsami.2c19758. Epub 2023 Feb 17. ACS Appl Mater Interfaces. 2023. PMID: 36800377 Free PMC article.

10

Minimally Invasive Inferior Intra-Articular Sacroiliac Joint Fusion: Successful Application of Osseous Stabilization Using Allograft Bone.

Lynch PJ, Tubic G, Foster JM, Puri S, Burnette CA, Block JE. Lynch PJ, et al. Orthop Res Rev. 2022 Nov 16;14:429-435. doi: 10.2147/ORR.S387104. eCollection 2022. Orthop Res Rev. 2022. PMID: 36420375 Free PMC article.

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