Wang J - Search Results

1

Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?

Baquero JL, Ayala RA, Wang J, Curless RG, Feero WG, Hoffman EP, Ebeid MR. Baquero JL, et al. Among authors: wang j. Ann Neurol. 1995 Mar;37(3):408-11. doi: 10.1002/ana.410370320. Ann Neurol. 1995. PMID: 7695243

2

Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families.

Feero WG, Wang J, Barany F, Zhou J, Todorovic SM, Conwit R, Galloway G, Hausmanowa-Petrusewicz I, Fidzianska A, Arahata K, et al. Feero WG, et al. Among authors: wang j. Neurology. 1993 Apr;43(4):668-73. doi: 10.1212/wnl.43.4.668. Neurology. 1993. PMID: 8385748

3

Duchenne-Becker muscular dystrophy and the nondystrophic myotonias. Paradigms for loss of function and change of function of gene products.

Hoffman EP, Wang J. Hoffman EP, et al. Among authors: wang j. Arch Neurol. 1993 Nov;50(11):1227-37. doi: 10.1001/archneur.1993.00540110101010. Arch Neurol. 1993. PMID: 8215981 Review.

4

Identification of a Thr-to-Met mutation in the skeletal muscle sodium channel gene in hyperkalemic periodic paralysis of a Japanese family.

Arahata K, Wang J, Feero WG, Hayakawa H, Honda K, Sugita H, Hoffman EP. Arahata K, et al. Among authors: wang j. Ann N Y Acad Sci. 1993 Dec 20;707:342-5. doi: 10.1111/j.1749-6632.1993.tb38065.x. Ann N Y Acad Sci. 1993. PMID: 9137564 No abstract available.

5

Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.

Wang J, Zhou J, Todorovic SM, Feero WG, Barany F, Conwit R, Hausmanowa-Petrusewicz I, Fidzianska A, Arahata K, Wessel HB, et al. Wang J, et al. Am J Hum Genet. 1993 Jun;52(6):1074-84. Am J Hum Genet. 1993. PMID: 8389097 Free PMC article.

6

The genomic structure of the human skeletal muscle sodium channel gene.

McClatchey AI, Lin CS, Wang J, Hoffman EP, Rojas C, Gusella JF. McClatchey AI, et al. Among authors: wang j. Hum Mol Genet. 1992 Oct;1(7):521-7. doi: 10.1093/hmg/1.7.521. Hum Mol Genet. 1992. PMID: 1339144

7

In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4.

Wang J, Dubowitz V, Lehmann-Horn F, Ricker K, Ptacek L, Hoffman EP. Wang J, et al. Soc Gen Physiol Ser. 1995;50:77-88. Soc Gen Physiol Ser. 1995. PMID: 7676326 Review.

8

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.

Wang J, Pegoraro E, Menegazzo E, Gennarelli M, Hoop RC, Angelini C, Hoffman EP. Wang J, et al. Hum Mol Genet. 1995 Apr;4(4):599-606. doi: 10.1093/hmg/4.4.599. Hum Mol Genet. 1995. PMID: 7543316

9

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T; PD GWAS Consortium. Pankratz N, et al. Ann Neurol. 2012 Mar;71(3):370-84. doi: 10.1002/ana.22687. Ann Neurol. 2012. PMID: 22451204 Free PMC article.

10

Effects of extended-release niacin with laropiprant in high-risk patients.

HPS2-THRIVE Collaborative Group; Landray MJ, Haynes R, Hopewell JC, Parish S, Aung T, Tomson J, Wallendszus K, Craig M, Jiang L, Collins R, Armitage J. HPS2-THRIVE Collaborative Group, et al. N Engl J Med. 2014 Jul 17;371(3):203-12. doi: 10.1056/NEJMoa1300955. N Engl J Med. 2014. PMID: 25014686 Free article. Clinical Trial.

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