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Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
PLoS Genet. 2017 Feb 27;13(2):e1006624. doi: 10.1371/journal.pgen.1006624. eCollection 2017 Feb.
PLoS Genet. 2017.
PMID: 28241013
Free PMC article.
ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
Zhang Y, Huang H, Zhao G, Yokoyama T, Vega H, Huang Y, Sood R, Bishop K, Maduro V, Accardi J, Toro C, Boerkoel CF, Lyons K, Gahl WA, Duan X, Malicdan MC, Lin S.
Zhang Y, et al. Among authors: accardi j.
PLoS Genet. 2017 Feb 3;13(2):e1006481. doi: 10.1371/journal.pgen.1006481. eCollection 2017 Feb.
PLoS Genet. 2017.
PMID: 28158191
Free PMC article.
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Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.
Albert JS, Bhattacharyya N, Wolfe LA, Bone WP, Maduro V, Accardi J, Adams DR, Schwartz CE, Norris J, Wood T, Gafni RI, Collins MT, Tosi LL, Markello TC, Gahl WA, Boerkoel CF.
Albert JS, et al. Among authors: accardi j.
Orphanet J Rare Dis. 2015 Mar 7;10:27. doi: 10.1186/s13023-015-0235-8.
Orphanet J Rare Dis. 2015.
PMID: 25888122
Free PMC article.
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Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Pierson TM, Markello T, Accardi J, Wolfe L, Adams D, Sincan M, Tarazi NM, Fajardo KF, Cherukuri PF, Bajraktari I, Meilleur KG, Donkervoort S, Jain M, Hu Y, Lehky TJ, Cruz P, Mullikin JC, Bonnemann C, Gahl WA, Boerkoel CF, Tifft CJ.
Pierson TM, et al. Among authors: accardi j.
Neuromuscul Disord. 2013 Jun;23(6):483-8. doi: 10.1016/j.nmd.2013.01.013. Epub 2013 Mar 1.
Neuromuscul Disord. 2013.
PMID: 23453856
Free PMC article.
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Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.
Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, Stoll M, Nicholson G, Gonzalez MA, Speziani F, Dürr A, Stevanin G, Biesecker LG; NIH Intramural Sequencing Center; Accardi J, Landis DM, Gahl WA, Traynor BJ, Marques W Jr, Züchner S, Blackstone C, Fischbeck KH, Burnett BG.
Landouré G, et al. Among authors: accardi j.
Hum Mutat. 2013 Oct;34(10):1357-60. doi: 10.1002/humu.22378. Epub 2013 Aug 12.
Hum Mutat. 2013.
PMID: 23857908
Free PMC article.
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Sitagliptin as combination therapy in the treatment of type 2 diabetes mellitus.
Miller SA, St Onge EL, Accardi JR.
Miller SA, et al. Among authors: accardi jr.
Diabetes Metab Syndr Obes. 2009 May 13;2:23-30. doi: 10.2147/dmsott.s4068.
Diabetes Metab Syndr Obes. 2009.
PMID: 21437116
Free PMC article.
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Angiotensin II vaccine: a novel approach in the treatment of hypertension.
Miller SA, Accardi JR, St Onge EL.
Miller SA, et al. Among authors: accardi jr.
Expert Opin Biol Ther. 2008 Nov;8(11):1669-73. doi: 10.1517/14712598.8.11.1669.
Expert Opin Biol Ther. 2008.
PMID: 18847303
Review.
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Attitudes and feelings of criminal justice personnel toward the mentally ill.
Silverman M, Nelson CE, Accardi J.
Silverman M, et al. Among authors: accardi j.
Am J Community Psychol. 1976 Jun;4(2):207-16. doi: 10.1007/BF00881943.
Am J Community Psychol. 1976.
PMID: 941878
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