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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 3
1997 2
2003 2
2005 2
2006 1
2007 2
2008 1
2009 4
2010 2
2011 4
2013 3
2014 1
2015 1
2017 2
2019 2
2020 2
2021 1
2022 1
2023 2
2024 0

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36 results

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Page 1
Pediatric joint hypermobility: a diagnostic framework and narrative review.
Tofts LJ, Simmonds J, Schwartz SB, Richheimer RM, O'Connor C, Elias E, Engelbert R, Cleary K, Tinkle BT, Kline AD, Hakim AJ, van Rossum MAJ, Pacey V. Tofts LJ, et al. Among authors: tinkle bt. Orphanet J Rare Dis. 2023 May 4;18(1):104. doi: 10.1186/s13023-023-02717-2. Orphanet J Rare Dis. 2023. PMID: 37143135 Free PMC article. Review.
Symptomatic joint hypermobility.
Tinkle BT. Tinkle BT. Best Pract Res Clin Rheumatol. 2020 Jun;34(3):101508. doi: 10.1016/j.berh.2020.101508. Epub 2020 Apr 3. Best Pract Res Clin Rheumatol. 2020. PMID: 32249022 Review.
GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
Platzer K, Yuan H, Schütz H, Winschel A, Chen W, Hu C, Kusumoto H, Heyne HO, Helbig KL, Tang S, Willing MC, Tinkle BT, Adams DJ, Depienne C, Keren B, Mignot C, Frengen E, Strømme P, Biskup S, Döcker D, Strom TM, Mefford HC, Myers CT, Muir AM, LaCroix A, Sadleir L, Scheffer IE, Brilstra E, van Haelst MM, van der Smagt JJ, Bok LA, Møller RS, Jensen UB, Millichap JJ, Berg AT, Goldberg EM, De Bie I, Fox S, Major P, Jones JR, Zackai EH, Abou Jamra R, Rolfs A, Leventer RJ, Lawson JA, Roscioli T, Jansen FE, Ranza E, Korff CM, Lehesjoki AE, Courage C, Linnankivi T, Smith DR, Stanley C, Mintz M, McKnight D, Decker A, Tan WH, Tarnopolsky MA, Brady LI, Wolff M, Dondit L, Pedro HF, Parisotto SE, Jones KL, Patel AD, Franz DN, Vanzo R, Marco E, Ranells JD, Di Donato N, Dobyns WB, Laube B, Traynelis SF, Lemke JR. Platzer K, et al. Among authors: tinkle bt. J Med Genet. 2017 Jul;54(7):460-470. doi: 10.1136/jmedgenet-2016-104509. Epub 2017 Apr 4. J Med Genet. 2017. PMID: 28377535 Free PMC article.
Joint hypermobility and headache.
Tinkle BT. Tinkle BT. Headache. 2014 Sep;54(8):1412-3. doi: 10.1111/head.12416. Headache. 2014. PMID: 25196367 No abstract available.
Oral and mandibular manifestations in the Ehlers-Danlos syndromes.
Mitakides J, Tinkle BT. Mitakides J, et al. Among authors: tinkle bt. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):220-225. doi: 10.1002/ajmg.c.31541. Epub 2017 Feb 13. Am J Med Genet C Semin Med Genet. 2017. PMID: 28192626 Review.
Health supervision for children with Marfan syndrome.
Tinkle BT, Saal HM; Committee on genetics. Tinkle BT, et al. Pediatrics. 2013 Oct;132(4):e1059-72. doi: 10.1542/peds.2013-2063. Epub 2013 Sep 30. Pediatrics. 2013. PMID: 24081994 Review.
Craniometaphyseal dysplasia-induced hearing loss.
Sun GH, Samy RN, Tinkle BT, Cornelius RS, Brown DK. Sun GH, et al. Among authors: tinkle bt. Otol Neurotol. 2011 Feb;32(2):e9-10. doi: 10.1097/MAO.0b013e3181d35e52. Otol Neurotol. 2011. PMID: 20351609 No abstract available.
36 results