Similar articles for PMID: 28838911

Year	Number of Results
2001	1
2006	1
2010	2
2011	7
2012	4
2013	4
2014	7
2015	11
2016	13
2017	19
2018	8
2019	9
2020	10
2021	11
2022	8
2023	1
2024	0

1

Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome.

Arrigoni F, Romaniello R, Peruzzo D, De Luca A, Parazzini C, Valente EM, Borgatti R, Triulzi F. Arrigoni F, et al. AJNR Am J Neuroradiol. 2017 Dec;38(12):2385-2390. doi: 10.3174/ajnr.A5360. Epub 2017 Aug 24. AJNR Am J Neuroradiol. 2017. PMID: 28838911 Free PMC article.

2

Interpeduncular Heterotopia and Brain Stem Cleft: An Isolated Finding Not Associated with Joubert Syndrome.

Sahap SK, Ucan B, Keskin DB, Goktas OA, Fitoz S. Sahap SK, et al. Neuropediatrics. 2021 Feb;52(1):62-64. doi: 10.1055/s-0040-1715487. Epub 2020 Oct 27. Neuropediatrics. 2021. PMID: 33111307

3

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome.

Epting D, Senaratne LDS, Ott E, Holmgren A, Sumathipala D, Larsen SM, Wallmeier J, Bracht D, Frikstad KM, Crowley S, Sikiric A, Barøy T, Käsmann-Kellner B, Decker E, Decker C, Bachmann N, Patzke S, Phelps IG, Katsanis N, Giles R, Schmidts M, Zucknick M, Lienkamp SS, Omran H, Davis EE, Doherty D, Strømme P, Frengen E, Bergmann C, Misceo D. Epting D, et al. Hum Mutat. 2020 Dec;41(12):2179-2194. doi: 10.1002/humu.24127. Epub 2020 Nov 1. Hum Mutat. 2020. PMID: 33131181 Free PMC article.

4

Sonographic 'molar tooth' sign in the diagnosis of Joubert syndrome.

Pugash D, Oh T, Godwin K, Robinson AJ, Byrne A, Van Allen MI, Osiovich H. Pugash D, et al. Ultrasound Obstet Gynecol. 2011 Nov;38(5):598-602. doi: 10.1002/uog.8979. Ultrasound Obstet Gynecol. 2011. PMID: 21370303 Free article.

5

Decaying molar tooth sign in Joubert syndrome and related disorders is correlated to a displacement of the corticospinal tract.

Alves CAPF, Ferraciolli S, Matsui C, Lucato LT. Alves CAPF, et al. Neuroradiology. 2017 Dec;59(12):1189-1191. doi: 10.1007/s00234-017-1940-x. Epub 2017 Oct 28. Neuroradiology. 2017. PMID: 29080037 No abstract available.

6

A characteristic image in Joubert syndrome: molar tooth sign.

Sghir M, Kesomtini W. Sghir M, et al. Pan Afr Med J. 2015 May 28;21:69. doi: 10.11604/pamj.2015.21.69.7068. eCollection 2015. Pan Afr Med J. 2015. PMID: 26491512 Free PMC article. No abstract available.

7

Defective ciliogenesis in INPP5E-related Joubert syndrome.

Hardee I, Soldatos A, Davids M, Vilboux T, Toro C, David KL, Ferreira CR, Nehrebecky M, Snow J, Thurm A, Heller T, Macnamara EF, Gunay-Aygun M, Zein WM, Gahl WA, Malicdan MCV. Hardee I, et al. Am J Med Genet A. 2017 Dec;173(12):3231-3237. doi: 10.1002/ajmg.a.38376. Epub 2017 Oct 20. Am J Med Genet A. 2017. PMID: 29052317 Free PMC article.

8

Novel CC2D2A compound heterozygous mutations cause Joubert syndrome.

Xiao D, Lv C, Zhang Z, Wu M, Zheng X, Yang L, Li X, Wu G, Chen J. Xiao D, et al. Mol Med Rep. 2017 Jan;15(1):305-308. doi: 10.3892/mmr.2016.6007. Epub 2016 Dec 7. Mol Med Rep. 2017. PMID: 27959436

9

Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia.

Enokizono M, Aida N, Niwa T, Osaka H, Naruto T, Kurosawa K, Ohba C, Suzuki T, Saitsu H, Goto T, Matsumoto N. Enokizono M, et al. J Neurol Sci. 2017 May 15;376:7-12. doi: 10.1016/j.jns.2017.02.065. Epub 2017 Mar 1. J Neurol Sci. 2017. PMID: 28431631

10

Fourth ventricle index: sonographic marker for severe fetal vermian dysgenesis/agenesis.

Haratz KK, Shulevitz SL, Leibovitz Z, Lev D, Shalev J, Tomarkin M, Malinger G, Lerman-Sagie T, Gindes L. Haratz KK, et al. Ultrasound Obstet Gynecol. 2019 Mar;53(3):390-395. doi: 10.1002/uog.19034. Epub 2019 Jan 31. Ultrasound Obstet Gynecol. 2019. PMID: 29484745 Free article.

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