Similar articles for PMID: 29759638

Year	Number of Results
2000	1
2006	2
2007	5
2008	4
2009	5
2010	9
2011	5
2012	6
2013	10
2014	9
2015	8
2016	10
2017	13
2018	11
2019	11
2020	12
2021	7
2022	7
2023	2
2024	0

1

A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature.

Brusa R, Magri F, Papadimitriou D, Govoni A, Del Bo R, Ciscato P, Savarese M, Cinnante C, Walter MC, Abicht A, Bulst S, Corti S, Moggio M, Bresolin N, Nigro V, Comi GP. Brusa R, et al. Neuromuscul Disord. 2018 Jun;28(6):532-537. doi: 10.1016/j.nmd.2018.04.006. Epub 2018 Apr 13. Neuromuscul Disord. 2018. PMID: 29759638 Review.

2

Conserved expression of truncated telethonin in a patient with limb-girdle muscular dystrophy 2G.

Barresi R, Morris C, Hudson J, Curtis E, Pickthall C, Bushby K, Davies NP, Straub V. Barresi R, et al. Neuromuscul Disord. 2015 Apr;25(4):349-52. doi: 10.1016/j.nmd.2014.12.006. Epub 2014 Dec 24. Neuromuscul Disord. 2015. PMID: 25724973

3

Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families.

Chen H, Xu G, Lin F, Jin M, Cai N, Qiu L, Ye Z, Wang L, Lin M, Wang N. Chen H, et al. Neuromuscul Disord. 2020 Feb;30(2):137-143. doi: 10.1016/j.nmd.2019.12.004. Epub 2019 Dec 17. Neuromuscul Disord. 2020. PMID: 32005491

4

Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient.

Ikenberg E, Karin I, Ertl-Wagner B, Abicht A, Bulst S, Krause S, Schoser B, Reilich P, Walter MC. Ikenberg E, et al. Neuromuscul Disord. 2017 Sep;27(9):856-860. doi: 10.1016/j.nmd.2017.05.017. Epub 2017 Jun 1. Neuromuscul Disord. 2017. PMID: 28666572

5

Novel mutation in TCAP manifesting with asymmetric calves and early-onset joint retractions.

de Fuenmayor-Fernández de la Hoz CP, Hernández-Laín A, Olivé M, Fernández-Marmiesse A, Domínguez-González C. de Fuenmayor-Fernández de la Hoz CP, et al. Neuromuscul Disord. 2016 Nov;26(11):749-753. doi: 10.1016/j.nmd.2016.07.003. Epub 2016 Jul 16. Neuromuscul Disord. 2016. PMID: 27618135

6

Limb-girdle muscular dystrophy in a Portuguese patient caused by a mutation in the telethonin gene.

Negrão L, Matos A, Geraldo A, Rebelo O. Negrão L, et al. Acta Myol. 2010 Jul;29(1):21-4. Acta Myol. 2010. PMID: 22029105 Free PMC article.

7

Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular center.

Huang K, Li QX, Duan HQ, Luo YB, Bi FF, Yang H. Huang K, et al. Neurogenetics. 2022 Jan;23(1):37-44. doi: 10.1007/s10048-021-00681-2. Epub 2022 Jan 4. Neurogenetics. 2022. PMID: 34982307

8

Unique Clinical, Radiological and Histopathological Characteristics of a Southeast Asian Cohort of Patients with Limb-Girdle Muscular Dystrophy 2G/LGMD-R7-Telethonin-Related.

Chen Z, Saini M, Koh JS, Prasad K, Koh SH, Tay KSS, Lee M, Tan YJ, Ng ASL, Tay SKH, Tan KB, Tandon A, Tan JMM, Chai JYH. Chen Z, et al. J Neuromuscul Dis. 2023;10(1):91-106. doi: 10.3233/JND-221517. J Neuromuscul Dis. 2023. PMID: 36463458

9

Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutation.

Chamova T, Bichev S, Todorov T, Gospodinova M, Taneva A, Kastreva K, Zlatareva D, Krupev M, Hadjiivanov R, Guergueltcheva V, Grozdanova L, Tzoneva D, Huebner A, V der Hagen M, Schoser B, Lochmüller H, Todorova A, Tournev I. Chamova T, et al. Neuromuscul Disord. 2018 Aug;28(8):625-632. doi: 10.1016/j.nmd.2018.05.005. Epub 2018 May 17. Neuromuscul Disord. 2018. PMID: 29935994

10

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.

Olivé M, Shatunov A, Gonzalez L, Carmona O, Moreno D, Quereda LG, Martinez-Matos JA, Goldfarb LG, Ferrer I. Olivé M, et al. Neuromuscul Disord. 2008 Dec;18(12):929-33. doi: 10.1016/j.nmd.2008.07.009. Epub 2008 Oct 22. Neuromuscul Disord. 2008. PMID: 18948002 Free PMC article.

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