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Quoted phrase not found in phrase index: "Juvenile-onset Steinert myotonic dystrophy"
Page 1
Differences in the pattern of cognitive impairments between juvenile and adult onset myotonic dystrophy type 1.
Woo J, Lee HW, Park JS. Woo J, et al. J Clin Neurosci. 2019 Oct;68:92-96. doi: 10.1016/j.jocn.2019.07.029. Epub 2019 Jul 29. J Clin Neurosci. 2019. PMID: 31371188
OBJECTIVE: To understand the different patterns of neuropsychological dysfunction observed between juvenile onset (jDM1) and adult onset (aDM1) myotonic dystrophy type 1. ...
OBJECTIVE: To understand the different patterns of neuropsychological dysfunction observed between juvenile onset (jDM1) and a …
White matter abnormalities and neurocognitive correlates in children and adolescents with myotonic dystrophy type 1: a diffusion tensor imaging study.
Wozniak JR, Mueller BA, Ward EE, Lim KO, Day JW. Wozniak JR, et al. Neuromuscul Disord. 2011 Feb;21(2):89-96. doi: 10.1016/j.nmd.2010.11.013. Epub 2010 Dec 18. Neuromuscul Disord. 2011. PMID: 21169018 Free PMC article.
Diffusion tensor imaging was used to evaluate cerebral white matter in eight patients (ages 10-17), with myotonic dystrophy type 1 (3 congenital-onset, 5 juvenile-onset) compared to eight controls matched for age and sex. Four regions of interest were …
Diffusion tensor imaging was used to evaluate cerebral white matter in eight patients (ages 10-17), with myotonic dystrophy ty …
Brain gray matter structural network in myotonic dystrophy type 1.
Sugiyama A, Sone D, Sato N, Kimura Y, Ota M, Maikusa N, Maekawa T, Enokizono M, Mori-Yoshimura M, Ohya Y, Kuwabara S, Matsuda H. Sugiyama A, et al. PLoS One. 2017 Nov 2;12(11):e0187343. doi: 10.1371/journal.pone.0187343. eCollection 2017. PLoS One. 2017. PMID: 29095898 Free PMC article.
This study aimed to investigate abnormalities in structural covariance network constructed from gray matter volume in myotonic dystrophy type 1 (DM1) patients by using graph theoretical analysis for further clarification of the underlying mechanisms of central nervo …
This study aimed to investigate abnormalities in structural covariance network constructed from gray matter volume in myotonic dys …
Characteristics of dynamic mutation in Japanese myotonic dystrophy.
Yamagata H, Miki T, Yamanaka N, Takemoto Y, Kanda F, Takahashi K, Inui T, Kinoshita M, Nakagawa M, Higuchi I, et al. Yamagata H, et al. Jpn J Hum Genet. 1994 Sep;39(3):327-35. doi: 10.1007/BF01874051. Jpn J Hum Genet. 1994. PMID: 7841443
To study the characteristics, if any, of unstable CTG repeat sequence in Japanese myotonic dystrophy (DM), we analyzed DNA from 351 at risk individuals (including affected and non-affected carriers and their descendants) from 105 families in Japan. ...There was a si …
To study the characteristics, if any, of unstable CTG repeat sequence in Japanese myotonic dystrophy (DM), we analyzed DNA fro …
Iris neovascular tufts. Relationship to rubeosis, insulin, and hypotony.
Mason GI. Mason GI. Arch Ophthalmol. 1979 Dec;97(12):2346-52. doi: 10.1001/archopht.1979.01020020562014. Arch Ophthalmol. 1979. PMID: 92984
This study searched for iris neovascular tufts by biomicroscopy and iris fluorescein angiography. They were found in two of 16 (12.5%) myotonic dystrophy patients, in two of 30 (6.7%) maturity-onset diabetics, and in zero of 14 (0%) juvenile-onset diab …
This study searched for iris neovascular tufts by biomicroscopy and iris fluorescein angiography. They were found in two of 16 (12.5%) my …