Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Myotonic Dystrophy and DMPK[original query] |
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| CTG repeat polymorphism in DMPK gene in healthy Yugoslav population. Acta neurologica Scandinavica 2002 Jan 105 (1): 55-8. Culjkovi? B, Stojkovi? O, Vukosavi? S, Savi? D, Rakocevic V, Apostolski S, Romac |
| 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1. Human mutation 2002 Feb 19 (2): 131-9. Savi? Dusanka, Rakocvic-Stojanovic Vidosava, Keckarevic Dusan, Culjkovic Biljana, Stojkovic Oliver, Mladenovic Jelena, Todorovic Slobodanka, Apostolski Slobodan, Romac Stan |
| [Polymorphism of CTG-repeats in the DMPK gene in populations of Yakutia and central Asia]. Molekuliarnaia biologiia 0 39 (3): 385-93. Fedorova S A, Khusainova R I, Kutuev I A, Sukhomiatova A L, Nikolaeva I A, Kulichkin S S, Akhmetova V L, Salimova A Z, Sviatova G S, Berezina G M, Platonov F A, Khusnutdinova E |
| Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population. Molecular and cellular probes 2005 Feb 19 (1): 71-4. Vallo L, Bonifazi E, Borgiani P, Novelli G, Botta |
| CTG repeats at the myotonic protein kinase gene in a healthy Chilean population sample. Acta neurologica Scandinavica 2009 May 119 (5): 321-4. Amenabar F, Jorquera H, Acuña M, Cifuentes |
| CTG expansion & haplotype analysis in DM1 gene in healthy Iranian population. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2008 May 35 (2): 216-9. Shojasaffar Bahareh, Moradin Neda, Kahrizi Kimia, Cobo Ana Maria, Najmabadi Hosse |
| Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans. The Korean journal of laboratory medicine 2008 Dec 28 (6): 483-92. Kim So Yeon, Kim Ji Yeon, Kim Gyoung Pyoung, Sung Jung-Jun, Lim Kyu Sang, Lee Kwang-Woo, Chae Jong Hee, Hong Yoon-Ho, Seong Moon-Woo, Park Sung S |
| CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2010 Dec 17 (12): 1520-2. Theerasasawat S, Papsing C, Pulkes |
| Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in the Korean population. Annals of clinical and laboratory science 2010 40 (2): 156-62. Kwon Min-Jung, Lee Seung-Tae, Kim Byoung Joon, Sung Duk Hyun, Kim Jong-Won, Ki Chang-Se |
| Mechanisms of statin-induced myalgia assessed by physiogenomic associations. Atherosclerosis 2011 Oct 218 (2): 451-6. Ruaño Gualberto, Windemuth Andreas, Wu Alan H B, Kane John P, Malloy Mary J, Pullinger Clive R, Kocherla Mohan, Bogaard Kali, Gordon Bruce R, Holford Theodore R, Gupta Ankur, Seip Richard L, Thompson Paul |
| MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1. Journal of neurology 2012 Nov . Huin V, Vasseur F, Schraen-Maschke S, Dhaenens CM, Devos P, Dupont K, Sergeant N, Buée L, Lacour A, Hofmann-Radvanyi H, Sablonnière B |
| [Genetic Variability and Structure of SNP Haplotypes in the DMPK Gene in Yakuts and Other Ethnic Groups of Northern Eurasia in Relation to Myotonic Dystrophy]. Genetika 2015 Jun 51 (6): 724-32. Swarovskaya M G, Stepanova S K, Marussin A V, Sukhomyasova A L, Maximova N R, Stepanov V |
| SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies. European journal of human genetics : EJHG 2015 Jun . Bissay Véronique, Van Malderen Sophie C H, Keymolen Kathelijn, Lissens Willy, Peeters Uschi, Daneels Dorien, Jansen Anna C, Pappaert Gudrun, Brugada Pedro, De Keyser Jacques, Van Dooren Son |
| Haplotype analysis and LD detection at DM1 locus. Gene 2015 Aug 567 (1): 45-50. Kumar Ashok, Agarwal Sarita, Pradhan Sun |
| Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy. Investigative ophthalmology & visual science 2017 Sep 58 (11): 4579-4585. Mootha V Vinod, Hansen Brock, Rong Ziye, Mammen Pradeep P, Zhou Zhengyang, Xing Chao, Gong X |
| Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution. Neuromuscular disorders : NMD 2017 10 27 (12): 1106-1114. Murillo-Melo N M, Márquez-Quiróz L C, Gómez R, Orozco L, Mendoza-Caamal E, Tapia-Guerrero Y S, Camacho-Mejorado R, Cortés H, López-Reyes A, Santana C, Noris G, Hernández-Hernández O, Cisneros B, Magaña J |
| Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1. Investigative ophthalmology & visual science 2018 Jun 59 (7): 3053-3057. Winkler Nelson S, Milone Margherita, Martinez-Thompson Jennifer M, Raja Harish, Aleff Ross A, Patel Sanjay V, Fautsch Michael P, Wieben Eric D, Baratz Keith |
| Genotype-phenotype correlations in pediatric patients with myotonic dystrophy type 1. Korean journal of pediatrics 2018 Sep . Kim Hyeong Jung, Na Ji-Hoon, Lee Young-Mo |
| Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1. PloS one 2019 5 14 (5): e0216407. Corrales Eyleen, Vásquez Melissa, Zhang Baili, Santamaría-Ulloa Carolina, Cuenca Patricia, Krahe Ralf, Monckton Darren G, Morales Fernan |
| Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations. European journal of human genetics : EJHG 2020 3 28 (7): 956-962. Joosten Isis B T, Hellebrekers Debby M E I, de Greef Bianca T A, Smeets Hubert J M, de Die-Smulders Christine E M, Faber Catharina G, Gerrits Monique |
| Intellectual Profile in Myotonic Dystrophy Type 1 and Its Association With Its Onset: A Systematic Review and Meta-Analysis. Pediatric neurology 2024 9 161 9-17. Carlos Pascual-Morena, Iván Cavero-Redondo, Alicia Saz-Lara, Irene Martínez-García, María Eugenia Visier-Alfonso, Vicente Martínez-Vizcaí |
- Page last reviewed:Feb 1, 2024
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