Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Hearing Loss and MELAS[original query] |
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Clinical features of A3243G mitochondrial tRNA mutation. Brain & development 2004 Oct 26 (7): 459-62. Chae Jong Hee, Hwang Hee, Lim Byung Chan, Cheong Hae Il, Hwang Yong Seung, Kim Ki Joo |
A novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS. Italian heart journal : official journal of the Italian Federation of Cardiology 2004 Jun 5 (6): 460-5. Menotti Francesca, Brega Agnese, Diegoli Marta, Grasso Maurizia, Modena Maria Grazia, Arbustini Eloi |
MELAS A3243G mitochondrial DNA mutation and age related maculopathy. American journal of ophthalmology 2004 Dec 138 (6): 1051-3. Jones Michael, Mitchell Paul, Wang Jie Jin, Sue Carol |
Population prevalence of the MELAS A3243G mutation. Mitochondrion 2007 May 7 (3): 230-3. Manwaring Neil, Jones Michael M, Wang Jie Jin, Rochtchina Elena, Howard Chris, Mitchell Paul, Sue Carolyn |
[Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate]. Zhonghua yi xue za zhi 2012 Oct 92 (40): 40. Xue JF, Chen L, Ma YN, Zhao DH, Duan JB, Wang ZX, Qi Y, Liu YH |
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management. Journal of neurology, neurosurgery, and psychiatry 2013 Jan . Nesbitt V, Pitceathly RD, Turnbull DM, Taylor RW, Sweeney MG, Mudanohwo EE, Rahman S, Hanna MG, McFarland R |
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? Journal of neurology 2014 Mar 261 (3): 504-10. Mancuso Michelangelo, Orsucci Daniele, Angelini Corrado, Bertini Enrico, Carelli Valerio, Comi Giacomo Pietro, Donati Alice, Minetti Carlo, Moggio Maurizio, Mongini Tiziana, Servidei Serenella, Tonin Paola, Toscano Antonio, Uziel Graziella, Bruno Claudio, Ienco Elena Caldarazzo, Filosto Massimiliano, Lamperti Costanza, Catteruccia Michela, Moroni Isabella, Musumeci Olimpia, Pegoraro Elena, Ronchi Dario, Santorelli Filippo Maria, Sauchelli Donato, Scarpelli Mauro, Sciacco Monica, Valentino Maria Lucia, Vercelli Liliana, Zeviani Massimo, Siciliano Gabrie |
Audiological and Vestibular Findings in Subjects with MELAS Syndrome. The journal of international advanced otology 2019 7 15 (2): 296-303. Hougaard Dan Dupont, Hestoy Danial Hofgaard, Hojland Allan Thomas, Gailhede Michael, Petersen Michael Bjo |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Journal of neurology 2021 1 268 (6): 2192-2207. Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet |
A retrospective cohort study exploring the association between different mitochondrial diseases and hearing loss. Molecular genetics and metabolism 2022 2 135 (4): 333-341. van Kempen Carlijn M A, Beynon Andy J, Smits Jeroen J, Janssen Mirian C |
[Epilepsy syndromes associated with hearing loss]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2023 1 123 (1): 28-33. Burd S G, Lebedeva A V, Rubleva Yu V, Pantina N V, Yurchenko A V, Bogomazova M A, Kovaleva I I, Karchevskaya A |
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