Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Atrophy and MFN2[original query] |
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[Update on hereditary neuropathy]. Rinsho shinkeigaku = Clinical neurology 2005 1 44 (11): 991-4. Nakagawa Masanori, Takashima Hiros |
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. BMC medical genetics 2009 10 91. Wolf Christiane, Gramer Eugen, Müller-Myhsok Bertram, Pasutto Francesca, Reinthal Eva, Wissinger Bernd, Weisschuh Nico |
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2. Journal of neurology 2011 1 258 (7): 1234-9. McCorquodale Donald S, Montenegro Gladys, Peguero Ainsley, Carlson Nicole, Speziani Fiorella, Price Justin, Taylor Sean W, Melanson Michel, Vance Jeffery M, Züchner Steph |
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
Association between Mitofusin 2 Gene Polymorphisms and Late-Onset Alzheimer's Disease in the Korean Population. Psychiatry investigation 2017 Jan 14 (1): 81-85. Kim Young Jong, Park Jin Kyung, Kang Won Sub, Kim Su Kang, Han Changsu, Na Hae Ri, Park Hae Jeong, Kim Jong Woo, Kim Young Youl, Park Moon Ho, Paik Jong-W |
Genetic epidemiology, demographic, and clinical characteristics of Charcot-Marie-tooth disease in the island of Gran Canaria (Spain). Journal of the peripheral nervous system : JPNS 2018 12 24 (1): 131-138. Lousa Manuel, Vázquez-Huarte-Mendicoa Carlos, Gutiérrez Antonio J, Saavedra Pedro, Navarro Beatriz, Tugores Anton |
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2. Neuromolecular medicine 2019 8 22 (1): 68-72. Deng Sheng, Feely Shawna M E, Shi Yong, Zhai Hong, Zhan Luna, Siddique Teepu, Deng Han-Xiang, Shy Michael |
Optic Neuropathy in Charcot-Marie-Tooth Disease. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2020 5 41 (2): 233-238. Hamedani Ali G, Wilson James A, Avery Robert A, Scherer Steven |
Associations between OPA1, MFN1, and MFN2 polymorphisms and primary open angle glaucoma in Polish participants of European ancestry. Ophthalmic genetics 2021 Aug 1-6. Milanowski Piotr, Kosior-Jarecka Ewa, ?ukasik Urszula, Wróbel-Dudzi?ska Dominika, Milanowska Joanna, Khor Chiea Chuen, Aung Tin, Kocki Janusz, ?arnowski Toma |
[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 10 54 (5): 874-883. Liu X X, Duan X H, Zhang S, Sun A P, Zhang Y S, Fan D |
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