Related content

Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia

By Ji Kunqian   Liu Kaiming   Lin Pengfei   Wen Bing   Luo Yue-Bei   Zhao Yuying   Yan Chuanzhu  

Neurological Sciences, Vol. 35, Iss. 3, 2014-03 ,pp. : 443-448

Springer Publishing Company

Access to resources Recommend Favorite

A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia

By Deschauer M.   Kiefer R.   Blakely E.L.   He L.   Zierz S.   Turnbull D.M.   Taylor R.W.  

Neuromuscular Disorders, Vol. 13, Iss. 7, 2003-09 ,pp. : 568-572

Elsevier

Access to resources Recommend Favorite

Progressive external ophthalmoplegia as initial manifestation of sporadic late-onset nemaline myopathy

By Wengert Oliver   Meisel Andreas   Kress Wolfram   Dekomien Gabriele   Angstwurm Klemens   Heppner Frank   Goebel Hans-Hilmar   Stenzel Werner  

Journal of Neurology, Vol. 258, Iss. 5, 2011-05 ,pp. : 915-917

Springer Publishing Company

Access to resources Recommend Favorite

Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns–Sayre syndrome

By Bosbach S.  

Brain, Vol. 126, Iss. 5, 2003-05 ,pp. : 1231-1240

Oxford University Press

Access to resources Recommend Favorite

Late onset autosomal dominant Charcot–Marie–Tooth 2 neuropathy in a Costa Rican family

By Berghoff Corinna   Berghoff Martin   Leal Alejandro   Morera Bernal   Contreras Carlos   Barrantes Ramiro   Rautenstrauss Bernd   Del Valle Gerardo   Heuss Dieter  

Neurological Research, Vol. 31, Iss. 3, 2009-04 ,pp. : 283-288

Maney Publishing

Access to resources Recommend Favorite