Your search returned 193 results.

Results
	1.	Primary optic atrophy and autosomal dominant osteopetrosis type II. [electronic resource] by Singh, S K Singh, Rina Maurya, V K Producer: 20021016 In: The Journal of the Association of Physicians of India vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	2.	Dominant optic atrophy. [electronic resource] by Lenaers, Guy Hamel, Christian Delettre, Cécile Amati-Bonneau, Patrizia Procaccio, Vincent Bonneau, Dominique Reynier, Pascal Milea, Dan Producer: 20130410 In: Orphanet journal of rare diseases vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics. [electronic resource] by Alavi, Marcel V Fuhrmann, Nico Producer: 20140801 In: Molecular neurodegeneration vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[The use of optical coherence tomography in hereditary optic neuropathies: description of a family]. [electronic resource] by Sánchez-Tocino, H Andrés-Santos, A Pascual-González, P Sanchidrián-Mayo, M Producer: 20080715 In: Archivos de la Sociedad Espanola de Oftalmologia vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Dominant hereditary optic atrophy with bitemporal field defects. [electronic resource] by MANCHESTER, P T CALHOUN, F P Producer: 20000701 In: A.M.A. archives of ophthalmology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Genetic basis of hereditary optic atrophies]. [electronic resource] by Wawrocka, Anna Krawczyński, Maciej R Producer: 20080617 In: Klinika oczna vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	7.	Optic atrophy and negative electroretinogram in a patient associated with a novel OPA1 mutation. [electronic resource] by Nakamura, Makoto Miyake, Yozo Producer: 20070510 In: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie vol. 244 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hereditary optic neuropathies: from the mitochondria to the optic nerve. [electronic resource] by Newman, Nancy J Producer: 20051004 In: American journal of ophthalmology vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Treatment strategies for inherited optic neuropathies: past, present and future. [electronic resource] by Yu-Wai-Man, P Votruba, M Moore, A T Chinnery, P F Producer: 20150114 In: Eye (London, England) vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates. [electronic resource] by Yu-Wai-Man, Patrick Chinnery, Patrick F Producer: 20131106 In: Ophthalmology vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Reply: 'Behr syndrome' with OPA1 compound heterozygote mutations. [electronic resource] by Yu-Wai-Man, Patrick Chinnery, Patrick F Producer: 20150302 In: Brain : a journal of neurology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy. [electronic resource] by Mayorov, Vladimir I Lowrey, Angela J Biousse, Valerie Newman, Nancy J Cline, Susan D Brown, Michael D Producer: 20081031 In: BMC biochemistry vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation. [electronic resource] by Pretegiani, Elena Rufa, Alessandra Gallus, Gian Nicola Cardaioli, Elena Malandrini, Alessandro Federico, Antonio Producer: 20120118 In: Brain : a journal of neurology vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Visual and psychological morbidity among patients with autosomal dominant optic atrophy. [electronic resource] by Bailie, Maura Votruba, Marcela Griffiths, Philip G Chinnery, Patrick F Yu-Wai-Man, Patrick Producer: 20131017 In: Acta ophthalmologica vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Sensorineural hearing loss in OPA1-linked disorders. [electronic resource] by Leruez, Stéphanie Milea, Dan Defoort-Dhellemmes, Sabine Colin, Estelle Crochet, Martine Procaccio, Vincent Ferré, Marc Lamblin, Julie Drouin, Valérie Vincent-Delorme, Catherine Lenaers, Guy Hamel, Christian Blanchet, Catherine Juul, Gitte Larsen, Michael Verny, Christophe Reynier, Pascal Amati-Bonneau, Patrizia Bonneau, Dominique Producer: 20130829 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Reply: Sensorineural hearing loss in OPA1-linked disorders. [electronic resource] by Yu-Wai-Man, Patrick Chinnery, Patrick F Producer: 20130829 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	'Behr syndrome' with OPA1 compound heterozygote mutations. [electronic resource] by Carelli, Valerio Sabatelli, Mario Carrozzo, Rosalba Rizza, Teresa Schimpf, Simone Wissinger, Bernd Zanna, Claudia Rugolo, Michela La Morgia, Chiara Caporali, Leonardo Carbonelli, Michele Barboni, Piero Tonon, Caterina Lodi, Raffaele Bertini, Enrico Producer: 20150302 In: Brain : a journal of neurology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	The OPA1 gene and optic neuropathy. [electronic resource] by Alward, W L M Producer: 20030220 In: The British journal of ophthalmology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy. [electronic resource] by Yu-Wai-Man, Patrick Trenell, Michael I Hollingsworth, Kieren G Griffiths, Philip G Chinnery, Patrick F Producer: 20110701 In: Brain : a journal of neurology vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	[Case report on OCT findings in a patient with hereditary optic neuropathy and a patient with autosomal dominant optic atrophy]. [electronic resource] by Schild, A M Fricke, J Liakopoulos, S Producer: 20120315 In: Klinische Monatsblatter fur Augenheilkunde vol. 228 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

1
2
3
4
5
6
7
8
9
10
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 193 results.