Electrophysiological findings in Dominant Optic Atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter

By Holder G.E.   Votruba M.   Carter A.C.   Bhattacharya S.S.   Fitzke F.W.   Moore A.T.  

Documenta Ophthalmologica, Vol. 95, Iss. 3, 1998-03 ,pp. : 217-228

Springer Publishing Company

Access to resources Recommend Favorite

The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene

By Amati-Bonneau P.   Odent S.   Derrien C.   Pasquier L.   Malthiery Y.   Reynier P.   Bonneau D.  

American Journal of Ophthalmology, Vol. 136, Iss. 6, 2003-12 ,pp. : 1170-1171

Elsevier

Access to resources Recommend Favorite

Water-soluble coenzyme Q10 formulation (Q-TER^®) in the treatment of presbycusis

By Salami Angelo   Mora Renzo   Dellepiane Massimo   Manini Giorgio   Santomauro Valentina   Barettini Luciano   Guastini Luca  

Acta Oto-Laryngologica, Vol. 130, Iss. 10, 2010-10 ,pp. : 1154-1162

Informa Healthcare

Access to resources Recommend Favorite

Optic nerve atrophy in propionic acidemia

By Ianchulev T.   Kolin T.   Moseley K.   Sadun A.  

Ophthalmology, Vol. 110, Iss. 9, 2003-09 ,pp. : 1850-1854

Elsevier

Access to resources Recommend Favorite

Optic neuritis in children – clinical and electrophysiological follow-up

By Tekavcic-Pompe M.   Stirn-Kranjc B.   Brecelj J.  

Documenta Ophthalmologica, Vol. 107, Iss. 3, 2003-11 ,pp. : 261-270

Springer Publishing Company

Access to resources Recommend Favorite