Fundus findings in Leber's hereditary optic neuroretinopathy. III: Fluorescein angiographic studiesNIKOSKELAINEN, E; HOYT, W. F; NUMMELIN, K et al.Archives of ophthalmology (1960). 1984, Vol 102, Num 7, pp 981-989, issn 0003-9950Article

DIE DIFFERENTIALDIAGNOSE DER KONGENITALEN AMAUROSE = LE DIAGNOSTIC DIFFERENTIEL DE L'AMAUROSE CONGENITALEZIEGLER EM; GODER G; COMBERG U et al.1972; DTSCHE GESUNDH.-WES.; DTSCH.; DA. 1972; VOL. 27; NO 30; PP. 1429-1432; ABS. RUSSE ANGL.; BIBL. 38 REF.Serial Issue

Névrite optique de Leber et micro-informatique = Leber amaurosis and micro-computerHEMERY, B; HACHE, J.-C; FRANCOIS, P et al.Bulletin des sociétés d'ophtalmologie de France. 1983, Vol 83, Num 6-7, pp 773-775, issn 0081-1270Article

Clinical and biochemical findings in Leber's hereditary optic atrophySYME, I. G; BRONTE-STEWART, J; FOULDS, W. S et al.Transactions of the Ophthalmological Societies of the United Kingdom. 1983, Vol 103, Num 5, pp 556-559, issn 0078-5334Article

UN CAS D'AMAUROSE CONGENITALE (LEBER)WATANABE I; OKOCHI Y; SAKAI T et al.1977; FOLIA OPHTHALMOL. JAP.; JAP.; DA. 1977; VOL. 28; NO 2; PP. 292-297; BIBL. 1 P. 1/2Article

AMAUROSIS CONGENITA (LEBER) = AMAUROSE CONGENITALE (LEBER)HIROSE T; WAND O.1975; ANN. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 7; NO 1; PP. 59-63; BIBL. 22REF.Article

MENTAL RETARDATION AND NEUROLOGIC INVOLVEMENT IN PATIENTS WITH CONGENITAL RETINAL BLINDNESS = RETARD MENTAL ET CONSEQUENCES NEUROLOGIQUES CHEZ LES SUJETS ATTEINTS DE CECITE RETINIENNE CONGENITALEDEKABAN AS.1972; DEVELOP. MED. CHILD NEUROL.; G.B.; DA. 1972; VOL. 14; NO 4; PP. 436-444; ABS. FR. ALLEM. ESP.; BIBL. 26REF.Serial Issue

LEBER'S OPTIC NEUROPATHY1980; BRIT. MED. J.; GBR; DA. 1980; NO 6222; PP. 1097-1098; BIBL. 19 REF.Article

THE EARLY PHASE IN LEBER HEREDITARY OPTIC ATROPHY.NIKOSKELAINEN E; SOGG RL; ROSENTHAL AR et al.1977; ARCH. OPHTHALMOL.; U.S.A.; DA. 1977; VOL. 95; NO 6; PP. 969-978; BIBL. 13 REF.Article

DYSTROPHIE VITELLIFORME DE LA MACULA ET DEGENERESCENCE TAPETO-RETINIENNE DE LEBER. (OBSERVATION D'UNE ASSOCIATION FAMILIALE).RISSE JF; FLAMENT J.1977; BULL. SOC. OPHTALMOL. FR.; FR.; DA. 1977; VOL. 77; NO 5-6; PP. 629-633; ABS. ANGL.; BIBL. 14 REF.Article

LEBER'S CONGENITAL AMAUROSIS. IS MENTAL RETARDATION A FREQUENT ASSOCIATED DEFECT.NICKEL B; HOYT CS.1982; ARCH. OPHTHALMOL.; ISSN 0003-9950; USA; DA. 1982; VOL. 100; NO 7; PP. 1089-1092; BIBL. 44 REF.Article

A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE AND LEBER'S OPTIC ATROPHY = UNE FAMILLE AVEC UNE MALADIE DE CHARCOT-MARIE-TOOTH ET ATROPHIE OPTIQUE DE LEBERMCLEOD JG; LOW PA; MORGAN JA et al.1975; PROC. AUSTRAL. ASS. NEUROLOGISTS; AUSTRAL.; DA. 1975; VOL. 12; PP. 23-25; BIBL. 18 REF.Article

DEUX CAS FAMILIAUX DE MALADIE DE LEBERBIGORGNE J; CORLAY; SOURDILLE et al.1974; BULL. SOC. OPHTALMOL. FR.; FR.; DA. 1974; VOL. 74; NO 3; PP. 353-357Article

ETUDE GENETIQUE ET ELECTROENCEPHALOGRAPHIQUE D'UNE NOUVELLE FAMILLE ATTEINTE DE NEVRITE OPTIQUE HEREDITAIRE DE LEBERSCOURAS J; CUENDET JF; HADJIANTONIOU J et al.1973; J. GENET. HUM.; SUISSE; DA. 1973; VOL. 21; NO 3; PP. 207-214; ABS. ANGL. ALLEM.; BIBL. 10REF.Article

LEBER'S CONGENITAL AMAUROSIS AS CONCEIVED BY LEBERPINCKERS AJL.1979; OPHTHALMOLOGICA; CHE; DA. 1979; VOL. 179; NO 1; PP. 48-51; ABS. FRE/GER; BIBL. 6 REF.Article

LES ATROPHIES OPTIQUES HEREDITAIRESFRANCOIS J.1976; ANN. OCULIST.; FR.; DA. 1976; VOL. 209; NO 3; PP. 169-179; ABS. ANGL.; BIBL. 2 P.Article

An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congénital amaurosisHEEGAARD, S; ROSENBERG, T; PREISING, M et al.British journal of ophthalmology. 2003, Vol 87, Num 8, pp 980-983, issn 0007-1161, 4 p.Article

La neurorétinite stellaire idiopathique de Leber : à propos de neuf cas = Leber's idiopathic stellate neuroretinitis. Report of nine casesHAMARD, P; HAMARD, H; NGOHOU, S et al.Journal français d'ophtalmologie. 1994, Vol 17, Num 2, pp 116-123, issn 0181-5512Article

Occurrence of a multiple sclerosis-like illness in women who have a leber's hereditary optic neuropathy mitochondrial DNA mutationHARDING, A. E; SWEENEY, M. G; MILLER, D. H et al.Brain. 1992, Vol 115, pp 979-989, issn 0006-8950, 4Article

Neuroretinite stellata idiopatica di Leber: a manifestazione bilaterale asincrona. Caso clinico = Leber's idiopathic stellate neuroretinitis with asynchronous bilateral onset: case reportCOLOMBATI, S; PASANISI, P; LOSAVIO, P et al.Annali di ottalmologia e clinica oculistica. 1993, Vol 119, Num 12, pp 853-856, issn 0003-4665Article

Evidence against an X-linked locus close to DX37 determining visual loss susceptibility in British and Italian families with leber hereditary optic neuropathySWEENEY, M. G; DAVIS, M. B; LASHWOOD, A et al.American journal of human genetics. 1992, Vol 51, Num 4, pp 741-748, issn 0002-9297Article

Does sporadic Leber's disease exist?NIKOSKELAINEN, E; NUMMELIN, K; SAVONTAUS, M.-L et al.Journal of clinical neuro-ophthalmology. 1988, Vol 8, Num 4, pp 225-229, issn 0272-846XArticle

Evolution de trois cas de dégénérescence tapéto-rétinienne congénitale dite de Leber diagnostiques en 1966 = Evolution of three cases of Leber congenital tapeto-retinal degeneration diagnosed in 1966EVRARD, J.-M; HULLO, A; DUCLAUX, R et al.Bulletin des sociétés d'ophtalmologie de France. 1987, Vol 87, Num 7-8, pp 1027-1029, issn 0081-1270Conference Paper

Les altérations de l'ADN mitochondrial dans la névrite optique de Leber : applications diagnostiques = Alterations of mitichondrial DNA in Leber's hereditary optic neuropathy diagnostical applicationsPUECH, B; DUMUR, V; HACHE, J.-C et al.Bulletin des sociétés d'ophtalmologie de France. 1991, Vol 91, Num 3, pp 313-317, issn 0081-1270Article

Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosisLAMBERT, S. R; KRISS, A; TAYLOR, D et al.American journal of ophthalmology. 1989, Vol 107, Num 6, pp 624-631, issn 0002-9394Article