128 related articles for article (PubMed ID: 7739437)
1. [Leber's optic atrophy (case report of progressive hereditary amaurosis].
Bozić K; Filipović D; Krkljes M; Kelemen A; Ivetić V
Med Pregl; 1994; 47(1-2):62-4. PubMed ID: 7739437
[TBL] [Abstract][Full Text] [Related]
2. Leber's hereditary optic neuropathy.
Letchavanakul A; Dechphongsaphilas W; Dhamcharee V
J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
[TBL] [Abstract][Full Text] [Related]
3. Late-onset Leber's hereditary optic neuropathy.
Ajax ET; Kardon R
J Neuroophthalmol; 1998 Mar; 18(1):30-1. PubMed ID: 9532536
[TBL] [Abstract][Full Text] [Related]
4. [Differential diagnosis of optic nerve atrophy].
Kommerell G
Bull Soc Belge Ophtalmol; 1990; 236():21-33. PubMed ID: 2093405
[TBL] [Abstract][Full Text] [Related]
5. [Leber's hereditary optic neuropathy].
Castier P; Francois P; Asseman R; Hemery B; Deleforge AM
Ophtalmologie; 1989; 3(3):199-202. PubMed ID: 2641110
[TBL] [Abstract][Full Text] [Related]
6. [Leber's hereditary optic neuropathy with onset at the age of 54 years].
Nakamura N; Furukawa Y; Fujiki K; Hayakawa M; Mizuno Y
Rinsho Shinkeigaku; 1994 Mar; 34(3):258-60. PubMed ID: 8200145
[TBL] [Abstract][Full Text] [Related]
7. The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease.
Nikoskelainen E
Trans Ophthalmol Soc U K (1962); 1985; 104 ( Pt 8)():845-52. PubMed ID: 3879564
[TBL] [Abstract][Full Text] [Related]
8. Optic nerve enhancement on orbital magnetic resonance imaging in Leber's hereditary optic neuropathy.
Vaphiades MS; Newman NJ
J Neuroophthalmol; 1999 Dec; 19(4):238-9. PubMed ID: 10608675
[TBL] [Abstract][Full Text] [Related]
9. [Leber's optic atrophy].
Kozuchowska I; Szymczak J
Klin Oczna; 1990 Oct; 92(7-8):149-51. PubMed ID: 2084314
[TBL] [Abstract][Full Text] [Related]
10. Does sporadic Leber's disease exist?
Nikoskelainen E; Nummelin K; Savontaus ML
J Clin Neuroophthalmol; 1988 Dec; 8(4):225-9. PubMed ID: 2977137
[TBL] [Abstract][Full Text] [Related]
11. [Positive diagnosis of Leber's hereditary optic neuropathy using molecular genetics].
Souied E; Pisella PJ; Ossareh B; Brézin A; Junes P; Wild-Decrette C; Munnich A; Bonnefont JP; Mondon H
J Fr Ophtalmol; 1997; 20(1):65-70. PubMed ID: 9099286
[TBL] [Abstract][Full Text] [Related]
12. [Clinical manifestation and molecular identification of patients with Leber's hereditary optic neuropathy in a national reference center for neuro-ophthalmology in Cuba].
Santiesteban-Freixas R; Rodríguez-Hernández M; Mendoza-Santiesteban CE; Carrero-Salgado M; Francisco-Plasencia M; Méndez-Larramendi I; Vidal-Casalís S; Rivero-Reyes R; Hirano M
Rev Neurol; 1999 Sep 1-15; 29(5):408-15. PubMed ID: 10584242
[TBL] [Abstract][Full Text] [Related]
13. [Hereditary optic neuropathies: from clinical signs to diagnosis].
Meunier I; Lenaers G; Hamel C; Defoort-Dhellemmes S
J Fr Ophtalmol; 2013 Dec; 36(10):886-900. PubMed ID: 24161764
[TBL] [Abstract][Full Text] [Related]
14. Leber's optic atrophy.
Beard D
Occup Health (Lond); 1990 Dec; 42(12):365. PubMed ID: 2255471
[No Abstract] [Full Text] [Related]
15. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
Yen MY; Wei YH; Liu JH
J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
[TBL] [Abstract][Full Text] [Related]
16. Leber's hereditary optic neuropathy: historical and contemporary considerations.
Kleiner L; Sherman J
Optom Clin; 1996; 5(3-4):77-112. PubMed ID: 8972510
[TBL] [Abstract][Full Text] [Related]
17. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
Lertrit P; Ruangvaravate N; Trongpanich Y; Imsumran A; Mungkornkarn C; Neungton N
J Med Assoc Thai; 1999 Jan; 82(1):59-64. PubMed ID: 10087740
[TBL] [Abstract][Full Text] [Related]
18. [Leber's optic neuropathy: a case report].
Pato-Pato A; Cimas-Hernando I; Lorenzo-González JR
Rev Neurol; 2006 Jan 1-15; 42(1):22-4. PubMed ID: 16402322
[TBL] [Abstract][Full Text] [Related]
19. Leber's hereditary optic atrophy: an atypical case with response to hydroxycobalamine therapy.
Chew SJ
Singapore Med J; 1990 Jun; 31(3):293-4. PubMed ID: 2392710
[TBL] [Abstract][Full Text] [Related]
20. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE
Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]