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Journal Abstract Search
127 related items for PubMed ID: 123591
1. A family with apparently sex-linked optic atrophy. Went LN, De Vries-De Mol EC, Völker-Dieben HJ. J Med Genet; 1975 Mar; 12(1):94-8. PubMed ID: 123591 [Abstract] [Full Text] [Related]
2. Neurological studies in families with Leber's optic atrophy. de Weerdt CJ, Went LN. Acta Neurol Scand; 1971 Mar; 47(5):541-54. PubMed ID: 5139723 [No Abstract] [Full Text] [Related]
3. The genetics of Leber's optic atrophy and its neurological sequelae. Went LN, Bruyn GW. J Genet Hum; 1966 Dec; 15(3):332-7. PubMed ID: 5987544 [No Abstract] [Full Text] [Related]
4. A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome. Assink JJ, Tijmes NT, ten Brink JB, Oostra RJ, Riemslag FC, de Jong PT, Bergen AA. Am J Hum Genet; 1997 Oct; 61(4):934-9. PubMed ID: 9382106 [Abstract] [Full Text] [Related]
5. Hereditary optic atrophy with onset in early childhood. Brodrick JD. Br J Ophthalmol; 1974 Sep; 58(9):817-22. PubMed ID: 4433496 [No Abstract] [Full Text] [Related]
7. [The heredo-degenerations of the optic nerve and their associations with systemic neurologic diseases. Complicated infantile optic atrophy (Behr's disease)]. Franceschetti A. J Genet Hum; 1966 Dec; 15(3):322-31. PubMed ID: 5987543 [No Abstract] [Full Text] [Related]
8. Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q. Votruba M, Moore AT, Bhattacharya SS. J Med Genet; 1997 Feb; 34(2):117-21. PubMed ID: 9039986 [Abstract] [Full Text] [Related]
10. Diagnostic criteria in cominantly inherited juvenile optic atrophy. A report of three new families. Smith DP. Am J Optom Arch Am Acad Optom; 1972 Mar; 49(3):183-200. PubMed ID: 4502353 [No Abstract] [Full Text] [Related]
12. Hereditary degeneration of the optic nerve (hereditary optic atrophy). Francois J. Int Ophthalmol Clin; 1968 Jan 29; 8(4):999-1054. PubMed ID: 4907160 [No Abstract] [Full Text] [Related]
13. Nerve deafness: optic nerve atrophy, and dementia: a new X-linked recessive syndrome? Jensen PK. Am J Med Genet; 1981 Jan 29; 9(1):55-60. PubMed ID: 7195649 [No Abstract] [Full Text] [Related]
14. Hereditary optic atrophy with probable association with a specific HLA haplotype. Stendahl-Brodin L, Möller E, Link H. J Neurol Sci; 1978 Aug 29; 38(1):11-21. PubMed ID: 151734 [Abstract] [Full Text] [Related]
15. Congenital tritanopia without neuroretinal disease. Smith DP, Cole BL, Isaacs A. Invest Ophthalmol; 1973 Aug 29; 12(8):608-17. PubMed ID: 4542649 [No Abstract] [Full Text] [Related]
16. Dominant juvenile optic atrophy. A study in two families and review of hereditary disease in childhood. Caldwell JB, Howard RO, Riggs LA. Arch Ophthalmol; 1971 Feb 29; 85(2):133-47. PubMed ID: 5545713 [No Abstract] [Full Text] [Related]
17. Association and linkage studies of Huntington's chorea in relation to fifteen genetic markers. Beckman L, Cedergren B, Mattsson B, Ottosson JO. Hereditas; 1974 Feb 29; 77(1):73-80. PubMed ID: 4278002 [No Abstract] [Full Text] [Related]