These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

61 related articles for article (PubMed ID: 18290960)

  • 21. [Bilateral macular placoid epitheliopathy in a rectangular form].
    Leopold P; Vianey-Passols E
    Bull Soc Ophtalmol Fr; 1982; 82(6-7):851-4. PubMed ID: 7172382
    [No Abstract]   [Full Text] [Related]  

  • 22. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M; Szczuciński A; Losy J
    Neurol Neurochir Pol; 2014; 48(2):150-3. PubMed ID: 24821643
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Epiretinal macular proliferation].
    Rencová E
    Cesk Oftalmol; 1987 May; 43(3):173-81. PubMed ID: 3594604
    [No Abstract]   [Full Text] [Related]  

  • 24. [Ultrastructural features of epiretinal membranes in spontaneous "macular pucker"].
    Bornfeld N; Laqua H; El-Hifnawi E
    Fortschr Ophthalmol; 1983; 80(4):326-8. PubMed ID: 6629261
    [No Abstract]   [Full Text] [Related]  

  • 25. Optical coherence tomography findings in acute macular neuroretinopathy.
    Shukla D; Arora A; Ambatkar S; Ramasamy K; Perumalsamy N
    Eye (Lond); 2005 Jan; 19(1):107-8. PubMed ID: 15094723
    [No Abstract]   [Full Text] [Related]  

  • 26. Mitochondrial DNA (mtDNA) A 3243G mutation associated with an annular perimacular retinal atrophy.
    Adjadj E; Mansouri K; Borruat FX
    Klin Monbl Augenheilkd; 2008 May; 225(5):462-4. PubMed ID: 18454399
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW; Huang CC; Tsai JL; Liu JY; Pang CY; Lee HC; Wang EK; Wei YH
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetically determined macular disorders.
    Reddy PS
    Indian J Ophthalmol; 1983 May; 31(3):254. PubMed ID: 6676231
    [No Abstract]   [Full Text] [Related]  

  • 29. Developmental macular disorders: phenotypes and underlying molecular genetic basis.
    Michaelides M; Jeffery G; Moore AT
    Br J Ophthalmol; 2012 Jul; 96(7):917-24. PubMed ID: 22517799
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Histopathological study of macular drusen].
    Bonnet M; Schiffer HP
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Apr; 34(4):251-65. PubMed ID: 4136374
    [No Abstract]   [Full Text] [Related]  

  • 31. Congenital and childhood macular lesions.
    Drack AV
    Int Ophthalmol Clin; 1995; 35(4):1-18. PubMed ID: 8847186
    [No Abstract]   [Full Text] [Related]  

  • 32. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
    Mimaki M; Hatakeyama H; Ichiyama T; Isumi H; Furukawa S; Akasaka M; Kamei A; Komaki H; Nishino I; Nonaka I; Goto Y
    Mitochondrion; 2009 Apr; 9(2):115-22. PubMed ID: 19460299
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A familial case of proliferative diabetic retinopathy associated with a mutation in the mitochondrial gene].
    Kuze M; Arima M; Saso M; Uji Y
    Nippon Ganka Gakkai Zasshi; 1998 Nov; 102(11):739-45. PubMed ID: 9852718
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Primary macular diseases in children].
    Turut P
    Annee Ther Clin Ophtalmol; 1984; 35():51-62. PubMed ID: 6443336
    [No Abstract]   [Full Text] [Related]  

  • 35. [Postoperative macular edema].
    Worst J
    Bull Mem Soc Fr Ophtalmol; 1976; 88():53-4. PubMed ID: 1029627
    [No Abstract]   [Full Text] [Related]  

  • 36. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T; Madden C; Dasgupta S; Saeed S; Das V
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis.
    Zhu V; Huang T; Wang D; Colville D; Mack H; Savige J
    Pediatr Nephrol; 2024 Mar; 39(3):655-679. PubMed ID: 37578539
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pearls & oy-sters: maternally inherited diabetes and deafness presenting with ptosis and macular pattern dystrophy.
    Ogun O; Sheldon C; Barton JJ
    Neurology; 2012 Aug; 79(6):e54-6. PubMed ID: 22869689
    [No Abstract]   [Full Text] [Related]  

  • 39. [Retinal pigment epithelium atrophy and hypacousia in monozygotic twin sisters].
    Oppermann T; Roider J; Hillenkamp J
    Ophthalmologe; 2010 Jan; 107(1):64-7. PubMed ID: 19756641
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.
    Sivaprasad S; Kung BT; Robson AG; Black G; Webster AR; Bird A; Egan C
    Clin Exp Ophthalmol; 2008; 36(1):92-3. PubMed ID: 18290960
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.