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 *

103 related articles for article (PubMed ID: 10522883)

  • 21. Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.
    Hirano M; Garcia-de-Yebenes J; Jones AC; Nishino I; DiMauro S; Carlo JR; Bender AN; Hahn AF; Salberg LM; Weeks DE; Nygaard TG
    Am J Hum Genet; 1998 Aug; 63(2):526-33. PubMed ID: 9683610
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
    Tabaku M; Legius E; Robberecht W; Sciot R; Fryns JP; Cassiman JJ; Matthijs G
    Genet Couns; 1999; 10(3):285-93. PubMed ID: 10546101
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
    Hanein S; Dürr A; Ribai P; Forlani S; Leutenegger AL; Nelson I; Babron MC; Elleuch N; Depienne C; Charon C; Brice A; Stevanin G
    Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.
    Federico A; Dotti MT; Cardaioli E; Grieco G; Malandrini A; Manneschi L; Plewnia K; Rufa A; Renieri A; Bruttini M; Perticoni GF
    J Submicrosc Cytol Pathol; 1998 Oct; 30(4):521-6. PubMed ID: 9851061
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Refinement of the adPEO linked locus on Chr10 and analysis of MRS4 and three other candidate genes.
    Lewis S; Hutchison W; Di Nezza L; Thyagarajan D; Marotta R; Dahl H
    FEBS Lett; 2001 Jul; 500(3):183-5. PubMed ID: 11445082
    [No Abstract]   [Full Text] [Related]  

  • 26. An autosomal locus predisposing to deletions of mitochondrial DNA.
    Suomalainen A; Kaukonen J; Amati P; Timonen R; Haltia M; Weissenbach J; Zeviani M; Somer H; Peltonen L
    Nat Genet; 1995 Feb; 9(2):146-51. PubMed ID: 7719341
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
    Meijer IA; Cossette P; Roussel J; Benard M; Toupin S; Rouleau GA
    Ann Neurol; 2004 Oct; 56(4):579-82. PubMed ID: 15455396
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.
    Nunes ME; Schutt G; Kapur RP; Luthardt F; Kukolich M; Byers P; Evans JP
    Hum Mol Genet; 1995 Nov; 4(11):2165-70. PubMed ID: 8589697
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.
    Yee RW; Sullivan LS; Lai HT; Stock EL; Lu Y; Khan MN; Blanton SH; Daiger SP
    Genomics; 1997 Nov; 46(1):152-4. PubMed ID: 9403072
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
    Luoma P; Melberg A; Rinne JO; Kaukonen JA; Nupponen NN; Chalmers RM; Oldfors A; Rautakorpi I; Peltonen L; Majamaa K; Somer H; Suomalainen A
    Lancet; 2004 Sep 4-10; 364(9437):875-82. PubMed ID: 15351195
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and molecular features of adPEO due to mutations in the Twinkle gene.
    Lewis S; Hutchison W; Thyagarajan D; Dahl HH
    J Neurol Sci; 2002 Sep; 201(1-2):39-44. PubMed ID: 12163192
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.
    Lossos A; Baala L; Soffer D; Averbuch-Heller L; Dotan S; Munnich A; Lyonnet S; Gomori JM; Genem A; Neufeld M; Abramsky O; Zlotogora J; Argov Z
    Brain; 2005 Jan; 128(Pt 1):42-51. PubMed ID: 15548556
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12.
    Engle EC; Kunkel LM; Specht LA; Beggs AH
    Nat Genet; 1994 May; 7(1):69-73. PubMed ID: 8075644
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
    Van Goethem G; Dermaut B; Löfgren A; Martin JJ; Van Broeckhoven C
    Nat Genet; 2001 Jul; 28(3):211-2. PubMed ID: 11431686
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chronic progressive external ophthalmoplegia with inflammatory myopathy.
    Chen T; Pu C; Shi Q; Wang Q; Cong L; Liu J; Luo H; Fei L; Tang W; Yu S
    Int J Clin Exp Pathol; 2014; 7(12):8887-92. PubMed ID: 25674260
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.
    Tyynismaa H; Sun R; Ahola-Erkkilä S; Almusa H; Pöyhönen R; Korpela M; Honkaniemi J; Isohanni P; Paetau A; Wang L; Suomalainen A
    Hum Mol Genet; 2012 Jan; 21(1):66-75. PubMed ID: 21937588
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G
    Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics.
    Lee JH; Mayeux R; Mayo D; Mo J; Santana V; Williamson J; Flaquer A; Ciappa A; Rondon H; Estevez P; Lantigua R; Kawarai T; Toulina A; Medrano M; Torres M; Stern Y; Tycko B; Rogaeva E; St George-Hyslop P; Knowles JA
    Mol Psychiatry; 2004 Nov; 9(11):1042-51. PubMed ID: 15241431
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletions.
    Moslemi AR; Melberg A; Holme E; Oldfors A
    Neurology; 1999 Jul; 53(1):79-84. PubMed ID: 10408540
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
    Lamantea E; Tiranti V; Bordoni A; Toscano A; Bono F; Servidei S; Papadimitriou A; Spelbrink H; Silvestri L; Casari G; Comi GP; Zeviani M
    Ann Neurol; 2002 Aug; 52(2):211-9. PubMed ID: 12210792
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.