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 *

108 related articles for article (PubMed ID: 10331707)

  • 61. Cochlear changes in serous labyrinthitis associated with silent otitis media: A human temporal bone study.
    Kaya S; Tsuprun V; Hızlı Ö; Schachern PA; Paparella MM; Cureoglu S
    Am J Otolaryngol; 2016; 37(2):83-8. PubMed ID: 26954857
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Lack of association between mitochondrial tRNA(Leu(UUR)) point mutation and cluster headache.
    Cortelli P; Zacchini A; Barboni P; Malpassi P; Carelli V; Montagna P
    Lancet; 1995 Apr; 345(8957):1120-1. PubMed ID: 7715370
    [No Abstract]   [Full Text] [Related]  

  • 63. Temporal Bone Histopathology in Cockayne Syndrome.
    Handzel O; Nadol JB
    Otol Neurotol; 2018 Jun; 39(5):e387-e391. PubMed ID: 29649050
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
    Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M; Klupa T; Wanic K; Frey J; Cyganek K; Sieradzki J
    Med Sci Monit; 2001; 7(2):246-50. PubMed ID: 11257730
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
    Kawakami Y; Sakuta R; Hashimoto K; Fujino O; Fujita T; Hida M; Horai S; Goto Y; Nonaka I
    Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Histopathology of the inner ear in DFNA9.
    Merchant SN; Linthicum FH; Nadol JB
    Adv Otorhinolaryngol; 2000; 56():212-7. PubMed ID: 10868238
    [No Abstract]   [Full Text] [Related]  

  • 68. Sleep-wake dysrhythm in mitochondrial diabetes mellitus.
    Suzuki Y; Taniyama M; Hata T; Miyaoka H; Atsumi Y; Matsuoka K
    Diabetes Res Clin Pract; 1997 Feb; 35(1):61-2. PubMed ID: 9113477
    [No Abstract]   [Full Text] [Related]  

  • 69. Age of onset possibly associated with the degree of heteroplasmy in two male siblings with diabetes mellitus having an A to G transition at 3243 of mitochondrial DNA.
    Kato Y; Miura Y; Inagaki A; Itatsu T; Oiso Y
    Diabet Med; 2002 Sep; 19(9):784-6. PubMed ID: 12207817
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Mitochondrial DNA defects in diabetes mellitus.
    Alcolado JC
    Diabetologia; 1993 Jun; 36(6):578-9. PubMed ID: 8335184
    [No Abstract]   [Full Text] [Related]  

  • 71. Temporal bone histopathology case of the month: Modiolar dehiscence associated with sensorineural hearing loss.
    Treadway JP; Doherty JK; Linthicum FH
    Otol Neurotol; 2013 Jan; 34(1):e4-5. PubMed ID: 23235552
    [No Abstract]   [Full Text] [Related]  

  • 72. Quantification of mitochondrial DNA heteroplasmy by temporal temperature gradient gel electrophoresis.
    Boles RG; Chaudhari D; Söderkvist J; Podberezin M; Ito M
    Clin Chem; 2003 Jan; 49(1):198-200. PubMed ID: 12507986
    [No Abstract]   [Full Text] [Related]  

  • 73. Mitochondrial DNA 3243 mutation is infrequent in Japanese diabetic patients with auditory disturbance.
    Fukunaga Y; Azuma N; Koshiyama H; Inoue D; Sato H; Yoshimasa Y; Nakao K
    Diabetes Care; 1997 Nov; 20(11):1800-3. PubMed ID: 9353631
    [No Abstract]   [Full Text] [Related]  

  • 74. Mitochondrial cytochrome oxidase immunolabeling in aged human temporal bones.
    Keithley EM; Harris B; Desai K; Linthicum F; Fischel-Ghodsian N
    Hear Res; 2001 Jul; 157(1-2):93-9. PubMed ID: 11470189
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A mutation in mt tRNALeu(UUR) causing a neuropsychiatric syndrome with depression and cataract.
    Jaksch M; Lochmuller H; Schmitt F; Volpel B; Obermaier-Kusser B; Horvath R
    Neurology; 2001 Nov; 57(10):1930-1. PubMed ID: 11723298
    [No Abstract]   [Full Text] [Related]  

  • 76. Autosomal dominant sensorineural hearing loss. Further temporal bone findings.
    Khetarpal U
    Arch Otolaryngol Head Neck Surg; 1993 Jan; 119(1):106-8. PubMed ID: 8417734
    [No Abstract]   [Full Text] [Related]  

  • 77. Congestive heart failure in mitochondrial diabetes mellitus.
    Yoshida R; Ishida Y; Hozumi T; Ueno H; Kishimoto M; Kasuga M; Kazumi T
    Lancet; 1994 Nov; 344(8933):1375. PubMed ID: 7968064
    [No Abstract]   [Full Text] [Related]  

  • 78. Impaired Hearing in MELAS.
    Finsterer J
    J Int Adv Otol; 2022 May; 18(3):276-277. PubMed ID: 35608499
    [No Abstract]   [Full Text] [Related]  

  • 79. Long-Term Progression and Rapid Decline in Hearing Loss in Patients with a Point Mutation at Nucleotide 3243 of the Mitochondrial DNA.
    Sakata A; Kashio A; Koyama H; Uranaka T; Iwasaki S; Fujimoto C; Kinoshita M; Yamasoba T
    Life (Basel); 2022 Apr; 12(4):. PubMed ID: 35455034
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Cochlear Implantation in Patients with Mitochondrial Gene Mutation: Decline in Speech Perception in Retrospective Long-Term Follow-Up Study.
    Kanemoto K; Kashio A; Ogata E; Akamatsu Y; Koyama H; Uranaka T; Hoshi Y; Iwasaki S; Yamasoba T
    Life (Basel); 2022 Mar; 12(4):. PubMed ID: 35454973
    [TBL] [Abstract][Full Text] [Related]  

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