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 *

141 related articles for article (PubMed ID: 18332579)

  • 1. [A case of maternally inherited diabetes with deafness (MIDD) occurring at an advanced age].
    Takeuchi J; Tashiro J; Nakagaki O; Yoshida M; Kamoshima H; Oku K; Yoshioka N
    Nihon Ronen Igakkai Zasshi; 2008 Jan; 45(1):95-9. PubMed ID: 18332579
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Visual, Ocular Motor, and Cochleo-Vestibular Loss in Patients With Heteroplasmic, Maternally-Inherited Diabetes Mellitus and Deafness (MIDD), 3243 Transfer RNA Mutation.
    Cardenas-Robledo S; Saber Tehrani A; Blume G; Kattah JC
    J Neuroophthalmol; 2016 Jun; 36(2):134-40. PubMed ID: 26741293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.
    Schleiffer T; 't Hart LM; Schürfeld C; Kraatz K; Riemann JF
    Exp Clin Endocrinol Diabetes; 2000; 108(2):81-5. PubMed ID: 10826513
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
    Laloi-Michelin M; Meas T; Ambonville C; Bellanné-Chantelot C; Beaufils S; Massin P; Vialettes B; Gin H; Timsit J; Bauduceau B; Bernard L; Bertin E; Blickle JF; Cahen-Varsaux J; Cailleba A; Casanova S; Cathebras P; Charpentier G; Chedin P; Crea T; Delemer B; Dubois-Laforgue D; Duchemin F; Ducluzeau PH; Bouhanick B; Dusselier L; Gabreau T; Grimaldi A; Guerci B; Jacquin V; Kaloustian E; Larger E; Lecleire-Collet A; Lorenzini F; Louis J; Mausset J; Murat A; Nadler-Fluteau S; Olivier F; Paquis-Flucklinger V; Paris-Bockel D; Raynaud I; Reznik Y; Riveline JP; Schneebeli S; Sonnet E; Sola-Gazagnes A; Thomas JL; Trabulsi B; Virally M; Guillausseau PJ;
    J Clin Endocrinol Metab; 2009 Aug; 94(8):3025-30. PubMed ID: 19470619
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Fukuda M; Nagao Y
    J Med Case Rep; 2019 Oct; 13(1):313. PubMed ID: 31630688
    [TBL] [Abstract][Full Text] [Related]  

  • 7. One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation.
    Esterhuizen K; Lindeque JZ; Mason S; van der Westhuizen FH; Rodenburg RJ; de Laat P; Smeitink JAM; Janssen MCH; Louw R
    Metabolomics; 2021 Jan; 17(1):10. PubMed ID: 33438095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brain anomalies in maternally inherited diabetes and deafness syndrome.
    Fromont I; Nicoli F; Valéro R; Felician O; Lebail B; Lefur Y; Mancini J; Paquis-Flucklinger V; Cozzone PJ; Vialettes B
    J Neurol; 2009 Oct; 256(10):1696-704. PubMed ID: 19536585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.
    Lien LM; Lee HC; Wang KL; Chiu JC; Chiu HC; Wei YH
    Acta Neurol Scand; 2001 Mar; 103(3):159-65. PubMed ID: 11240563
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.
    Oishi N; Kubota D; Nakamoto K; Takeda Y; Hayashi M; Gocho K; Yamaki K; Igarashi T; Takahashi H; Kameya S
    Ophthalmic Genet; 2021 Jun; 42(3):304-311. PubMed ID: 33541179
    [No Abstract]   [Full Text] [Related]  

  • 11. MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.
    de Wit HM; Westeneng HJ; van Engelen BG; Mudde AH
    Neth J Med; 2012 Dec; 70(10):460-2. PubMed ID: 23230016
    [TBL] [Abstract][Full Text] [Related]  

  • 12. THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS.
    Robinson KN; Terrazas S; Giordano-Mooga S; Xavier NA
    Endocr Pract; 2020 Feb; 26(2):241-246. PubMed ID: 31682520
    [No Abstract]   [Full Text] [Related]  

  • 13. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
    Tabebi M; Charfi N; Kallabi F; Alila-Fersi O; Ben Mahmoud A; Tlili A; Keskes-Ammar L; Kamoun H; Abid M; Mnif M; Fakhfakh F
    J Diabetes Complications; 2017 Jan; 31(1):253-259. PubMed ID: 27422531
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness.
    Tsang SH; Aycinena ARP; Sharma T
    Adv Exp Med Biol; 2018; 1085():163-165. PubMed ID: 30578504
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.
    Murphy R; Turnbull DM; Walker M; Hattersley AT
    Diabet Med; 2008 Apr; 25(4):383-99. PubMed ID: 18294221
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Outer retinal tubulations in maternally inherited diabetes & deafness - associated macular dystrophy: case report.
    Syriga M; Soumplis V; Kapernopoulos C; Kleftogiannis D; Karampelas M
    Ophthalmic Genet; 2020 Dec; 41(6):606-611. PubMed ID: 32720551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.
    Mory PB; Santos MC; Kater CE; Moisés RS
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):574-7. PubMed ID: 23295301
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).
    Guillausseau PJ; Dubois-Laforgue D; Massin P; Laloi-Michelin M; Bellanné-Chantelot C; Gin H; Bertin E; Blickle JF; Bauduceau B; Bouhanick B; Cahen-Varsaux J; Casanova S; Charpentier G; Chedin P; Derrien C; Grimaldi A; Guerci B; Kaloustian E; Lorenzini F; Murat A; Olivier F; Paques M; Paquis-Flucklinger V; Tielmans A; Vincenot M; Vialettes B; Timsit J;
    Diabetes Metab; 2004 Apr; 30(2):181-6. PubMed ID: 15223991
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes.
    Zhu J; Yang P; Liu X; Yan L; Rampersad S; Li F; Li H; Sheng C; Cheng X; Zhang M; Qu S
    J Diabetes Complications; 2017 Aug; 31(8):1354-1359. PubMed ID: 28599824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mother and a child with maternally inherited diabetes and deafness (MIDD) showing atrophy of the cerebrum, cerebellum and brainstem on magnetic resonance imaging (MRI).
    Kobayashi Z; Tsunemi T; Miake H; Tanaka S; Watabiki S; Morokuma Y
    Intern Med; 2005 Apr; 44(4):328-31. PubMed ID: 15897646
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.