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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 1658240

  • 1. Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.
    Bresolin N, Martinelli P, Barbiroli B, Zaniol P, Ausenda C, Montagna P, Gallanti A, Comi GP, Scarlato G, Lugaresi E.
    J Neurol Sci; 1991 Aug; 104(2):182-9. PubMed ID: 1658240
    [Abstract] [Full Text] [Related]

  • 2. Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine.
    Uncini A, Lodi R, Di Muzio A, Silvestri G, Servidei S, Lugaresi A, Iotti S, Zaniol P, Barbiroli B.
    J Neurol Sci; 1995 Apr; 129(2):214-22. PubMed ID: 7608738
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopy.
    Lodi R, Taylor DJ, Tabrizi SJ, Hilton-Jones D, Squier MV, Seller A, Styles P, Schapira AH.
    Brain; 1998 Nov; 121 ( Pt 11)():2119-26. PubMed ID: 9827771
    [Abstract] [Full Text] [Related]

  • 5. A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigation.
    Hayes DJ, Hilton-Jones D, Arnold DL, Galloway G, Styles P, Duncan J, Radda GK.
    J Neurol Sci; 1985 Nov; 71(1):105-18. PubMed ID: 4087016
    [Abstract] [Full Text] [Related]

  • 6. Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura.
    Barbiroli B, Montagna P, Cortelli P, Funicello R, Iotti S, Monari L, Pierangeli G, Zaniol P, Lugaresi E.
    Neurology; 1992 Jun; 42(6):1209-14. PubMed ID: 1603349
    [Abstract] [Full Text] [Related]

  • 7. Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Vialettes B, Paquis-Fluckinger V, Silvestre-Aillaud P, Ben Dahan D, Pelissier JF, Etchary-Bouyx F, Raccah D, Gin H, Guillausseau PJ, Vanuxen D.
    Diabetes Care; 1995 Jul; 18(7):1023-8. PubMed ID: 7555536
    [Abstract] [Full Text] [Related]

  • 8. Complicated migraine studied by phosphorus magnetic resonance spectroscopy.
    Barbiroli B, Montagna P, Cortelli P, Martinelli P, Sacquegna T, Zaniol P, Lugaresi E.
    Cephalalgia; 1990 Oct; 10(5):263-72. PubMed ID: 2272097
    [Abstract] [Full Text] [Related]

  • 9. MELAS syndrome with mitochondrial tRNA(Leu)(UUR) mutation: correlation of clinical state, nerve conduction, and muscle 31P magnetic resonance spectroscopy during treatment with nicotinamide and riboflavin.
    Penn AM, Lee JW, Thuillier P, Wagner M, Maclure KM, Menard MR, Hall LD, Kennaway NG.
    Neurology; 1992 Nov; 42(11):2147-52. PubMed ID: 1436526
    [Abstract] [Full Text] [Related]

  • 10. Deficit of brain and skeletal muscle bioenergetics and low brain magnesium in juvenile migraine: an in vivo 31P magnetic resonance spectroscopy interictal study.
    Lodi R, Montagna P, Soriani S, Iotti S, Arnaldi C, Cortelli P, Pierangeli G, Patuelli A, Zaniol P, Barbiroli B.
    Pediatr Res; 1997 Dec; 42(6):866-71. PubMed ID: 9396571
    [Abstract] [Full Text] [Related]

  • 11. 31P-magnetic resonance spectroscopy in migraine without aura.
    Montagna P, Cortelli P, Monari L, Pierangeli G, Parchi P, Lodi R, Iotti S, Frassineti C, Zaniol P, Lugaresi E.
    Neurology; 1994 Apr; 44(4):666-9. PubMed ID: 8164822
    [Abstract] [Full Text] [Related]

  • 12. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
    Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Lovelace RE, Rowland LP, Schon EA, DiMauro S.
    J Clin Invest; 1993 Dec; 92(6):2906-15. PubMed ID: 8254046
    [Abstract] [Full Text] [Related]

  • 13. In vivo magnetic resonance spectroscopy of brain and muscle in a type of mitochondrial encephalomyopathy (MERRF).
    Matthews PM, Berkovic SF, Shoubridge EA, Andermann F, Karpati G, Carpenter S, Arnold DL.
    Ann Neurol; 1991 Apr; 29(4):435-8. PubMed ID: 1929212
    [Abstract] [Full Text] [Related]

  • 14. Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome.
    Lodi R, Montagna P, Iotti S, Zaniol P, Barboni P, Puddu P, Barbiroli B.
    J Neurol Neurosurg Psychiatry; 1994 Dec; 57(12):1492-6. PubMed ID: 7798979
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).
    Shaag A, Saada A, Steinberg A, Navon P, Elpeleg ON.
    Biochem Biophys Res Commun; 1997 Apr 28; 233(3):637-9. PubMed ID: 9168904
    [Abstract] [Full Text] [Related]

  • 16. Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family.
    Cortelli P, Montagna P, Avoni P, Sangiorgi S, Bresolin N, Moggio M, Zaniol P, Mantovani V, Barboni P, Barbiroli B.
    Neurology; 1991 Aug 28; 41(8):1211-5. PubMed ID: 1866007
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
    Shoffner JM, Bialer MG, Pavlakis SG, Lott M, Kaufman A, Dixon J, Teichberg S, Wallace DC.
    Neurology; 1995 Feb 28; 45(2):286-92. PubMed ID: 7854527
    [Abstract] [Full Text] [Related]

  • 20. Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation.
    Barbiroli B, Montagna P, Cortelli P, Iotti S, Lodi R, Barboni P, Monari L, Lugaresi E, Frassineti C, Zaniol P.
    Neurology; 1995 Jul 28; 45(7):1364-9. PubMed ID: 7617199
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.