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 *

152 related articles for article (PubMed ID: 8015633)

  • 1. [MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics].
    Damian MS; Reichmann H; Seibel P; Bachmann G; Schachenmayr W; Dorndorf W
    Nervenarzt; 1994 Apr; 65(4):258-63. PubMed ID: 8015633
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y; Guo Z; Chen L; Zhang J; Wang W; Liu X; Ren H; Gao S
    Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Follow-up studies and disorders of endocrinologic function in MELAS syndrome].
    Robeck S; Stefan H; Engelhardt A; Neundörfer B
    Nervenarzt; 1996 Jun; 67(6):465-70. PubMed ID: 8767201
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Di Trapani G; Gregori B; Servidei S; Ricci E; Sabatelli M; Tonali P
    Clin Neuropathol; 1997; 16(4):195-200. PubMed ID: 9266144
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diversity of clinical symptoms in A3243G mitochondrial DNA mutation (MELAS syndrome mutation).
    Pronicki M; Sykut-Cegielska J; Mierzewska H; Tońska K; Karczmarewicz E; Iwanicka K; Bartnik E; Pronicka E
    Med Sci Monit; 2002 Nov; 8(11):CR767-73. PubMed ID: 12444382
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy.
    Nicoll JA; Moss TH; Love S; Campbell MJ; Schutt WH
    Clin Neuropathol; 1993; 12(1):38-43. PubMed ID: 8382573
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Auditory symptoms: a critical clue for diagnosis of MELAS.
    Tawankanjanachot I; Channarong NS; Phanthumchinda K
    J Med Assoc Thai; 2005 Nov; 88(11):1715-20. PubMed ID: 16471125
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [MELAS syndrome as a differential diagnosis of ischemic stroke].
    Finsterer J
    Fortschr Neurol Psychiatr; 2009 Jan; 77(1):25-31. PubMed ID: 19012224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnosis and management of MELAS.
    Thambisetty M; Newman NJ
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree.
    Dubeau F; De Stefano N; Zifkin BG; Arnold DL; Shoubridge EA
    Ann Neurol; 2000 Feb; 47(2):179-85. PubMed ID: 10665488
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA; Wang N
    Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MELAS and L-arginine therapy: pathophysiology of stroke-like episodes.
    Koga Y; Povalko N; Nishioka J; Katayama K; Kakimoto N; Matsuishi T
    Ann N Y Acad Sci; 2010 Jul; 1201():104-10. PubMed ID: 20649546
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].
    Pérez López-Fraile MI; Barrena R; Montoya J; Marta E
    Neurologia; 2006; 21(6):327-32. PubMed ID: 16799910
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P; Ziegler F; Sternberg D; Rouche A; Frachon P; Fardeau M; Eymard B; Lombès A
    Rev Neurol (Paris); 2000 Dec; 156(12):1136-47. PubMed ID: 11139730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Chen JC; Tsai TC; Liu CS; Lu CT
    Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H; Sugimura T; Yamada T; Hayashi K; Kobayashi T
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
    Degoul F; Diry M; Pou-Serradell A; Lloreta J; Marsac C
    Ann Neurol; 1994 Mar; 35(3):365-70. PubMed ID: 8122891
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Donegal kindred--clinical features and molecular genetic analysis.
    McEntagart M; Droogan O; Burke M; Brett F; Murphy S; Farrell M
    Ir Med J; 1997; 90(4):144-5. PubMed ID: 9267093
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Depressive episode with catatonic features in a case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Ju Seok Ryu ; Sook Joung Lee ; In Young Sung ; Tae Sung Ko ; Han Ik Yoo
    J Child Neurol; 2009 Oct; 24(10):1307-9. PubMed ID: 19451268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.