Artigos de revistas sobre o tema "Mitochondriopathies"
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Finsterer, J. "Mitochondriopathies". European Journal of Neurology 11, n.º 3 (março de 2004): 163–86. http://dx.doi.org/10.1046/j.1351-5101.2003.00728.x.
Chinnery, P. F., e P. G. Griffiths. "Optic mitochondriopathies". Neurology 64, n.º 6 (21 de março de 2005): 940–41. http://dx.doi.org/10.1212/01.wnl.0000157285.93611.b2.
Swerdlow, Russell H. "The Neurodegenerative Mitochondriopathies". Journal of Alzheimer's Disease 17, n.º 4 (23 de julho de 2009): 737–51. http://dx.doi.org/10.3233/jad-2009-1095.
Tardieu, M., B. Barret e S. Blanche. "Antiviraux et mitochondriopathies". Archives de Pédiatrie 8 (maio de 2001): 327–28. http://dx.doi.org/10.1016/s0929-693x(01)80062-2.
Gomes, Sérgio. "A review of mitochondrial disease in dogs". Companion Animal 26, n.º 11 (2 de dezembro de 2021): 257–64. http://dx.doi.org/10.12968/coan.2021.0018.
Ben Chehida, A., E. Ben Arab, S. Khatrouch, M. Zribi, H. Boudabous e M. S. Abdelmoula. "Manifestations endocriniennes dans les mitochondriopathies". Annales d'Endocrinologie 83, n.º 5 (outubro de 2022): 301–2. http://dx.doi.org/10.1016/j.ando.2022.07.074.
Griggs, Robert C., e George Karpati. "Muscle Pain, Fatigue, and Mitochondriopathies". New England Journal of Medicine 341, n.º 14 (30 de setembro de 1999): 1077–78. http://dx.doi.org/10.1056/nejm199909303411411.
Ruitenbeek, W., R. Sengers, R. Van Laack, F. Trijbels, J. Bakkeren, A. Janssen e O. Van Diggelen. "150 ANTENATAL DIAGNOSIS OF MITOCHONDRIOPATHIES". Pediatric Research 20, n.º 10 (outubro de 1986): 1059. http://dx.doi.org/10.1203/00006450-198610000-00205.
Liskova, Alena, Marek Samec, Lenka Koklesova, Erik Kudela, Peter Kubatka e Olga Golubnitschaja. "Mitochondriopathies as a Clue to Systemic Disorders—Analytical Tools and Mitigating Measures in Context of Predictive, Preventive, and Personalized (3P) Medicine". International Journal of Molecular Sciences 22, n.º 4 (18 de fevereiro de 2021): 2007. http://dx.doi.org/10.3390/ijms22042007.
Swerdlow, Russell. "Mitochondrial Medicine and the Neurodegenerative Mitochondriopathies". Pharmaceuticals 2, n.º 3 (3 de dezembro de 2009): 150–67. http://dx.doi.org/10.3390/ph2030150.
Taibi, B., N. Allali e L. Chat. "Apport de l’IRM cérébrale dans les mitochondriopathies". Journal of Neuroradiology 47, n.º 2 (março de 2020): 125. http://dx.doi.org/10.1016/j.neurad.2020.01.064.
Koklesova, Lenka, Alena Liskova, Marek Samec, Kevin Zhai, Raghad Khalid AL-Ishaq, Ondrej Bugos, Miroslava Šudomová et al. "Protective Effects of Flavonoids Against Mitochondriopathies and Associated Pathologies: Focus on the Predictive Approach and Personalized Prevention". International Journal of Molecular Sciences 22, n.º 16 (11 de agosto de 2021): 8649. http://dx.doi.org/10.3390/ijms22168649.
Byrne, Edward, Sangot Marzuki e Xenia Dennett. "Current perspectives in the study of human mitochondriopathies". Medical Journal of Australia 149, n.º 1 (julho de 1988): 30–33. http://dx.doi.org/10.5694/j.1326-5377.1988.tb120480.x.
Kraoua, I., H. Benrhouma, I. Marouani, S. Hamdi, N. Fradj, A. Rouissi, S. Zekri, N. Kaabachi, M. Jaafoura e N. Gouider-Khouja. "PO17-TU-14 Diagnosis of mitochondriopathies in Tunisia". Journal of the Neurological Sciences 285 (outubro de 2009): S243. http://dx.doi.org/10.1016/s0022-510x(09)70926-8.
Huizing, Marjan, Vito DePinto, Wim Ruitenbeek, Frans J. M. Trijbels, Lambert P. van den Heuvel e Udo Wendel. "Importance of mitochondrial transmembrane processes in human mitochondriopathies". Journal of Bioenergetics and Biomembranes 28, n.º 2 (abril de 1996): 109–14. http://dx.doi.org/10.1007/bf02110640.
Nagahashi-Marie, Suely Kazue. "Mitochondriopathies: contribution to the study of mitochondrial DNA mutations". Arquivos de Neuro-Psiquiatria 55, n.º 2 (junho de 1997): 340. http://dx.doi.org/10.1590/s0004-282x1997000200029.
Swerdlow, Russell H. "Mitochondria in cybrids containing mtDNA from persons with mitochondriopathies". Journal of Neuroscience Research 85, n.º 15 (2007): 3416–28. http://dx.doi.org/10.1002/jnr.21167.
Bosche, Jürgen, Wolfgang Hammerstein, Eva Neuen-Jacob e Ralf Schober. "Variation in retinal changes and muscle pathology in mitochondriopathies". Graefe's Archive for Clinical and Experimental Ophthalmology 227, n.º 6 (novembro de 1989): 578–83. http://dx.doi.org/10.1007/bf02169456.
Iommarini, L., A. Maresca, L. Caporali, M. L. Valentino, R. Liguori, C. Giordano e V. Carelli. "Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies". Neurology 79, n.º 14 (19 de setembro de 2012): 1517–19. http://dx.doi.org/10.1212/wnl.0b013e31826d5f72.
Ruitenbeek, W., R. C. A. Sengers, J. M. F. Trijbels, A. J. M. Janssen e J. A. J. M. Bakkeren. "The use of chorionic villi in prenatal diagnosis of mitochondriopathies". Journal of Inherited Metabolic Disease 15, n.º 3 (maio de 1992): 303–6. http://dx.doi.org/10.1007/bf02435962.
Wilkins, Heather M., Steven M. Carl e Russell H. Swerdlow. "Cytoplasmic hybrid (cybrid) cell lines as a practical model for mitochondriopathies". Redox Biology 2 (2014): 619–31. http://dx.doi.org/10.1016/j.redox.2014.03.006.
N., Santosh, Prahlad Kadambi, Ravi Kyaddigeri, Radha Rao e Hemanth Kumar N. "Rare case report of mitochondriopathy". International Journal of Contemporary Pediatrics 10, n.º 6 (26 de maio de 2023): 969–71. http://dx.doi.org/10.18203/2349-3291.ijcp20231512.
Beaudonnet, G., C. Denier, C. Lacroix, A. Slama e D. Adams. "Les neuropathies des mitochondriopathies : étude de 18 cas et revue de la littérature". Revue Neurologique 169 (abril de 2013): A42. http://dx.doi.org/10.1016/j.neurol.2013.01.091.
Das, Anibh M., Ulrike Steuerwald e Sabine Illsinger. "Inborn Errors of Energy Metabolism Associated with Myopathies". Journal of Biomedicine and Biotechnology 2010 (2010): 1–19. http://dx.doi.org/10.1155/2010/340849.
Citrigno, Luigi, Antonio Qualtieri, Annamaria Cerantonio, Selene De Benedittis, Olivier Gallo, Gemma Di Palma, Patrizia Spadafora e Francesca Cavalcanti. "Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies". Journal of the Neurological Sciences 457 (fevereiro de 2024): 122869. http://dx.doi.org/10.1016/j.jns.2024.122869.
Dongre, Kanchan, Anja Jungo, Selina Späni, Yvonne Zysset e Anne Leuppi-Taegtmeyer. "Disease-Drug Interactions Requiring Special Attention". Praxis 111, n.º 12 (setembro de 2022): 700–705. http://dx.doi.org/10.1024/1661-8157/a003923.
Koklesova, Lenka, Marek Samec, Alena Liskova, Kevin Zhai, Dietrich Büsselberg, Frank A. Giordano, Peter Kubatka e Olga Golunitschaja. "Mitochondrial impairments in aetiopathology of multifactorial diseases: common origin but individual outcomes in context of 3P medicine". EPMA Journal 12, n.º 1 (março de 2021): 27–40. http://dx.doi.org/10.1007/s13167-021-00237-2.
Fu, X., P. Rinaldo, S. H. Hahn, H. Kodama e S. Packman. "Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes". Journal of Inherited Metabolic Disease 26, n.º 1 (julho de 2003): 55–66. http://dx.doi.org/10.1023/a:1024027630589.
Lehmann Urban, Diana, Leila Motlagh Scholle, Kerstin Alt, Albert C. Ludolph e Angela Rosenbohm. "Camptocormia as a Novel Phenotype in a Heterozygous POLG2 Mutation". Diagnostics 10, n.º 2 (26 de janeiro de 2020): 68. http://dx.doi.org/10.3390/diagnostics10020068.
Paoli, Antonio, Antonino Bianco, Ernesto Damiani e Gerardo Bosco. "Ketogenic Diet in Neuromuscular and Neurodegenerative Diseases". BioMed Research International 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/474296.
Ramakrishna, Ramprasad, Jeremy S. Edwards, Andrew McCulloch e Bernhard O. Palsson. "Flux-balance analysis of mitochondrial energy metabolism: consequences of systemic stoichiometric constraints". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 280, n.º 3 (1 de março de 2001): R695—R704. http://dx.doi.org/10.1152/ajpregu.2001.280.3.r695.
Khoreva, M. A., e I. V. Smagina. "Basal Ganglia Calcification. Aetiopathogenesis, Diagnostics, Clinical Manifestations". Russian neurological journal 25, n.º 4 (19 de outubro de 2020): 4–13. http://dx.doi.org/10.30629/2658-7947-2020-25-4-4-13.
Elsnicova, Barbara, Daniela Hornikova, Veronika Tibenska, David Kolar, Tereza Tlapakova, Benjamin Schmid, Markus Mallek et al. "Desmin Knock-Out Cardiomyopathy: A Heart on the Verge of Metabolic Crisis". International Journal of Molecular Sciences 23, n.º 19 (10 de outubro de 2022): 12020. http://dx.doi.org/10.3390/ijms231912020.
Averina, Olga A., Ivan G. Laptev, Mariia A. Emelianova, Oleg A. Permyakov, Sofia S. Mariasina, Alyona I. Nikiforova, Vasily N. Manskikh et al. "Mitochondrial rRNA Methylation by Mettl15 Contributes to the Exercise and Learning Capability in Mice". International Journal of Molecular Sciences 23, n.º 11 (27 de maio de 2022): 6056. http://dx.doi.org/10.3390/ijms23116056.
Rafai, Mohammed Abdoh, Habtany Younes, Jardel Claude, Slassi Ilham, Dehbi Hind e Bouche Pierre. "Le « SMANDOP » un nouveau phénotype des mitochondriopathies liées aux mutations POLG1 ou un simple profil évolutif du classique syndrome SANDO ?" Revue Neurologique 175 (abril de 2019): S127. http://dx.doi.org/10.1016/j.neurol.2019.01.334.
Novosel, Dinko, Vladimir Brajković, Mojca Simčič, Minja Zorc, Tanja Svara, Karmen Branovic Cakanic, Andreja Jungić et al. "The Consequences of Mitochondrial T10432C Mutation in Cika Cattle: A “Potential” Model for Leber’s Hereditary Optic Neuropathy". International Journal of Molecular Sciences 23, n.º 11 (6 de junho de 2022): 6335. http://dx.doi.org/10.3390/ijms23116335.
Golubnitschaja, Olga, Peter Kubatka, Alena Mazurakova, Marek Samec, Abdullah Alajati, Frank A. Giordano, Vincenzo Costigliola, Jörg Ellinger e Manuel Ritter. "Systemic Effects Reflected in Specific Biomarker Patterns Are Instrumental for the Paradigm Change in Prostate Cancer Management: A Strategic Paper". Cancers 14, n.º 3 (28 de janeiro de 2022): 675. http://dx.doi.org/10.3390/cancers14030675.
Eichwald, Tuany, Lucila de Bortoli da da Silva, Ananda Christina Staats Staats Pires, Laís Niero, Erick Schnorrenberger, Clovis Colpani Filho, Gisele Espíndola et al. "Tetrahydrobiopterin: Beyond Its Traditional Role as a Cofactor". Antioxidants 12, n.º 5 (3 de maio de 2023): 1037. http://dx.doi.org/10.3390/antiox12051037.
Salvan, Anne-Marie, Jean Vion-Dury, Sylviane Confort-Gouny, Iban Sangla, Jean Pouget e Patrick J. Cozzone. "Brain Metabolic Profiles Obtained by Proton MRS in Two Forms of Mitochondriopathies: Leber’s Hereditary Optic Neuropathy and Chronic Progressive External Ophthalmoplegia". European Neurology 40, n.º 1 (1998): 46–49. http://dx.doi.org/10.1159/000007955.
Suzuki, Yoshihiko, Motoaki Sano, Junichihro Irie, Toshihide Kawai, Shu Meguro e Nobuhiro Ikemura. "A case of mitochondrial diabetes associated with 3243 bp tRNA Leu (UUR) mutation, who suffered from the rapid appearance of “mitochondriopathies”". Diabetes Research and Clinical Practice 120 (outubro de 2016): S81. http://dx.doi.org/10.1016/s0168-8227(16)31108-1.
Finsterer, J. "Mitochondriopathien". Aktuelle Neurologie 24, n.º 06 (dezembro de 1997): 231–41. http://dx.doi.org/10.1055/s-2007-1017815.
Roesti, Andreas. "MITOCHONDRIOPATHIEN". Akupunktur & Aurikulomedizin 42, n.º 2 (junho de 2016): 24–29. http://dx.doi.org/10.1007/s15009-016-5392-x.
Sperl, W., H. Prokisch, D. Karall, J. A. Mayr e P. Freisinger. "Mitochondriopathien". Monatsschrift Kinderheilkunde 159, n.º 9 (31 de agosto de 2011): 848–54. http://dx.doi.org/10.1007/s00112-011-2447-x.
Feldhaus, Simon. "Mitochondriopathie". Erfahrungsheilkunde 73, n.º 02 (abril de 2024): 56–61. http://dx.doi.org/10.1055/a-2264-5078.
Schmidt, Robert. "Mitochondriopathie". Erfahrungsheilkunde 73, n.º 02 (abril de 2024): 53. http://dx.doi.org/10.1055/a-2252-6231.
Fingerhut, R., W. Schmitz, B. Garavaglia, H. Reichmann e E. Conzelmann. "Impaired degradation of phytanic acid in cells from patients with mitochondriopathies: Evidence for the involvement of ETF and the respiratory chain in phytanic acid ?-oxidation". Journal of Inherited Metabolic Disease 17, n.º 5 (1994): 527–32. http://dx.doi.org/10.1007/bf00711585.
Ost, Bernhard. "Multifunktionsstörungen durch Mitochondriopathien". gynäkologie + geburtshilfe 25, n.º 6 (dezembro de 2020): 58–59. http://dx.doi.org/10.1007/s15013-020-3154-2.
Eugorisse, Alfred. "Mitochondriopathie und Anorexie". psychopraxis. neuropraxis 18, n.º 5 (11 de agosto de 2015): 168–71. http://dx.doi.org/10.1007/s00739-015-0277-7.
Mörkl, Sabrina, Adelina Tmava, Claudia Blesl, Franziska Schmiedhofer, Walter E. Wurm, Anna Holl e Annamaria Painold. "Die Kraftwerke der Zellen- über die Behandlung von psychiatrischen Symptomen bei Patienten mit Mitochondriopathien". Fortschritte der Neurologie · Psychiatrie 85, n.º 08 (agosto de 2017): 474–78. http://dx.doi.org/10.1055/s-0043-113824.
Mende, S., A. Storch e H. Reichmann. "Genexpressionsstudien bei klassischen Mitochondriopathien". Der Nervenarzt 78, n.º 10 (26 de abril de 2007): 1155–59. http://dx.doi.org/10.1007/s00115-007-2266-4.