Journal articles on the topic 'Mitochondriopathies'
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Finsterer, J. "Mitochondriopathies." European Journal of Neurology 11, no. 3 (March 2004): 163–86. http://dx.doi.org/10.1046/j.1351-5101.2003.00728.x.
Chinnery, P. F., and P. G. Griffiths. "Optic mitochondriopathies." Neurology 64, no. 6 (March 21, 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, no. 4 (July 23, 2009): 737–51. http://dx.doi.org/10.3233/jad-2009-1095.
Tardieu, M., B. Barret, and S. Blanche. "Antiviraux et mitochondriopathies." Archives de Pédiatrie 8 (May 2001): 327–28. http://dx.doi.org/10.1016/s0929-693x(01)80062-2.
Ben Chehida, A., E. Ben Arab, S. Khatrouch, M. Zribi, H. Boudabous, and M. S. Abdelmoula. "Manifestations endocriniennes dans les mitochondriopathies." Annales d'Endocrinologie 83, no. 5 (October 2022): 301–2. http://dx.doi.org/10.1016/j.ando.2022.07.074.
Griggs, Robert C., and George Karpati. "Muscle Pain, Fatigue, and Mitochondriopathies." New England Journal of Medicine 341, no. 14 (September 30, 1999): 1077–78. http://dx.doi.org/10.1056/nejm199909303411411.
Ruitenbeek, W., R. Sengers, R. Van Laack, F. Trijbels, J. Bakkeren, A. Janssen, and O. Van Diggelen. "150 ANTENATAL DIAGNOSIS OF MITOCHONDRIOPATHIES." Pediatric Research 20, no. 10 (October 1986): 1059. http://dx.doi.org/10.1203/00006450-198610000-00205.
Gomes, Sérgio. "A review of mitochondrial disease in dogs." Companion Animal 26, no. 11 (December 2, 2021): 257–64. http://dx.doi.org/10.12968/coan.2021.0018.
Liskova, Alena, Marek Samec, Lenka Koklesova, Erik Kudela, Peter Kubatka, and 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, no. 4 (February 18, 2021): 2007. http://dx.doi.org/10.3390/ijms22042007.
Swerdlow, Russell. "Mitochondrial Medicine and the Neurodegenerative Mitochondriopathies." Pharmaceuticals 2, no. 3 (December 3, 2009): 150–67. http://dx.doi.org/10.3390/ph2030150.
Taibi, B., N. Allali, and L. Chat. "Apport de l’IRM cérébrale dans les mitochondriopathies." Journal of Neuroradiology 47, no. 2 (March 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, no. 16 (August 11, 2021): 8649. http://dx.doi.org/10.3390/ijms22168649.
Byrne, Edward, Sangot Marzuki, and Xenia Dennett. "Current perspectives in the study of human mitochondriopathies." Medical Journal of Australia 149, no. 1 (July 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, and N. Gouider-Khouja. "PO17-TU-14 Diagnosis of mitochondriopathies in Tunisia." Journal of the Neurological Sciences 285 (October 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, and Udo Wendel. "Importance of mitochondrial transmembrane processes in human mitochondriopathies." Journal of Bioenergetics and Biomembranes 28, no. 2 (April 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, no. 2 (June 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, no. 15 (2007): 3416–28. http://dx.doi.org/10.1002/jnr.21167.
Bosche, Jürgen, Wolfgang Hammerstein, Eva Neuen-Jacob, and Ralf Schober. "Variation in retinal changes and muscle pathology in mitochondriopathies." Graefe's Archive for Clinical and Experimental Ophthalmology 227, no. 6 (November 1989): 578–83. http://dx.doi.org/10.1007/bf02169456.
Iommarini, L., A. Maresca, L. Caporali, M. L. Valentino, R. Liguori, C. Giordano, and V. Carelli. "Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies." Neurology 79, no. 14 (September 19, 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, and J. A. J. M. Bakkeren. "The use of chorionic villi in prenatal diagnosis of mitochondriopathies." Journal of Inherited Metabolic Disease 15, no. 3 (May 1992): 303–6. http://dx.doi.org/10.1007/bf02435962.
Wilkins, Heather M., Steven M. Carl, and 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.
Beaudonnet, G., C. Denier, C. Lacroix, A. Slama, and D. Adams. "Les neuropathies des mitochondriopathies : étude de 18 cas et revue de la littérature." Revue Neurologique 169 (April 2013): A42. http://dx.doi.org/10.1016/j.neurol.2013.01.091.
Das, Anibh M., Ulrike Steuerwald, and 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.
Dongre, Kanchan, Anja Jungo, Selina Späni, Yvonne Zysset, and Anne Leuppi-Taegtmeyer. "Disease-Drug Interactions Requiring Special Attention." Praxis 111, no. 12 (September 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, and Olga Golunitschaja. "Mitochondrial impairments in aetiopathology of multifactorial diseases: common origin but individual outcomes in context of 3P medicine." EPMA Journal 12, no. 1 (March 2021): 27–40. http://dx.doi.org/10.1007/s13167-021-00237-2.
Fu, X., P. Rinaldo, S. H. Hahn, H. Kodama, and S. Packman. "Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes." Journal of Inherited Metabolic Disease 26, no. 1 (July 2003): 55–66. http://dx.doi.org/10.1023/a:1024027630589.
Lehmann Urban, Diana, Leila Motlagh Scholle, Kerstin Alt, Albert C. Ludolph, and Angela Rosenbohm. "Camptocormia as a Novel Phenotype in a Heterozygous POLG2 Mutation." Diagnostics 10, no. 2 (January 26, 2020): 68. http://dx.doi.org/10.3390/diagnostics10020068.
Paoli, Antonio, Antonino Bianco, Ernesto Damiani, and 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, and 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, no. 3 (March 1, 2001): R695—R704. http://dx.doi.org/10.1152/ajpregu.2001.280.3.r695.
Khoreva, M. A., and I. V. Smagina. "Basal Ganglia Calcification. Aetiopathogenesis, Diagnostics, Clinical Manifestations." Russian neurological journal 25, no. 4 (October 19, 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, no. 19 (October 10, 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, no. 11 (May 27, 2022): 6056. http://dx.doi.org/10.3390/ijms23116056.
Rafai, Mohammed Abdoh, Habtany Younes, Jardel Claude, Slassi Ilham, Dehbi Hind, and 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 (April 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, no. 11 (June 6, 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, and Manuel Ritter. "Systemic Effects Reflected in Specific Biomarker Patterns Are Instrumental for the Paradigm Change in Prostate Cancer Management: A Strategic Paper." Cancers 14, no. 3 (January 28, 2022): 675. http://dx.doi.org/10.3390/cancers14030675.
Finsterer, J. "Mitochondriopathien." Aktuelle Neurologie 24, no. 06 (December 1997): 231–41. http://dx.doi.org/10.1055/s-2007-1017815.
Roesti, Andreas. "MITOCHONDRIOPATHIEN." Akupunktur & Aurikulomedizin 42, no. 2 (June 2016): 24–29. http://dx.doi.org/10.1007/s15009-016-5392-x.
Sperl, W., H. Prokisch, D. Karall, J. A. Mayr, and P. Freisinger. "Mitochondriopathien." Monatsschrift Kinderheilkunde 159, no. 9 (August 31, 2011): 848–54. http://dx.doi.org/10.1007/s00112-011-2447-x.
Salvan, Anne-Marie, Jean Vion-Dury, Sylviane Confort-Gouny, Iban Sangla, Jean Pouget, and 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, no. 1 (1998): 46–49. http://dx.doi.org/10.1159/000007955.
Suzuki, Yoshihiko, Motoaki Sano, Junichihro Irie, Toshihide Kawai, Shu Meguro, and 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 (October 2016): S81. http://dx.doi.org/10.1016/s0168-8227(16)31108-1.
Fingerhut, R., W. Schmitz, B. Garavaglia, H. Reichmann, and 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, no. 5 (1994): 527–32. http://dx.doi.org/10.1007/bf00711585.
Ost, Bernhard. "Multifunktionsstörungen durch Mitochondriopathien." gynäkologie + geburtshilfe 25, no. 6 (December 2020): 58–59. http://dx.doi.org/10.1007/s15013-020-3154-2.
Eugorisse, Alfred. "Mitochondriopathie und Anorexie." psychopraxis. neuropraxis 18, no. 5 (August 11, 2015): 168–71. http://dx.doi.org/10.1007/s00739-015-0277-7.
Mende, S., A. Storch, and H. Reichmann. "Genexpressionsstudien bei klassischen Mitochondriopathien." Der Nervenarzt 78, no. 10 (April 26, 2007): 1155–59. http://dx.doi.org/10.1007/s00115-007-2266-4.
Mörkl, Sabrina, Adelina Tmava, Claudia Blesl, Franziska Schmiedhofer, Walter E. Wurm, Anna Holl, and Annamaria Painold. "Die Kraftwerke der Zellen- über die Behandlung von psychiatrischen Symptomen bei Patienten mit Mitochondriopathien." Fortschritte der Neurologie · Psychiatrie 85, no. 08 (August 2017): 474–78. http://dx.doi.org/10.1055/s-0043-113824.
Gröber, Uwe. "Long-COVID – eine Mitochondriopathie?" Zeitschrift für Orthomolekulare Medizin 19, no. 04 (December 2021): 24–29. http://dx.doi.org/10.1055/a-1700-8588.
Gröber, Uwe. "Long-COVID – Eine Mitochondriopathie?" Erfahrungsheilkunde 70, no. 04 (August 2021): 225–30. http://dx.doi.org/10.1055/a-1528-4310.
Freisinger, Peter, Christine Makowski, and Wolfgang Sperl. "Mitochondriopathien im Kindes- und Jugendalter." Pädiatrie up2date 10, no. 04 (December 3, 2015): 323–40. http://dx.doi.org/10.1055/s-0041-103529.
Yien, Yvette Y., Caiyong Chen, Jiahai Shi, Liangtao Li, Daniel E. Bauer, Nicholas Huston, Paul D. Kingsley, et al. "Fam210b Is Required for Optimal Cellular and Mitochondrial Iron Uptake during Erythroid Differentiation." Blood 126, no. 23 (December 3, 2015): 405. http://dx.doi.org/10.1182/blood.v126.23.405.405.
Prokisch, H., K. Oexle, and T. Meitinger. "Exomdiagnostik verändert die Sicht auf Mitochondriopathien." medizinische genetik 24, no. 3 (September 2012): 183–86. http://dx.doi.org/10.1007/s11825-012-0348-6.