Articoli di riviste sul tema "Mitochondriopathies"
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Finsterer, J. "Mitochondriopathies". European Journal of Neurology 11, n. 3 (marzo 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. 6 (21 marzo 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. 4 (23 luglio 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 (maggio 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 e M. S. Abdelmoula. "Manifestations endocriniennes dans les mitochondriopathies". Annales d'Endocrinologie 83, n. 5 (ottobre 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. 14 (30 settembre 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. 10 (ottobre 1986): 1059. http://dx.doi.org/10.1203/00006450-198610000-00205.
Gomes, Sérgio. "A review of mitochondrial disease in dogs". Companion Animal 26, n. 11 (2 dicembre 2021): 257–64. http://dx.doi.org/10.12968/coan.2021.0018.
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. 4 (18 febbraio 2021): 2007. http://dx.doi.org/10.3390/ijms22042007.
Swerdlow, Russell. "Mitochondrial Medicine and the Neurodegenerative Mitochondriopathies". Pharmaceuticals 2, n. 3 (3 dicembre 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. 2 (marzo 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. 16 (11 agosto 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. 1 (luglio 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 (ottobre 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. 2 (aprile 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. 2 (giugno 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. 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. 6 (novembre 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. 14 (19 settembre 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. 3 (maggio 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.
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 (aprile 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.
Dongre, Kanchan, Anja Jungo, Selina Späni, Yvonne Zysset e Anne Leuppi-Taegtmeyer. "Disease-Drug Interactions Requiring Special Attention". Praxis 111, n. 12 (settembre 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. 1 (marzo 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. 1 (luglio 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. 2 (26 gennaio 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. 3 (1 marzo 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. 4 (19 ottobre 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. 19 (10 ottobre 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. 11 (27 maggio 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 (aprile 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. 11 (6 giugno 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. 3 (28 gennaio 2022): 675. http://dx.doi.org/10.3390/cancers14030675.
Finsterer, J. "Mitochondriopathien". Aktuelle Neurologie 24, n. 06 (dicembre 1997): 231–41. http://dx.doi.org/10.1055/s-2007-1017815.
Roesti, Andreas. "MITOCHONDRIOPATHIEN". Akupunktur & Aurikulomedizin 42, n. 2 (giugno 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. 9 (31 agosto 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 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. 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 (ottobre 2016): S81. http://dx.doi.org/10.1016/s0168-8227(16)31108-1.
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. 5 (1994): 527–32. http://dx.doi.org/10.1007/bf00711585.
Ost, Bernhard. "Multifunktionsstörungen durch Mitochondriopathien". gynäkologie + geburtshilfe 25, n. 6 (dicembre 2020): 58–59. http://dx.doi.org/10.1007/s15013-020-3154-2.
Eugorisse, Alfred. "Mitochondriopathie und Anorexie". psychopraxis. neuropraxis 18, n. 5 (11 agosto 2015): 168–71. http://dx.doi.org/10.1007/s00739-015-0277-7.
Mende, S., A. Storch e H. Reichmann. "Genexpressionsstudien bei klassischen Mitochondriopathien". Der Nervenarzt 78, n. 10 (26 aprile 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 e Annamaria Painold. "Die Kraftwerke der Zellen- über die Behandlung von psychiatrischen Symptomen bei Patienten mit Mitochondriopathien". Fortschritte der Neurologie · Psychiatrie 85, n. 08 (agosto 2017): 474–78. http://dx.doi.org/10.1055/s-0043-113824.
Gröber, Uwe. "Long-COVID – eine Mitochondriopathie?" Zeitschrift für Orthomolekulare Medizin 19, n. 04 (dicembre 2021): 24–29. http://dx.doi.org/10.1055/a-1700-8588.
Gröber, Uwe. "Long-COVID – Eine Mitochondriopathie?" Erfahrungsheilkunde 70, n. 04 (agosto 2021): 225–30. http://dx.doi.org/10.1055/a-1528-4310.
Freisinger, Peter, Christine Makowski e Wolfgang Sperl. "Mitochondriopathien im Kindes- und Jugendalter". Pädiatrie up2date 10, n. 04 (3 dicembre 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, n. 23 (3 dicembre 2015): 405. http://dx.doi.org/10.1182/blood.v126.23.405.405.
Prokisch, H., K. Oexle e T. Meitinger. "Exomdiagnostik verändert die Sicht auf Mitochondriopathien". medizinische genetik 24, n. 3 (settembre 2012): 183–86. http://dx.doi.org/10.1007/s11825-012-0348-6.