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Auswahl der wissenschaftlichen Literatur zum Thema „Autoimmune and idiopathic organic disease“
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Zeitschriftenartikel zum Thema "Autoimmune and idiopathic organic disease"
Keda, YM, IV Krjukova, IA Ilovaiskaia, MS Morozova, OV Fofanova, MB Babarina, EI Marova, YA Pankov und VI Kandror. „Antibodies to pituitary surface antigens during various pituitary disease states“. Journal of Endocrinology 175, Nr. 2 (01.11.2002): 417–23. http://dx.doi.org/10.1677/joe.0.1750417.
Der volle Inhalt der QuelleKrug, Susanne M. „Solving the Puzzle: Molecular Research in Inflammatory Bowel Diseases“. International Journal of Molecular Sciences 24, Nr. 17 (29.08.2023): 13389. http://dx.doi.org/10.3390/ijms241713389.
Der volle Inhalt der QuelleMeunier, Lucy, und Dominique Larrey. „Hepatotoxicity of Drugs Used in Multiple Sclerosis, Diagnostic Challenge, and the Role of HLA Genotype Susceptibility“. International Journal of Molecular Sciences 24, Nr. 1 (03.01.2023): 852. http://dx.doi.org/10.3390/ijms24010852.
Der volle Inhalt der QuelleFukushima, Kiyoharu, Kazuyuki Tsujino, Shinji Futami und Hiroshi Kida. „Natural Autoantibodies in Chronic Pulmonary Diseases“. International Journal of Molecular Sciences 21, Nr. 3 (08.02.2020): 1138. http://dx.doi.org/10.3390/ijms21031138.
Der volle Inhalt der QuellePulito-Cueto, Verónica, Fernanda Genre, Raquel López-Mejías, Víctor Manuel Mora-Cuesta, David Iturbe-Fernández, Virginia Portilla, María Sebastián Mora-Gil et al. „Endothelin-1 as a Biomarker of Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease Associated with Autoimmune Diseases“. International Journal of Molecular Sciences 24, Nr. 2 (09.01.2023): 1275. http://dx.doi.org/10.3390/ijms24021275.
Der volle Inhalt der QuelleKageyama, Reiko, Tetsuya Honda und Yoshiki Tokura. „Acquired Idiopathic Generalized Anhidrosis (AIGA) and Its Complications: Implications for AIGA as an Autoimmune Disease“. International Journal of Molecular Sciences 22, Nr. 16 (04.08.2021): 8389. http://dx.doi.org/10.3390/ijms22168389.
Der volle Inhalt der QuelleLöfdahl, Anna, Göran Tornling, Jenny Wigén, Anna-Karin Larsson-Callerfelt, Christina Wenglén und Gunilla Westergren-Thorsson. „Pathological Insight into 5-HT2B Receptor Activation in Fibrosing Interstitial Lung Diseases“. International Journal of Molecular Sciences 22, Nr. 1 (28.12.2020): 225. http://dx.doi.org/10.3390/ijms22010225.
Der volle Inhalt der QuelleKim, Ji-Won, Mi-Hyun Ahn, Ju-Yang Jung, Chang-Hee Suh und Hyoun-Ah Kim. „An Update on the Pathogenic Role of Neutrophils in Systemic Juvenile Idiopathic Arthritis and Adult-Onset Still’s Disease“. International Journal of Molecular Sciences 22, Nr. 23 (02.12.2021): 13038. http://dx.doi.org/10.3390/ijms222313038.
Der volle Inhalt der QuelleRawanduzy, Cameron A., Alexander Winkler-Schwartz und William T. Couldwell. „Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities“. International Journal of Molecular Sciences 24, Nr. 6 (21.03.2023): 5917. http://dx.doi.org/10.3390/ijms24065917.
Der volle Inhalt der QuelleEngin, Muhammet Mesut Nezir, und Öner Özdemir. „Current mechanisms in the pathogenesis of lung fibrosis“. Trends in Immunotherapy 7, Nr. 1 (17.07.2023): 2028. http://dx.doi.org/10.24294/ti.v7.i1.2028.
Der volle Inhalt der QuelleDissertationen zum Thema "Autoimmune and idiopathic organic disease"
Malichin, Aikaterini. „Jouissance, écriture et nombre dans les maladies auto-immune et idiopathique : l'assomption de la métaphore subjective par l'organisme“. Sorbonne Paris Cité, 2015. http://www.theses.fr/2015USPCC317.
Der volle Inhalt der QuelleThe present clinical and bibliographical research is articulated on three points and constitutes the tripartite undertaking of this doctoral thesis. The first relates to the study closely the Freudian theory and the Lacanian teaching and the concept of phenomenon psychosomatic, in order to approach the auto-immune and idiopathic organic disease, the Multiple Sclerosis and the disease of Crohn, on two suffering subjects within an analytical cure. The second relates to the investigation of the objects of construction in their discourses and their caused positions, and the third the investigation of knowing if exists pause of symptom and failure of signifying induction, i. E. Failure of the subjective metaphor, as to know if the disease of the suffering subjects fills the criteria of the phenomenon psychosomatic and if is held assumption of subjective metaphor by the organism. The qualitative analysis of the enunciate and the enunciation of the subjects through the sessions is carried out with an analysis of discourses structural criticism and an analysis of their speech during one period of cure exceeding the four years, by making a comparison with former research. We conclude that the disease fills the criteria of the phenomenon psychosomatic and that the assumption of the subjective metaphor it is held by the organism, thus confirming our hypothesis. We also arrive at conclusions which are mainly in agreement with preliminary research. Finally, we note the improvement of the health of the subjects and the stabilization or the disappearance of the repetitions during their analysis, in parallel with their medical care, which that had not been observed before, and the appropriation of the points of the pain and the suffering of their history so that it does not lead to the way of pathological pulsing’s acts and the discharge by the organism
Liley, Albert James. „Statistical co-analysis of high-dimensional association studies“. Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/270628.
Der volle Inhalt der QuelleAlves, André Oliveira. „Polimiosite - Fisiopatologia e Terapêutica“. Master's thesis, 2018. http://hdl.handle.net/10316/84581.
Der volle Inhalt der QuelleA Polimiosite é uma doença que se inclui no grupo das Miopatias Inflamatórias Idiopáticase cuja etiologia continua desconhecida até ao momento. Contudo, a presença de anticorpose linfócitos T nos músculos, acompanhada por respostas positivas à terapêutica imunológica,constituem evidência de que podemos estar perante uma doença autoimune.As vias imunitárias e não imunitárias são a base do estudo da Polimiosite, sendo que aevolução destes conceitos foi crucial para uma melhor compreensão e distinção entre asdiferentes Miopatias Inflamatórias Idiopáticas.Apesar de nem sempre ser detetada morte ou degeneração celular, a nível muscular, éeste o processo que está na origem da fraqueza e diminuição do desempenho muscularcaraterísticas desta doença, sendo por isso, o primeiro alvo de estudo em caso de suspeita amesma.Ao longo dos anos foram vários os avanços ao nível do diagnóstico e terapêutica, de talforma que, ao exame físico inicial, indicativo da progressão da fraqueza muscular, foramacrescentados outros critérios de diagnóstico, tais como os níveis séricos das enzimasmusculares, características da distrofia muscular, presença de anticorpos específicos da mioseno soro e, por fim, a biópsia muscular, peça fundamental na distinção entre a Polimiosite e asrestantes Miopatias Inflamatórias Idiopáticas.A base do tratamento da Polimiosite continua a ser o reforço e eliminação da inflamaçãomuscular, em que o tratamento de primeira linha são os corticosteroides. No entanto, novasalternativas terapêuticas têm surgido, tais como a utilização de agentes imunossupressores e,mais recentemente, a bioterapia.A presente monografia consiste, assim, numa revisão da literatura sobre os estudos eavanços alcançados ao nível da fisiopatologia e terapêutica da Polimiosite, doença muito poucoconhecida atualmente.
Polymyositis is a disease included in the group of the Idiopathic Inflammatory Myopathiesand whose etiology remains unknown, so far. However, the presence of antibodies and Tlymphocytes in the muscles, accompanied by positive responses to the immunological therapy,evidence that this might be an autoimmune disease.The immune and non-immune pathways are the basis of the study of Polymyositis, beingthat the evolution of these concepts was crucial for a better understanding and distinctionbetween the different Idiopathic Inflammatory Myopathies.Although death or cell degeneration are not always detected at the muscular level, theyconstitute the source of weakness and decrease of muscular performance, characteristics ofthis disease, being therefore the first target of study in case of suspicion.Over the years there have been several advances in diagnosis and therapy, in such a waythat the initial physical examination, indicative of the progression of muscle weakness, is nowcomplemented by other diagnostic criteria, such as serum levels of muscle enzymes, musculardystrophy, the presence of myositis specific antibodies in the serum and, finally, muscle biopsy,a key element in the distinction between Polymyositis and the remaining IdiopathicInflammatory Myopathies.The basis for Polymyositis treatment continues to be the strengthening and eliminationof muscle inflammation, where the first treatment line are the corticosteroids. However, newtherapeutic alternatives have emerged, such as the use of immunosuppressive agents and,more recently, biotherapy.The present monography consists in a review of the literature on the studies and advancesachieved in the pathophysiology and therapeutics of Polymyositis, a disease that remains littleknown nowadays.
Bücher zum Thema "Autoimmune and idiopathic organic disease"
Bending, David, Kiran Nistala und Lucy R. Wedderburn. Pathogenesis of juvenile idiopathic arthritis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0060.
Der volle Inhalt der QuelleGraham, Andrew. Neurological dementias. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199644957.003.0037.
Der volle Inhalt der QuelleParkes, Joanna E., Simon Rothwell und Janine A. Lamb. Aetiology and pathogenesis. Herausgegeben von Hector Chinoy und Robert Cooper. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198754121.003.0003.
Der volle Inhalt der QuelleSteensma, David P. Benign Hematology. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0294.
Der volle Inhalt der QuelleForsyth, Rob, und Richard Newton. Specific conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198784449.003.0004.
Der volle Inhalt der QuelleLimaye, Vidya Sadanand. Overview and epidemiology. Herausgegeben von Hector Chinoy und Robert Cooper. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198754121.003.0001.
Der volle Inhalt der QuelleClunie, Gavin P. R., Nick Wilkinson, Elena Nikiphorou und Deepak Jadon, Hrsg. Oxford Handbook of Rheumatology. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198728252.001.0001.
Der volle Inhalt der QuelleChinoy, Hector, und Robert G. Cooper. Polymyositis and dermatomyositis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0124.
Der volle Inhalt der QuelleBuchteile zum Thema "Autoimmune and idiopathic organic disease"
Gartler, Stanley M., R. Scott Hansen, Vinzenz Oji, Heiko Traupe, Julia Horn, Bodo Grimbacher, Srijita Sen-Chowdhry et al. „Idiopathic Autoimmune Hamolytic“. In Encyclopedia of Molecular Mechanisms of Disease, 1023. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7096.
Der volle Inhalt der QuelleFroehlich, Stephan J., Carlo A. Lackerbauer, Guenter Rudolph, Jan Rémi, Soheyl Noachtar, Werner J. Heppt, Annette Cryer et al. „Neuromyotonia, Autoimmune and Idiopathic“. In Encyclopedia of Molecular Mechanisms of Disease, 1458–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1276.
Der volle Inhalt der QuellePretis, Nicolo’ de, Yan Bi, Saurabh Mukewar und Suresh Chari. „Steroid-Responsive Chronic Pancreatitides: Autoimmune Pancreatitis and Idiopathic Duct-Centric Chronic Pancreatitis“. In Pancreas and Biliary Disease, 83–101. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28089-9_5.
Der volle Inhalt der QuelleBrodehl, Johannes, und P. F. Hoyer. „Ciclosporin Treatment of Idiopathic Nephrotic Syndrome in Children (Minimal Change Disease and Focal Segmental Glomerulosclerosis)“. In Ciclosporin in Autoimmune Diseases, 329–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70607-3_64.
Der volle Inhalt der QuelleCorbridge, Rogan, und Nicholas Steventon. „The inner ear“. In Oxford Handbook of ENT and Head and Neck Surgery, 109–48. Oxford University Press, 2009. http://dx.doi.org/10.1093/med/9780199550791.003.07.
Der volle Inhalt der QuelleLundberg, Ingrid E., Hector Chinoy und Robert Cooper. „Inflammatory myopathies“. In Oxford Textbook of Medicine, herausgegeben von Richard A. Watts, 4537–46. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0457.
Der volle Inhalt der QuelleGelbman, Brian, und Ronald G. Crystal. „Idiopathic and Autoimmune Interstitial Lung Disease“. In The Autoimmune Diseases, 1335–54. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-812102-3.00067-1.
Der volle Inhalt der QuelleGelbman, Brian, und Ronald G. Crystal. „Idiopathic and Autoimmune Interstitial Lung Disease“. In The Autoimmune Diseases, 1105–23. Elsevier, 2014. http://dx.doi.org/10.1016/b978-0-12-384929-8.00074-5.
Der volle Inhalt der QuelleSpickett, Gavin P. „Autoimmune eye disease“. In Oxford Handbook of Clinical Immunology and Allergy, 251–56. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199603244.003.0011.
Der volle Inhalt der QuelleOyama, Yu, Walter G. Barr und Richard K. Burt. „Autologous Hematopoietic Stem Cell Transplantation for Idiopathic Inflammatory Myositis“. In Stem Cell Therapy for Autoimmune Disease, 437–41. CRC Press, 2019. http://dx.doi.org/10.1201/9780367813895-52.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Autoimmune and idiopathic organic disease"
Romagnoli, Micaela, Carlotta Nannini, Sara Piciucchi, Francesco Girelli, Carlo Gurioli, Gianluca Casoni, Sara Tomassetti et al. „Idiopathic Nonspecific Interstitial Pneumonia (NSIP): Early Lung Manifestation Of An Autoimmune Disease?“ In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6002.
Der volle Inhalt der QuelleHayton, Conal, Dayle Terrington, Waqar Ahmed, Iain White, Max Wilkinson, Kirti Vekaria, Nazia Chaudhuri, Andrew Wilson, Colm Leonard und Stephen Fowler. „Exhaled volatile organic compounds in idiopathic pulmonary fibrosis and disease progression“. In ERS International Congress 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/13993003.congress-2020.727.
Der volle Inhalt der QuelleRemuzgo-Martínez, S., B. Atienza-Mateo, V. Pulito-Cueto, F. Genre, V. M. Mora-Cuesta, D. Iturbe-Fernández, V. Portilla et al. „Endothelin-1 for the differential diagnosis between interstitial lung disease associated with autoimmune diseases and idiopathic pulmonary fibrosis“. In ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.2310.
Der volle Inhalt der QuelleVergara, Karen, Silvana Saavedra, Felipe Reyes, Annelise Goecke, Caterina Chesta und Sebastian Chavez. „AB1109 CHARACTERIZATION OF PATIENTS WITH INTERSTITIAL PNEUMONIA WITH AUTOIMMUNE FEATURES (IPAF) AND ITS COMPARISON WITH PATIENTS WITH SCLERODERMA-RELATED INTERSTITIAL LUNG DISEASE AND WITH IDIOPATHIC FIBROSIS“. In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.7794.
Der volle Inhalt der QuelleMoraes, Marianna, Fabiano Abrantes, José Luiz Pedroso und Orlando Graziani Povoas Barsottini. „Etiological evaluation of hypertrophic pachymeningitis in a tertiary general neurology department“. In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.665.
Der volle Inhalt der QuelleSantos, João Vitor Ribeiro dos, Mariana Spitz und Ana Carolina Andorinho. „Stroke secondary to thrombotic microangiopathy“. In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.300.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Autoimmune and idiopathic organic disease"
Zhang, Yingrong, Sanchun Tan, Jieyu Wang, Yanji Zhang, Mengyuan Huang, Hongjie Xia, Yaxin Hu, Yinyue Rao und Zhongyu Zhou. A scoping review protocol of systematic reviews and meta-analyses to acupuncture for the treatment of peripheral facial paralysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, März 2022. http://dx.doi.org/10.37766/inplasy2022.3.0084.
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