Academic literature on the topic 'Eosinophilic granuloma'

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Journal articles on the topic "Eosinophilic granuloma"

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Baş, Burcu, Hatice Duran, Özgün Şenyurt, and Ömer Günhan. "Eosinophilic Granuloma." Journal of Craniofacial Surgery 22, no. 6 (November 2011): 2409–12. http://dx.doi.org/10.1097/scs.0b013e318231febe.

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Plasschaert, F., C. Craig, R. Bell, W. G. Cole, J. S. Wunder, and B. A. Alman. "Eosinophilic granuloma." Journal of Bone and Joint Surgery. British volume 84-B, no. 6 (August 2002): 870–72. http://dx.doi.org/10.1302/0301-620x.84b6.0840870.

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Jordan, David R. "Eosinophilic Granuloma." Archives of Ophthalmology 111, no. 1 (January 1, 1993): 134. http://dx.doi.org/10.1001/archopht.1993.01090010138040.

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Hashimoto, Ken. "Eosinophilic Granuloma." Archives of Dermatology 121, no. 6 (June 1, 1985): 770. http://dx.doi.org/10.1001/archderm.1985.01660060084027.

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Duncan, William K., A. Charles Post, and Bruce P. McCoy. "Eosinophilic granuloma." Oral Surgery, Oral Medicine, Oral Pathology 65, no. 6 (June 1988): 736–41. http://dx.doi.org/10.1016/0030-4220(88)90020-5.

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VanderWilde, Russell S., Lester E. Wold, Richard A. McLeod, and Franklin H. Sim. "EOSINOPHILIC GRANULOMA." Orthopedics 13, no. 11 (November 1990): 1301–3. http://dx.doi.org/10.3928/0147-7447-19901101-20.

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Milosevic, Rajko, Danijela Lekovic, Nebojsa Antonijevic, and Andrija Bogdanovic. "Eosinophilia as a first sign of Hodgkin´s lymphoma: A case report." Vojnosanitetski pregled 74, no. 6 (2017): 581–84. http://dx.doi.org/10.2298/vsp150604245m.

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Introduction. It is well known that eosinophilia appears in a malignant disease. Frequency of all Hodgkin`s lymphoma patients is estimated to about 15%. Prognostic importance of this phenomenon is not completely investigated. Therefore we decided to present a female patient with eosinophilia, six months before lymphoma appearance. Case report. We presented a 51- years old female, from Serbia, who had eosinophilia (1,530?2,040 eosinophils per ?L of blood), six months before Hodgkin's lymphoma appearance. Eosinophilic granuloma was confirmed by tumor?s biopsy and histopathologic examination, from the right femoral region. As eosinophilia was increasing, lymph nodes became enlarged (120 ? 65 mm diameter), in the right parailiac region. All infectious and allergic examinations did not reveal eosinophilia's cause. Histopathologic revision was made with added immunohistochemical stains 17 months after tumor's biopsy. The diagnosis was changed from eosinophilic granuloma to mixed cellularity Hodgkin's lymphoma. After conducted Ann Arbor staging classification, II B clinical stage was established. The treatment was done by chemotherapy according to adriamycin, bleomycin, vinblastine, dacarbarine (ABVD) protocol, with 6 courses. Complete remission of the disease was achieved after 4 courses. Eosinophils number dropped to 640 per ?l blood. Conclusion. Eosinophilia without revealed cause can precede Hodgkin's lymphoma. We suggest careful search for enlarged lymph nodes, anywhere in the patients? body who suffer from eosinophilia. Timely and accurate histopathologic diagnostic is a right way to resolve such conditions.
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Penar, Paul L., Jung H. Kim, and Douglas Chyatte. "Solitary Eosinophilic Granuloma of the Frontal Lobe." Neurosurgery 21, no. 4 (October 1, 1987): 566–68. http://dx.doi.org/10.1227/00006123-198710000-00024.

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Abstract Solitary intracranial eosinophilic granulomas are rare and most frequently involve the hypothalamus. We report an unusual case of solitary eosinophilic granuloma of the frontal lobe in a patient without evidence of systemic disease. Previously reported cases of solitary intracranial nonhypothalamic lesions are reviewed, and the clinical, radiographic, and histological features of this case are discussed.
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Gervais, D. A., G. J. Whitman, and F. S. Chew. "Pulmonary eosinophilic granuloma." American Journal of Roentgenology 161, no. 6 (December 1993): 1158. http://dx.doi.org/10.2214/ajr.161.6.8249718.

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CAÑADELL, J., C. VILLAS, J. MARTÍNEZ-DENEGRI, J. AZCARATE, and A. IMIZCOZ. "Vertebral Eosinophilic Granuloma." Spine 11, no. 7 (September 1986): 767–69. http://dx.doi.org/10.1097/00007632-198609000-00023.

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Dissertations / Theses on the topic "Eosinophilic granuloma"

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Fondati, Alessandra. "Pathogenetic studies on feline eosinophilic granuloma complex." Doctoral thesis, Universitat Autònoma de Barcelona, 2003. http://hdl.handle.net/10803/3658.

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En el gat, encara que amb freqüència es parla dels desordres associats a eosinòfils, inclòs el EGC, són poc coneguts i en general s'associen a causes immuno-mediades o parasitàries, anàlegs als seus equivalents humans. Tot i així, el contingut i les funcions dels eosinòfils dels gats, encara que es consideren similars als eosinòfils humans, no es coneixen. Per tot això, els objectius d'aquesta tesi varen ser estudiar el EGC felí i obtenir informació específica de la biologia dels eosinòfils del gat.
En aquesta tesi, es varen estudiar els signes histopatològics de les diferents lesions clíniques del EGC amb seccions de H & E i tinció tricròmica. A H & E, totes les lesiones del EGC examinades es varen caracteritzar per un infiltrat dèrmic eosinofílic, de intensitat variable, i per la presència de petits a grans focus de material eosinofìlic que amb la tinció tricròmica, semblaren estar constituïts per fibres de col·lagen normals rodejades per restes de material amb el mateix aspecte tintorial dels grànuls dels eosinòfils. Aquests resultats indiquen que les lesiones del EGC amb diferent aspecte clínic histopatològicament són indistingibles i que els focus dèrmics de material eosinofílic, petits i grans, tenen una histogènesi similar. A més, les figures amb flama, utilitzades per definir petits focus de material eosinofílic amb analogia amb les figures amb flama de la síndrome de Wells, es poden utilitzar també per parlar de dipòsits de material eosinofílic de gran tamany.
A més, es va investigar la ultraestructura de les figures en flama, petites i grans, de les lesions del EGC. Estan formades per fibrilles de col·lagen morfològicament inalterades, fibres de col·lagen parcialment separades per edema i restes cel·lulars i eosinòfils desgranulats via ECL i PMD. La ultraestructura de les figures en flama al EGC va ser similar al que es descriu a les figures en flama de la síndrome de Wells humana. Això suggereix que en el gat els eosinòfils juguen un paper primari en la formació de les figures en flama, anàlogues a les descrites als humans. A més, aquest estudi demostra que al EGC felí, en els teixits, els eosinòfils alliberen el contingut dels seus grànuls per ECL i PMD, igual que els eosinòfils tisulars humans en inflamacions mediades per eosinòfils. El mecanisme de desgranulació predominant va ser ECL.
Es va realitzar un estudi ultraestructural de eosinòfils circulants de gats amb diferents recomptes de eosinòfils i diferents malalties asociades a eosinofília. Als eosinòfils perifèrics es va observar morfologia de PMD, indicativa d'activació i desgranulació. No es va observar correlació directa entre en numero de eosinòfils que presentaven canvis de PMD i el nivell de eosinofília sanguínia. Aquesta última observació suggereix que el recompte del número total de eosinofils circulants no representa el millor criteri per avaluar la participació dels eosinòfils en una malaltia eosinofílica.
Finalment, es va realitzar un estudi sobre les proteïnes dels grànuls dels eosinòfils del gat. Es varen estudiar les proteïnes dels grànuls extretes de eosinòfils obtinguts per inducció experimental de eosinofilia peritoneal. Les proteïnes es varen analitzar per cromatografia de gel-filtració i es varen estudiar les seves activitats biològiques. Les proteïnes dels grànuls dels eosinòfils del gat tenen activitats peroxidasa, RNasa i bactericida. La EAR felina presenta una homologia de la seqüència N-terminal amb les proteïnes de la superfamília de la RNasa A, incloses les RNases de eosinòfils i la seqüència N-terminal de la MBP felina va ser homòloga a la de la MBP-1 humana i murina. Aquest resultats indiquen que les proteïnes dels grànuls del eosinòfil felí tenen un paper biològic similar als descrits als humans i a altres espècies animals i evidencien que el gat pot ser una espècie adequada per l'estudi de les malalties eosinofíliques humanes.
Despite being commonly reported, feline eosinophil-associated disorders, including EGC, are poorly understood and generally associated to immune-mediated or parasitic causes, analogous to their human counterparts. Nevertheless, cat eosinophil functions and contents, although considered similar to those of human eosinophils, are currently unknown. Hence, the objectives of this thesis were to study feline EGC and to obtain specific information on the cat eosinophil biology.
In this thesis, the histopathological features of clinically different EGC lesions were studied on H & E and trichrome stained sections. With H & E stain, all the EGC lesions examined were characterised by a dermal eosinophilic infiltration of variable intensity and the presence of small- to large-sized foci of eosinophilic debris that, with trichrome stain, appeared to consist of normally stained collagen fibres surrounded by a debris showing the same tinctorial properties as eosinophil granules. These results showed that EGC lesions with different clinical appearance are histopathologically indistinguishable and that small- and large-sized dermal foci of eosinophilic debris have similar histogenesis. Hence, the term flame figures, normally used to define small foci of eosinophilic debris by analogy with flame figures in Wells' syndrome, may be employed also to designate large-sized focal depositions of this debris.
Furthermore, the ultrastructure of small- and large-sized flame figures in EGC lesions was investigated. They comprised morphologically unaltered collagen fibrils, collagen fibres partly disrupted by oedema and cellular debris, and degranulating eosinophils via ECL and PMD. The ultrastructure of flame figures in EGC was similar to that reported in flame figures of human Wells' syndrome. This suggested that eosinophils play a primary role in flame figures formation in cats, analogous to what reported in humans. In addition, this study demonstrated that tissue eosinophils in feline EGC release their granule contents by ECL and PMD, analogous to human tissue eosinophils at sites of eosinophil-mediated inflammation. ECL was the predominant mode of degranulation.
An ultrastructural study of feline circulating eosinophils from cats with various blood eosinophil counts and different eosinophil-associated diseases was also performed. PMD morphology, indicative of eosinophil activation and degranulation, was recognised in peripheral eosinophils. No direct correlation was found between the number of eosinophils showing PMD changes and the level of blood eosinophilia. This latter finding suggested that total blood eosinophil count might not represent the best criterion to evaluate the contribution of eosinophils to the ongoing eosinophil-associated disease.
Finally, a study on cat eosinophil granule proteins was conducted. Granule proteins, extracted from cat eosinophils obtained by experimentally induced peritoneal eosinophilia, were analysed by gel-filtration chromatography and their biological activities were studied. Cat eosinophil granule proteins possessed peroxidase, RNase and bactericidal activities. Feline EAR showed N-terminal sequence homology with proteins of the RNase A superfamily, including eosinophil RNases, and the N-terminal sequence of feline MBP was homologue to that of human and murine MBP-1. These findings indicated that feline eosinophil granule proteins have biological roles similar to those reported in humans and other animal species and highlighted that the cat might represent a suitable species for studying human eosinophil-mediated diseases.
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Al-Khabuli, Jumaʾ. "Role of eosinophil in oral squamous cell carcinoma and traumatic ulcerative granuloma with stromal eosinophilia." Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418167.

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GRISONI, FRANCE PATRICIA. "Le granulome eosinophile facial de type lever : revue de la litterature a propos de quatre cas." Nice, 1990. http://www.theses.fr/1990NICE6015.

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LE, MOAL NOEL. "Granulome eosinophile de la selle turcique : a propos d'un cas." Amiens, 1988. http://www.theses.fr/1988AMIEM128.

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MICHAUD, BEAUPERE MARIE-JOSE. "Signification d'un granulome eosinophile arteriel temporal dans la maladie de horton." Nantes, 1988. http://www.theses.fr/1988NANT022M.

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PAVEC, ERIC. "Les localisations rachidiennes du granulome eosinophile chez l'enfant et l'adolescent : a propos de 7 observations et d'une revue de la litterature." Reims, 1991. http://www.theses.fr/1991REIMM028.

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Amaral, Kátia Batista do. "Estudo comparativo da esquistossomose mansônica no reservatório silvestre Nectomys squamipes naturalmente infectado e no modelo experimental camundongo Swiss: análises histopatológicas, bioquímicas e ultraestruturais." Universidade Federal de Juiz de Fora (UFJF), 2015. https://repositorio.ufjf.br/jspui/handle/ufjf/2561.

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O roedor Nectomys squamipes, também conhecido como rato d’água, é considerado o mais importante reservatório silvestre do parasito Schistosoma mansoni no Brasil, contribuindo para a epidemiologia da esquistossomose mansônica humana. Além disso, quando infectado, não apresenta sinais clínicos da doença, apresentando lesões teciduais extremamente brandas decorrentes da infecção. Parâmetros relacionados à infecção esquistossomótica em modelos murinos de infecção experimental já foram bem documentados; porém, em modelos de infecção natural, ainda são pouco conhecidos. A relação parasito-hospedeiro neste modelo de infecção natural é de grande relevância e motivou o desenvolvimento deste trabalho. Foi realizado estudo comparativo da esquistossomose mansônica em N. squamipes naturalmente infectado pelo parasito S. mansoni e no camundongo Swiss experimentalmente infectado, nas fases aguda e crônica da infecção, através de análises histopatológicas, bioquímicas e ultraestruturais, objetivando obter uma melhor compreensão de como o rato d’água lida com o parasitismo pelo S. mansoni. Foram realizadas análises de frequências e tipos de granulomas, suas áreas médias e do comprometimento tecidual dos órgãos alvos da infecção (fígado e intestinos), nos dois modelos experimentais. A participação dos eosinófilos durante a resposta inflamatória granulomatosa também foi avaliada, visto que estas células estão presentes em grandes números nos granulomas. Dosagens bioquímicas das transaminases hepáticas auxiliaram na avaliação do dano hepatocelular. Além disso, a influência da esteatose hepática neste modelo de infecção natural foi estudada, visto que seus efeitos não são conhecidos em animais silvestres. Assim, dosagens séricas de glicose, colesterol total e triglicerídeos foram importantes para avaliar o perfil glicêmico e lipídico dos animais estudados. Os tecidos hepáticos dos animais foram submetidos à espectroscopia Raman, para avaliar o grau de insaturação presente. Finalmente, análises ultraestruturais ajudaram a aprofundar o conhecimento sobre os papéis dos eosinófilos e dos corpúsculos lipídicos presentes nos hepatócitos nestes dois modelos de esquistossomose mansônica. Os resultados revelaram que N. squamipes apresentou excelente modulação das lesões teciduais no fígado, com baixo comprometimento tecidual neste órgão e uma reação granulomatosa mais exacerbada no intestino delgado, favorável à eliminação dos ovos do parasito nas fezes. Além disso, os níveis séricos das transaminases não se alteraram em decorrência da infecção neste roedor silvestre, ao contrário do que ocorreu no camundongo Swiss. N. squamipes infectados e não infectados apresentaram os maiores graus de insaturação presentes nos tecidos hepáticos. Características ultraestruturais intrigantes dos eosinófilos de N. squamipes foram observadas por MET. Através dos dados obtidos, concluímos que o rato d’água apresenta uma relação ecológica bem estabelecida com o parasito S. mansoni, sendo que esta adaptação ao parasitismo pode estar relacionada ao metabolismo lipídico deste reservatório silvestre.
The rodent Nectomys squamipes, also known as water rat, is considered the most important wild reservoir of the parasite Schistosoma mansoni in Brazil, contributing to the epidemiology of human schistosomiasis. Furthermore, when infected, it shows no clinical signs of the disease with extremely soft tissue injuries resulting from infection. Parameters related to the infection in murine models of experimental infection have been well documented; however, in natural infection models, they are still largely unknown. The host-parasite relationship in this model of natural infection is highly relevant and motivated the development of this work. So, It was conducted a comparative study of schistosomiasis in N. squamipes naturally infected by the parasite Schistosoma mansoni and in Swiss experimentally infected mice, at the acute and chronic phases of the infection through histological, biochemical and ultrastructural analysis, aiming to gain a better understanding of how the water rat handles with parasitism by S. mansoni. Analysis of frequencies and types of granulomas were held, their average areas and tissue impairment of the target organs of infection (liver and intestines) in both experimental models. The involvement of eosinophils during granulomatous inflammatory response was also evaluated, as these cells are present in large numbers in the granulomas. Biochemical testing of liver transaminases contributed to the evaluation of hepatocellular damage. Furthermore, the influence of hepatic steatosis in the natural infection model was studied, since their effects are not known in wild animals. Thus, serum levels of glucose, total cholesterol and triglycerides were important to assess the glycemic and lipid profile of the animals studied. The liver tissues of animals were subjected to Raman spectroscopy, to assess the degree of unsaturation. Finally, ultrastructural analysis helped to deepen understanding of the roles of eosinophils and lipid bodies present in hepatocytes in these two models of schistosomiasis. The results revealed that N. squamipes showed excellent modulation of tissue lesions in the liver, with low tissue impairment and a more exacerbated granulomatous reaction in the small intestine, favoring the elimination of the parasite eggs in feces. Furthermore, serum transaminases levels did not change as a result of the infection in wild rodents, unlike what occurred in Swiss mice. N. squamipes infected and uninfected showed the highest degree of unsaturation present in liver tissue. Intriguing ultrastructural characteristics of N. squamipes eosinophils were observed by TEM. Through the data obtained, we concluded that the water rat has a wellestablished ecological relationship with the parasite Schistosoma mansoni, and this adaptation to parasitism may be related to lipid metabolism of this wild reservoir.
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Arndt, Kirsten [Verfasser]. "Immunhistochemisch morphologische Untersuchung eosinophiler nekrotischer Granulome in Darm und Leber bei akuter Schistosomiasis (Katayama Krankheit) : zur Bedeutung der Nekrose eosinophiler Granulozyten in vivo / vorgelegt von Kirsten Arndt." 2004. http://d-nb.info/970905289/34.

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Books on the topic "Eosinophilic granuloma"

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Lindberg, Ronny. On granulomatous enteritis and eosinophilic granulomatosis in the horse. Uppsala: Sveriges Lantbruksuniveristet, 1985.

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Crawshaw, Anjali. Sarcoidosis and other granulomatous lung disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0138.

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Sarcoidosis is a multisystem disorder characterized by the formation of non-caseating granulomas in many tissues. A granuloma is an organized aggregate of immune cells; it forms in response to an antigenic stimulus. It contains abnormal macrophages (epithelioid histiocytes, which often fuse to form multinucleated giant cells), lymphocytes, neutrophils, eosinophils, fibroblasts, and collagen.
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Barsoum, Rashad S. Schistosomiasis. Edited by Neil Sheerin. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0181_update_001.

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AbstractSchistosomes are blood flukes that parasitize humans, apes, cattle, and other animals. In these definitive hosts they are bisexual, and lay eggs which are shed to fresh water where they complete an asexual cycle in different snails, ending in the release of cercariae which infect the definitive hosts to complete the life cycle.Seven of over 100 species of schistosomes are human pathogens, causing disease in different organs depending on the parasite species. Racial and genetic factors are involved in susceptibility, severity, and sequelae of infection.Morbidity is induced by the host’s immune response to schistosomal antigens. The latter include tegument, microsomal, gut, and oval antigens. The former are important in the process of invasion and establishment of infection, oval antigens in formation of granulomata which lead to fibrosis in different sites, and the gut antigens constitute the main circulating antigens in established infection, leading to immune-complex disease, particularly in the kidneys. The host immunological response includes innate and adaptive mechanisms, the former being the front line responsible for removing 90% of the infecting cercarial load. Adaptive immunity includes a Th1 phase, dominated by activation of an acute inflammatory response, followed by a prolonged Th2 phase which is responsible for immunity to re-infection as well as progression of tissue injury. Switching from Th1 to Th2 phases is controlled by functional and morphological change in the antigen-presenting cells, which is achieved by molecules of host as well as parasitic origin.Many cells participate in parasite killing, but also in the induction of tissue injury. The most potent of these is the eosinophil, which by binding antibodies to the parasite, particularly immunoglobulin E, facilitates parasite elimination. However, this process is complex, including agonist as well as antagonist pathways, which provide escape mechanisms for the parasite to survive, thereby achieving a delicate balance that permits schistosomes to live for decades in the infected host.
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Book chapters on the topic "Eosinophilic granuloma"

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Prein, Joachim, Wolfgang Remagen, Bernd Spiessl, and Erwin Uehlinger. "Eosinophilic Granuloma." In Atlas of Tumors of the Facial Skeleton, 114–18. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70949-4_27.

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Timson, David J., Richard J. Reece, James B. Thoden, Hazel M. Holden, Andrea L. Utz, Beverly M. K. Biller, Eugen-Matthias Strehle, et al. "Granuloma, Eosinophilic." In Encyclopedia of Molecular Mechanisms of Disease, 748–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_564.

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Inai, Kei, Alexander K. C. Leung, Jouni Uitto, Gerhard-Paul Diller, Michael A. Gatzoulis, John-John B. Schnog, Victor E. A. Gerdes, et al. "Eosinophilic Granuloma." In Encyclopedia of Molecular Mechanisms of Disease, 585. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_9156.

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De Schepper, A. M. A., and H. R. M. Degryse. "Eosinophilic Granuloma." In Magnetic Resonance Imaging of Bone and Soft Tissue Tumors and Their Mimics, 58–59. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0997-7_11.

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Henderson, William R., and Emil Y. Chi. "Eosinophilic Granuloma." In Local Invasion and Spread of Cancer, 172–77. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1093-5_14.

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Cheng, Xiaoguang, Yongbin Su, and Mingqian Huang. "Eosinophilic Granuloma: Case 18." In Bone Tumor Imaging, 91–94. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9927-5_18.

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Cheng, Xiaoguang, Yongbin Su, and Mingqian Huang. "Eosinophilic Granuloma: Case 19." In Bone Tumor Imaging, 95–99. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9927-5_19.

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Inai, Kei, Alexander K. C. Leung, Jouni Uitto, Gerhard-Paul Diller, Michael A. Gatzoulis, John-John B. Schnog, Victor E. A. Gerdes, et al. "Eosinophilic Granuloma (Single-Organ Involvement)." In Encyclopedia of Molecular Mechanisms of Disease, 585. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_6024.

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Wallace, S., C. H. Carrasco, C. Charnsangavej, and M. Cohen. "Eosinophilic granuloma of bone: direct steroid injection." In Interventional Radiology in Bone and Joint, 244–49. Vienna: Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-8948-1_18.

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Colombo, Silvia, and Alessandra Fondati. "Plaques, Nodules and Eosinophilic Granuloma Complex Lesions." In Feline Dermatology, 123–36. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-29836-4_6.

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Conference papers on the topic "Eosinophilic granuloma"

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Czyz, Marcin. "Diagnosis and Management of Eosinophilic Granuloma of the Spine." In eccElearning Postgraduate Diploma in Spine Surgery. eccElearning, 2017. http://dx.doi.org/10.28962/01.3.127.

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Kooragayalu, Shravan, Purvi Parikh, Golda Hudes, and David L. Rosenstreich. "All That Glitters Is Not Gold: Hypersensitivity Pneumonitis (HP) Presenting As Eosinophilic Non-Necrotizing Granuloma Masquerading As Sarcoidosis In An African American Female." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3216.

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Larkin, Allyson S., Samuel A. Yousem, and Sally E. Wenzel. "Small Airway Obstruction, Eosinophilia And Airway Granulomas: A New Phenotype Of Severe Asthma?" In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3723.

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