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1.

001-es BibID:BIBFORM007053
Első szerző:Bodolay Edit (belgyógyász, allergológus és klinikai immunológus)
Cím:Angiogenesis and chemokines in rheumatoid arthritis and other systemic inflammatory rheumatic diseases / Bodolay, E., Koch, A. E., Kim, J., Szegedi, G., Szekanecz, Z.
Dátum:2002
ISSN:1582-1838 (Print)
Megjegyzések:Angiogenesis, the formation of new vessels, is important in the pathogenesis of rheumatoid arthritis (RA) and other inflammatory diseases. Chemotactic cytokines termed chemokines mediate the ingress of leukocytes, including neutrophils and monocytes into the inflamed synovium. In this review, authors discuss the role of the most important angiogenic factors and angiogenesis inhibitors, as well as relevant chemokines and chemokine receptors involved in chronic inflammatory rheumatic diseases. RA was chosen as a prototype to discuss these issues, as the majority of studies on the role of angiogenesis and chemokines in inflammatory diseases were carried out in arthritis. However, other systemic inflammatory (autoimmune) diseases including systemic lupus erythematosus (SLE), systemic sclerosis (SSc), Sjogren's syndrome (SS), mixed connective tissue disease (MCTD), polymyositis/dermatomyositis (PM/DM) and systemic vasculites are also discussed in this context. As a number of chemokines may also play a role in neovascularization, this issue is also described here. Apart from discussing the pathogenic role of angiogenesis and chemokines, authors also review the regulation of angiogenesis and chemokine production by other inflammatory mediators, as well as the important relevance of neovascularization and chemokines for antirheumatic intervention.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Angiogenesis Inhibitors
Arthritis, Rheumatoid
Autoimmune Diseases
Chemokines
Growth Substances
Humans
Neovascularization, Pathologic
Receptors, Chemokine
Megjelenés:Journal of Cellular and Molecular Medicine. - 6 : 3 (2002), p. 357-376. -
További szerzők:Koch, Alisa E. Kim, Joon Szegedi Gyula (1936-2013) (belgyógyász, immunológus) Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus)
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2.

001-es BibID:BIBFORM046367
Első szerző:Halloran, Margaret M.
Cím:Cellular adhesion molecules in rat adjuvant arthritis / Halloran M. M., Szekanecz Z., Barquin N., Haines G. K., Koch A. E.
Dátum:1996
ISSN:0004-3591
Megjegyzések:To examine adhesion molecule expression during the progression of inflammation in a rheumatoid arthritis model of adjuvant-induced arthritis (AIA) in rats. METHODS: Immunohistochemical analysis was used to determine the distribution of the following adhesion molecules: lymphocyte function-associated antigen 1 (LFA-1; CD11a/CD18), Mac-1 and p150/95 (CD11bc/CD18), intercellular adhesion molecule 1 (ICAM-1), and CD44 in tissue sections from the ankle joints of rats with AIA. Control animals and those with AIA were killed at intervals over a 54-day period after injection with mineral oil and Mycobacterium butyricum, respectively. RESULTS: CD44 and LFA-1 were expressed on lymphocytes, macrophages, and synovial (ST) lining cells. CD44 expression on macrophages was found to be increased compared with control animals by day 18, and was significantly increased by day 41. CD44 expression on lymphocytes significantly increased earlier, on days 11-18. Increased LFA-1 expression on macrophages occurred late, on day 41. LFA-1 expression on lymphocytes was significantly increased on days 25, 47, and 54. ST lining cells exhibited two distinct periods of increased expression, one early, on days 11-25 and one later, on days 41-54. CD11b/c was expressed on macrophages and ST lining cells, showing a significant increase on AIA rat ST lining cells compared with control animals on day 4. No differences in ICAM-1 expression on endothelial cells between rats with AIA and controls were found on any of the days examined. CONCLUSION: CD44 expression is up-regulated on macrophages and lymphocytes during the early development of AIA, while LFA-1 expression is up-regulated later in the development of AIA. The up-regulation of CD44 and LFA-1 at different times in the development of AIA suggests an important role for these adhesion molecules in establishing and sustaining an inflammatory response in the AIA joint.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Arthritis and Rheumatism. - 39 : 5 (1996), p. 810-819. -
További szerzők:Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus) Barquin, Nora Haines, G. Kenneth Koch, Alisa E.
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3.

001-es BibID:BIBFORM007064
Első szerző:Halloran, Margaret M.
Cím:The role of an epithelial neutrophil-activating peptide-78-like protein in rat adjuvant-induced arthritis / Margaret M. Halloran, James M. Woods, Robert M. Strieter, Zoltan Szekanecz, Michael V. Volin, Shigeru Hosaka, G. Kenneth Haines III, Steven L. Kunkel, Marie D. Burdick, Alfred Walz, Alisa E. Koch
Dátum:1999
ISSN:0022-1767 (Print)
Megjegyzések:The chemokine, epithelial neutrophil-activating peptide-78 (ENA-78), is a potent neutrophil chemotaxin whose expression is increased in inflamed synovial tissue and fluid in human rheumatoid arthritis compared with osteoarthritis. Since ENA-78 has been implicated in the pathogenesis of RA, we examined the expression of an ENA-78-like protein during the development of rat adjuvant-induced arthritis (AIA). Using an ELISA assay, we found increased levels of antigenic ENA-78-like protein in the sera of AIA animals compared with control normal animals by day 7 postadjuvant injection. ENA-78-like protein levels continued to increase as AIA developed. ENA-78-like protein levels in joint homogenates were increased in AIA animals later in the development of the disease, by day 18 during maximal arthritis, compared with control animals. Expression of ENA-78-like protein in both the AIA serum and joint correlated with the progression of inflammation of the joints. Anti-human ENA-78 administered before disease onset modified the severity of AIA, while administration of anti-ENA-78 after clinical onset of AIA did not modify the disease. These data support a role for an ENA-78-like protein as an important chemokine in the progression and maintenance of AIA.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Animals
Arthritis, Experimental
Cell Movement
Chemokine CXCL5
Chemokines, CXC
Epithelial Cells
Female
Immune Sera
Injections, Intraperitoneal
Interleukin-8
derivatives
Neutrophil Activation
Neutrophils
Peritoneum
Rats
Rats, Inbred Lew
Synovial Fluid
Tarsus, Animal
Time Factors
Megjelenés:The Journal of Immunology 162 : 12 (1999), p. 7492-7500. -
További szerzők:Woods, James M. Strieter, Robert M. Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus) Volin, Michael V. Hosaka, Shigeru Haines, Kenneth G. III. Kunkel, Steven L. Burdick, Marie D. Walz, Alfred Koch, Alisa E.
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4.

001-es BibID:BIBFORM007073
Első szerző:Koch, Alisa E.
Cím:Effects of thrombospondin-1 on disease course and angiogenesis in rat adjuvant-induced arthritis / Koch, A. E., Szekanecz, Z., Friedman, J., Haines, G. K., Langman, C. B., Bouck, N. P.
Dátum:1998
ISSN:0090-1229 (Print)
Megjegyzések:Leukocyte extravasation into the synovium is important in rheumatoid arthritis (RA). Thrombospondin (TSP)-1 mediates cell adhesion and migration and inhibits angiogenesis, and it has been implicated in RA. However, little information is available on the role of TSP-1 in arthritis-associated inflammation and neovascularization. Therefore, we analyzed the effects of TSP-1 in adjuvant-induced arthritis (AIA), a rat model for RA. Hydron pellets containing TSP-1 were implanted in one ankle of AIA rats post-adjuvant injection, while the contralateral ankle received sham implants. Body weight loss and joint swelling were determined in comparison to nonimplanted AIA controls. In addition, synovial vessel counts were obtained in TSP-1-versus sham-implanted ankles of the same rat. The implantation of TSP-1 pellets into one ankle resulted in an enhancement of swelling in both ankles. Furthermore, TSP-1 exhibited a biphasic modulatory effect on synovial vessel counts (P < 0.05). In conclusion, TSP-1 implanted into one ankle of AIA rats may augment the severity of the disease. One possible explanation, among others, for the modulating effect of TSP-1 on inflammation may be its effect on arthritis-related angiogenesis.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Animals
Arthritis, Experimental
Arthritis, Rheumatoid
Body Weight
Disease Models, Animal
Dose-Response Relationship, Drug
Joints
Neovascularization, Pathologic
Rats
Rats, Inbred Lew
Tarsus, Animal
Thrombospondin 1
Megjelenés:Clinical Immunology and Immunopathology. - 86 : 2 (1998), p. 199-208. -
További szerzők:Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus) Friedman, J. Haines, G. Kenneth Langman, C. B. Bouck, N. P.
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5.

001-es BibID:BIBFORM007072
Első szerző:Koch, Alisa E.
Cím:In situ expression of cytokines and cellular adhesion molecules in the skin of patients with systemic sclerosis : their role in early and late disease / Koch, A. E., Kronfeld-Harrington, L. B., Szekanecz, Z., Cho, M. M., Haines, G. K., Harlow, L. A., Strieter, R. M., Kunkel, S. L., Massa, M. C., Barr, W. G., Jimenez, S. A.
Dátum:1993
ISSN:1015-2008 (Print)
Megjegyzések:Cytokines and cellular adhesion molecules (CAMs) may play a role in the inflammatory and fibrotic processes underlying systemic sclerosis (SSc). We compared the immunohistological distribution of cytokines and CAMs in skin biopsies from 12 SSc patients and 14 normal (NL) individuals. Among CAMs, vascular cell adhesion molecule-1 (VCAM-1), which mediates leukocyte-endothelial adhesion, showed increased expression on SSc versus NL endothelium and stratum granulosum. P-selectin was up-regulated in SSc versus NL stratum granulosum. The CD44 lymphocyte homing receptor showed the most striking differences between SSc and NL: its expression was increased in SSc stratum granulosum, stratum spinosum, on lymphocytes, and macrophages. Regarding cytokines, interleukin-6 (IL-6) expression was increased on SSc versus NL endothelium and fibroblasts. Tumor necrosis factor-alpha (TNF-alpha) reactivity was more prevalent in SSc than NL stratum granulosum, whereas IL-8 expression was higher on SSc compared to NL endothelium. Some CAMs, such as VCAM-1 and P-selectin, and cytokines, namely TNF-alpha and IL-8, were more commonly found in skin biopsies taken from early (< or = 1 year's duration) SSc, while others, such as IL-6, showed up-regulation in the late stage of the disease. The results suggest that certain CAMs and cytokines may play a differential role in both the early, inflammatory, and the late, fibrotic stage of SSc.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Adult
Aged
Antigens, CD44
Biopsy
Carrier Proteins
Cell Adhesion
Cell Adhesion Molecules
Cytokines
Endothelium
Female
Fibroblasts
Humans
Immunohistochemistry
Interleukin-6
Interleukin-8
Male
Middle Aged
P-Selectin
Platelet Membrane Glycoproteins
Receptors, Cell Surface
Receptors, Lymphocyte Homing
Scleroderma, Systemic
Skin
Tumor Necrosis Factor-alpha
Vascular Cell Adhesion Molecule-1
Megjelenés:Pathobiology. - 61 : 5-6 (1993), p. 239-246. -
További szerzők:Kronfeld-Harrington, Lisa B. Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus) Cho, Michael M. Haines, G. Kenneth Harlow, Lisa A. Strieter, Robert M. Kunkel, Steven L. Massa, Mary C. Barr, Walter G. Jimenez, Sergio A.
Internet cím:elektronikus változat
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6.

001-es BibID:BIBFORM010151
Első szerző:Pákozdi Angéla
Cím:Endothelial progenitor cells in arthritis-associated vasculogenesis and atherosclerosis / Pákozdi Angéla, Besenyei Tímea, Paragh György, Koch Alisa E., Szekanecz Zoltán
Dátum:2009
ISSN:1297-319X (Print)
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Joint, Bone, Spine. - 76 : 6 (2009), p. 581-583. -
További szerzők:Besenyei Tímea (1980-) (reumatológus, belgyógyász) Paragh György (1953-) (belgyógyász) Koch, Alisa E. Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus)
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7.

001-es BibID:BIBFORM001945
Első szerző:Szekanecz Éva (onkológus szakorvos)
Cím:Increased production of the soluble tumor-associated antigens CA19-9, CA125, and CA15-3 in rheumatoid arthritis : potential adhesion molecules in synovial inflammation? / Szekanecz E., Sándor Z., Antal-Szalmás P., Soós L., Lakos G., Besenyei T., Szentpétery A., Simkovics E., Szántó J., Kiss E., Koch A. E., Szekanecz Z.
Dátum:2007
Megjegyzések:Some tumor-associated antigens (TAAs) are expressed on inflammatory cells. We previously detected carcinoembryonic antigen (CEA; CD66) in the rheumatoid (RA) synovium. The production of CEA, CA19-9, CA125, and CA15.3, may be increased in patients with RA, scleroderma, lupus, and Sjogren's syndrome (SS). Some of these TAAs contain sialylated carbohydrate motifs and they are involved in tumor-associated cell adhesion and metastasis. We assessed levels of TAAs in the sera of RA patients and healthy subjects. Serum TAA levels were correlated with disease markers including serum rheumatoid factor (RF), C-reactive protein (CRP), and anti-CCP antibody levels, DAS28, age disease duration. TAAs including CEA, CA15-3, CA72-4, CA125, and CA19-9, and neuron-specific enolase (NSE) were assessed by immunoassay in the sera of 75 patients with RA and 50 age- and sex-matched healthy controls. Normal upper limits for these TAAs were 3.4 microg/L, 25 kU/L, 6.9 kU/L, 35 kU/L, 34 kU/L, and 16.3 microg/L, respectively. There were significantly more RA patients showing abnormally high levels of CA125 (10.8% versus 7.1%), CA19-9 (8.1% versus 0%), and CA15-3 (17.6% versus 14.3%) in comparison to controls (P < 0.05). The mean absolute serum levels of CA125 (23.9 +/- 1.8 versus 16.8 +/- 2.2 kU/L) and CA19-9 (14.2 +/- 1.2 versus 10.5 +/- 1.6 kU/L) were also significantly higher in RA compared to controls (P < 0.05). Among RA patients, serum CEA showed significant correlation with RF (r = 0.270; P < 0.05). None of the assessed TAAs showed any correlation with CRP, anti-CCP, DAS28, age or disease duration. The concentration of some TAAs may be elevated in the sera of patients with established RA in comparison to healthy subjects. CEA, CA19-9, CA125, and CA15-3 contain carbohydrate motifs and thus they may be involved in synovitis-associated adhesive events. Furthermore, some TAAs, such as CEA, may also correlate with prognostic factors, such as serum RF levels.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
rheumatoid arthritis
tumor antigens
anti-CCP antibody
rheumatoid factor
carcinoembryonic antigen
Megjelenés:Annals of the New York Academy of Sciences 1108 (2007), p. 359-371. -
További szerzők:Sándor Zsuzsa (1980-) (pathológus) Antal-Szalmás Péter (1968-) (laboratóriumi szakorvos) Soós Lilla Lakos Gabriella (1963-) (laboratóriumi szakorvos, transzfúziológus, immunológus) Besenyei Tímea (1980-) (reumatológus, belgyógyász) Szentpétery Ágnes (1978-) (reumatológus) Simkovics Enikő Szántó János (1949-) (onkológus szakorvos) Kiss Emese (1960-) (belgyógyász, immunológus) Koch, Alisa E. Szekanecz Zoltán (1964-) (reumatológus, belgyógyász, immunológus)
Internet cím:elektronikus változat
DOI
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8.

001-es BibID:BIBFORM094141
Első szerző:Szekanecz Zoltán (reumatológus, belgyógyász, immunológus)
Cím:Chemokinek patogenetikai és klinikai szerepe rheumatoid arthritisben / Szekanecz Zoltán, Alisa E. Koch, Szegedi Gyula
Dátum:1998
Megjegyzések:A leukocyták bejutása a synoviumba alapvető jelentőségű a rheumatoid arthritis patogenesisében. A chemokinek olyan chemotaktikus gyulladásos mediátorok, melyek elősegítik a lymphocyták, monocyták és granulocyták synovialis membránba történő kivándorlását. A szerzők áttekintik a rheumatoid arthritis patogenesisében szerepet játszó főbb chernokineket. Összefoglalják a chemokinek és más mediátorok közti komplex kölcsönhatásokon alapuló szabályozó mechanizmusokat. Végül tárgyalják a chemokinek termelődésére irányuló intervenciós lehetőségeket, melyeknek szerepe lehet a jövő antirheumatikus terápiájában. Pathogenetic and clinical roles of chemokines in rheumatoid arthritis The migration of leukocytes into the synovium is crucial in the pathogenesis of rheumatoid arthritis. Chernokínes are chemotactic inflarnrnatcry mediators which facilitate the invasion of the synovial tissue by Iymphocytes, monocytes and neutrophils. The authors review the role of the most relevant chemokines in the pathogenesis of rheumatoid arthritis. They summarise the regulatory mechanisms which are based on the complex interactions among chemokines and other mediators. Finally they discuss the possibilities of interventions against chemokine production which might have a role in the future anti rheumatic therapies.
Tárgyszavak:Orvostudományok Klinikai orvostudományok magyar nyelvű folyóiratközlemény hazai lapban
folyóiratcikk
chemokin
rheumatoid arthritis
synovium
makrofágok
chemokine
Macrophage
Megjelenés:Magyar reumatológia. - 39 : 2 (1998), p. 86-93. -
További szerzők:Koch, Alisa E. Szegedi Gyula (1936-2013) (belgyógyász, immunológus)
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9.

001-es BibID:BIBFORM094102
Első szerző:Szekanecz Zoltán (reumatológus, belgyógyász, immunológus)
Cím:Angiogenesis in rheumatoid anhritis / Zoltán Szekanecz, Joon Kim, Alisa E. Koch
Dátum:2002
Megjegyzések:Angiogenesis, the formation of new blood vessels, enables the emigration of leukocytes into tissues. Neovascularization is a crucial process in the pathogenesis of inflammatory and malignant disorders. Rheumatoid arthritis (RA) is considered by many as an "angiogenic disease". A number of angiogenic mediators including cytokines, chemokines, growth factors, matrix components, adhesion molecules, proteolytic enzymes and others are abundantly produced in the RA synovium. These factors stimulate the proliferation and migration of endothelial cells followed by capillary formation.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Recent Res. Devel. lmmunology. - 4 (2002), p. 523-533. -
További szerzők:Kim, Joon Koch, Alisa E.
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10.

001-es BibID:BIBFORM077208
Első szerző:Szekanecz Zoltán (reumatológus, belgyógyász, immunológus)
Cím:Angiogenesis and vasculogenesis in rheumatoid arthritis / Zoltán Szekanecz, Emese Balogh, Alisa E. Koch
Dátum:2019
Tárgyszavak:Orvostudományok Klinikai orvostudományok könyvfejezet
Megjelenés:Rheumatology / Ed. Marc C. Hochberg, Alan J. Silman, Josef S. Smolen, Michael E. Weinblatt, Michael H. Weisman. - p. 764-767. -
További szerzők:Balogh Emese (reumatológus) Koch, Alisa E.
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
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11.

001-es BibID:BIBFORM046369
Első szerző:Szekanecz Zoltán (reumatológus, belgyógyász, immunológus)
Cím:Differential distribution of intercellular adhesion molecules (ICAM-1, ICAM-2, and ICAM-3) and the MS-1 antigen in normal and diseased human synovia : their possible pathogenetic and clinical significance in rheumatoid arthritis / Szekanecz Z., Haines G. K., Lin T. R., Harlow L. A., Goerdt S., Rayan G., Koch A. E.
Dátum:1994
ISSN:0004-3591
Megjegyzések:Cellular adhesion and differentiation molecules (CAMs) may play a role in the recruitment and retention of inflammatory cells into rheumatoid arthritis synovial tissue (RA ST). In order to determine if certain CAMs are up-regulated in RA ST compared with normal ST, we studied the distribution of intercellular adhesion molecules (ICAMs) 1, 2, and 3 in ST. We also studied the MS-1 antigen since it is preferentially expressed on discontinuous endothelia, such as those found in RA ST; MS-1 is also expressed differentially upon cytokine activation of cells in vitro or in pathologic conditions in situ. Thus, we postulated a possible similarity between MS-1 and ICAM-1 expression in inflamed ST. METHODS. Immunohistochemical analysis was used to determine the distribution of ICAMs and MS-1 in ST from 10 patients with RA, 10 with osteoarthritis (OA), and 4 normal individuals. RESULTS. ICAM-1 expression was found on significantly more RA ST endothelial cells compared with normal cells, as well as on RA ST macrophages and lining cells. ICAM-2, also found on endothelial cells, showed no differential staining pattern. ICAM-3 was present on RA ST macrophages and lining cells as well as on some RA and OA endothelial cells. The MS-1 antigen was present on most RA and OA ST endothelia, lining cells, and macrophages. ICAM-1 expression and MS-1 expression in the lining layer were positively correlated in both RA and OA. CONCLUSION. ICAM-1, while found mainly on endothelial cells, is up-regulated on RA ST macrophages and lining cells, suggesting a role for these cells in the infiltration and tissue damage seen in the RA ST. ICAM-3, which is present mainly on normal resting leukocytes but not on normal endothelium, is expressed by some diseased ST leukocytes and endothelial cells. MS-1 is also found on the RA ST specialized, fenestrated endothelium, on macrophages, and in the lining layer. These results suggest that the differential expression of ICAMs and MS-1 in RA ST compared with normal ST might play a special role in the pathogenesis of RA.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Arthritis and Rheumatism. - 37 : 2 (1994), p. 221-231. -
További szerzők:Haines, G. Kenneth Lin, Theodore R. Harlow, Lisa A. Goerdt, Sergij Rayan, Ghazi Koch, Alisa E.
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12.

001-es BibID:BIBFORM063072
Első szerző:Szekanecz Zoltán (reumatológus, belgyógyász, immunológus)
Cím:Successes and failures of chemokine-pathway targeting in rheumatoid arthritis / Zoltán Szekanecz, Alisa E. Koch
Dátum:2015
ISSN:1759-4790 1759-4804
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Nature Reviews Rheumatology. - 12 : 1 (2015), p. 5-13. -
További szerzők:Koch, Alisa E.
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