Artículo
Meiorin, S.M.; Espada, G.; Costa, C.E.; Tartara, A.; De Matteo, E.; Wouters, C.; Martin, T.M.; Rose, C.D. "Granulomatous nephritis associated with R334Q mutation in NOD2 [5]" (2007) Journal of Rheumatology. 34(9):1945-1947
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Registro:
| Documento: | Artículo |
| Título: | Granulomatous nephritis associated with R334Q mutation in NOD2 [5] |
| Autor: | Meiorin, S.M.; Espada, G.; Costa, C.E.; Tartara, A.; De Matteo, E.; Wouters, C.; Martin, T.M.; Rose, C.D. |
| Filiación: | Department of Rheumatology, Buenos Aires, Argentina Department of Ophthalmology, Buenos Aires, Argentina Hospital de Niños Ricardo Gutierrez, Buenos Aires, Argentina University Hospital Gasthuisberg, Leuven, Belgium Casey Eye Institute, Oregon Health and Science University, Portland, OR, United States Thomas Jefferson University, Department of Pediatrics, Wilmington, DE, United States Department of Rheumatology, Hospital de Niños Ricardo Gutierrez, Pabellón L, Gallo 1330, Buenos Aires 1425, Argentina |
| Palabras clave: | arginine; caspase recruitment domain protein 15; corticosteroid; etanercept; glutamine; infliximab; methotrexate; amino acid substitution; arthropathy; atrophy; combination chemotherapy; disease association; granulomatosis; human; kidney biopsy; letter; nephritis; priority journal; Arthritis; Child, Preschool; Female; Genetic Predisposition to Disease; Granuloma; Humans; Nephritis; Nod2 Signaling Adaptor Protein; Polymorphism, Single Nucleotide; Uveitis |
| Año: | 2007 |
| Volumen: | 34 |
| Número: | 9 |
| Página de inicio: | 1945 |
| Página de fin: | 1947 |
| Título revista: | Journal of Rheumatology |
| Título revista abreviado: | J. Rheumatol. |
| ISSN: | 0315162X |
| CODEN: | JRHUA |
| CAS: | arginine, 1119-34-2, 15595-35-4, 7004-12-8, 74-79-3; etanercept, 185243-69-0, 200013-86-1; glutamine, 56-85-9, 6899-04-3; infliximab, 170277-31-3; methotrexate, 15475-56-6, 59-05-2, 7413-34-5; CARD15 protein, human; Nod2 Signaling Adaptor Protein |
| Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0315162X_v34_n9_p1945_Meiorin |
Referencias:
- Blau, E.B., Familial granulomatous arthritis, iritis, and rash (1985) J Pediatr, 107, pp. 689-693
- Jabs, D.A., Houk, J.L., Bias, W.B., Arnett, F.C., Familial granulomatous synovitis, uveitis, and cranial neuropathies (1985) Am J Med, 78, pp. 801-804
- Miceli-Richard, C., Lesage, S., Rybojad, M., CARD15 mutations in Blau syndrome (2001) Nat Genet, 29, pp. 19-20
- Saini, S.K., Rose, C.D., Liver involvement in familial granulomatous arthritis (Blau syndrome) (1996) J Rheumatol, 23, pp. 396-399
- Rotenstein, D., Gibbas, D.L., Majmudar, B., Chastain, E.A., Familial granulomatous arteritis and polyarthritis of juvenile onset (1982) New Engl J Med, 306, pp. 86-90
- Rose, C.D., Wouters, C.H., Meiorin, S., Pediatric granulomatous artritis (2006) An international registry. Arthritis Rheum, 54, pp. 3337-3344
- Ting, S.S., Ziegler, J., Fischer, E., Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions (1998) J Pediatr, 133, pp. 450-452
- Coutant, R., Leroy, B., Niaudet, P., Renal granulomatous sarcoidosis in childhood: A report of 11 cases and a review of the literature (1999) Eur J Pediatr, 158, pp. 154-159
- Wang, X., Kuivaniemi, H., Bonavita, G., CARD15 mutations in familial granulomatous syndromes: A study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy (2002) Arthritis Rheum, 46, pp. 3041-3045
- Kanazawa, N., Okafuji, I., Kambe, N., Early-onset sarcoidosis and CARD15 mutations with consecutive nuclear factor kB activation: Common genetic etiology with Blau syndrome (2005) Blood, 105, pp. 1195-1197
Citas:
---------- APA ----------
Meiorin, S.M., Espada, G., Costa, C.E., Tartara, A., De Matteo, E., Wouters, C., Martin, T.M.,..., Rose, C.D. (2007) . Granulomatous nephritis associated with R334Q mutation in NOD2 [5]. Journal of Rheumatology, 34(9), 1945-1947.Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0315162X_v34_n9_p1945_Meiorin [ ]
---------- CHICAGO ----------
Meiorin, S.M., Espada, G., Costa, C.E., Tartara, A., De Matteo, E., Wouters, C., et al. "Granulomatous nephritis associated with R334Q mutation in NOD2 [5]" . Journal of Rheumatology 34, no. 9 (2007) : 1945-1947.Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0315162X_v34_n9_p1945_Meiorin [ ]
---------- MLA ----------
Meiorin, S.M., Espada, G., Costa, C.E., Tartara, A., De Matteo, E., Wouters, C., et al. "Granulomatous nephritis associated with R334Q mutation in NOD2 [5]" . Journal of Rheumatology, vol. 34, no. 9, 2007, pp. 1945-1947.Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0315162X_v34_n9_p1945_Meiorin [ ]
---------- VANCOUVER ----------
Meiorin, S.M., Espada, G., Costa, C.E., Tartara, A., De Matteo, E., Wouters, C., et al. Granulomatous nephritis associated with R334Q mutation in NOD2 [5]. J. Rheumatol. 2007;34(9):1945-1947.Available from: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0315162X_v34_n9_p1945_Meiorin [ ]
