The IL-17A rs2275913 single nucleotide polymorphism is associated with protection to tuberculosis but related to higher disease severity in Argentina

por Rolandelli, A., Del Pino, R.E.H., Pellegrini, J.M., Tateosian, N.L., Amiano, N.O., De La Barrera, S., Casco, N., Gutiérrez, M., Palmero, D.J., García, V.E.

Histopathology of Sclerotinia sclerotiorum attack on flower parts of Helianthus annuus heads in tolerant and susceptible varieties

por Rodríguez, M.A., Venedikian, N., Bazzalo, M.E., Godeas, A.

The IL-17A rs2275913 single nucleotide polymorphism is associated with protection to tuberculosis but related to higher disease severity in Argentina

por Amiano, Nicolás Oscar, García, Verónica Edith
Publicado 2017

Histopathology of Sclerotinia sclerotiorum attack on flower parts of Helianthus annuus heads in tolerant and susceptible varieties

por Rodríguez, María Alejandra, Venedikian, Nadia, Bazzalo, María Eugenia, Godeas, Alicia Margarita
Publicado 2004

Somatic Hypermutation Defects in Common Variable Immune Deficiency

por Almejun, M.B., Borge, M.

Somatic Hypermutation Defects in Common Variable Immune Deficiency

Publicado 2017

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.
Publicado 2011

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.
Publicado 2011

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, Carolina, Nadra, Alejandro Daniel, Taboas, Melisa, Charreau, Eduardo Hernán
Publicado 2011

Granulomatous nephritis associated with R334Q mutation in NOD2 [5]

por 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]

Publicado 2007

Response to comment on "Gender differences in 1,25 dihydroxyvitamin D 3 immunomodulatory effects in multiple sclerosis patients and healthy subjects"

por Correale, J., Ysrraelit, M.C., Gaitán, M.I.

Response to comment on "Gender differences in 1,25 dihydroxyvitamin D 3 immunomodulatory effects in multiple sclerosis patients and healthy subjects"

Publicado 2011

Survey of genetic counselors and clinical geneticists regarding recurrence risks for families with nonsyndromic cleft lip with or without cleft palate

por Wyszynski, D.F., Zeiger, J., Tilli, M.T., Bailey-Wilson, J.E., Beaty, T.H.

Survey of genetic counselors and clinical geneticists regarding recurrence risks for families with nonsyndromic cleft lip with or without cleft palate

Publicado 1998

Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: An international collaborative study

por Daly, A.F., Tichomirowa, M.A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M.-L., Barlier, A., Naves, L.A., Ebeling, T., Karhu, A., Raappana, A., Cazabat, L., De Menis, E., Montañana, C.F., Raverot, G., Weil, R.J., Sane, T., Maiter, D., Neggers, S., Yaneva, M., Tabarin, A., Verrua, E., Eloranta, E., Murat, A., Vierimaa, O., Salmela, P.I., Emy, P., Toledo, R.A., Sabaté, M.I., Villa, C., Popelier, M., Salvatori, R., Jennings, J., Longás, Á.F., Aizpún, J.I.L., Georgitsi, M., Paschke, R., Ronchi, C., Valimaki, M., Saloranta, C., De Herder, W., Cozzi, R., Guitelman, M., Magri, F., Lagonigro, M.S., Halaby, G., Corman, V., Hagelstein, M.-T., Vanbellinghen, J.-F., Barra, G.B., Gimenez-Roqueplo, A.-P., Cameron, F.J., Borson-Chazot, F., Holdaway, I., Toledo, S.P.A., Stalla, G.K., Spada, A., Zacharieva, S., Bertherat, J., Brue, T., Bours, V., Chanson, P., Aaltonen, L.A., Beckers, A.

Toll-like receptor 4 D299G polymorphism in metabolic disorders: A meta-analysis

por S. Belforte, F., Coluccio Leskow, F., Poskus, E., Penas Steinhardt, A.

Molecular analysis of the UROD gene in 17 Argentinean patients with familial porphyria cutanea tarda: Characterization of four novel mutations

por Méndez, M., Rossetti, M.V., Gómez-Abecia, S., Morán-Jiménez, M.-J., Parera, V., Batlle, A., Enríquez de Salamanca, R.