Congenital Malaria

Por Eckstein, A., Nixon, W. C. W.
Publicado em 1946

Treatment of ocular symptoms of Behçet's disease with interferon α(2a): a pilot study

Por Kotter, I., Eckstein, A., Stubiger, N., Zierhut, M.
Publicado em 1998

Direct measurement of the biphoton Wigner function through two-photon interference

Por Douce, T., Eckstein, A., Walborn, S. P., Khoury, A. Z., Ducci, S., Keller, A., Coudreau, T., Milman, P.
Publicado em 2013

Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.

Por Weber, B H, Sander, S, Kopp, C, Walker, D, Eckstein, A, Wissinger, B, Zrenner, E, Grimm, T
Publicado em 1996

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.

Por Kohl, S, Christ-Adler, M, Apfelstedt-Sylla, E, Kellner, U, Eckstein, A, Zrenner, E, Wissinger, B
Publicado em 1997

Impact of smoking on the response to treatment of thyroid associated ophthalmopathy

Por Eckstein, A, Quadbeck, B, Mueller, G, Rettenmeier, A W, Hoermann, R, Mann, K, Steuhl, P, Esser, J
Publicado em 2003

Efficacy of recombinant human interferon-alfa2a on ocular and extra-ocular manifestations of Behçet's disease and influence on cells of the immune system: results of an open four c...

Por Kötter, I, Treusch, M, Vonthein, R, Zierhut, M, Eckstein, A, Ness, T, Günaydin, I, Grimbacher, B, Blaschke, S, Peter, HH, Stübiger, N
Publicado em 2003

Thyroid associated ophthalmopathy: evidence for CD4(+) γδ T cells; de novo differentiation of RFD7(+) macrophages, but not of RFD1(+) dendritic cells; and loss of γδ and αβ T cell...

Por Eckstein, A K, Quadbeck, B, Tews, S, Mann, K, Krüger, C, Mohr, C H, Steuhl, K-P, Esser, J, Gieseler, R K
Publicado em 2004

HHV8 associated Kaposi's sarcoma during triple immunosuppressive treatment with cyclosporin A, azathioprine, and prednisolone for ocular Behçet's disease and complete remission of...

Por Kotter, I, Aepinus, C, Graepler, F, Gartner, V, Eckstein, A, Stubiger, N, Kaskas, B, Zierhut, M, Bultmann, B, Kandolf, R, Kanz, L
Publicado em 2001

Human recombinant interferon alfa-2a for the treatment of Behçet's disease with sight threatening posterior or panuveitis

Por Kötter, I, Zierhut, M, Eckstein, A K, Vonthein, R, Ness, T, Günaydin, I, Grimbacher, B, Blaschke, S, Meyer-Riemann, W, Peter, H H, Stübiger, N
Publicado em 2003

Genetic immunization with mouse thyrotrophin hormone receptor plasmid breaks self‐tolerance for a murine model of autoimmune thyroid disease and Graves' orbitopathy

Por Schlüter, A., Horstmann, M., Diaz‐Cano, S., Plöhn, S., Stähr, K., Mattheis, S., Oeverhaus, M., Lang, S., Flögel, U., Berchner‐Pfannschmidt, U., Eckstein, A., Banga, J. P.
Publicado no Clin Exp Immunol (2017)

Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa.

Por Wroblewski, J J, Wells, J A, Eckstein, A, Fitzke, F W, Jubb, C, Keen, T J, Inglehearn, C F, Bhattacharya, S S, Arden, G B, Jay, M R
Publicado em 1994

Detector-Independent Verification of Quantum Light

Por Sperling, J., Clements, W. R., Eckstein, A., Moore, M., Renema, J. J., Kolthammer, W. S., Nam, S. W., Lita, A., Gerrits, T., Vogel, W., Agarwal, G. S., Walmsley, I. A.
Publicado no Phys Rev Lett (2017)

Identification of nonclassical properties of light with multiplexing layouts

Por Sperling, J., Eckstein, A., Clements, W. R., Moore, M., Renema, J. J., Kolthammer, W. S., Nam, S. W., Lita, A., Gerrits, T., Walmsley, I. A., Agarwal, G. S., Vogel, W.
Publicado no Phys Rev A (Coll Park) (2017)

Graves’ orbitopathy as a rare disease in Europe: a European Group on Graves’ Orbitopathy (EUGOGO) position statement

Por Perros, P., Hegedüs, L., Bartalena, L., Marcocci, C., Kahaly, G. J., Baldeschi, L., Salvi, M., Lazarus, J. H., Eckstein, A., Pitz, S., Boboridis, K., Anagnostis, P., Ayvaz, G., Boschi, A., Brix, T. H., Currò, N., Konuk, O., Marinò, M., Mitchell, A. L., Stankovic, B., Törüner, F. B., von Arx, G., Zarković, M., Wiersinga, W. M.
Publicado no Orphanet J Rare Dis (2017)

Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity

Por Hornig, N. C., Ukat, M., Schweikert, H. U., Hiort, O., Werner, R., Drop, S. L. S., Cools, M., Hughes, I. A., Audi, L., Ahmed, S. F., Demiri, J., Rodens, P., Worch, L., Wehner, G., Kulle, A. E., Dunstheimer, D., Müller-Roßberg, E., Reinehr, T., Hadidi, A. T., Eckstein, A. K., van der Horst, C., Seif, C., Siebert, R., Ammerpohl, O., Holterhus, P.-M.
Publicado no J Clin Endocrinol Metab (2016)