Cerebral atrophy and nephropathic cystinosis.

Por Cochat, P, Drachman, R, Gagnadoux, M F, Pariente, D, Broyer, M
Publicado em 1986

Inheritance of abnormal erythrocyte cation transport in essential hypertension.

Por Meyer, P, Garay, R P, Nazaret, C, Dagher, G, Bellet, M, Broyer, M, Feingold, J
Publicado em 1981

Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assay.

Por Forestier, L, Jean, G, Attard, M, Cherqui, S, Lewis, C, van't Hoff, W, Broyer, M, Town, M, Antignac, C
Publicado em 1999

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Por Jean, G., Fuchshuber, A., Town, M. M., Gribouval, O., Schneider, J. A., Broyer, M., van't Hoff, W., Niaudet, P., Antignac, C.
Publicado em 1996

Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression.

Por Antignac, C, Knebelmann, B, Drouot, L, Gros, F, Deschênes, G, Hors-Cayla, M C, Zhou, J, Tryggvason, K, Grünfeld, J P, Broyer, M
Publicado em 1994

Thrombosis in systemic lupus erythematosus: a French collaborative study.

Por Montes de Oca, M A, Babron, M C, Blétry, O, Broyer, M, Courtecuisse, V, Fontaine, J L, Loirat, C, Méry, J P, Reinert, P, Wechsler, B
Publicado em 1991

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Por Knebelmann, B., Breillat, C., Forestier, L., Arrondel, C., Jacassier, D., Giatras, I., Drouot, L., Deschênes, G., Grünfeld, J. P., Broyer, M., Gubler, M. C., Antignac, C.
Publicado em 1996