论文信息 - Familial, recurrent haemolytic-uraemic syndrome with hypocomplementaemia - 字舞流文

Familial, recurrent haemolytic-uraemic syndrome with hypocomplementaemia

J. Maciejewski | K. Strzykala | J. Zachwieja | Wanda Golda

[1] R. Bogdanović,et al. Recurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report , 1988, Pediatric Nephrology.

[2] R. Wyatt,et al. Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement. , 1985, The Journal of pediatrics.

[3] R. Thompson,et al. Hypocomplementaemia due to a genetic deficiency of beta 1H globulin. , 1981, Clinical and experimental immunology.

[4] R. Chesney,et al. Hemolytic uremic syndrome in families. , 1975, The New England journal of medicine.

[5] B. Kaplan,et al. SERUM-COMPLEMENT LEVELS IN HÆMOLYTIC-URÆMIC SYNDROME , 1973 .

[6] J. Cameron,et al. PLASMA-C3 IN HÆMOLYTIC-URÆMIC SYNDROME AND THROMBOTIC THROMBOCYTOPENIC PURPURA , 1973 .

[7] M. Ognjanović,et al. Haemolytic-uraemic syndrome associated with Aeromonas hydrophila enterocolitis. , 1991, Pediatric nephrology.

[8] J. Cameron,et al. Letter: Plasma-C3 in haemolytic-uraemic syndrome and thrombotic thrombocytopenic purpura. , 1973, Lancet.