Déficit héréditaire en inhibiteur de la C1 estérase Lupus et glomérulonéphrite

[1]  A. Cameron,et al.  A genetic defect of the C1q subcomponent of complement associated with childhood (immune complex) nephritis. , 1980, The New England journal of medicine.

[2]  J. Gelfand,et al.  Replacement therapy in hereditary angioedema: successful treatment of acute episodes of angioedema with partly purified C1 inhibitor. , 1980, The New England journal of medicine.

[3]  B. Pussell,et al.  COMPLEMENT DEFICIENCY AND NEPHRITIS A Report of a Family , 1980, The Lancet.

[4]  A. Steinberg,et al.  Systemic Lupus Erythematosus: Evolving Concepts , 1979 .

[5]  G. Boss,et al.  Acquired C1 Esterase Inhibitor Deficiency and Angioedema: A Review , 1979, Medicine.

[6]  E. Rayfield,et al.  Viruses and the Pathogenesis of Diabetes Mellitus , 1978, Diabetes.

[7]  A. Huellmantel,et al.  Immunopathology of Juvenile-onset Diabetes Mellitus: I. IgA Deficiency and Juvenile Diabetes , 1978, Diabetes.

[8]  V. Agnello COMPLEMENT DEFICIENCY STATES , 1978, Medicine.

[9]  A. J. Mcadams,et al.  Lupus-erythematosus-like disease in three unrelated women with hereditary angioneurotic edema. , 1977, Annals of internal medicine.

[10]  D. Alling,et al.  Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities. , 1976, The New England journal of medicine.

[11]  J. Atkinson,et al.  Hereditary angioedema: the clinical syndrome and its management. , 1976, Annals of internal medicine.

[12]  B. Boucher,et al.  The complement abnormalities of lipodystrophy. , 1976, The New England journal of medicine.

[13]  P. Kohler Inherited complement deficiencies and systemic lupus erythematosus: an immunogenetic puzzle. , 1975, Annals of internal medicine.

[14]  J. Starr,et al.  Erythema marginatum preceding hereditary angioedema. , 1974, The Journal of allergy and clinical immunology.

[15]  W. M. Campion,et al.  Hereditary angioedema and "familial" lupus erythematosus in identical twin boys. , 1974, The American journal of medicine.

[16]  D. Evans,et al.  Mesangiocapillary nephritis, partial lipodystrophy, and hypocomplementaemia. , 1973, Lancet.

[17]  R. Faivre,et al.  Néphropathie à complexes immuns et déficit héréditaire en inhibiteur de la C1 estérase. , 1981 .

[18]  A. Van Gossum,et al.  Gallstones and acute hepatitis. , 1981, Lancet.

[19]  R. Thompson,et al.  Plasmapheresis in hereditary angioneurotic edema and systemic lupus erythematosus. , 1980, Archives of internal medicine.

[20]  M. Kazatchkine,et al.  La voie alterne du complément , 1979 .

[21]  W. Fridman,et al.  Déficit génétique de la deuxième fraction du complément avec manifestations lupiques. Etude clinique et immunologique d'une nouvelle observation familiale. , 1977 .

[22]  J. Bach,et al.  [Disseminated lupus erythematosus: etiopathogenic factors]. , 1977, Annales de medecine interne.

[23]  V. Nussenzweig Receptors for immune complexes on lymphocytes. , 1974, Advances in immunology.

[24]  A. Michael,et al.  The complement system in chronic glomerulonephritis: three newly associated aberrations. , 1971, The Journal of pediatrics.