G Lehner-Netsch

Familial Hemolytic-Uremic Syndrome and Homozygous Factor H Deficiency

Vincent Pichette, Serge Quérin, Walter Schürch et al. · American Journal of Kidney Diseases · 1994 · 123 citations

Down Syndrome, Anemia, Urology +6

Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian family.

J.-M. Del′ge, Patrice Bergeron, Jacques Simard et al. · Journal of Clinical Investigation · 1977 · 33 citations · Full text

C3b inactivator deficiency with immune complex manifestations.

P Solal-Céligny, Michel Laviolette, Jacques Hébert et al. · PubMed · 1982 · 30 citations · Full text

Primary Immunodeficiency, Recurrent Infections, Autoimmune Disease +13

Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.

J Delage, G Lehner-Netsch, Rhonda L. LaFleur et al. · PubMed · 1979 · 22 citations

Immunohematology, Family Members, Genetics +19

[Leukemias and autoimmune diseases: Sjogren's syndrome and hemolytic anemia associated with chronic lymphocytic anemia].

G Lehner-Netsch, Aïssata Barry, J Delage · PubMed · 1969 · 10 citations

Immunohematology, Autoimmune Disease, Sjögren’s Syndrome +12