HLA-Linked Complement Markers in Narcolepsy

[1]  M. Satake,et al.  Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics. , 1985, The Journal of clinical investigation.

[2]  M. Satake,et al.  EXTRAORDINARY ASSOCIATION BETWEEN HLA-DR2 AND NARCOLEPSY , 1985, The Lancet.

[3]  M. Billiard,et al.  Possible association between HLA-B7 and narcolepsy. , 2008, Tissue antigens.

[4]  R. Vaughan,et al.  GENETIC MARKERS IN NARCOLEPSY , 1984, The Lancet.

[5]  M. Satake,et al.  HLA antigens in Japanese patients with narcolepsy , 1984 .

[6]  L. Strong,et al.  Human C4 haplotypes with duplicated C4A or C4B. , 1984, American journal of human genetics.

[7]  E. Yunis,et al.  An unusual "morphologic" variant of BF S. , 1984, American journal of human genetics.

[8]  D. Bentley,et al.  A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B , 1984, Nature.

[9]  Porter Rr Complement polymorphism, the major histocompatibility complex and associated diseases: a speculation. , 1983 .

[10]  B. Olaisen,et al.  Statement on the nomenclature of human C4 allotypes. , 1983, Immunobiology.

[11]  M. Walport,et al.  Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility. , 1983, British medical journal.

[12]  J. McCluskey,et al.  Disease Associations with Complotypes, Supratypes and Haplotypes , 1983, Immunological reviews.

[13]  C. Rittner,et al.  On the significance of C2, C4, and factor B polymorphisms in disease , 1981, Human Genetics.

[14]  G. Hauptmann,et al.  A hemolytically inactive gene product of factor B. , 1980, Immunobiology.

[15]  C. Alper,et al.  Inherited structural polymorphism of the fourth component of human complement. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[16]  G. Hauptmann,et al.  The nomenclature of properdin factor B allotypes. , 1978, Zeitschrift fur Immunitatsforschung. Immunobiology.

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

[18]  J. Atkinson,et al.  Mapping of the HLA locus controlling C2 structural variants and linkage disequilibrium between alleles C22 and Bw15 , 1976 .

[19]  C. Alper Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf , 1976, The Journal of experimental medicine.

[20]  C. Alper,et al.  GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN , 1972, The Journal of experimental medicine.