Hereditary C1q deficiency and secondary Sjögren's syndrome

Ítems similars

• Secondary C1q Deficiency in Activated PI3Kδ Syndrome Type 2
  per: Hong, Ying, et al.
  Publicat: (2019)
• An immunohistological study of secondary Sjögren's syndrome.
  per: Isenberg, D A, et al.
  Publicat: (1984)
• RFC1 expansions can mimic hereditary sensory neuropathy with cough and Sjögren syndrome
  per: Kumar, Kishore R, et al.
  Publicat: (2020)
• SLE like syndrome and functional deficiency of C1q in members of a large family.
  per: Hannema, A J, et al.
  Publicat: (1984)
• Sub-units of the first complement component in immunologic deficiency syndromes: independence of C1s and C1q
  per: Stroud, R. M., et al.
  Publicat: (1970)