Literature DB >> 28435995

Hereditary Homozygous C3 Deficiency.

Jigna N Bathia1,2, Priyankar Pal3, Mandira Roy4, Souvik Guha4.   

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Year:  2017        PMID： 28435995     DOI： 10.1007/s12098-017-2350-0

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Global study of primary immunodeficiency diseases (PI)--diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation.

Authors:  Vicki Modell; Bonnie Gee; David B Lewis; Jordan S Orange; Chaim M Roifman; John M Routes; Ricardo U Sorensen; Luigi D Notarangelo; Fred Modell
Journal:  Immunol Res       Date:  2011-10       Impact factor: 2.829

Review 2.  Clinical and laboratory evaluation of complement deficiency.

Authors:  Leana Wen; John P Atkinson; Patricia C Giclas
Journal:  J Allergy Clin Immunol       Date:  2004-04       Impact factor: 10.793

Review 3.  Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.

Authors:  E S Reis; D A Falcão; L Isaac
Journal:  Scand J Immunol       Date:  2006-03       Impact factor: 3.487

Review 4.  Clinical significance of complement deficiencies.

Authors:  H David Pettigrew; Suzanne S Teuber; M Eric Gershwin
Journal:  Ann N Y Acad Sci       Date:  2009-09       Impact factor: 5.691

Review 5.  Complement in human diseases: Lessons from complement deficiencies.

Authors:  Marina Botto; Michael Kirschfink; Paolo Macor; Matthew C Pickering; Reinhard Würzner; Francesco Tedesco
Journal:  Mol Immunol       Date:  2009-05-28       Impact factor: 4.407
  5 in total

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