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Mutations in IAPP and NEUROG3 genes are not a common cause of permanent neonatal/infancy/childhood‐onset diabetes
Author(s) -
Nocerino V.,
Colombo C.,
Bonfanti R.,
Iafusco D.,
Barbetti F.
Publication year - 2009
Publication title -
diabetic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 145
eISSN - 1464-5491
pISSN - 0742-3071
DOI - 10.1111/j.1464-5491.2009.02726.x
Subject(s) - medicine , diabetes mellitus , pediatrics , gene , mutation , genetics , endocrinology , biology
1 Heinzerling L, Raile K, Rochlitz H, Zuberbier T, Worm M. Insulin allergy: clinical manifestations and management strategies. Allergy 2008; 63: 148–155. 2 Greenfield JR, Tuthill A, Soos MA, Semple RK, Halsall DJ, Chaudhry A et al. Severe insulin resistance due to anti-insulin antibodies: response to plasma exchange and immunosuppressive therapy. Diabet Med 2009; 26: 79–82. 3 Shemin D, Briggs D, Greenan M. Complications of therapeutic plasma exchange: a prospective study of 1,727 procedures. J Clin Apher 2007; 22: 270–276. 4 Nicholls AJ, Platts MM. Anaphylactoid reactions due to haemodialysis, haemofiltration, or membrane plasma separation. Br Med J (Clin Res Ed) 1982; 285: 1607–1609.

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