Publications on PID

CID with associated or syndromic features

Rapid Transition of Facial Features from Early to Mid - Adolescence in Autosomal Dominant Hyper IgE Syndrome with a STAT3 Variation.
Geeta MG, A. Riyaz, C. Krishnan, Scaria V.
Indian J Pediatr (2018) 85:595-596.

Pan-Hammarstrom, Q., H. Abolhassani, and L. Hammarström, Defects in plasma cell differentiation are associated with primary immunodeficiency in humans. J Allergy Clin Immunol, 141, 1217, 2018.

Abolhassani, H., A. Aghamohammadi, M. Fang, N. Rezaei, C. Jiang, X. Liu, Q. Pan-Hammarström, and L. Hammarström, Clinical Implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency. In press: Genet Med, 2018.

King, J., S. Borte, N. Brodsky, U. von Döbeln, C.I.E. Smith, and L. Hammarström, Kappa-deleting recombination excision circle levels remain low or absent throughout life in patients with X-linked agammaglobulinemia. Ped Allergy Immunol, 29, 453, 2018.

Gardulf, A., R. Gustafson, L.E. Eriksson, H. Abolhassani, and L. Hammarström, Predictive markers for humoral influenza vaccine response in patients with common variable immunodeficiency. In press: J Allergy Clin Immunol, 2018.

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