B. Sánchez

Diagnostic and therapeutic challenges in a child with complete Interferon‐γ Receptor 1 deficiency

J. Casanova, C. Deswarte, J. Bustamante, 2015, Pediatric blood & cancer.

Newborn Screening for Primary T- and B-Cell Immune Deficiencies—A Prospective Study in Andalucía

J. Soto, O. Neth, P. Olbrich, 2017 .

[A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia].

R. Rodero, S. Borte, P. Ybot‐González, 2014, Anales de pediatria.

X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world

A. Plebani, C. Pignata, H. Kanegane, 2019, The World Allergy Organization Journal.

Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity.

Q. Pan-Hammarström, L. Hammarström, S. Burns, 2018, Clinical immunology.

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.

A. Schäffer, E. Gertz, A. Plebani, 2010, The Journal of allergy and clinical immunology.

Activated PI3Kδ syndrome type 2: Two patients, a novel mutation, and review of the literature

K. Schwarz, C. Speckmann, O. Neth, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Immune deficiencies , infection , and systemic immune disorders Mutations in STAT 3 and diagnostic guidelines for hyper-IgE syndrome

A. Schäffer, A. Plebani, C. Pignata, 2010 .

A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopaenia

R. Rodero, S. Borte, P. Ybot‐González, 2014 .

Association of Human Beta-Defensin-2 Serum Levels and Sepsis in Preterm Neonates*

O. Neth, P. Olbrich, J. Praena-Fernández, 2013, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.