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Clinical Immunology (Orlando, Fla.)|March 18, 2018
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complicationsDomenico Umberto De Rose, Silvia Giliani, Lucia Dora Notarangelo, et al.
European Journal of Immunology|March 17, 2005
Damaging-agent sensitivity of Artemis-deficient cell linesAntonio Musio, Veronica Marrella, Cristina Sobacchi, et al.
Blood|September 25, 2007
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutationsPonpan Matangkasombut, Muriel Pichavant, Doris E Saez, et al.
Haematologica|April 13, 2004
Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic outputSilvia Pirovano, Luigi Daniele Notarangelo, Fabio Malacarne, et al.
Journal of Clinical Immunology|February 1, 2014
Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experienceSrdjan Pasic, Dragana Vujic, Dobrila Veljković, et al.
Current Opinion in Immunology|July 31, 2012
The role of induced pluripotent stem cells in research and therapy of primary immunodeficienciesKatja G Weinacht, Patrick M Brauer, Kerstin Felgentreff, et al.
Clinical Pharmacology and Therapeutics|April 4, 2020
Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From PatientsElena Genova, Federica Cavion, Marianna Lucafò, et al.
Stem Cell Research|November 4, 2019
Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2BRosalba Monica Ferraro, Stefania Masneri, Gaetana Lanzi, et al.
Dermatology and Therapy|November 7, 2019
Incontinentia Pigmenti Associated with Aplasia Cutis Congenita in a Newborn Male with Klinefelter Syndrome: Is the Severity of Neurological Involvement Linked to Skin Manifestations?Ruggero Moro, Antonella Fabiano, Piergiacomo Calzavara-Pinton, et al.
Stem Cell Research|October 24, 2019
Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1Rosalba Monica Ferraro, Gaetana Lanzi, Stefania Masneri, et al.
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