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1.
Transplantation after CD45-ADC corrects Rag1 immunodeficiency in congenic and haploidentical settings.
J Allergy Clin Immunol
; 153(1): 341-348.e3, 2024 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37567393
2.
Efficacy and safety of anti-CD45-saporin as conditioning agent for RAG deficiency.
J Allergy Clin Immunol
; 147(1): 309-320.e6, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32387109
3.
Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.
Minerva Pediatr
; 72(5): 393-407, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-32960006
4.
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy.
Clin Immunol
; 173: 121-123, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27713031
5.
Defining a new immune deficiency syndrome: MAN2B2-CDG.
J Allergy Clin Immunol
; 145(3): 1008-1011, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31775018
6.
F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.
J Allergy Clin Immunol
; 143(6): 2317-2321.e12, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30822429
7.
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency.
Sci Transl Med
; 16(733): eadh8162, 2024 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38324638
8.
Artificial thymic organoids represent a reliable tool to study T-cell differentiation in patients with severe T-cell lymphopenia.
Blood Adv
; 4(12): 2611-2616, 2020 06 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-32556283
9.
Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.
Front Pediatr
; 7: 353, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31508401
10.
Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.
Front Pediatr
; 7: 295, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31440487
11.
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.
Front Immunol
; 8: 1244, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-29042861
12.
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.
Front Immunol
; 8: 798, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28769923
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