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Unbiased assessment of genome integrity and purging of adverse outcomes at the target locus upon editing of CD4+ T‐cells for the treatment of Hyper IgM1

The EMBO journal, 2023-12, Vol.42 (23), p.e114188-n/a

2023

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The lack of either IRF9, or STAT2, has surprisingly little effect on human natural killer cell development and function

Immunology, 2024-07, Vol.172 (3), p.440-450

2024

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The complex nature of CXCR4 mutations in WHIM syndrome

Frontiers in immunology, 2024-07, Vol.15, p.1406532

2024

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Minimal-moderate variation of human oral virome and microbiome in IgA deficiency

Scientific reports, 2021-07, Vol.11 (1), p.14913-7, Article 14913

2021

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Prospective neonatal screening for severe T‐ and B‐lymphocyte deficiencies in Seville

Pediatric allergy and immunology, 2016-02, Vol.27 (1), p.70-77

2016

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Pyomyositis and bacteremia due to Staphylococcus aureus as onset of acute promyelocytic leukemia

Pediatrics international, 2015-10, Vol.57 (5), p.1053-1054

2015

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Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency

Journal of clinical immunology, 2022-04, Vol.42 (3), p.512-513

2022

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Acquired and Innate Immunity Impairment and Severe Disseminated Mycobacterium genavense Infection in a Patient With a NF-κB1 Deficiency

Frontiers in immunology, 2019-01, Vol.9, p.3148

2019

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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

Journal of allergy and clinical immunology, 2021-02, Vol.147 (2), p.520-531

2021

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Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

Scandinavian journal of immunology, 2019-06, Vol.89 (6), p.e12763-n/a

2019

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Extreme Phenotypes With Identical Mutations: Two Patients With Same Non-sense NHEJ1 Homozygous Mutation

Frontiers in immunology, 2019-01, Vol.9, p.2959-2959

2019

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Mendelian susceptibility to mycobacterial infection should be ruled out in Mycobacterium chelonae empyema

Annals of thoracic medicine, 2010-01, Vol.5 (1), p.55-55

González-Granado, Luis Ignacio

2010

Volltextzugriff (PDF)

Subcutaneous Route for Refractory Epilepsy

Pediatric neurology, 2013, Vol.48 (1), p.79-79

2013

Volltextzugriff (PDF)

Case report: Novel treatment regimen for enterovirus encephalitis in SCID

Frontiers in immunology, 2022-09, Vol.13

2022

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In Nonendemic Areas, Is Microscopy Better than Polymerase Chain Reaction for Diagnosis of Congenital Chagas Disease?

Clinical infectious diseases, 2010-01, Vol.50 (2), p.279-279

2010

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Altered CXCR4 dynamics at the cell membrane impairs directed cell migration in WHIM syndrome patients

Proceedings of the National Academy of Sciences - PNAS, 2022-05, Vol.119 (21), p.e2119483119-e2119483119

2022

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Impact of cytomegalovirus infection prior to hematopoietic stem cell transplantation in children with inborn errors of immunity

European journal of pediatrics, 2022-11, Vol.181 (11), p.3889-3898

2022

Volltextzugriff (PDF)

Fatal Pneumocystis jirovecii and Cytomegalovirus Infections in an Infant With Normal TRECs Count: Pitfalls of Newborn Screening for Severe Combined Immunodeficiency

The Pediatric infectious disease journal, 2019-02, Vol.38 (2), p.157

2019

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Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome

Journal of clinical immunology, 2016-05, Vol.36 (4), p.363-365

2016

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Primary immunodeficiency diseases in lung disease: warning signs, diagnosis and management

Respiratory research, 2018-11, Vol.19 (1), p.219-219, Article 219

2018

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Acute bacterial meningitis

The Lancet infectious diseases, 2010-09, Vol.10 (9), p.596-596

Gonzalez-Granado, Luis Ignacio

2010

Volltextzugriff (PDF)

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

iScience, 2023-06, Vol.26 (6), p.106818-106818, Article 106818

2023

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Subcutaneous Immunoglobulin in Refractory Juvenile Dermatomyositis

Pediatrics (Evanston), 2016-04, Vol.137 (4)

2016

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Chronic granulomatous disease caused by maternal uniparental isodisomy of chromosome 16

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2017-07, Vol.5 (4), p.1146-1148

2017

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Unbiased assessment of genome integrity and purging of adverse outcomes at the target locus upon editing of CD4+ T‐cells for the treatment of Hyper IgM1

The lack of either IRF9, or STAT2, has surprisingly little effect on human natural killer cell development and function

The complex nature of CXCR4 mutations in WHIM syndrome

Minimal-moderate variation of human oral virome and microbiome in IgA deficiency

Prospective neonatal screening for severe T‐ and B‐lymphocyte deficiencies in Seville

Pyomyositis and bacteremia due to Staphylococcus aureus as onset of acute promyelocytic leukemia

Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency

Acquired and Innate Immunity Impairment and Severe Disseminated Mycobacterium genavense Infection in a Patient With a NF-κB1 Deficiency

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

Extreme Phenotypes With Identical Mutations: Two Patients With Same Non-sense NHEJ1 Homozygous Mutation

Mendelian susceptibility to mycobacterial infection should be ruled out in Mycobacterium chelonae empyema

A Validated Highly Sensitive Microsatellite Instability Assay Accurately Identifies Individuals Harboring Biallelic Germline PMS2 Pathogenic Variants in Constitutional Mismatch Repair Deficiency

Subcutaneous Route for Refractory Epilepsy

Case report: Novel treatment regimen for enterovirus encephalitis in SCID

In Nonendemic Areas, Is Microscopy Better than Polymerase Chain Reaction for Diagnosis of Congenital Chagas Disease?

Altered CXCR4 dynamics at the cell membrane impairs directed cell migration in WHIM syndrome patients

Impact of cytomegalovirus infection prior to hematopoietic stem cell transplantation in children with inborn errors of immunity

Fatal Pneumocystis jirovecii and Cytomegalovirus Infections in an Infant With Normal TRECs Count: Pitfalls of Newborn Screening for Severe Combined Immunodeficiency

Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome

Primary immunodeficiency diseases in lung disease: warning signs, diagnosis and management

Acute bacterial meningitis

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

Subcutaneous Immunoglobulin in Refractory Juvenile Dermatomyositis

Chronic granulomatous disease caused by maternal uniparental isodisomy of chromosome 16

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