C. Cancrini

发表

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

F. Alt, M. Vihinen, L. Notarangelo, 2013, The Journal of allergy and clinical immunology.

Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome

C. Cancrini, S. C. Mannurita, E. Gambineri, 2012, Journal of autoimmunity.

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

Ivan K. Chinn, Eric A. Smith, J. Lupski, 2017, The Journal of allergy and clinical immunology.

In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells

C. Cancrini, L. Biasco, M. Roncarolo, 2015, Science Translational Medicine.

Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia

C. Cancrini, L. Racioppi, G. Matarese, 2001, Clinical and experimental immunology.

Analysis of HIV-1 reverse transcriptase gene mutations in infected children treated with zidovudine.

C. Cancrini, P. Orlandi, P. Rossi, 1998, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.

Evidence of Clonotypic Pattern of T‐Cell Repertoire in Synovial Fluid of Children with Juvenile Rheumatoid Arthritis at the Onset of the Disease

C. Cancrini, P. Rossi, F. Angelini, 2002, Scandinavian journal of immunology.

Liver transplantation: expanding the donor pool.

C. Cancrini, P. Berloco, R. Cortesini, 2001, Transplantation proceedings.

Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome

C. Cancrini, F. Candotti, C. Granata, 2019, Journal of Clinical Immunology.

NK cell effector functions in a Chédiak-Higashi patient undergoing cord blood transplantation: Effects of in vitro treatment with IL-2.

C. Cancrini, A. Santoni, A. Gismondi, 2016, Immunology letters.

In vivo T-cell dynamics during immune reconstitution after hematopoietic stem cell gene therapy in adenosine deaminase severe combined immune deficiency.

C. Cancrini, A. Aiuti, B. Cassani, 2011, The Journal of allergy and clinical immunology.

Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID

C. Cancrini, M. Roncarolo, A. Aiuti, 2010, Haematologica.

Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections

C. Cancrini, P. Rossi, F. Angelini, 2002, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Inborn errors of immunity with atopic phenotypes: A practical guide for allergists

G. Giardino, V. Lougaris, C. Cancrini, 2021, The World Allergy Organization journal.

How to dissect the plasticity of antigen‐specific immune response: a tissue perspective

P. Palma, C. Cancrini, P. Rossi, 2020, Clinical and experimental immunology.

Consensus statement of the Italian society of pediatric allergy and immunology for the pragmatic management of children and adolescents with allergic or immunological diseases during the COVID-19 pandemic

S. Rizzi, Paolo Rosso, D. Caimmi, 2020, Italian Journal of Pediatrics.

First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia

C. Cancrini, M. Chiriacò, A. Aiuti, 2019, Front. Immunol..

Rapid disease progression in HIV-1 perinatally infected children born to mothers receiving zidovudine monotherapy during pregnancy. The Italian register for HIV Infection in Children.

R. Consolini, C. Pignata, C. Cancrini, 1999, AIDS.

The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)

G. Giardino, E. Cirillo, V. Lougaris, 2022, Journal of Clinical Immunology.

Successful Allogeneic Hemopoietic Stem Cell Transplantation in a Child Who Had Anhidrotic Ectodermal Dysplasia With Immunodeficiency

A. Fischer, C. Bodemer, J. Casanova, 2006, Pediatrics.

A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency.

A. Fischer, A. Smahi, G. Courtois, 2003, The Journal of clinical investigation.

Virological and immunological features of SARS-CoV-2-infected children who develop neutralizing antibodies

A. Jenkner, C. Giaquinto, P. Palma, 2021, Cell Reports.

IgE Immunoadsorption Knocks Down the Risk of Food-Related Anaphylaxis

C. Cancrini, A. Fiocchi, L. Dahdah, 2015, Pediatrics.

Successful simplification of protease inhibitor-based HAART with triple nucleoside regimens in children vertically infected with HIV

P. Palma, C. Cancrini, C. Montesano, 2007, AIDS.

Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations.

L. Notarangelo, C. Picard, P. Soler-Palacín, 2019, Clinical immunology.

Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients

C. Cancrini, M. Chiriacò, P. Merli, 2021, Journal of clinical immunology.

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

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

Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma.

C. Cancrini, F. Locatelli, A. Aiuti, 2016, The Journal of allergy and clinical immunology.

Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients

C. Cancrini, M. Digilio, R. Capolino, 2015, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment.

E. Stupka, D. Lazarević, P. Palma, 2017, Clinical immunology.

Wiskott-Aldrich syndrome protein–mediated actin dynamics control type-I interferon production in plasmacytoid dendritic cells

M. van der Burg, L. Notarangelo, C. Cancrini, 2013, The Journal of experimental medicine.

Prognostic Value of a CCR5 Defective Allele in Pediatric HIV-1 Infection

C. Cancrini, A. Amoroso, P. Orlandi, 2000, Molecular medicine.

The Impact of TACI Mutations: From Hypogammaglobulinemia in Infancy to Autoimmunity in Adulthood

C. Cancrini, M. Bengala, R. Miniero, 2012, International journal of immunopathology and pharmacology.

NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential.

V. Lougaris, A. Plebani, C. Cancrini, 2019, Clinical immunology.

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

A. Schulz, C. Cancrini, J. Litzman, 2009, The Journal of experimental medicine.

Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

D. Lazarević, C. Pignata, S. Giliani, 2019, Front. Immunol..

Structural defects and variations in the HIV‐1 nef gene from rapid, slow and non‐progressor children

C. Cancrini, G. Scarlatti, A. Plebani, 2003, AIDS.

JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long‐known gene

C. Cancrini, M. Chiriacò, A. Aiuti, 2018, Molecular genetics & genomic medicine.

Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants

C. Cancrini, M. Tartaglia, A. Yoshimi, 2022, Human Genomics.

Prognostic value of the stromal cell-derived factor 1 3'A mutation in pediatric human immunodeficiency virus type 1 infection.

C. Cancrini, A. Amoroso, M. Boniotto, 2002, The Journal of infectious diseases.

Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report

P. Palma, C. Cancrini, A. Deodati, 2022, Frontiers in Immunology.

Effect of HLA compatibility, pregnancies, blood transfusions, and taboo mismatches in living unrelated kidney transplantation.

C. Cancrini, P. Berloco, R. Cortesini, 2001, Transplantation proceedings.

A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation

A. Fischer, J. Casanova, C. Cancrini, 2020, Journal of Clinical Immunology.

Relapsing Campylobacter jejuni Systemic Infections in a Child with X-Linked Agammaglobulinemia

C. Cancrini, C. Russo, P. D’argenio, 2013, Case reports in pediatrics.

Thymic Epithelium Abnormalities in DiGeorge and Down Syndrome Patients Contribute to Dysregulation in T Cell Development

L. Notarangelo, C. Cancrini, S. Bergante, 2019, Front. Immunol..

Schimke immunoosseous dysplasia: suggestions of genetic diversity

C. Cancrini, C. Boerkoel, J. Ehrich, 2007, Human mutation.

Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene

S. Giliani, P. Palma, C. Cancrini, 2020, Journal of leukocyte biology.

Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency

P. Palma, C. Cancrini, A. Aiuti, 2015, Journal of Clinical Immunology.

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)

C. Cancrini, R. Carsetti, P. Rossi, 2006, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome

C. Cancrini, R. Carsetti, P. Rossi, 2006 .

Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency

G. Giardino, E. Cirillo, V. Lougaris, 2021, bioRxiv.

Targeted treatment of autoimmune cytopenias in primary immunodeficiencies

G. Giardino, C. Pignata, P. Palma, 2022, Frontiers in Immunology.

Update in primary immunodeficiencies

C. Cancrini, G. Marseglia, S. Manti, 2020, Acta bio-medica : Atenei Parmensis.

Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies

P. Palma, C. Cancrini, M. Chiriacò, 2019, Front. Immunol..

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis

K. Schwarz, A. Fischer, A. Schulz, 2017, The Journal of allergy and clinical immunology.

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

G. Scarano, V. Gallo, G. Giardino, 2014, BMC Medical Genetics.

Bruton's tyrosine kinase defect in dendritic cells from X‐linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen‐presenting cell function

C. Cancrini, T. Miyawaki, M. Gagliardi, 2003, Clinical and experimental immunology.

Early-onset monocyte-B-natural killer-dendritic cells' deficiency successfully treated with hematopoietic stem cell transplantation.

A. Fischer, P. Palma, C. Cancrini, 2011, The Journal of allergy and clinical immunology.

Serum leptin and CD4+ T lymphocytes in HIV+ children during highly active antiretroviral therapy

C. Cancrini, L. Racioppi, G. Matarese, 2002, Clinical endocrinology.

Restriction in T‐Cell Receptor Repertoire in a Patient Affected by Trichothiodystrophy and CD4+ Lymphopenia

C. Cancrini, L. Racioppi, P. Rossi, 2002, Scandinavian journal of immunology.

HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders.

C. Cancrini, S. Rutella, F. Locatelli, 2014, Blood.

Case Report: Successful Treatment With Monoclonal Antibodies in One APDS Patient With Prolonged SARS-CoV-2 Infection Not Responsive to Previous Lines of Treatment

P. Palma, C. Cancrini, C. Russo, 2022, Frontiers in Immunology.

B‐cell activation with CD40L or CpG measures the function of B‐cell subsets and identifies specific defects in immunodeficient patients

C. Cancrini, M. Scarsella, O. Grimsholm, 2017, European journal of immunology.

Long Term Longitudinal Follow up of AD-HIES Cohort: Impact of Early Diagnosis and Enrolment to IPINet Centres on Natural History of Job Syndrome

L. Dotta, G. Giardino, E. Cirillo, 2022 .

In Search for the Missing Link in APECED-like Conditions: Analysis of the AIRE Gene in a Series of 48 Patients

C. Cancrini, M. Cappa, A. Fierabracci, 2022, Journal of clinical medicine.

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

A. Fischer, C. Picard, P. Soler-Palacín, 2018, Front. Immunol..

Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature

C. Cancrini, M. Tartaglia, M. Chiriacò, 2021, Journal of Clinical Immunology.

Accumulation of peripheral autoreactive B cells in the absence of functional human regulatory T cells.

H. Ochs, T. Torgerson, C. Cancrini, 2013, Blood.

Urogenital Abnormalities in Adenosine Deaminase Deficiency

A. Salonia, C. Cancrini, A. Aiuti, 2020, Journal of 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.

Hematopoietic stem cell gene therapy for the cure of blood diseases: primary immunodeficiencies

C. Cancrini, A. Aiuti, F. Ferrua, 2018, Rendiconti Lincei. Scienze Fisiche e Naturali.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature

C. Cancrini, P. Williamson, L. Romani, 2021, Frontiers in Immunology.

One-lung Ventilation in a Child with Hyper-IgE Syndrome

R. Badolato, P. Palma, C. Cancrini, 2018, Annals of Case Reports.

A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function

Ivan K. Chinn, J. Lupski, R. Gibbs, 2019, The Journal of experimental medicine.

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

Bodo Grimbacher, James Curtis, Siobhan O. Burns, 2017, The Journal of allergy and clinical immunology.

Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders

C. Cancrini, A. Nordgren, M. Irving, 2021, American journal of medical genetics. Part A.

Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience.

C. Cancrini, S. Martelossi, A. Barabino, 2020, Inflammatory bowel diseases.

Immune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO gene.

Douglas R. McDonald, L. Notarangelo, R. Geha, 2010, The Journal of allergy and clinical immunology.

A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

A. Fischer, F. Deist, A. Smahi, 2003 .

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

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.

A. Fischer, W. Friedrich, L. Notarangelo, 2012, Blood.

Humoral and Cellular Response Following Vaccination With the BNT162b2 mRNA COVID-19 Vaccine in Patients Affected by Primary Immunodeficiencies

P. Palma, C. Cancrini, M. L. Ciofi Degli Atti, 2021, Frontiers in Immunology.

Waning of vaccine-induced immunity to measles in kidney transplanted children

P. Palma, C. Cancrini, L. Dello Strologo, 2016, Medicine.

Premature Senescence and Increased Oxidative Stress in the Thymus of Down Syndrome Patients

C. Cancrini, S. Bergante, M. Genua, 2021, Frontiers in Immunology.

Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency

P. Palma, C. Cancrini, A. Aiuti, 2015, Journal of Clinical Immunology.

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, J. Casanova, 2022, medRxiv.

The Interplay between CD27dull and CD27bright B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory.

A. N. Davydov, V. Lougaris, A. Plebani, 2020, Cell reports.

Human B‐cell memory is shaped by age‐ and tissue‐specific T‐independent and GC‐dependent events

C. Cancrini, M. Scarsella, S. Ceccarelli, 2017, European journal of immunology.

Etiology, clinical outcome, and laboratory features in children with neutropenia: Analysis of 104 cases

P. Palma, C. Cancrini, A. Aiuti, 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Rapid T-cell Receptor CD4+ Repertoire Reconstitution and Immune Recovery in Unrelated Umbilical Cord Blood Transplanted Pediatric Leukemia Patients

C. Cancrini, P. Rossi, M. Caniglia, 2006, Journal of pediatric hematology/oncology.

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

J. B. Oliveira, R. Gelman, L. Notarangelo, 2015, The Journal of clinical investigation.

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.

E. Cirillo, R. Consolini, A. Plebani, 2014, The Journal of pediatrics.

Post-Natal Ontogenesis of the T-Cell Receptor CD4 and CD8 Vβ Repertoire and Immune Function in Children with DiGeorge Syndrome

C. Cancrini, P. Rossi, S. Pahwa, 2005, Journal of Clinical 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 .

Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?

P. Palma, C. Cancrini, A. Bruselles, 2022, Frontiers in Immunology.

Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience

P. Palma, C. Cancrini, M. Chiriacò, 2017, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

G. Giardino, E. Cirillo, V. Lougaris, 2019, Front. Immunol..

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency.

L. Notarangelo, J. Walter, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Characterization of T and B cell repertoire diversity in patients with RAG deficiency

Hao Wu, L. Notarangelo, J. Walter, 2016, Science Immunology.

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

J. B. Oliveira, R. Gelman, L. Notarangelo, 2016, The Journal of clinical investigation.

Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement

Massimiliano Valeriani, C. Saunders, G. Giardino, 2017, Front. Immunol..

The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant.

C. Cancrini, F. Di Girolamo, E. Bellacchio, 2014, Gene.

Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

D. Lazarević, C. Pignata, S. Giliani, 2019, Front. Immunol..

The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)

V. Lougaris, R. Consolini, A. Plebani, 2020, Journal of Clinical Immunology.

Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells

C. Cancrini, M. Pastore, M. Chiriacò, 2017, Front. Immunol..

DNAM-1 Activating Receptor and Its Ligands: How Do Viruses Affect the NK Cell-Mediated Immune Surveillance during the Various Phases of Infection?

P. Palma, C. Cancrini, S. Zicari, 2019, International journal of molecular sciences.

Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.

L. Dotta, G. Giardino, A. Plebani, 2019, The journal of allergy and clinical immunology. In practice.

Delayed early antiretroviral treatment is associated with an HIV-specific long-term cellular response in HIV-1 vertically infected infants.

P. Palma, C. Cancrini, C. Montesano, 2008, Vaccine.

Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality.

E. Cirillo, V. Lougaris, R. Consolini, 2020, The Journal of allergy and clinical immunology.

Mechanisms of genotype‐phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

J. Casanova, R. Geha, H. Kanegane, 2017, The Journal of allergy and clinical immunology.

disease and greater impairment of NF-κB activation in IκBa point mutants versus truncation mutants in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

J. Casanova, R. Geha, H. Kanegane, 2017 .

Host Defenses to Viruses: Lessons from Inborn Errors of Immunity

C. Cancrini, G. Marseglia, C. Caffarelli, 2022, Medicina.

Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anticytokine antibodies.

J. Walter, P. Palma, C. Cancrini, 2018, The journal of allergy and clinical immunology. In practice.

How CD4+ T Cells Transcriptional Profile Is Affected by Culture Conditions: Towards the Design of Optimal In Vitro HIV Reactivation Assays

P. Palma, C. Cancrini, M. Lichterfeld, 2023, Biomedicines.

Rituximab unveils hypogammaglobulinemia and immunodeficiency in children with autoimmune cytopenia.

V. Gallo, C. Pignata, C. Cancrini, 2019, The journal of allergy and clinical immunology. In practice.

Inherited defects in the complement system

G. Giardino, V. Lougaris, C. Cancrini, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome.

G. Giardino, R. Consolini, A. Plebani, 2019, The journal of allergy and clinical immunology. In practice.

Cardiopulmonary anomalies in incontinentia pigmenti patients

C. Cancrini, P. D’argenio, L. Iughetti, 2018, International journal of dermatology.

Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature

C. Cancrini, M. Tartaglia, M. Chiriacò, 2021, Journal of Clinical Immunology.

Consensus of the Italian Primary Immunodeficiency Network on Transition Management from Pediatric to Adult Care in Patients Affected with Childhood Onset Inborn Errors of Immunity.

L. Dotta, G. Giardino, E. Cirillo, 2020, The Journal of allergy and clinical immunology.

Late‐onset combined immune deficiency due to LIGIV mutations in a 12‐year‐old patient

C. Cancrini, A. Antoccia, M. Chiriacò, 2017, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Lymphocytes are a major source of circulating soluble dipeptidyl peptidase 4

C. Cancrini, A. Casrouge, S. Sánchez-Ramón, 2018, Clinical and experimental immunology.

Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies

P. Soler-Palacín, C. Cancrini, S. Ehl, 2020, The Journal of Immunology.

Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches.

G. Giardino, V. Lougaris, C. Pignata, 2023, Clinical immunology.

Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up

P. Palma, C. Cancrini, M. Chiriacò, 2021, Frontiers in Pediatrics.

Theophylline as a precision therapy in a young girl with PIK3R1 immunodeficiency.

C. Cancrini, M. Lucafò, A. Tommasini, 2018, The journal of allergy and clinical immunology. In practice.

Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature.

C. Pignata, C. Cancrini, A. Ugazio, 2013, Journal of biological regulators and homeostatic agents.

Consanguinity and Polygenic Diseases: A Model for Antibody Deficiencies

C. Cancrini, P. Rossi, S. Ferrari, 2014, Human Heredity.

Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment

P. Palma, C. Cancrini, M. Chiriacò, 2019, Front. Immunol..

Role of immunity in maternal—infant HIV‐1 transmission

E. Halapi, C. Cancrini, P. Orlandi, 1997, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Kinetics of the T-cell receptor CD4 and CD8 Vβ repertoire in HIV-1 vertically infected infants early treated with HAART

E. Halapi, C. Cancrini, P. Rossi, 2001, AIDS.

Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia.

C. Cancrini, L. Chessa, S. Di Cesare, 2021, Clinical immunology.

Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity

G. Giardino, V. Lougaris, A. Plebani, 2021, The Journal of Allergy and Clinical Immunology: In Practice.

Tailored treatments in inborn errors of immunity associated with atopy (IEIs-A) with skin involvement

C. Cancrini, A. Finocchi, M. El Hachem, 2023, Frontiers in Pediatrics.

Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network

G. Giardino, E. Cirillo, V. Lougaris, 2022, Journal of Clinical Immunology.

Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child With Intermittent Neutropenia

P. Palma, C. Cancrini, M. Chiriacò, 2019, Journal of pediatric hematology/oncology.

Serratia marcescens osteomyelitis in a newborn with chronic granulomatous disease.

P. Palma, C. Cancrini, Valentina Capo, 2013, The Pediatric infectious disease journal.

[Relationship between blood fibrinogen and plasma lipoproteins in patients with hypercholesterolemia].

C. Cancrini, S. Basili, M. Vieri, 1994, Minerva medica.

The Role of NK Cells in EBV Infection and Related Diseases: Current Understanding and Hints for Novel Therapies

C. Cancrini, M. Doria, D. Covino, 2023, Cancers.

Activated phosphoinositide 3‐dinase delta syndrome (APDS): An update

G. Giardino, V. Lougaris, C. Cancrini, 2022, Pediatric Allergy and Immunology.

Switching from protease inhibitor-based-HAART to a protease inhibitor-sparing regimen is associated with improved specific HIV-immune responses in HIV-infected children

P. Palma, C. Cancrini, P. Rossi, 2006, AIDS.

Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome

C. Cancrini, F. Candotti, C. Granata, 2019, Journal of Clinical Immunology.

Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection

A. Jenkner, E. Stupka, D. Lazarević, 2016, Journal of Clinical Immunology.

Immunological basis of virus‐host interaction in COVID‐19

G. Giardino, V. Lougaris, C. Cancrini, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[Perinatal infections of B19 Parvoviruses]

A. Di Paolo, C. Cancrini, P. Rossi, 2002, Igiene e sanita pubblica.

Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy.

L. Notarangelo, C. Cancrini, Y. Yamazaki, 2016, Clinical immunology.

Severe Toxoplasma gondii infection in a member of a NFKB2-deficient family with T and B cell dysfunction.

C. Cancrini, G. Colafati, M. Chiriacò, 2017, Clinical Immunology.

SARS‐CoV‐2 infection and treatment in a cohort of patients with inborn errors of immunity

P. Palma, C. Cancrini, A. Pession, 2022, Pediatric Allergy and Immunology.

Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept.

R. Cozza, C. Cancrini, M. Rinelli, 2021, European journal of gastroenterology & hepatology.

Immune reconstitution in paediatric patients with acquired immunodeficiency

C. Cancrini, F. Chiodi, S. Pensieroso, 2008 .