E. Cirillo

发表

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

Carol J. Saunders, E. Farrow, C. Saunders, 2016, Front. Immunol..

Clinical Manifestations of 22q11.2 Deletion Syndrome.

G. Giardino, E. Cirillo, C. Pignata, 2021, Heart failure clinics.

Efficacy of very‐low‐dose betamethasone on neurological symptoms in ataxia‐telangiectasia

G. Giardino, E. Cirillo, C. Pignata, 2011, European journal of neurology.

Genetic Basis of Altered Central Tolerance and Autoimmune Diseases: A Lesson from AIRE Mutations

V. Gallo, G. Giardino, E. Cirillo, 2012, International reviews of immunology.

NADPH Oxidase Deficiency: A Multisystem Approach

V. Gallo, G. Giardino, E. Cirillo, 2017, Oxidative medicine and cellular longevity.

DiGeorge‐like syndrome in a child with a 3p12.3 deletion involving MIR4273 gene born to a mother with gestational diabetes mellitus

V. Gallo, G. Giardino, E. Cirillo, 2017, American journal of medical genetics. Part A.

Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey

V. Gallo, E. Cirillo, C. Pignata, 2018, American journal of medical genetics. Part A.

Complement system network in cell physiology and in human diseases

G. Giardino, E. Cirillo, C. Pignata, 2020, International reviews of immunology.

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.

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

A. Fischer, E. Cirillo, A. Plebani, 2011, Blood.

Different Degrees of NADPH Oxidase 2 Regulation and In Vivo Platelet Activation: Lesson From Chronic Granulomatous Disease

E. Cirillo, A. Plebani, C. Pignata, 2014, Journal of the American Heart Association.

Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET).

V. Gallo, E. Cirillo, R. Badolato, 2018, Vaccine.

In ataxia‐teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity

E. Cirillo, C. Pignata, A. Fusco, 2009, European journal of neurology.

Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies

V. Gallo, G. Giardino, E. Cirillo, 2015, International reviews of immunology.

Unbalanced Immune System: Immunodeficiencies and Autoimmunity

V. Gallo, G. Giardino, E. Cirillo, 2016, Front. Pediatr..

Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet)

E. Cirillo, A. Plebani, C. Pignata, 2019, Journal of Clinical Immunology.

B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand.

F. Fusco, V. Gallo, G. Giardino, 2015, Clinical immunology.

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

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

Recurrent Cold Suppurative Granulomatous Lymphadenitis

V. Gallo, G. Giardino, E. Cirillo, 2019, Pediatric Immunology.

Altered signaling through IL-12 receptor in children with very high serum IgE levels.

G. Giardino, E. Cirillo, C. Pignata, 2010, Cellular immunology.

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

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

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 .

Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet)

E. Cirillo, A. Plebani, C. Pignata, 2019, Journal of Clinical Immunology.

Oral Thrush and Onychomycosis

V. Gallo, G. Giardino, E. Cirillo, 2019, Pediatric Immunology.

Reduced Atherosclerotic Burden in Subjects With Genetically Determined Low Oxidative Stress

E. Cirillo, A. Plebani, C. Pignata, 2013, Arteriosclerosis, thrombosis, and vascular biology.

T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy

V. Gallo, G. Giardino, E. Cirillo, 2022, Genetic Syndromes.

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

F. Benfenati, A. E. Sousa, G. Giardino, 2021, Journal of Clinical Immunology.

T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features

G. Giardino, E. Cirillo, C. Pignata, 2020, Frontiers in Immunology.

Rare inborn errors of immunity: new insights in molecular basis, diagnosis and treatment

E. Cirillo, 2017 .

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches

V. Gallo, G. Giardino, E. Cirillo, 2017, Journal of Clinical Immunology.

Severe combined immunodeficiency—an update

V. Gallo, G. Giardino, E. Cirillo, 2015, Annals of the New York Academy of Sciences.

Severe Combined Immunodeficiences: New and Old Scenarios

V. Gallo, G. Giardino, E. Cirillo, 2012, International reviews of immunology.

Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination

S. Pittaluga, L. Notarangelo, G. Giardino, 2022, Frontiers in Immunology.

Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task.

G. Giardino, E. Cirillo, C. Pignata, 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Novel Findings into AIRE Genetics and Functioning: Clinical Implications

E. Cirillo, C. Pignata, M. Salerno, 2016, Front. Pediatr..

Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels

C. Saunders, V. Gallo, G. Giardino, 2020, Journal of clinical medicine.

Epigenetic Alterations in Inborn Errors of Immunity

N. Brunetti‐Pierri, G. Giardino, E. Cirillo, 2022, Journal of clinical medicine.

De novo 13q12.3–q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A‐T like phenotype

G. Giardino, E. Cirillo, C. Pignata, 2012, American journal of medical genetics. Part A.

γ Chain transducing element: a shared pathway between endocrine and immune system.

E. Cirillo, C. Pignata, L. Palamaro, 2011, Cellular immunology.

1-1-2016 Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

Alessandro, E. Farrow, C. Saunders, 2019 .

Novel STAT1 gain‐of‐function mutation and suppurative infections

G. Giardino, E. Cirillo, A. Leonardi, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

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

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..

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

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

Clinical phenotype, immunological abnormalities and genomic findings in patients with DiGeorge spectrum phenotype without 22q11.2 deletion.

G. Giardino, E. Cirillo, C. Pignata, 2020, The journal of allergy and clinical immunology. In practice.

Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children

V. Gallo, E. Cirillo, C. Pignata, 2018, European Journal of Pediatrics.

Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature

E. Cirillo, C. Pignata, M. Salerno, 2014, BMC Pediatrics.

Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome

V. Gallo, G. Giardino, E. Cirillo, 2014, Scandinavian journal of gastroenterology.

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.

Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause

V. Poggi, V. Gallo, G. Giardino, 2013, British journal of haematology.

SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways

G. Giardino, E. Cirillo, C. Pignata, 2021, The Journal of Allergy and Clinical Immunology: In Practice.

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.

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.

Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts

E. Cirillo, C. Pignata, P. Soler-Palacín, 2023, Cancer medicine.

In Ataxia-Telangiectasia, Oral Betamethasone Administration Ameliorates Lymphocytes Functionality through Modulation of the IL-7/IL-7Rα Axis Paralleling the Neurological Behavior: A Comparative Report of Two Cases

V. Gallo, G. Giardino, E. Cirillo, 2020, Immunological investigations.

Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia‐telangiectasia: a multicenter observer‐blind study

E. Cirillo, C. Pignata, R. Micheli, 2018, European journal of neurology.

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches

V. Gallo, G. Giardino, E. Cirillo, 2017, Journal of Clinical Immunology.

Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort.

G. Giardino, E. Cirillo, C. Pignata, 2021, Archivos de bronconeumologia.

CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations

G. Giardino, E. Cirillo, C. Pignata, 2020, Frontiers in Immunology.

Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature

G. Giardino, E. Cirillo, C. Pignata, 2023, Frontiers in Immunology.

Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job’s syndrome

L. Dotta, G. Giardino, E. Cirillo, 2023, Allergy, Asthma & Clinical Immunology.

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

A. Fischer, E. Cirillo, A. Plebani, 2011, Blood.

A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype-phenotype Association.

E. Cirillo, R. Badolato, C. Pignata, 2023, Journal of clinical immunology.