M. Kanariou

发表

DOCK8 Functions as an Adaptor that Links TLR–MyD88 Signaling to B Cell Activation

Schneider, Douglas R. McDonald, Ghassan, 2012 .

DOCK 8 functions as an adaptor that links Toll-like receptor – MyD 88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012 .

Severe Combined Immunodeficiency in Greek Children over a 20-Year Period

S. Giliani, G. Chrousos, A. Villa, 2011, Journal of Clinical Immunology.

Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

L. Notarangelo, R. Geha, J. Chou, 2015, The Journal of allergy and clinical immunology.

Phenotype, penetrance, and treatment of 133 cytotoxic T‐lymphocyte antigen 4–insufficient subjects

O. Elemento, T. Giese, A. Schulz, 2018, The Journal of allergy and clinical immunology.

The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency.

T. Morio, A. Worth, Sophie Jung, 2016, The Journal of allergy and clinical immunology.

Factors for thyroid autoimmunity in children and adolescents with type 1 diabetes mellitus

K. Karavanaki, M. Kanariou, A. Fotinou, 2009, Upsala journal of medical sciences.

Successful Management of Cryopyrin-Associated Periodic Syndrome With Canakinumab in Infancy

M. Kanariou, I. Varela, I. Nikas, 2014, Pediatrics.

Absence of Bruton's tyrosine kinase (Btk) mutations in patients with acute myeloid leukaemia

G. Bourikas, P. Orlandi, P. Sideras, 1998, British journal of haematology.

Primary Immunodeficiency Diseases: A 30-year Patient Registry from the Referral Center for Primary Immunodeficiencies in Greece

M. Kanariou, A. Michos, M. Tzanoudaki, 2014, Journal of Clinical Immunology.

Is Rituximab-Associated Hypogammaglobulinemia Always Linked to B-Cell Depletion?

A. Soldatou, M. Kanariou, M. Tzanoudaki, 2022, Children.

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses

K. Stefanaki, M. Kanariou, M. Tzanoudaki, 2019, Journal of Clinical Immunology.

Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH

M. Tzetis, E. Kanavakis, P. Makrythanasis, 2010, Journal of Human Genetics.

Prevalence of antibodies to ganglioside and Hep 2 in Gaucher, Niemann – Pick type C and Sanfilippo diseases

M. Kanariou, H. Michelakakis, E. Dimitriou, 2019, Molecular genetics and metabolism reports.

Association of allergic sensitization with infectious diseases burden in Roma and non‐Roma children

E. Petridou, M. Giannaki, M. Kanariou, 2011, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Erythropoiesis defect observed in STAT3 GOF patients with severe anaemia.

E. Haralambieva, A. Šedivá, S. Ehl, 2019, The Journal of allergy and clinical immunology.

Schimke immunoosseous dysplasia: suggestions of genetic diversity

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

Serum immunoglobulin G subclasses in healthy infants and children in Greece

D. Trichopoulos, E. Petridou, M. Kanariou, 1997, European Journal of Epidemiology.

Therapeutic options for CTLA-4 Insufficiency.

V. Lougaris, T. Morio, K. Sullivan, 2021, The Journal of allergy and clinical immunology.

Long‐term outcomes of 176 patients with X‐linked hyper‐IgM syndrome treated with or without hematopoietic cell transplantation

L. Notarangelo, J. Chou, C. Cunningham-Rundles, 2017, The Journal of allergy and clinical immunology.

Serum eosinophil cationic protein and CD23 in acute RSV bronchiolitis.

A. Papadopoulou, M. Kanariou, P. Nicolaidou, 2005, Medical science monitor : international medical journal of experimental and clinical research.

The role of basophil activation test in allergic bronchopulmonary aspergillosis and Aspergillus fumigatus sensitization in cystic fibrosis patients.

E. Kanavakis, S. Doudounakis, C. Kanaka-Gantenbein, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Factors influencing serum immunoglobulin E levels in Greek children

D. Trichopoulos, E. Petridou, M. Kanariou, 1995, Allergy.

Elevated IgG4 Serum Levels Among Primary Sjögren's Syndrome Patients: Do They Unmask Underlying IgG4‐Related Disease?

D. Rontogianni, H. Moutsopoulos, M. Kanariou, 2014, Arthritis care & research.

Analysis of Btk Mutations in Patients with X‐Linked Agammaglobulinaemia (XLA) and Determination of Carrier Status in Normal Female Relatives: a Nationwide Study of Btk Deficiency in Greece

M. Vihinen, P. Sideras, M. Kanariou, 2001, Scandinavian journal of immunology.

A study on the effects of seasonal solar radiation on exposed populations.

S. Piperakis, M. Kanariou, S. Tsilimigaki, 2003, Mutagenesis.

Immunosuppression by immunoglobulin deaggregation is not effective in reducing the anti-xenogeneic immunoglobulin response: experimental and clinical studies.

M. Ritter, M. Kanariou, G. Sivolapenko, 1989, British Journal of Cancer.

Immune responses in children infected with the pinworm Enterobius vermicularis in central Greece

M. Kanariou, E. Piperaki, C. Tzoumaka-Bakoula, 2015, Journal of Helminthology.

CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome.

A. Villa, M. Vihinen, S. Giliani, 1996, Immunology today.

X‐linked thrombocytopenia in three males with normal sized platelets due to novel WAS gene mutations

M. Kanariou, E. Mantadakis, M. Tzanoudaki, 2014, Pediatric blood & cancer.

Screening for Associated Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus (T1DM)

K. Karavanaki, M. Kanariou, K. Kakleas, 2009, Hormone Research in Paediatrics.

Subacute vertebral osteomyelitis in a child with diabetes mellitus associated with Fusarium

F. Tzortzatou-Stathopoulou, M. Moschovi, M. Kanariou, 2004, Pediatrics International.

Long-term observational studies of chronic granulomatous disease

M. Kanariou, K. Spanou, Sofia Tantou, 2018, Current opinion in hematology.

Next Generation Sequencing Reveals Skewing of the T and B Cell Receptor Repertoires in Patients with Wiskott–Aldrich Syndrome

L. Notarangelo, K. Dobbs, S. Pai, 2014, Front. Immunol..

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.

Case Report: A Novel Synonymous ARPC1B Gene Mutation Causes a Syndrome of Combined Immunodeficiency, Asthma, and Allergy With Significant Intrafamilial Clinical Heterogeneity

J. Traeger-Synodinos, C. Kanaka-Gantenbein, M. Kanariou, 2021, Frontiers in Immunology.

Erratum to: Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece

D. Roos, M. Kanariou, M. Tzanoudaki, 2013, Journal of Clinical Immunology.

Novel genetic risk variants for pediatric celiac disease

B. Peters, R. Drmanac, G. Patrinos, 2016, Human Genomics.

Mechanisms of tolerance to parental parathyroid tissue when combined with human allogeneic thymus transplantation.

J. Olson, I. Chinn, F. Bonilla, 2010, The Journal of allergy and clinical immunology.

Temporal nutritional and inflammatory changes in children with severe head injury fed a regular or an immune-enhancing diet: A randomized, controlled trial

I. Papassotiriou, M. Kanariou, G. Briassoulis, 2006, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

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..

Ex Vivo Evaluation of Glutamine Treatment in Sepsis and Trauma in a Human Peripheral Blood Mononuclear Cells Model

G. Daikos, M. Kanariou, M. Tzanoudaki, 2023, Nutrients.

Modeling, optimization, and comparable efficacy of T cell and hematopoietic stem cell gene editing for treating hyper‐IgM syndrome

V. Lougaris, A. Plebani, P. Rancoita, 2021, EMBO molecular medicine.

Autosomal-dominant immune dysregulation syndrome in humans with CTLA4 mutations

A. Schäffer, R. Backofen, S. Ehl, 2014, Nature Medicine.

Primary Immunodeficiency Diseases: A 30-year Patient Registry from the Referral Center for Primary Immunodeficiencies in Greece

M. Kanariou, A. Michos, M. Tzanoudaki, 2014, Journal of Clinical Immunology.

Children with frequent infections: A proposal for a stepwise assessment and investigation of the immune system

D. Cassimos, M. Kanariou, M. Liatsis, 2009, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Erratum to: Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece

D. Roos, M. Kanariou, M. Tzanoudaki, 2014, Journal of Clinical Immunology.

Alopecia, Hypothyroidism, Leukopenia and Hypogammaglobulinemia

M. Kanariou, M. Tzanoudaki, Sofia Tantou, 2019, Pediatric Immunology.

Transporter Associated with Antigen Processing Deficiency Syndrome: Case Report of an Adolescent with Chronic Perforated Granulomatous Skin Lesions Due to TAP2 Mutation

A. Tosca, M. Kanariou, Athanasios Kokolakis, 2013, Pediatric dermatology.

Dock8 Functions as an Adaptor That Links Toll-like Receptor– Myd88 Signaling to B Cell Activation Hhs Public Access

Alessandro Plebani, Rima Wakim, Kate Fitzgerald, 2022 .

Hypogammaglobulinaemia associated with normal or increased IgM (the hyper IgM syndrome): a case series review.

N. Banatvala, R. Levinsky, S. Strobel, 1994, Archives of disease in childhood.

Mutation in the Class II trans-Activator Leading to a Mild Immunodeficiency1

N. Brousse, W. Wiszniewski, G. Barbieri, 2001, The Journal of Immunology.

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.

Mycophenolate mofetil as an alternate immunosuppressor for autoimmune lymphoproliferative syndrome.

F. Rieux-Laucat, M. Kanariou, F. Le Deist, 2006, Journal of pediatric hematology/oncology.

Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia

A. Plebani, C. Pignata, S. Reda, 2021, Journal of Clinical Immunology.

Abnormalities of T-cell receptor repertoire in CD4+ regulatory and conventional T cells in patients with RAG mutations: Implications for autoimmunity.

L. Notarangelo, J. Walter, L. Henderson, 2017, The Journal of allergy and clinical immunology.

M. Kanariou, C. Pitsios, G. Chouliaras, 2011, European Journal of Pediatrics.

Successful long-term immunologic reconstitution by allogeneic hematopoietic stem cell transplantation cures patients with autosomal dominant hyper-IgE syndrome.

F. Tzortzatou-Stathopoulou, E. Kanavakis, J. Traeger-Synodinos, 2010, The Journal of allergy and clinical immunology.

HLA class II high-resolution genotyping in Greek children with celiac disease and impact on disease susceptibility

E. Roma, M. Kanariou, J. Panayiotou, 2012, Pediatric Research.

Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

J. Litzman, Hanns-Martin Lorenz, G. Häcker, 2022, Frontiers in Immunology.

Short Stature, Prolonged Fever and Lymphoproliferation

M. Kanariou, K. Kotsonis, Sofia Tantou, 2019, Pediatric Immunology.

TNFRSF13B/TACI Alterations in Greek Patients with Antibody Deficiencies

M. Kanariou, M. Speletas, A. Germenis, 2011, Journal of Clinical Immunology.

Age patterns of immunoglobulins G, A & M in healthy children and the influence of breast feeding and vaccination status

D. Trichopoulos, E. Petridou, M. Kanariou, 1995, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

DOCK8 and STAT3 dependent inhibition of IgE isotype switching by TLR9 ligation in human B cells.

R. Geha, W. Al-Herz, T. Chatila, 2017, Clinical immunology.

Flow cytometric analysis of the CD4+ TCR Vβ repertoire in the peripheral blood of children with type 1 diabetes mellitus, systemic lupus erythematosus and age-matched healthy controls

G. Chrousos, C. Kanaka-Gantenbein, M. Kanariou, 2013, BMC Immunology.

Comparative effects of early randomized immune or non-immune-enhancing enteral nutrition on cytokine production in children with septic shock

M. Kanariou, G. Briassoulis, T. Hatzis, 2005, Intensive Care Medicine.

Glutamine May Repress the Weak LPS and Enhance the Strong Heat Shock Induction of Monocyte and Lymphocyte HSP72 Proteins but May Not Modulate the HSP72 mRNA in Patients with Sepsis or Trauma

G. Daikos, M. Kanariou, M. Tzanoudaki, 2015, BioMed research international.

Erratum: Mutation in the class II trans-activator leading to a mild immunodeficiency (The Journal of Immunology (2001) 167 (1787-1794))

A. Fischer, F. Deist, N. Brousse, 2002 .

Twenty Year Follow up of a Patient with a New De-Novo NLRP3 Mutation (S595G) and CINCA Syndrome

A. Rösen‐Wolff, V. Schuster, J. Roesler, 2009, Klinische Padiatrie.