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4123 POSTER “The Breathing Tree Project” Biofeedback and Stress Mitigation in Children With Cancer

European journal of cancer (1990), 2011, Vol.47, p.S290-S290

2011

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Reversible Severe Combined Immunodeficiency Phenotype Secondary to a Mutation of the Proton-Coupled Folate Transporter

Journal of allergy and clinical immunology, 2009-02, Vol.123 (2), p.S67-S67

2009

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Hypomorphic Rag1 mutations alter the preimmune repertoire at early stages of lymphoid development

Blood, 2018-07, Vol.132 (3), p.281-292

2018

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Novel Presentation of Omenn Syndrome in Association with Aniridia

Journal of allergy and clinical immunology, 2008-02, Vol.121 (2), p.S89-S89

2008

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Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)

Blood cells, molecules, & diseases, 2024-09, Vol.108, p.102860, Article 102860

2024

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PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients

Genes and immunity, 2010-12, Vol.11 (8), p.665-670

2010

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A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation

Genes and immunity, 2015-03, Vol.16 (2), p.151-161

2015

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First report of successful stem cell transplantation in a child with CD40 deficiency

Bone marrow transplantation (Basingstoke), 2007-08, Vol.40 (3), p.279-281

2007

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Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism

Human genetics, 2000-01, Vol.106 (1), p.73-79

2000

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Organization of the Human CD40L Gene: Implications for Molecular Defects in X Chromosome-Linked Hyper-IgM Syndrome and Prenatal Diagnosis

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (6), p.2110-2114

1994

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Incest by father or by brother? A case report

International Congress series, 2006-04, Vol.1288, p.453-455

2006

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Frasier syndrome with childhood-onset renal failure

Hormone research, 2001-01, Vol.55 (2), p.77-80

2001

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Immune reconstitution after in utero bone marrow transplantation in a fetus with severe combined immunodeficiency with natural killer cells

Transplantation proceedings, 1999-09, Vol.31 (6), p.2581-2581

1999

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Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis

Prenatal diagnosis, 2000-10, Vol.20 (10), p.822-823

2000

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Primary immunodeficiency with microcephalia: Report of eight cases

Molecular immunology, 1998-08, Vol.35 (11), p.743-743

1998

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Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome

Molecular immunology, 1998-08, Vol.35 (11), p.796-796

1998

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Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome

Molecular immunology, 1998-08, Vol.35 (11), p.665-665

1998

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The spleen in the wiskott-aldrich syndrome: White pulp changes correlate with the clinical phenotype of the disease

Molecular immunology, 1998-08, Vol.35 (11), p.733-733

1998

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Defective actin polymerization in patients with the Wiskott-Aldrich syndrome

Molecular immunology, 1998-08, Vol.35 (11), p.734-734

1998

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Molecular analysis in X-linked agamaglobulinemia: Results of an Italian multicenter study

Molecular immunology, 1998-08, Vol.35 (11), p.719-719

1998

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Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism

Human genetics, 2000-01, Vol.106 (1), p.73-79

2000

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Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole

Molecular immunology, 1998-08, Vol.35 (11), p.786-786

1998

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Identification of novel RFLPs in the vicinity of CpG islands in Xq28 : application to the analysis of the pattern of X chromosome inactivation

American journal of human genetics, 1992, Vol.50 (1), p.156-163

1992

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Mutations in the JAK3-gene in children with autosomal recessive T-B+ SCIDin the JAK3-gene in children with autosomal recessive T-B+ SCID

Molecular immunology, 1998-08, Vol.35 (11), p.713-713

1998

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Successful haploidentical transplant in a SCID T-B-NK+ by coinfusion of purified CD34+ and stromal cells

Molecular immunology, 1998-08, Vol.35 (11), p.771-771

1998

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4123 POSTER “The Breathing Tree Project” Biofeedback and Stress Mitigation in Children With Cancer

Reversible Severe Combined Immunodeficiency Phenotype Secondary to a Mutation of the Proton-Coupled Folate Transporter

Hypomorphic Rag1 mutations alter the preimmune repertoire at early stages of lymphoid development

Novel Presentation of Omenn Syndrome in Association with Aniridia

Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)

PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients

A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation

First report of successful stem cell transplantation in a child with CD40 deficiency

Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism

Organization of the Human CD40L Gene: Implications for Molecular Defects in X Chromosome-Linked Hyper-IgM Syndrome and Prenatal Diagnosis

Incest by father or by brother? A case report

Frasier syndrome with childhood-onset renal failure

Immune reconstitution after in utero bone marrow transplantation in a fetus with severe combined immunodeficiency with natural killer cells

Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis

Primary immunodeficiency with microcephalia: Report of eight cases

Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome

Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome

The spleen in the wiskott-aldrich syndrome: White pulp changes correlate with the clinical phenotype of the disease

Defective actin polymerization in patients with the Wiskott-Aldrich syndrome

Molecular analysis in X-linked agamaglobulinemia: Results of an Italian multicenter study

Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism

Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole

Identification of novel RFLPs in the vicinity of CpG islands in Xq28 : application to the analysis of the pattern of X chromosome inactivation

Mutations in the JAK3-gene in children with autosomal recessive T-B+ SCIDin the JAK3-gene in children with autosomal recessive T-B+ SCID

Successful haploidentical transplant in a SCID T-B-NK+ by coinfusion of purified CD34+ and stromal cells

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