394 results on '"Soresina, Annarosa"'
Search Results
52. Prospective Study on CVID Patients with Adverse Reactions to Intravenous or Subcutaneous IgG Administration
53. La sindrome di Chediak-Higashi a esordio tardivo
54. Long-Term Follow-Up and Outcome of a Large Cohort of Patients with Common Variable Immunodeficiency
55. Mutational Analysis of Human BLyS in Patients with Common Variable Immunodeficiency
56. Mutational Analysis of Human BAFF Receptor TNFRSF13C (BAFF-R) in Patients with Common Variable Immunodeficiency
57. Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency
58. Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients
59. A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia
60. 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
61. Use of linezolid in infants and children: a retrospective multicentre study of the Italian Society for Paediatric Infectious Diseases
62. 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
63. Two X‐linked agammaglobulinemia patients develop pneumonia as COVID‐19 manifestation but recover
64. Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome
65. Unrelated hematopoietic stem cell transplantation for Cernunnos-XLF deficiency
66. Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings.
67. Primary atopic disorders and chronic skin disease.
68. Inherited defects in the complement system.
69. Sensorineural Hearing Loss in Primary Antibody Deficiency Disorders
70. Double-Blind, Placebo-Controlled Randomized Trial on Low Dose Azithromycin Prophilaxis in Primary Antibody Deficiencies
71. A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG
72. Genetic Causes of Bronchiectasis: Primary Immune Deficiencies and the Lung
73. The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency
74. Search for poliovirus long-term excretors among patients affected by agammaglobulinemia
75. Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay
76. Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients
77. 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)
78. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
79. Primary Immunodeficiencies and Oncological Risk: The Experience of the Children's Hospital of Brescia
80. Clinical, Immunological, and Molecular Analysis in a Large Cohort of Patients with X-Linked Agammaglobulinemia: An Italian Multicenter Study
81. Il contributo dell’Associazione italiana di ematologia e oncologia pediatrica (AIEOP) - The contribution of the Italian Association of paediatric haematology and oncology (AIEOP)
82. Immunological basis of virus‐host interaction in COVID‐19.
83. Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
84. Circulating Follicular Helper and Follicular Regulatory T Cells Are Severely Compromised in Human CD40 Deficiency: A Case Report
85. Oral Azitromycin Prophylaxis, 250 Mg Once Daily Three-Times a Week, in Primary Antibody Deficiencies: A Multicenter, Double-Blind, Placebo-Controlled Randomized Clinical Trial
86. Neurovisual Assessment in Children with Ataxia Telangiectasia
87. Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations
88. ATM splicing variants as biomarkers for low dose dexamethasone treatment of A-T
89. Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force
90. Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders
91. Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography
92. Impaired platelet activation in patients with hereditary deficiency of p47phox
93. Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease
94. Safety and Efficacy of Gadoxetate Disodium-enhanced Liver Mri in Pediatric Patients Aged >2 Months to <18 Years—Results of a Retrospective, Multicenter Study
95. NOX 5 is expressed in platelets from patients with chronic granulomatous disease
96. In vivo effects of dexamethasone on blood gene expression in ataxia telangiectasia.
97. Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia
98. Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial
99. Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects
100. Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study
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