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1. Full Text X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
by Aadam, Zahra and Kechout, Nadia and Barakat, Abdelhamid and Chan, Koon-Wing and Ben-Ali, Meriem and Ben-Mustapha, Imen and Zidi, Fethi and Ailal, Fatima and Attal, Nabila and Doudou, Fatouma and Abbadi, Mohamed-Cherif and Kaddache, Chawki and Smati, Leila and Touri, Nabila and Chemli, Jalel and Gargah, Tahar and Brini, Ines and Bakhchane, Amina and Charoute, Hicham and Jeddane, Leila and El Atiqi, Sara and El Hafidi, Naïma and Hida, Mustapha and Saile, Rachid and Alj, Hanane Salih and Boukari, Rachida and Bejaoui, Mohamed and Najib, Jilali and Barbouche, Mohamed-Ridha and Lau, Yu-Lung and Mellouli, Fethi and Bousfiha, Ahmed Aziz
Journal of clinical immunology, ISSN 0271-9142, 4/2016, Volume 36, Issue 3, pp. 187 - 194
Medical Microbiology | north african population | Biomedicine | Immunology | novel mutations | BTK | Infectious Diseases | Internal Medicine | XLA | Life Sciences & Biomedicine | Science & Technology | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Humans | Child, Preschool | Genetic Diseases, X-Linked - complications | Agammaglobulinemia - diagnosis | Infant | Male | Genetic Counseling | Protein-Tyrosine Kinases - immunology | Protein-Tyrosine Kinases - genetics | Morocco | Adult | Genetic Diseases, X-Linked - genetics | Algeria | Opportunistic Infections - immunology | B-Lymphocytes - pathology | Child | Tunisia | Opportunistic Infections - complications | Gene Expression | Agammaglobulinemia - complications | Genetic Association Studies | Gene Frequency | Opportunistic Infections - genetics | Sequence Analysis, DNA | Genetic Diseases, X-Linked - diagnosis | Opportunistic Infections - diagnosis | Genetic Diseases, X-Linked - immunology | B-Lymphocytes - immunology | Age of Onset | Alleles | Heterozygote | Mutation | Genetic research | Genetic aspects | B cells | Index Medicus | Agammaglobulinemia/diagnosis | Protein-Tyrosine Kinases/genetics | Agammaglobulinemia/complications | Life Sciences | Agammaglobulinemia/genetics | Genetic Diseases, X-Linked/complications | Opportunistic Infections/complications | Biochemistry, Molecular Biology | Agammaglobulinemia/immunology | Genetic Diseases, X-Linked/immunology | B-Lymphocytes/pathology | Genetic Diseases, X-Linked/diagnosis | Opportunistic Infections/diagnosis | B-Lymphocytes/immunology | Protein-Tyrosine Kinases/immunology | Agammaglobulinaemia Tyrosine Kinase | Opportunistic Infections/immunology | Opportunistic Infections/genetics | Genetic Diseases, X-Linked/genetics
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2. Full Text Helicobacter bilis-Associated Suppurative Cholangitis in a Patient with X-Linked Agammaglobulinemia
by Degand, Nicolas and Dautremer, Justine and Pilmis, Benoît and Ferroni, Agnès and Lanternier, Fanny and Bruneau, Julie and Hermine, Olivier and Blanche, Stéphane and Nassif, Xavier and Lortholary, Olivier and Lecuit, Marc
Journal of clinical immunology, ISSN 0271-9142, 10/2017, Volume 37, Issue 7, pp. 727 - 731
Medical Microbiology | Biomedicine | Immunology | agammaglobulinemia | Infectious Diseases | Internal Medicine | Helicobacter bilis | cholangitis | Bruton’s disease | Life Sciences & Biomedicine | Science & Technology | Helicobacter - genetics | Liver - pathology | Humans | Male | Agammaglobulinemia - microbiology | Helicobacter Infections - pathology | Cholangitis - drug therapy | Young Adult | Anti-Bacterial Agents - therapeutic use | Agammaglobulinemia - pathology | Agammaglobulinemia - drug therapy | DNA, Bacterial - genetics | Genetic Diseases, X-Linked - drug therapy | Helicobacter Infections - drug therapy | Cholangitis - microbiology | Genetic Diseases, X-Linked - pathology | Genetic Diseases, X-Linked - microbiology | Cholangitis - pathology | DNA, Ribosomal - genetics | Helicobacter Infections - microbiology | Hepatitis | Colitis | Agammaglobulinemia | Liver | rRNA 16S | Azithromycin | Cholangitis | Moxifloxacin | Ceftriaxone | X-linked agammaglobulinemia | Biopsy | Etiology | Metronidazole | Index Medicus | Helicobacter Infections/drug therapy | Genetic Diseases, X-Linked/pathology | Helicobacter/genetics | Helicobacter Infections/pathology | Helicobacter Infections/microbiology | DNA, Ribosomal/genetics | Cholangitis/pathology | Life Sciences | Genetic Diseases, X-Linked/drug therapy | Agammaglobulinemia/drug therapy | Cholangitis/drug therapy | Agammaglobulinemia/microbiology | Agammaglobulinemia/pathology | Cholangitis/microbiology | Bacteriology | Liver/pathology | Human health and pathology | Microbiology and Parasitology | Infectious diseases | Genetic Diseases, X-Linked/microbiology | Anti-Bacterial Agents/therapeutic use | DNA, Bacterial/genetics
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3. Full Text X-linked agammaglobulinemia (XLA) clinical profile
by Vaz, Fernanda and Marino, Luiza and Manhães, Isabella and Moraes, Marilia and Saldanha, Rafael and Anjos-Roque, Raissa and Bubach, Pedro and Vital, Nathalia and Ferreira, Caroline and Pimentel, Mariana and Aranda, Carolina and Sole, Dirceu
Journal of allergy and clinical immunology, ISSN 0091-6749, 02/2020, Volume 145, Issue 2, p. AB125
X-linked agammaglobulinemia | Agammaglobulinemia
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4. Full Text Effectiveness of Immunoglobulin Replacement Therapy on Clinical Outcome in Patients with Primary Antibody Deficiencies: Results from a Multicenter Prospective Cohort Study
by Quinti, Isabella and Soresina, Annarosa and Guerra, Andrea and Rondelli, Roberto and Spadaro, Giuseppe and Agostini, Carlo and Milito, Cinzia and Trombetta, Amelia Chiara and Visentini, Marcella and Martini, Helene and Plebani, Alessandro and Fiorilli, Massimo and IPINet Investigators
Journal of clinical immunology, ISSN 0271-9142, 6/2011, Volume 31, Issue 3, pp. 315 - 322
effectiveness | Medical Microbiology | Immunoglobulin replacement | IgA | Biomedicine | Immunology | Internal Medicine | Infectious Diseases | common variable immunodeficiency | X-linked agammaglobulinemia | bronchiectasis | Life Sciences & Biomedicine | Science & Technology | Common Variable Immunodeficiency - immunology | Agammaglobulinemia - immunology | Injections, Intravenous | Prospective Studies | Agammaglobulinemia - genetics | Common Variable Immunodeficiency - drug therapy | Follow-Up Studies | Humans | Middle Aged | Pneumonia - pathology | Child, Preschool | Infant | Male | Bronchiectasis - immunology | Incidence | Bronchiectasis - pathology | Agammaglobulinemia - pathology | Agammaglobulinemia - drug therapy | Genes, X-Linked | Common Variable Immunodeficiency - epidemiology | Immunoglobulin G - immunology | Pneumonia - immunology | Adult | Female | Child | Databases, Factual | Bronchiectasis - drug therapy | Comorbidity | Pneumonia - epidemiology | Risk Factors | Common Variable Immunodeficiency - pathology | Immunoglobulin G - therapeutic use | Treatment Outcome | Immunoglobulin G - administration & dosage | Disease-Free Survival | Pneumonia - drug therapy | Bronchiectasis - epidemiology | Immunoglobulin A - immunology | Adolescent | Italy | Aged | Agammaglobulinemia - epidemiology | Index Medicus
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5. Full Text Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency
by Cicalese, Maria Pia and Ferrua, Francesca and Castagnaro, Laura and Pajno, Roberta and Barzaghi, Federica and Giannelli, Stefania and Dionisio, Francesca and Brigida, Immacolata and Bonopane, Marco and Casiraghi, Miriam and Tabucchi, Antonella and Carlucci, Filippo and Grunebaum, Eyal and Adeli, Mehdi and Bredius, Robbert G and Puck, Jennifer M and Stepensky, Polina and Tezcan, Ilhan and Rolfe, Katie and De Boever, Erika and Reinhardt, Rickey R and Appleby, Jonathan and Ciceri, Fabio and Roncarolo, Maria Grazia and Aiuti, Alessandro
Blood, ISSN 0006-4971, 07/2016, Volume 128, Issue 1, pp. 45 - 54
Life Sciences & Biomedicine | Hematology | Science & Technology | Genetic Therapy | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Humans | Severe Combined Immunodeficiency - mortality | Child, Preschool | Infant | Male | Recovery of Function | CD4-Positive T-Lymphocytes - immunology | Female | Adenosine Deaminase - deficiency | Child | Adenosine Deaminase - genetics | Agammaglobulinemia - therapy | Agammaglobulinemia - mortality | Retroviridae | Severe Combined Immunodeficiency - therapy | Survival Rate | Severe Combined Immunodeficiency - immunology | Disease-Free Survival | Severe Combined Immunodeficiency - genetics | B-Lymphocytes - immunology | CD8-Positive T-Lymphocytes - immunology | Adenosine Deaminase - immunology | Index Medicus | Abridged Index Medicus | 100 | Gene Therapy
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6. Full Text Impact of trough IgG on pneumonia incidence in primary immunodeficiency: A meta-analysis of clinical studies
by Orange, Jordan S and Grossman, William J and Navickis, Roberta J and Wilkes, Mahlon M
Clinical immunology (Orlando, Fla.), ISSN 1521-6616, 2010, Volume 137, Issue 1, pp. 21 - 30
Allergy and Immunology | Pneumonia | Trough concentration | Common variable immunodeficiency | Intravenous immunoglobulin | IVIG | X-linked agammaglobulinemia | Dose | Incidence | Primary immunodeficiency | Meta-analysis | Life Sciences & Biomedicine | Immunology | Science & Technology | Fundamental and applied biological sciences. Psychology | Fundamental immunology | Immunopathology | Biological and medical sciences | Medical sciences | Immunodeficiencies. Immunoglobulinopathies | Immunodeficiencies | Agammaglobulinemia - immunology | Immunoglobulin G - blood | Humans | Middle Aged | Pneumonia - prevention & control | Child, Preschool | Immunoglobulins, Intravenous - administration & dosage | Infant | Male | Young Adult | Immunoglobulin G - immunology | Pneumonia - immunology | Adult | Female | Immunologic Deficiency Syndromes - blood | Immunoglobulins, Intravenous - blood | Immunologic Deficiency Syndromes - immunology | Agammaglobulinemia - prevention & control | Child | Immunologic Deficiency Syndromes - therapy | Agammaglobulinemia - complications | Immunologic Deficiency Syndromes - complications | Agammaglobulinemia - therapy | Treatment Outcome | Clinical Trials as Topic | Immunoglobulins, Intravenous - therapeutic use | Adolescent | Pneumonia - complications | Aged | Medicine, Experimental | Medical colleges | Medical research | Bacterial pneumonia | Immunoglobulin G | Hypogammaglobulinemia | Index Medicus
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7. Full Text The expanding field of secondary antibody deficiency: Causes, diagnosis, and management
by Patel, Smita Y and Carbone, Javier and Jolles, Stephen
Frontiers in immunology, ISSN 1664-3224, 2019, Volume 10, pp. 33 - 33
Chronic lymphocytic leukemia | Immunoglobulin replacement (IgRT) | Secondary antibody deficiency | Lymphoma | Solid organ transplant | Multiple myeloma | Life Sciences & Biomedicine | Immunology | Science & Technology | Agammaglobulinemia - etiology | Disease Susceptibility | Agammaglobulinemia - therapy | Humans | Agammaglobulinemia - diagnosis | Disease Management | Evidence-Based Medicine | Agammaglobulinemia - prevention & control | Practice Guidelines as Topic | Care and treatment | Research | Diagnosis | Biological markers | Agammaglobulinemia | Index Medicus | secondary antibody deficiency | multiple myeloma | chronic lymphocytic leukemia | immunoglobulin replacement (IgRT) | solid organ transplant | lymphoma
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