scholarly article | Q13442814 |
P356 | DOI | 10.1097/00005792-200005000-00003 |
P698 | PubMed publication ID | 10844935 |
P50 | author | Harry Malech | Q42654598 |
P2093 | author name string | S M Holland | |
J I Gallin | |||
S J Chanock | |||
R H Buckley | |||
J Boyle | |||
J A Winkelstein | |||
R B Johnston | |||
H Ochs | |||
J Curnutte | |||
C B Foster | |||
H Dickler | |||
M C Marino | |||
P Quie | |||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 155-169 | |
P577 | publication date | 2000-05-01 | |
P1433 | published in | Medicine | Q15716652 |
P1476 | title | Chronic granulomatous disease. Report on a national registry of 368 patients | |
P478 | volume | 79 |
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Q35011464 | Killing of Aspergillus fumigatus by alveolar macrophages is mediated by reactive oxidant intermediates |
Q38835840 | LC3-associated phagocytosis: a crucial mechanism for antifungal host defence against Aspergillus fumigatus |
Q36753685 | Lack of p47(phox) in Akita Diabetic Mice Is Associated with Interstitial Pneumonia, Fibrosis, and Oral Inflammation |
Q39561887 | Lentiviral Vector Gene Therapy Protects XCGD Mice From Acute Staphylococcus aureus Pneumonia and Inflammatory Response. |
Q92979235 | Lentiviral gene therapy for X-linked chronic granulomatous disease |
Q38195200 | Lentiviral vectors for the treatment of primary immunodeficiencies |
Q35778617 | Lessons about the pathogenesis and management of aspergillosis from studies in chronic granulomatous disease. |
Q43779609 | Lessons learned from phagocytic function studies in a large cohort of patients with recurrent infections |
Q34182786 | Lineage- and stage-restricted lentiviral vectors for the gene therapy of chronic granulomatous disease |
Q35408185 | Lipid- and polymer-based drug delivery carriers for eradicating microbial biofilms causing medical device-related infections. |
Q34429033 | Live attenuated S. Typhimurium vaccine with improved safety in immuno-compromised mice |
Q35789900 | Long polymerase chain reaction-based fluorescence in situ hybridization analysis of female carriers of X-linked chronic granulomatous disease deletions. |
Q50104585 | Long-term follow-up and prognosis of chronic granulomatous disease in Yugoslavia: is there a role for early bone marrow transplantation? |
Q40526315 | Long-term interferon-gamma therapy for patients with chronic granulomatous disease |
Q35553610 | Long-term outcome of patients with p22 (phox) -deficient chronic granulomatous disease on Jeju Island, Korea |
Q41353450 | Low-dose total-body irradiation and alemtuzumab-based reduced-intensity conditioning regimen results in durable engraftment and correction of clinical disease among children with chronic granulomatous disease |
Q33703196 | Lupus and proliferative nephritis are PAD4 independent in murine models. |
Q35673745 | Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase |
Q37577712 | Making sense of the cause of Crohn's - a new look at an old disease |
Q39684886 | Managing Inflammatory Manifestations in Patients with Chronic Granulomatous Disease |
Q50093392 | Mastoidectomy in a child with chronic granulomatous disease. |
Q28066193 | Mechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary Immunodeficiencies |
Q34792962 | Mechanisms of NDV-3 vaccine efficacy in MRSA skin versus invasive infection. |
Q49923802 | Mechanisms to Evade the Phagocyte Respiratory Burst Arose by Convergent Evolution in Typhoidal Salmonella Serovars. |
Q27022250 | Mendelian genetics of human susceptibility to fungal infection |
Q26862947 | Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity |
Q36906968 | Methods for defining distinct bioenergetic profiles in platelets, lymphocytes, monocytes, and neutrophils, and the oxidative burst from human blood |
Q27336723 | Mice chronically fed high-fat diet have increased mortality and disturbed immune response in sepsis |
Q37064440 | Modern management of chronic granulomatous disease |
Q38950276 | Modern management of phagocyte defects |
Q47334511 | Modulating Host Signaling Pathways to Promote Resistance to Infection by Candida albicans |
Q90322108 | Modulation of the Oxidative Stress and Lipid Peroxidation by Endocannabinoids and Their Lipid Analogues |
Q33654713 | Molecular analysis of X-linked chronic granulomatous disease in five unrelated Korean patients |
Q37273205 | Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome |
Q36965983 | Molecular identification of bacterial DNA in the chorioretinal scars of chronic granulomatous disease |
Q37974983 | Molecular mechanisms of the immunological abnormalities in hyper-IgE syndrome |
Q30538643 | Monocyte- and macrophage-targeted NADPH oxidase mediates antifungal host defense and regulation of acute inflammation in mice. |
Q38911356 | Monocyte/macrophage-specific NADPH oxidase contributes to antimicrobial host defense in X-CGD. |
Q36372960 | Monogenic forms of systemic lupus erythematosus: new insights into SLE pathogenesis |
Q64231080 | Mucormycotic Osteomyelitis Involving the Maxilla: A Rare Case Report and Review of the Literature |
Q37224540 | Multiple pericardial abscesses in a child with known chronic granulomatous disease |
Q44318186 | Multiple-azole-resistant Aspergillus fumigatus osteomyelitis in a patient with chronic granulomatous disease successfully treated with long-term oral posaconazole and surgery. |
Q90066827 | Munchausen syndrome mimicking refractory subcutaneous abscess with bacteremia, diagnosed by repetitive element sequence-based polymerase chain reaction: a case report |
Q53545782 | Mutations of chronic granulomatous disease in Turkish families. |
Q36517880 | Myeloablative transplantation using either cord blood or bone marrow leads to immune recovery, high long-term donor chimerism and excellent survival in chronic granulomatous disease |
Q49422978 | NADPH Oxidase Deficiency: A Multisystem Approach. |
Q37713391 | NADPH oxidase promotes neutrophil extracellular trap formation in pulmonary aspergillosis |
Q36302873 | NADPH oxidases: an overview from structure to innate immunity-associated pathologies |
Q36647903 | NETosis and NADPH oxidase: at the intersection of host defense, inflammation, and injury |
Q35977261 | NOX Modifiers-Just a Step Away from Application in the Therapy of Airway Inflammation? |
Q33840366 | NOX2 protects against progressive lung injury and multiple organ dysfunction syndrome |
Q42264626 | NOX2 protects against prolonged inflammation, lung injury, and mortality following systemic insults. |
Q33911333 | NOX2-dependent regulation of inflammation |
Q37601820 | Necrotizing Liver Granuloma/Abscess and Constrictive Aspergillosis Pericarditis with Central Nervous System Involvement: Different Remarkable Phenotypes in Different Chronic Granulomatous Disease Genotypes. |
Q40052231 | Neutrophil Evolution and Their Diseases in Humans |
Q54261956 | Neutrophil-generated HOCl leads to non-specific thiol oxidation in phagocytized bacteria. |
Q49570630 | Neutrophils and neutrophil extracellular traps in the liver and gastrointestinal system. |
Q38221176 | Neutrophils at work |
Q28087227 | Neutrophils: Between host defence, immune modulation, and tissue injury |
Q27002519 | New insights into innate immune control of systemic candidiasis |
Q55282167 | New onset colitis in an adult patient with chronic granulomatous disease treated with hematopoietic stem cell transplantation: a diagnostic dilemma. |
Q36698099 | Newly diagnosed chronic granulomatous disease in a 44 year old male presenting with recurrent groin cellulitis and colitis |
Q46682211 | Newly diagnosed chronic granulomatous disease in a 53-year-old woman with Crohn disease |
Q40126607 | Nine patients with chronic granulomatous disease having selective neck dissection for severe cervical lymphadenitis. |
Q34141669 | Nocardia infection in chronic granulomatous disease |
Q38078056 | Non-Aspergillus fungal infections in chronic granulomatous disease |
Q55021826 | Noninfectious Manifestations and Complications of Chronic Granulomatous Disease. |
Q38167633 | Ocular involvement in primary immunodeficiency diseases |
Q38363105 | Opportunistic yeast pathogens: reservoirs, virulence mechanisms, and therapeutic strategies |
Q33531937 | Orofacial findings in chronic granulomatous disease: report of twelve patients and review of the literature |
Q33851299 | Osteomyelitis and lung abscess due to Aspergillus fumigatus in a chronic granulomatous disease patient |
Q37880202 | Osteomyelitis due to Aspergillus species in chronic granulomatous disease: an update of the literature |
Q37304752 | Otitis media as a presenting complaint in childhood immunodeficiency diseases |
Q33357224 | Otolaryngologic manifestations of immunodeficiency |
Q37684019 | Otolaryngologic manifestations of pediatric immunodeficiency |
Q35030912 | Oxidase-deficient neutrophils from X-linked chronic granulomatous disease iPS cells: functional correction by zinc finger nuclease-mediated safe harbor targeting |
Q60907100 | Oxidative Stress in Poultry: Lessons from the Viral Infections |
Q33715508 | Oxidative stress in the pathology and treatment of systemic lupus erythematosus |
Q34238532 | P67-phox (NCF2) lacking exons 11 and 12 is functionally active and leads to an extremely late diagnosis of chronic granulomatous disease (CGD) |
Q47913800 | Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease |
Q38916325 | Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience. |
Q35227431 | Peculiarities of cell death mechanisms in neutrophils. |
Q34584769 | Penicillium piceum infection: diagnosis and successful treatment in chronic granulomatous disease |
Q73293990 | Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease |
Q37161242 | Persistence of the bacterial pathogen Granulibacter bethesdensis in chronic granulomatous disease monocytes and macrophages lacking a functional NADPH oxidase |
Q38373915 | Phagocyte NADPH oxidase and specific immunity |
Q35027263 | Phagocyte NADPH oxidase restrains the inflammasome in ANCA-induced GN |
Q37141844 | Phagocyte dysfunction and inflammatory bowel disease |
Q33420369 | Phagocytic superoxide specifically damages an extracytoplasmic target to inhibit or kill Salmonella |
Q34141420 | Pharmacokinetics and safety of intravenous voriconazole in children after single- or multiple-dose administration |
Q33840702 | Phellinus tropicalis abscesses in a patient with chronic granulomatous disease |
Q26825944 | Pneumococcal vaccine and patients with pulmonary diseases |
Q38798358 | Polymorphonuclear neutrophils in periodontitis and their possible modulation as a therapeutic approach |
Q28306873 | Population prevalence of diagnosed primary immunodeficiency diseases in the United States |
Q43708431 | Posaconazole for treatment of refractory invasive fungal disease. |
Q34532546 | Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America |
Q29042159 | Practice parameter for the diagnosis and management of primary immunodeficiency |
Q48653640 | Preimplantation genetic diagnosis for HLA typing in a case of X-linked chronic granulomatous disease. |
Q58735127 | Preliminary study on chronic granulomatous disease in Sri Lanka |
Q50084357 | Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections. |
Q36763235 | Prevalence and morbidity of primary immunodeficiency diseases, United States 2001-2007. |
Q44832666 | Prevalence of chronic granulomatous disease in pediatric patients diagnosed with Crohn's disease |
Q54973296 | Prevention of Infectious Complications in Patients With Chronic Granulomatous Disease. |
Q56941015 | Primary Immune Deficiencies Presenting in Adults: Seven Years of Experience from Iran |
Q97067634 | Primary Immunodeficiencies With Defects in Innate Immunity: Focus on Orofacial Manifestations |
Q62658778 | Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID Registry |
Q39027692 | Primary immune deficiencies with defects in neutrophil function. |
Q33902831 | Primary immunodeficiencies underlying fungal infections |
Q36371000 | Primary immunodeficiency diseases in oman: five years' experience at sultan qaboos university hospital |
Q34114555 | Primary phagocytic disorders of childhood |
Q56941385 | Propionibacterium acnes Chest Infections in Patients with Chronic Granulomatous Disease: Case Reports |
Q57173966 | Prédisposition mendélienne aux infections mycobactériennes et défaut de l’explosion oxydative des macrophages |
Q40216978 | Pseudomonas aeruginosa Effector ExoS Inhibits ROS Production in Human Neutrophils. |
Q45400331 | Psychrobacter immobilis septicemia in a boy with X-linked chronic granulomatous disease and fulminant hepatic failure |
Q36996797 | Pulmonary Aspergillosis in a Previously Healthy 13-Year-Old Boy. |
Q35674223 | Pulmonary complications of primary immunodeficiencies |
Q38079835 | Pulmonary manifestations of chronic granulomatous disease |
Q36973074 | Rapid determination of chimerism status using dihydrorhodamine assay in a patient with X-linked chronic granulomatous disease following hematopoietic stem cell transplantation. |
Q33813874 | Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution melting |
Q40200333 | Rare diagnosis in a neonate who presents with fever |
Q38851117 | Reactive oxygen homeostasis - the balance for preventing autoimmunity. |
Q36593591 | Reactive oxygen species produced by the NADPH oxidase 2 complex in monocytes protect mice from bacterial infections. |
Q37098488 | Reactive oxygen species regulate neutrophil recruitment and survival in pneumococcal pneumonia |
Q24624942 | Reactive oxygen species-independent activation of the IL-1beta inflammasome in cells from patients with chronic granulomatous disease |
Q90383809 | Recent advances in chronic granulomatous disease |
Q38119863 | Recent advances in transplantation for primary immune deficiency diseases: a comprehensive review |
Q40059524 | Recent advances in understanding and treating chronic granulomatous disease |
Q41929675 | Recognition and Clinical Presentation of Invasive Fungal Disease in Neonates and Children. |
Q34429384 | Recognizing primary immune deficiency in clinical practice |
Q30435963 | Recurrent Burkholderia infection in patients with chronic granulomatous disease: 11-year experience at a large referral center |
Q34132929 | Recurrent Granulibacter bethesdensis infections and chronic granulomatous disease |
Q46085453 | Recurrent streptococcal hepatic abscesses in a 46-year-old woman |
Q43640569 | Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study |
Q37247851 | Redundant hydrogen peroxide scavengers contribute to Salmonella virulence and oxidative stress resistance. |
Q36040945 | Regulation of innate immunity by NADPH oxidase |
Q60300625 | Regulation of mycobacterial infection by macrophage Gch1 and tetrahydrobiopterin |
Q34832611 | Relevance of laboratory testing for the diagnosis of primary immunodeficiencies: a review of case-based examples of selected immunodeficiencies |
Q89440609 | Renal Disease in Chronic Granulomatous Disease: Data from the USIDNET Registry |
Q40429733 | Renal amyloidosis in a child with chronic granulomatous disease and invasive aspergillosis |
Q41614325 | Renal transplantation in a patient with chronic granulomatous disease: case report |
Q36410497 | Residual NADPH oxidase activity and isolated lung involvement in x-linked chronic granulomatous disease |
Q28301969 | Residual NADPH oxidase and survival in chronic granulomatous disease |
Q54290737 | Resistant invasive aspergillosis in an autosomal recessive chronic granulomatous disease. |
Q37372812 | Restoration of NET formation by gene therapy in CGD controls aspergillosis |
Q35568541 | Retroviral gene therapy for X-linked chronic granulomatous disease: results from phase I/II trial |
Q33387329 | Retrovirus gene therapy for X-linked chronic granulomatous disease can achieve stable long-term correction of oxidase activity in peripheral blood neutrophils |
Q47133379 | Review: Metabolic Control of Immune System Activation in Rheumatic Diseases |
Q37349116 | Rheumatologic and autoimmune manifestations of primary immunodeficiency disorders |
Q39140136 | Robust T cell responses to aspergillosis in chronic granulomatous disease: implications for immunotherapy |
Q33864943 | Role of NADPH oxidase in host defense against aspergillosis |
Q34098141 | Role of NADPH oxidase versus neutrophil proteases in antimicrobial host defense |
Q33552201 | Role of Protein Kinase C and Nox2-Derived Reactive Oxygen Species Formation in the Activation and Maturation of Dendritic Cells by Phorbol Ester and Lipopolysaccharide. |
Q39299815 | Role of apoptosis and autophagy in tuberculosis |
Q52733597 | Role of gp91phox in hepatic macrophage programming and alcoholic liver disease. |
Q35217529 | Role of inducible nitric oxide synthase and NADPH oxidase in early control of Burkholderia pseudomallei infection in mice |
Q34862986 | Roles of the host oxidative immune response and bacterial antioxidant rubrerythrin during Porphyromonas gingivalis infection. |
Q36521306 | SNaPBceBcon: a Practical Tool for Identification and Genotyping of Burkholderia cepacia and Burkholderia contaminans |
Q50043378 | Salmonella detoxifying enzymes are sufficient to cope with the host oxidative burst. |
Q34611825 | Salmonella evades D-amino acid oxidase to promote infection in neutrophils. |
Q24610283 | Serologic reactivity to the emerging pathogen Granulibacter bethesdensis |
Q90259713 | Serum Biomarkers for Early Diagnosis of Chinese X-CGD Children: Case Reports and a Literature Review |
Q54572514 | Severe X-linked chronic granulomatous disease in two unrelated females. |
Q37226837 | Simian immunodeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft |
Q34489893 | Simultaneous Host-Pathogen Transcriptome Analysis during Granulibacter bethesdensis Infection of Neutrophils from Healthy Subjects and Patients with Chronic Granulomatous Disease |
Q30303140 | Single amino acid substitution in homogentisate 1,2-dioxygenase is responsible for pigmentation in a subset of Burkholderia cepacia complex isolates |
Q57121572 | Single centre experience of umbilical cord stem cell transplantation for primary immunodeficiency |
Q38113986 | Skin manifestations of primary immune deficiency |
Q37426267 | Skin ulcers and disseminated abscesses are characteristic of Serratia marcescens infection in older patients with chronic granulomatous disease |
Q24655272 | Special article: chronic granulomatous disease in the United Kingdom and Ireland: a comprehensive national patient-based registry |
Q47166455 | Spectrum of imaging findings of chronic granulomatous disease: a single center experience |
Q37107790 | Spectrum of primary immune deficiency at a tertiary care hospital |
Q93645648 | Spoken sessions |
Q39534623 | Sporothrix schenckii lymphadentitis in a male with X-linked chronic granulomatous disease. |
Q91900034 | Staphylococcus aureus Lipoic Acid Synthesis Limits Macrophage Reactive Oxygen and Nitrogen Species Production To Promote Survival during Infection |
Q39037945 | Staphylococcus aureus, phagocyte NADPH oxidase and chronic granulomatous disease |
Q38735833 | Stem cell transplantation for the treatment of immunodeficiency in children: current status and hopes for the future |
Q46871937 | Stem-cell transplantation for chronic granulomatous disease |
Q38984645 | Study of naïve and memory cells in a cohort of Egyptian chronic granulomatous disease patients. |
Q40896765 | Subclinical intestinal inflammation in chronic granulomatous disease patients |
Q41534196 | Subcutaneous abscess due to the basidiomycete Phellinus mori in a patient with chronic granulomatous disease |
Q39809887 | Subspecialty evaluation of chronically ill hospitalized patients with suspected immune defects |
Q64100149 | Successful application of next-generation sequencing for pre-natal diagnosis in a pedigree with chronic granulomatosis disease |
Q33606830 | Successful hepatectomy for hepatic abscess with chronic granulomatous disease: a case report |
Q46936602 | Successful renal transplantation in patients with chronic granulomatous disease |
Q46788388 | Successful treatment of chronic granulomatous disease with fludarabine-based reduced-intensity conditioning and unrelated bone marrow transplantation |
Q36244604 | Successful treatment of fungal osteomyelitis with voriconazole in a patient with chronic granulomatous disease |
Q51682318 | Successful umbilical cord blood stem cell transplantation for chronic granulomatous disease. |
Q43703233 | Successful unrelated bone marrow transplantation for a patient with chronic granulomatous disease and associated resistant pneumonitis and Aspergillus osteomyelitis |
Q48370654 | Successful unrelated bone marrow transplantation in a child with chronic granulomatous disease complicated by pulmonary and cerebral granuloma formation |
Q42113918 | Superoxide production and expression of NAD(P)H oxidases by transformed and primary human colonic epithelial cells |
Q84446170 | Suppurative lymphadenitis |
Q35070983 | Synaptic plasticity deficits and mild memory impairments in mouse models of chronic granulomatous disease |
Q35608083 | Systemic lupus erythematosus-associated neutrophil cytosolic factor 2 mutation affects the structure of NADPH oxidase complex |
Q37962982 | Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century |
Q33743570 | Th17 cytokines and the gut mucosal barrier |
Q49960282 | The Changing Paradigm of Management of Liver Abscesses in Chronic Granulomatous Disease. |
Q35851420 | The Endoplasmic Reticulum Stress Sensor Inositol-Requiring Enzyme 1α Augments Bacterial Killing through Sustained Oxidant Production |
Q50181582 | The European internet-based patient and research database for primary immunodeficiencies: results 2004-06. |
Q37204038 | The NADPH oxidase NOX2 plays a role in periodontal pathologies |
Q59326775 | The Plasma Membrane: A Platform for Intra- and Intercellular Redox Signaling |
Q36635676 | The Relationship Between Invasive Nontyphoidal Salmonella Disease, Other Bacterial Bloodstream Infections, and Malaria in Sub-Saharan Africa |
Q46349699 | The Role of NrF2 in the Regulation of Periodontal Health and Disease |
Q34052242 | The blessings and curses of intestinal inflammation |
Q37962986 | The demographics of primary immunodeficiency diseases across the unique ethnic groups in Iran, and approaches to diagnosis and treatment |
Q42688094 | The glycosylphosphatidylinositol-anchored protease Sap9 modulates the interaction of Candida albicans with human neutrophils |
Q37825925 | The human NADPH oxidase: primary and secondary defects impairing the respiratory burst function and the microbicidal ability of phagocytes |
Q34454572 | The immunologic workup of the child suspected of immunodeficiency |
Q37783925 | The many roles of NOX2 NADPH oxidase-derived ROS in immunity |
Q36531751 | The role of Candida albicans AP-1 protein against host derived ROS in in vivo models of infection. |
Q89181533 | The role of neutrophil extracellular traps in rheumatic diseases |
Q33904653 | The role of neutrophils and NETosis in autoimmune and renal diseases |
Q90266811 | The role of neutrophils in host defense against invasive fungal infections |
Q36759569 | The role of surgery in the management of patients with refractory chronic granulomatous disease colitis |
Q34786696 | The role of the gut flora in health and disease, and its modification as therapy |
Q36872083 | The role of the innate immune system in granulomatous disorders |
Q37722665 | Therapeutic effects of proteoliposomes on X-linked chronic granulomatous disease: proof of concept using macrophages differentiated from patient-specific induced pluripotent stem cells. |
Q38920756 | Thoracic Surgery in Chronic Granulomatous Disease: a 25-Year Single-Institution Experience. |
Q41994928 | Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease. |
Q36942513 | Tolerance and autoimmunity: lessons at the bedside of primary immunodeficiencies |
Q39941137 | Transgene optimization significantly improves SIN vector titers, gp91phox expression and reconstitution of superoxide production in X-CGD cells. |
Q41994355 | Transition From Pediatric to Adult Care by Young Adults With Chronic Granulomatous Disease: The Patient's Viewpoint. |
Q54347197 | Treatment With Anakinra, a Recombinant IL-1 Receptor Antagonist, Unlikely to Induce Lasting Remission in Patients With CGD Colitis. |
Q38048853 | Treatment of candidiasis: insights from host genetics |
Q43252991 | Treosulfan-based conditioning regimen in a second matched unrelated peripheral blood stem cell transplantation for a pediatric patient with CGD and invasive aspergillosis, who experienced initial graft failure after RIC. |
Q87696079 | Two Chronic Granulomatous Disease Diagnosed in Adult Age |
Q40289910 | Two siblings with prolonged fever and pneumonia |
Q33716493 | USIDNET: a strategy to build a community of clinical immunologists |
Q36006149 | Ulcerative colitis associated with chronic granulomatous disease: case report |
Q36480989 | Umbilical cord stem cell transplantation for primary immunodeficiencies |
Q37135419 | Understanding systemic lupus erythematosus physiopathology in the light of primary immunodeficiencies. |
Q33410503 | Undiagnosed Chronic Granulomatous Disease, Burkholderia cepacia complex Pneumonia, and Acquired Hemophagocytic Lymphohistiocytosis: A Deadly Association |
Q34310579 | Urinary tract infection by chromobacterium violaceum |
Q52575536 | Use of Genetic Testing for Primary Immunodeficiency Patients. |
Q39093281 | Using dendritic cells to evaluate how Burkholderia cenocepacia clonal isolates from a chronically infected cystic fibrosis patient subvert immune functions. |
Q36560699 | Utility of fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography in a child with chronic granulomatous disease |
Q82535300 | Utility of screening for chronic granulomatous disease in patients with inflammatory bowel disease |
Q50092440 | Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET). |
Q38212512 | Vaccine use in primary immunodeficiency disorders |
Q89848736 | Variable Presentation of the CYBB Mutation in One Family, Approach to Management, and a Review of the Literature |
Q41987460 | Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease |
Q38430977 | Very early-onset inflammatory bowel disease: gaining insight through focused discovery |
Q30436584 | Virulence and cellular interactions of Burkholderia multivorans in chronic granulomatous disease |
Q64950468 | X-Linked Chronic Granulomatous Disease: Initial Presentation with Intracranial Hemorrhage from Vitamin K Deficiency in Infant. |
Q37008479 | X-linked chronic granulomatous disease secondary to skewed X chromosome inactivation in a female with a novel CYBB mutation and late presentation |
Q35841384 | Zinc sequestration by the neutrophil protein calprotectin enhances Salmonella growth in the inflamed gut. |
Q83367731 | [Primary immune deficiencies in neutrophil functioning] |
Q37073789 | p47phox deficiency induces macrophage dysfunction resulting in progressive crystalline macrophage pneumonia |
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