Disease: Childhood interstitial lung disease (chILD Syndrome)
- <em>NKX2-1</em>-Related Disorders
- A 5-year follow-up of pulmonary function tests in childhood-onset systemic lupus erythematosus: a single-center retrospective study
- A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy
- A Novel <em>STAT3</em> Gain-of-Function Mutation in Fatal Infancy-Onset Interstitial Lung Disease
- A rare association of Down syndrome with Dandy -Walker variant, pulmonary hypertension and childhood interstitial lung disease: A case report of a prognostic dilemma
- ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease
- ABCA3 mutations led to pulmonary fibrosis and emphysema with pulmonary hypertension in an 8-year-old girl
- Adult-onset eosinophilic airway diseases
- An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy
- An unprecedented COPA gene mutation in two patients in the same family: comparative clinical analysis of newly reported patients with other known COPA gene mutations
- Analysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved Proteases
- ANCA-associated vasculitis in childhood: recent advances
- Atypical Presentation of Systemic Arthritis in a Toddler with Down Syndrome
- Biologic characterization of ABCA3 variants in lung tissue from infants and children with ABCA3 deficiency
- Brain-lung-thyroid syndrome in a newborn with deletion 14q12-q21.1
- Cardiac involvement as a presenting feature of eosinophilic granulomatosis with polyangiitis in childhood
- Case Report: Activating <em>PIK3CD</em> Mutation in Patients Presenting With Granulomatosis With Polyangiitis
- Case report: Filamin A mutation lung disease recognized in an 11-year-old child
- Childhood interstitial lung disease: A systematic review
- Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experience
- Childhood sarcoidosis: Louisiana experience
- Childhood-Onset ANCA- Associated Vasculitis: single center experience from Central California
- Childhood-Onset Eosinophilic Granulomatosis with Polyangiitis with a Vulvar Granuloma: A Case Report and Review of the Literature
- Childhood-Onset Sjögren Syndrome Presenting as Pulmonary Hemorrhage
- Classification, presentation, and initial treatment of Wegener's granulomatosis in childhood
- Clinical analysis of heterozygous ABCA3 mutations in children
- Comparing Presenting Clinical Features in 48 Children With Microscopic Polyangiitis to 183 Children Who Have Granulomatosis With Polyangiitis (Wegener's): An ARChiVe Cohort Study
- Congenital Surfactant C Deficiency with Pulmonary Hypertension-A Case Report
- Cutaneous manifestations of childhood Eosinophilic Granulomatosis with Polyangiitis (cEGPA): A case-based review
- Cyclophosphamide-induced liver injury during treatment of interstitial lung disease in juvenile dermatomyositis
- Diffuse alveolar hemorrhage in childhood-onset systemic lupus erythematosus: a severe disease flare with serious outcome
- Efficacy of mycophenolate on lung disease and autoimmunity in children with immunodeficiency
- Epidemiology of primary systemic vasculitis in children: a population-based study from southern Sweden
- Epistaxis due to Wegener's granulomatosis in a pediatric patient
- Establishment of a pilot pediatric registry for chronic vasculitis is both essential and feasible: a Childhood Arthritis and Rheumatology Alliance (CARRA) survey
- Etiologic Profile of Older Children With Diffuse Radiological Changes in Eastern China
- Etiologic spectrum of interstitial lung diseases in Chinese children older than 2 years of age
- Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy
- Exposure to inorganic particles in paediatric sarcoidosis: the PEDIASARC study
- Fanconi syndrome-associated interstitial lung disease
- Fatal pulmonary fibrosis after rituximab administration
- First patient with ILNEB syndrome due to pathogenic variants in ITGA3 surviving to adulthood
- French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial management
- Functional characterization of four ATP-binding cassette transporter A3 gene (ABCA3) variants
- Gene Therapy Potential for Genetic Disorders of Surfactant Dysfunction
- Genetic disorders of surfactant protein dysfunction: when to consider and how to investigate
- Genetic testing for diffuse lung diseases in children
- Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
- Genotype-phenotype correlations for infants and children with ABCA3 deficiency
- Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood
- Heterogeneity of lung disease associated with NK2 homeobox 1 mutations
- Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1
- High-Content Screening Identifies Cyclosporin A as a Novel ABCA3-Specific Molecular Corrector
- Hydroxychloroquine, a successful treatment for lung disease in ABCA3 deficiency gene mutation: a case report
- Imaging findings in systemic childhood diseases presenting with dermatologic manifestations
- Imaging findings of COPA Syndrome
- Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3
- Increased sensitivity of the European medicines agency algorithm for classification of childhood granulomatosis with polyangiitis
- Interstitial lung disease in autoinflammatory disease in childhood: A systematic review of the literature
- Interstitial lung disease in children with Rubinstein-Taybi syndrome
- Interstitial processes of the lungs in childhood
- Langerhans cell histiocytosis in a pediatric patient with thrombocytopenia-absent radius syndrome and 1q21.1 deletion: case report and proposal of a rapid molecular diagnosis of 1q21.1 deletion
- Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findings
- Lung disease caused by <em>ABCA3</em> mutations
- Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series
- Measles-induced respiratory distress, air-leak and ARDS
- Neonatal Onset Interstitial Lung Disease as a Primary Presenting Manifestation of Mucopolysaccharidosis Type I
- NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
- Oral Juvenile Xanthogranuloma: a case report of gingival hyperplasia and osteolysis in male adult patient
- Out of the box diagnosis in a child treated as childhood interstitial lung disease- William-Campbell syndrome
- Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism
- Pediatric Case Report on an Interstitial Lung Disease with a Novel Mutation of <em>SFTPC</em> Successfully Treated with Lung Transplantation
- Primary childhood vasculitis--new classification criteria
- Primary Immunodeficiency: Primary Antibody Disorders in Respiratory Medicine
- Primary vasculitides in childhood and adulthood
- Pulmonary hypertension and other potentially fatal pulmonary complications in systemic juvenile idiopathic arthritis
- Pulmonary interstitial glycogenosis in a patient with trisomy 21
- Pulmonary manifestations of childhood-onset primary Sjogren's syndrome (SS) masquerading as reactive airways disease in a male patient and review of interstitial lung disease associated with SS
- Pulmonary renal syndrome in a child with coexistence of anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane disease: case report and literature review
- Pulmonary vasodilators can lead to various complications in pulmonary "arterial" hypertension associated with congenital heart disease
- Renal Involvement as Rare Acute Tubulointerstitial Nephritis in a Patient with Eosinophilic Disorder Treated with Early Add-on Administration of Mepolizumab
- Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
- Simulated Assessment of Pharmacokinetically Guided Dosing for Investigational Treatments of Pediatric Patients With Coronavirus Disease 2019
- Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With Polyangiitis
- Surfactant lipidomics in healthy children and childhood interstitial lung disease
- Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD)
- Surfactant protein disorders in childhood interstitial lung disease
- Systemic inflammatory syndrome in children with FARSA deficiency
- The clinical phenotypes of the juvenile idiopathic inflammatory myopathies
- The common ABCA3<sup>E292V</sup> variant disrupts AT2 cell quality control and increases susceptibility to lung injury and aberrant remodeling
- The Common Among the Rare: A Pictorial Essay of the Most Common Diffuse Lung Diseases in Children
- Therapeutic options for CTLA-4 insufficiency
- Thymus and mediastinal node involvement in childhood Langerhans cell histiocytosis: long-term follow-up from the French national cohort
- Treatment of telomeropathies
- Type I Interferonopathies in Children: An Overview
- Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family
- Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children
- Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutations
- Wegener's granulomatosis in pediatric patients
- What triggered massive hemoptysis in Goodpasture syndrome with isolated pulmonary involvement in a 14-year-old boy?