Myositis-Associated ILD: Clinical Manifestations and Diagnosis
Wednesday, January 15, 7:00 am EST, 2025
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- Project ECHO for ILD
- 2022-2023 Curriculum
- Idiopathic Pulmonary Fibrosis: A Diagnostic Approach
- Shifting Paradigms of IPF Pathogenesis
- Treatments for Idiopathic Pulmonary Fibrosis
- Overview of Autoimmune ILD
- Scleroderma-Associated ILD: Clinical Manifestations and Diagnosis
- Idiopathic Pulmonary Fibrosis: Natural History and Survival
- Myositis-Associated ILD: Clinical Manifestations and Diagnosis
- Lung Biopsy in the Diagnosis of Fibrotic ILD
- Sarcoidosis: Overview, Diagnosis and Monitoring
- Rethinking Classification Criteria for Connective Tissue Diseases
- Post-acute Sequelae of COVID-19 (PASC)
- Acute Exacerbations of ILD
- Scleroderma-Associated ILD: Treatment Approaches and Challenges
- Myositis-Associated ILD: Treatment Approaches and Challenges
- Pulmonary Hypertension Associated with ILD
- More Than Meds: Nonpharmacologic Treatments for ILD
- Hypersensitivity Pneumonitis: Approach and Challenges
- Lung Transplant for ILD: When to Refer and What to Expect
- Sarcoidosis: Beyond First Line Therapy
- Genetics and the Development of Pulmonary Fibrosis
- Hypersensitivity Pneumonitis: Treatment Approach and Challenges
- HRCT Patterns and Pitfalls: Approach to Fibrotic Lung Disease
- Common Comorbidities of ILD
- Quality of Life and ILD: Palliative Care Along the Trajectory of Illness
- 2024-2025 Curriculum
- Rheumatoid Arthritis-Associated ILD
- Shifting Paradigms of IPF Pathogenesis
- HRCT Patterns and Pitfalls: Approach to Fibrotic Lung Disease
- Myositis-Associated ILD: Clinical Manifestations and Diagnosis
- Emerging Treatments for Pulmonary Fibrosis and Active Clinical Trials
- Lung Cancer in Patients with ILD: Diagnostic and Management Considerations
- Rethinking Classification Criteria for Connective Tissue Diseases
- A Guide to Immunosuppression
- Lung Biopsy in the Diagnosis of ILD
- Hypersensitivity Pneumonitis: Diagnostic Approach and Challenges
- Pulmonary Manifestations of ANCA Vasculitis
- Acute Exacerbations of ILD
- Scleroderma-Associated ILD: Treatment Approaches and Challenges
- Pulmonary Complications of Immunotherapy
- Post-acute Sequelae of COVID-19 (PASC): “Long-haulers” and Pulmonary Disease
- Hypersensitivity Pneumonitis: Update on Treatment Approaches
- Pulmonary Hypertension Associated with ILD: Diagnosis and Management
- Occupational Lung Disease
- Myositis-Associated ILD: Treatment Approaches and Challenges
- Lung Transplant for ILD: When to Refer and What to Expect
- Obliterative Bronchiolitis
- Sarcoidosis: Conventional and Evolving Treatments
- Quality of Life and ILD: The Role of Palliative Care
- Genetics and the Development of Pulmonary Fibrosis
- Common Comorbidities of ILD
- Project ECHO for ILD
- Registration
- 2022-2023 Curriculum
- Virtual Meetings
- Air Filtration
- Air Pollution and Interstitial Lung Disease
- Airway Clearance
- Anesthesia for People With Interstitial Lung Disease
- Art Therapy in Chronic Illness
- Cough in ILD: Its Causes and Management
- Eight Active Ingredients of Tai Chi
- Gastroesophageal Reflux Disease (GERD) and ILD
- Hypersensitivity Pneumonitis
- Immunomodulatory Agents in the Treatment of ILD
- Implementing Energy Conservation Strategies
- Interstitial Lung Disease: The Journey to Diagnosis and Treatment
- Living Better with ILD
- Lung Transplant: Eligibility and Evaluation
- Monthly Oxygen Therapy Series: Is It Time to Use Oxygen?
- Monthly Oxygen Therapy Series: Portable Oxygen Concentrators and Travel
- Monthly Palliative Care Series: Palliative Care and QoL in ILD
- Nutritional Considerations for ILD
- Pulmonary Hypertension: Diagnosis and Management
- Sarcoidosis: Is There Better Treatment?
- The Lived Experience Series: Financial and Tax Planning
- Understanding Autoimmune-Related ILD
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- Updates on Clinical Research for IPF and Other Forms of ILD (2023)
- Updates on Clinical Research for IPF and Other Forms of ILD
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- Basics of ILDs
- Basics of IPF
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- Genetics of Familial Idiopathic Interstitial Pneumonia
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- IPF and PF-ILD Clinical Trials
- Monitoring Disease Progression in Idiopathic Pulmonary Fibrosis
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- Phase IV IPF Clinical Trials
- Pulmonary Function Testing
- Starting Oxygen Therapy
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