CheckRare CME Exchange

CheckRare CME Exchange

Continuing medical education for healthcare professionals caring for patients with rare diseases. The CheckRare CME Exchange delivers non-accredited and accredited continuing medical education (CME) featuring leading experts in rare diseases. Through interviews, case-based discussions, panel conversations, and evidence-based educational programs, these episodes explore the latest advances in diagnosis, treatment, clinical research, and patient care. Designed for healthcare professionals, CheckRare CME Exchange provides practical, balanced education that can be applied directly to clinical practice while helping listeners stay current with the rapidly evolving rare disease landscape.

Episodes

Myasthenia Gravis Clinical Research Highlights

August 2, 2026 • 34 mins
This program is supported by educational grants from argenx and UCB, Inc.

This accredited CME program highlights the latest clinical research about myasthenia gravis, a rare, autoimmune disease that targets the neuromuscular junction. To obtain CME credit for this activity, visit https://checkrare.com/learning/p-myasthenia-gravis-clinical-research-highlights-2026/

Management of myasthenia gravis is highly individualiz...
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Current Issues in Gene Therapies for Lysosomal Disorders

December 31, 2025 • 106 mins
Shunji Tomatsu, MD, PhD, Professor and Head, Nemours Children’s Health, Delaware, USA; Alessandra d’Azzo, PhD, Emerita Faculty, Genetics, St. Jude Children’s Research Hospital, Tennessee, USA; Merve Emecen Sanli, MD, Associate Professor, Department of Pediatrics, University of Texas Southwestern Medical Center, Texas, USA; and Ryan Colburn, patient with Pompe disease and president of Odimm Inc, discuss new and eme...
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Theranostics and Lysosomal Disorders

December 31, 2025 • 106 mins
Duarte C. Barral, PhD, Associate Professor, NOVA Medical School, NOVA University of Lisbon, Portugal; Nuno Raimundo, PhD, Associate Professor, Department of Cellular and Molecular Physiology; Penn State College of Medicine, Pennsylvania, USA; Betul Celik, PhD, Postdoctoral Fellow, Nemours Children’s Health, Delaware, USA; and Gregory Newby, PhD, Assistant Professor, Department of Genetic Medicine, Johns Hopkins School of Medi...
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Expanded Applications of AI in Lysosomal Disorders

December 31, 2025 • 121 mins
Oral Alpan, MD, Immunologist, Amerimmune, Virginia, USA; Svenja Keller, PhD student, University of Zurich, Switzerland; Shoshana Revel-Vilk, MD, PhD, Director, Gaucher Unit & Pediatric Hematology/Oncology Unit, Shaare Zedek Medical Center, Jerusalem, Israel; Patrick Deegan, MD, Consultant Metabolic Physician, University of Cambridge, UK; and Ravi Kamath, MD, PhD, Head of Musculoskeletal Radiology, Inova Health System, Virginia,...
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Organoids and Lab-Grown Models in Lysosomal Disorders

December 31, 2025 • 96 mins
Mia Horowitz, PhD, Tel Aviv University; Aitor Aguirre, PhD, Michigan State University, Michigan, USA; and Ying Sun, PhD, University of Cincinnati, discuss the use of organoid models in lysosomal disorder research and drug development.

This continuing education activity is provided through collaboration between the Lysosomal and Rare Disorders Research and Treatment Center (LDRTC), CheckRare CE, and AffinityCE. This activity ...
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Nanotechnology and Lysosomal Disorders

December 31, 2025 • 50 mins
Stephan Stern, PhD, DABT, Director of Research and Development, Nanotechnology Characterization Lab (NCL), Frederick National Laboratory for Cancer Research, Maryland, USA; and Ruben Boado, PhD, Professor of Medicine, University of California at Los Angeles, California, USA, discuss the use of nanotechnology in the treatment of lysosomal disorders.

This continuing education activity is provided through collaboration bet...
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AI in Medicine: Transforming the Landscape of Tissue-Based Diagnostics

December 31, 2025 • 52 mins
Behzad Najafian, MD, Professor, Department of Laboratory Medicine & Pathology, Department of Medicine at the University of Washington, Washington, USA discusses the use of artificial intelligence in identifying and managing lysosomal disorders.

This continuing education activity is provided through collaboration between the Lysosomal and Rare Disorders Research and Treatment Center (LDRTC), CheckRare CE, and AffinityCE. ...
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Consider Rare: Suspecting and Diagnosing CIDP

November 15, 2025 • 28 mins
This accredited continuing education program is supported by an educational grant from Sanofi. Credit for the program can be obtained by visiting https://checkrare.com/learning/p-consider-rare-suspecting-and-diagnosing-cidp/ . 

This program, led by Jeffrey Allen, MD, Professor of Neurology at the University of Minnesota provides an overview on the diagnostic delays that often occur in patients with CIDP as well as best ...
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Lysosomal Disorders and the Brain

October 14, 2025 • 58 mins
Ozlem Goker-Alpan, MD, Founder and President, Lysosomal & Rare Disorders Research & Treatment Center (LDRTC) and Raphael Schiffmann, MD, of the Texas Christian University, discuss best practices to identify and treat neurologic problems associated with lysosomal disorders.

This continuing education activity is provided through collaboration between the Lysosomal and Rare Disorders Research and Treatment Center (LDRTC...
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Case Studies in Diagnosing and Managing FOP

October 1, 2025 • 50 mins
This program, led by Christiaan Scott, MD, Professor of Pediatric Rheumatology at the University of Ottawa and Raphaella Stander, MBCHB, Pediatrician at Atlantic Children’s Practice, focused  on three case studies to provide physicians with education on best practices to: 1) suspect and diagnose FOP, 2) monitor and manage younger children with FOP, and 3) monitor and manage older children and adults with FOP. 
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Immune Thrombocytopenia (ITP) Research Highlights: ISTH 2025

September 15, 2025 • 27 mins
This accredited CME program highlights the latest clinical research about immune thrombocytopenia (ITP), a rare thrombotic disorder.
 
Led by Shruti Chaturvedi, MD, this program provides a summary of clinically relevant data presented at the International Society of Thrombosis and Haemostatis Congress (ISTH 2025) that can enhance the care of patients with ITP. 

This program is supported by an educational gran...
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Immune Thrombotic Thrombocytopenic Purpura (iTTP) Research Highlights: ISTH 2025

September 15, 2025 • 25 mins
The accredited CME program highlights the latest clinical research about iTTP, a rare thrombotic disorder.
 
Led by Shruti Chaturvedi, MD, this activity provides a summary of clinically relevant data presented at the International Society of Thrombosis and Haemostatis Congress (ISTH 2025) that can enhance the care of patients with iTTP. 

This program is supported by an educational grant from Sanofi.

To...
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Hemophilia Research Highlights: ISTH 2025

September 15, 2025 • 44 mins
The accredited CME program highlights the latest clinical research about hemophilia, a rare, genetic bleeding disorder.
 
Led by Dr. Steven Pipe, MD, this activity provides a summary of clinically relevant data presented at the International Society of Thrombosis and Haemostatis Congress (ISTH 2025) that can enhance the care of patients with hemophilia. 

This program is supported by an educational grant from ...
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Skeletal Involvement in Lysosomal Disorders

June 18, 2025 • 56 mins
Ozlem Goker-Alpan, MD, Founder and President, Lysosomal & Rare Disorders Research & Treatment Center (LDRTC) and Ravi Kamath, MD, PhD, of Fairfax Radiological Consultants & Inova Health System and University of Virginia School of Medicine Fairfax, Virginia, USA discuss best practices to identify and treat bone problems associated with lysosomal disorders.

This continuing education activity is provided through col...
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