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The Latest Insights into Rare Blood Disorders: Diagnosis and Treatment Strategies
David J. Kuter, MD, DPhil
Spero R. Cataland, MD
Catherine Broome, MD
Cindy Neunert, MD, MSCS
Diagnostic Delay and the Critical Role of Personalized Screening Approaches in Cushing’s Syndrome
Maria Fleseriu, MD, FACE
Martin Reincke, MD
Recurrence of Cushing’s and the Changing Landscape of Medical Management
Richard Auchus, MD
Comprehensive Care and Medical Management of Acromegaly: Achieving an Earlier Diagnosis and Biochemical Control
Susan L Samson, MD, PhD, FRCPC, FACE
Eliza B. Geer, MD
Kevin C.J. Yuen, MD
Could Your Patient’s Symptoms Be Acromegaly?
Refining Screening and Referral in Frontline Care Settings
Making a Definitive Diagnosis
Guideline and Evidence-Based Best Practices for Treatment Sequencing
Understanding Trial Data
Best Practices for Individualizing Treatment Selection
Managing TRAEs and Minimizing Hyperglycemia
How Would You Treat?
Idiopathic Multicentric Castleman Disease Patient Journey: Optimizing Best Practices to Improve Patient-Centric Outcomes
Corey Casper, MD, MPH
Sudipto Mukherjee, MD, PhD, MPH
Jovanna De La Pena
Hiding in Plain Sight: Could This Be Castleman Disease?
Climbing the Long, Winding Stairs to the Diagnosis of Castleman Disease
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