Available courses

A Tailored Approach to Diagnosis and Early Treatment in Patients with Duchenne Muscular Dystrophy: A Real-World View of Quality of Life

Program Introduction

A detailed, modern digest of key advances in the diagnosis, treatment, and management of patients with Duchenne muscular dystrophy.

Learning Objective

After completing this educational activity, you should be able to: 

  • Use expert-guided treatment strategies for patients with Duchenne muscular dystrophy. 

Available Credit

  • 0.50 AMA PRA Category 1 Credit™
  • 0.50 Participation
Best Practices for Management of Mental Health in Women: Focusing on Mood Disorders Throughout the Lifespan

Program Introduction

Diagnosis and tailored treatment of menstrual cycle- and menopausal-related mood disorders are key factors in helping women live the lives they want to live.

Learning Objectives

  • Appraise the influence of the reproductive stage on mood disorders and comorbid psychiatric conditions in women.
  • Assess factors involved in the diagnoses of mood disorders in women and the differential diagnoses and common comorbidities.
  • Summarize evidence-based approaches for diagnosing and treating mood disorders in women.

Available Credit

  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation
Comparing LAI and Oral Antipsychotic Options: Expert Discussions with Schizophrenia Case Reports

Program Introduction

LAI antipsychotics are often initiated late in adults with schizophrenia, despite evidence supporting early use. Experts discuss the barriers to initiating LAI treatment, as well as adherence, efficacy and safety data.

Learning Objectives

After completing this educational activity, you should be able to:

  • Examine data comparing the efficacy of LAIAs and oral medications.  
  • Analyze the clinical trial data and unique considerations of available LAIAs.  
  • Implement early integration of LAIA therapies in appropriate patients.  

Available Credit

  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation
Case Studies in HAE: Diagnosing, Treating, and Managing the Patient With Hereditary Angioedema

Program Introduction

Explore Hereditary Angioedema treatment, emphasizing individualized care, first-line therapeutic options and investigational agents in clinical development. 

Learning Objectives

  • Analyze Hereditary Angioedema’s (HAE) pathophysiology to explain its underlying mechanisms.
  • Evaluate the impact of HAE on affected individuals to appreciate the condition's severity and implications.
  • Compare and contrast different therapeutic options available for HAE to determine their effectiveness.
  • Investigate and predict developments in future therapies for HAE to understand the direction of medical research and potential innovations.

Available Credit

  • 1.00 AMA PRA Category 1 Credit
  • 1.00 Participation
Untangling the Complexity of Alzheimer Disease With Effective Diagnostic Tools and Novel Treatment Options

Program Introduction

New biomarker technology and advancements in treatment options can lead to earlier diagnosis of Alzheimer disease and initiation of appropriate disease modifying therapies.

Learning Objectives

  • Identify biomarkers used in the early identification of Alzheimer disease
  • Assess the efficacy and safety data of novel investigational therapies for the management of Alzheimer disease
  • Implement advancements in diagnostic and screening tools for early Alzheimer disease assessment

Available Credit

  • 1.25 AMA PRA Category 1 Credits
  • 1.25 Participation
Optimizing Mental Health for Women: Recognizing and Treating Mood Disorders Throughout the Lifespan

Program Introduction

Mood disorders throughout women's reproductive stages require comprehensive care to alleviate unnecessary suffering, comorbidities, and unwanted outcomes.

Learning Objectives

After completing this educational activity, you should be able to:

  • Appraise the influence of the reproductive stage on mood disorders and comorbid psychiatric conditions in women
  • Assess factors involved in the diagnoses of mood disorders in women and the differential diagnoses and common comorbidities
  • Summarize evidence-based approaches for diagnosing and treating mood disorders in women

Available Credit

  • 1.00 AMA PRA Category 1 Credit
  • 1.00 Participation
Staying Up to Date with Evolving Postpartum Depression Pathophysiology and Treatment Research

Program Introduction

Early diagnosis of PPD is critical for mother-infant outcomes, and new hypotheses in its pathophysiology has led to novel and emerging therapies that can improve these outcomes.

Learning Objectives

After completing this educational activity, you should be able to: 

  • Examine the impact of delayed diagnosis on outcomes in PPD and best practices for management 
  • Explore pathophysiological mechanisms related to the expression of PPD symptoms 
  • Review clinical trial safety, efficacy, and dosing for current and emerging therapeutics for PPD 

Available Credit

  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation
Reviewing Non-Dopaminergic Mechanisms for Positive and Negative Schizophrenia Symptom Management

Program Introduction

What is the future of schizophrenia treatment? An in-depth exploration of novel, non-dopaminergic therapies transforming the standard of care for patients with schizophrenia’s positive and negative symptoms. 

Learning Objectives

After completing this educational activity, you should be able to: 

  • Outline current medication classes used in the treatment of schizophrenia 
  • Articulate side effect development and negative symptom control challenges associated with standard-of-care antipsychotics 
  • Review the latest research describing the biologic rationale of novel non-dopaminergic pathways in schizophrenia 
  • Analyze emerging clinical trial data for non-dopamine-targeting schizophrenia therapies 

Available Credit

  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation
Neuropsychiatric Complications of Parkinson’s Disease Psychosis

Program Introduction

Join us for a dynamic one-hour CME activity on Parkinson’s Disease Psychosis (PDP) with top experts Mark F. Lew, MD, and Jennifer Hui, MD. Unlock the latest best practices for diagnosing PDP and implementing cutting-edge therapies. The session kicks off with a deep dive into Parkinson’s Disease, covering its prevalence, motor and nonmotor symptoms, and the unique challenges of PDP. Next, master the intricacies of recognizing and diagnosing PDP with the newest diagnostic criteria and screening tools. Finally, conquer PDP treatment and management strategies, including behavioral approaches, medication adjustments, and safe antipsychotic options. Plus, gain invaluable insights from the caregiver of a real-world patient with PDP, providing a firsthand perspective on managing this complex condition. Boost your clinical expertise and transform patient care with this essential update on managing Parkinson’s Disease Psychosis.

Learning Objectives

  • Identify appropriate best practices for the diagnosis of PDP
  • Implement evidence-based current therapies for patients with PDP

Available Credit

  • 1.00 AMA PRA Category 1 CreditTM
  • 1.00 Participation

Advancements in Understanding Facioscapulohumeral Muscular Dystrophy (FSHD) and What Clinically Meaningful Outcomes Look Like

Program Introduction

Delve into the cutting-edge advancements in Facioscapulohumeral Muscular Dystrophy (FSHD) alongside the dynamic duo of Dr. Leo H. Wang and Dr. Maya N. Hatch in this symposium recorded at the 2024 MDA Clinical & Scientific Conference Summit. Positioned as the third most prevalent muscular dystrophy, FSHD stands as a genetic enigma with intricate roots, showcasing a progressive saga of asymmetrical muscle weakness. Initially targeting the facial and shoulder muscles before spreading its grip onto the extremities, this disorder's clinical narrative presents a formidable challenge in quantifying outcomes. It's an imperative moment to unearth dependable and sensitive metrics for clinical trials, navigating the labyrinthine landscape of FSHD. Acquire invaluable insights into mastering daily functionalities, tackling complications head-on, and remain abreast of the latest breakthroughs in establishing rock-solid measures for gauging progress.

Learning Objectives

  • Evaluate the use of RWS as an outcome measure for FSHD clinical trials and translate changes in RWS to clinically meaningful outcomes
  • Discuss the mechanism of FSHD disease that leads to challenges in DUX4 biomarker detection

Available Credit

  • 1.00 AMA PRA Category 1 CreditTM
  • 1.00 Participation