Gerald Pfeffer
Biographic Data
| ID | 8981212 |
|---|---|
| NAME | Gerald Pfeffer |
| GIVEN NAMES | Gerald |
| FAMILY NAME | Pfeffer |
| SIGNATURE | PFEFFER G |
| AFFILIATIONS | Department of Clinical Neurosciences Hotchkiss Brain Institute Calgary Alberta Canada |
| ORCID | 0000-0002-7657-7098 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 2 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
From Doubt to Diagnosis
INTRODUCTION: Limb-girdle muscular dystrophies (LGMDs) encompass a rare and genetically diverse set of disorders, posing challenges in diagnosis due to the absence of distinct pathological features, leading to frequent misdiagnoses and inadequate symptom management. Yet, there is a scarcity of published data on how patients perceive the diagnostic journey of LGMD. Our aim was to unveil the firsthand experiences of individuals with LGMD to gain in…
Counting the Cost
INTRODUCTION: Neuromuscular diseases (NMDs) impose multifaceted challenges on individuals and their families, often resulting in significant medical and non-medical expenses. While cost-of-illness (COI) studies provide valuable quantitative data, few explore the lived experience of financial strain. This study aims to identify the complex, often hidden, financial impacts experienced by individuals with NMDs and their families. METHODS: We conduct…
No prominent works on this page.
From Doubt to Diagnosis
INTRODUCTION: Limb-girdle muscular dystrophies (LGMDs) encompass a rare and genetically diverse set of disorders, posing challenges in diagnosis due to the absence of distinct pathological features, leading to frequent misdiagnoses and inadequate symptom management. Yet, there is a scarcity of published data on how patients perceive the diagnostic journey of LGMD. Our aim was to unveil the firsthand experiences of individuals with LGMD to gain in…
Counting the Cost
INTRODUCTION: Neuromuscular diseases (NMDs) impose multifaceted challenges on individuals and their families, often resulting in significant medical and non-medical expenses. While cost-of-illness (COI) studies provide valuable quantitative data, few explore the lived experience of financial strain. This study aims to identify the complex, often hidden, financial impacts experienced by individuals with NMDs and their families. METHODS: We conduct…
Neurogenetic and Muscular Disorders Research (2 works) · Qualitative research (2 works) · Amyotrophic Lateral Sclerosis Research (1 work) · Anxiety (1 work) · Clinical Psychology (1 work) · Distress (1 work) · Feeling (1 work) · Focus group (1 work) · General partnership (1 work) · Genetic Neurodegenerative Diseases (1 work)