F Mutschler
Biographic Data
| ID | 8253371 |
|---|---|
| NAME | F Mutschler |
| GIVEN NAMES | F |
| FAMILY NAME | Mutschler |
| SIGNATURE | MUTSCHLER F |
| AFFILIATIONS | Medizinische Hochschule Hannover |
| ORCID | 0000-0003-1313-5863 |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
Ileal Bile Acid Transporter Inhibition Reduces Post-Transplant Diarrhea and Growth Failure in FIC1 Disease—A Case Report
Familial intrahepatic cholestasis 1 (FIC1) disease is a genetic disorder characterized by hepatic and gastrointestinal disease due to ATP8B1 deficiency, often requiring liver transplantation (LT). Extrahepatic symptoms, such as diarrhea, malabsorption, and failure to thrive, do not improve and instead may be aggravated after LT. We describe a patient with FIC1 disease who underwent LT at 2 years, 8 months of age. After LT, the child developed sev…
No prominent works on this page.
Ileal Bile Acid Transporter Inhibition Reduces Post-Transplant Diarrhea and Growth Failure in FIC1 Disease—A Case Report
Familial intrahepatic cholestasis 1 (FIC1) disease is a genetic disorder characterized by hepatic and gastrointestinal disease due to ATP8B1 deficiency, often requiring liver transplantation (LT). Extrahepatic symptoms, such as diarrhea, malabsorption, and failure to thrive, do not improve and instead may be aggravated after LT. We describe a patient with FIC1 disease who underwent LT at 2 years, 8 months of age. After LT, the child developed sev…
Bile acid (1 work) · Cholestasis (1 work) · Diarrhea (1 work) · Disease (1 work) · Drug Transport and Resistance Mechanisms (1 work) · Failure to thrive (1 work) · Gastroenterology (1 work) · Internal Medicine (1 work) · Liver disease (1 work) · Liver Diseases and Immunity (1 work)