A 60-year-old man was admitted in the intensive care unit (ICU) for a rapidly progressive respiratory failure due to SARS-CoV-2 infection. He developed numerous complications including acute kidney injury (AKI) requiring prolonged continuous renal replacement therapy (CRRT). Enteral feeding was initiated on day 8. Despite nutritional management, there was a remarkable amyotrophy and weight loss. On day 85 in the ICU, the patient became progressively unresponsive. An extensive metabolic workup was performed, and blood results showed hyperammoniemia and hypertriglyceridemia. Plasma free carnitine level was low, as was also copper. After carnitine supplementation, the neurological condition rapidly improved, and metabolic perturbations regress...
Carnitine is a conditionally essential metabolite that plays a critical role in cell physiology. Car...
© 2022 American Society for Parenteral and Enteral Nutrition.Background: Acute kidney injury (AKI) t...
BACKGROUND: Cystinosis is an autosomal recessive disorder marked by intralysosomal cystine accumulat...
A 60-year-old man was admitted in the intensive care unit (ICU) for a rapidly progressive respirator...
Plasma carnitine levels were studied in 14 uremic patients before, during, and after hemodialysis. T...
Chronic kidney failure is associated with many kinds of metabolic disorders caused by the kidney dis...
The purpose of the study was to find out an eventual relation beΩween the carnitine levels and the d...
Abstract Background l-carnitine is essential for lipid metabolism, and lack of l-carnitine intake an...
Background. Functional carnitine deficiency [as indicated by an abnormal acyl-carnitine/free-carniti...
A stay in intensive care unit (ICU) exposes patients to a risk of carnitine deficiency. Moreover, ac...
Acute renal failure (ARF) is rarely an isolated process but is often a complication of underlying co...
peer reviewedA stay in intensive care unit (ICU) exposes patients to a risk of carnitine deficiency....
BACKGROUND: Carnitine palmitoyltransferase II deficiency (CPT II) is an autosomal recessive disorder...
The aim of the present study was to investigate the effects of continuous and acute L-carnitine supp...
WOS: 000175543600014PubMed ID: 11982875Background: Impaired structural and metabolic integrity of th...
Carnitine is a conditionally essential metabolite that plays a critical role in cell physiology. Car...
© 2022 American Society for Parenteral and Enteral Nutrition.Background: Acute kidney injury (AKI) t...
BACKGROUND: Cystinosis is an autosomal recessive disorder marked by intralysosomal cystine accumulat...
A 60-year-old man was admitted in the intensive care unit (ICU) for a rapidly progressive respirator...
Plasma carnitine levels were studied in 14 uremic patients before, during, and after hemodialysis. T...
Chronic kidney failure is associated with many kinds of metabolic disorders caused by the kidney dis...
The purpose of the study was to find out an eventual relation beΩween the carnitine levels and the d...
Abstract Background l-carnitine is essential for lipid metabolism, and lack of l-carnitine intake an...
Background. Functional carnitine deficiency [as indicated by an abnormal acyl-carnitine/free-carniti...
A stay in intensive care unit (ICU) exposes patients to a risk of carnitine deficiency. Moreover, ac...
Acute renal failure (ARF) is rarely an isolated process but is often a complication of underlying co...
peer reviewedA stay in intensive care unit (ICU) exposes patients to a risk of carnitine deficiency....
BACKGROUND: Carnitine palmitoyltransferase II deficiency (CPT II) is an autosomal recessive disorder...
The aim of the present study was to investigate the effects of continuous and acute L-carnitine supp...
WOS: 000175543600014PubMed ID: 11982875Background: Impaired structural and metabolic integrity of th...
Carnitine is a conditionally essential metabolite that plays a critical role in cell physiology. Car...
© 2022 American Society for Parenteral and Enteral Nutrition.Background: Acute kidney injury (AKI) t...
BACKGROUND: Cystinosis is an autosomal recessive disorder marked by intralysosomal cystine accumulat...