carnitine has been researched along with Enlarged Liver in 11 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Carnitine deficiency in the serum was found in 5 infants with cystic fibrosis, impaired liver function and neurological symptoms." | 7.69 | [Total carnitine level in infants with cystic fibrosis and deficit supplementation by means of pharmacologic preparations and diet. Introductory remarks]. ( Bujniewicz, E; Chlebowczyk, U; Krauze, M; Maliszewska, I; Mastalerz, Z; Szymańska, M; Woś, H, 1995) |
| "Massive hepatomegaly and steatosis developed in the baby at a time of severe viral respiratory illness, prolonged fasting, hypoglycemia, and hypoketonuria." | 5.28 | Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis. ( Stanley, CA; Treem, WR, 1989) |
| " Investigations revealed non-ketotic hypoglycemia suggesting FAOD which was later confirmed as carnitine uptake defect with gas chromatography and mass spectrometry and mutation analysis." | 3.85 | Infant with hepatomegaly and hypoglycemia: A setting for fatty acid oxidation defects. ( Pai, G; Poddar, U; Ravindranath, A; Srivastava, A; Yachha, SK, 2017) |
| "Here, we report the case of a 17-year-old girl who presented in both ten months and five years of age a clinical picture characterized by lethargy leading to apnea and coma, hepatomegaly, hypoglycemia, metabolic acidosis, hyperammoniemia, elevated serum transaminases and absence of ketonuria." | 3.70 | [3-hydroxy-3-methylglutaric aciduria and recurrent Reye-like syndrome]. ( Castro-Gago, M; Eirís, J; Fernández-Prieto, R; Ribes, A; Rodríguez-García, J; Rodríguez-Segade, S, 1998) |
| " Significant laboratory findings included elevated plasma levels of creatine phosphokinase and acyl-carnitine and a fatty liver at biopsy suggesting a diagnosis of VLCAD deficiency." | 3.70 | Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy. ( Abo, W; Doi, T; Fukao, T; Hayashi, K; Hori, T; Nakada, T; Takahashi, Y; Tateno, M; Terada, N, 2000) |
| "Carnitine deficiency in the serum was found in 5 infants with cystic fibrosis, impaired liver function and neurological symptoms." | 3.69 | [Total carnitine level in infants with cystic fibrosis and deficit supplementation by means of pharmacologic preparations and diet. Introductory remarks]. ( Bujniewicz, E; Chlebowczyk, U; Krauze, M; Maliszewska, I; Mastalerz, Z; Szymańska, M; Woś, H, 1995) |
| "The FF-treated rats developed hepatomegaly associated with increased hepatic carnitine and ATP and AMP concentrations, decreased protein breakdown, and decreased concentrations of DNA and triglycerides." | 1.56 | Effects of low and high doses of fenofibrate on protein, amino acid, and energy metabolism in rat. ( Holeček, M; Vodeničarovová, M, 2020) |
| "Massive hepatomegaly and steatosis developed in the baby at a time of severe viral respiratory illness, prolonged fasting, hypoglycemia, and hypoketonuria." | 1.28 | Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis. ( Stanley, CA; Treem, WR, 1989) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (18.18) | 18.7374 |
| 1990's | 2 (18.18) | 18.2507 |
| 2000's | 2 (18.18) | 29.6817 |
| 2010's | 4 (36.36) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Holeček, M | 1 |
| Vodeničarovová, M | 1 |
| Ravindranath, A | 1 |
| Pai, G | 1 |
| Srivastava, A | 1 |
| Poddar, U | 1 |
| Yachha, SK | 1 |
| Deswal, S | 1 |
| Bijarnia-Mahay, S | 1 |
| Manocha, V | 1 |
| Hara, K | 1 |
| Shigematsu, Y | 1 |
| Saxena, R | 1 |
| Verma, IC | 1 |
| Bouchireb, K | 1 |
| Teychene, AM | 1 |
| Rigal, O | 1 |
| de Lonlay, P | 1 |
| Valayannopoulos, V | 1 |
| Gaudelus, J | 1 |
| Sellier, N | 1 |
| Bonnefont, JP | 1 |
| Brivet, M | 1 |
| de Pontual, L | 1 |
| Răşanu, T | 1 |
| Mehedinţi-Hâncu, M | 1 |
| Alexianu, M | 1 |
| Mehedinţi, T | 1 |
| Gheorghe, E | 1 |
| Damian, I | 1 |
| Boles, RG | 1 |
| Woś, H | 1 |
| Krauze, M | 1 |
| Bujniewicz, E | 1 |
| Chlebowczyk, U | 1 |
| Mastalerz, Z | 1 |
| Szymańska, M | 1 |
| Maliszewska, I | 1 |
| Eirís, J | 1 |
| Ribes, A | 1 |
| Fernández-Prieto, R | 1 |
| Rodríguez-García, J | 1 |
| Rodríguez-Segade, S | 1 |
| Castro-Gago, M | 1 |
| Doi, T | 1 |
| Abo, W | 1 |
| Tateno, M | 1 |
| Hayashi, K | 1 |
| Hori, T | 1 |
| Nakada, T | 1 |
| Fukao, T | 1 |
| Takahashi, Y | 1 |
| Terada, N | 1 |
| Engel, AG | 1 |
| Banker, BQ | 1 |
| Eiben, RM | 1 |
| Treem, WR | 1 |
| Stanley, CA | 1 |
11 other studies available for carnitine and Enlarged Liver
| Article | Year |
|---|---|
Effects of low and high doses of fenofibrate on protein, amino acid, and energy metabolism in rat.
Topics: Amino Acids; Amino Acids, Branched-Chain; Animals; Carnitine; Energy Metabolism; Fenofibrate; Glycin | 2020 |
Infant with hepatomegaly and hypoglycemia: A setting for fatty acid oxidation defects.
Topics: Cardiomyopathies; Carnitine; Chromatography, Gas; DNA Mutational Analysis; Early Diagnosis; Hepatome | 2017 |
Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive Hepatomegaly.
Topics: Cardiomyopathies; Carnitine; Hepatomegaly; Humans; Hyperammonemia; Infant; Male; Muscular Diseases | 2017 |
Post-mortem MRI reveals CPT2 deficiency after sudden infant death.
Topics: Carnitine; Carnitine O-Palmitoyltransferase; Cause of Death; Diagnosis; Fatty Liver; Hepatomegaly; H | 2010 |
Carnitine deficiency.
Topics: Biopsy; Carnitine; Child; Diagnosis, Differential; Disease Progression; Electromyography; Female; He | 2012 |
Very long-chain acyl-CoA dehydrogenase deficiency in an infant presenting with massive hepatomegaly.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Cardiomyopathies; Carnitine; Diet; Gastroenteritis; Hepatomegaly | 2002 |
[Total carnitine level in infants with cystic fibrosis and deficit supplementation by means of pharmacologic preparations and diet. Introductory remarks].
Topics: Cardiomegaly; Carnitine; Cystic Fibrosis; Enteral Nutrition; Food, Fortified; Hepatomegaly; Humans; | 1995 |
[3-hydroxy-3-methylglutaric aciduria and recurrent Reye-like syndrome].
Topics: Acidosis; Adolescent; Apnea; Carnitine; Coma; Diagnosis, Differential; Fatty Liver; Female; Fibrobla | 1998 |
Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Cardiomegaly; Carnitine; Child; Fatty Liver; Heart Failure; Hepa | 2000 |
Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.
Topics: Acidosis; Carnitine; Child; Hepatomegaly; Humans; Male; Mitochondria, Muscle; Muscles; Muscular Dise | 1977 |
Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis.
Topics: Carnitine; Combined Modality Therapy; Cystic Fibrosis; Fatty Liver; Glycine max; Hepatomegaly; Human | 1989 |