carnitine has been researched along with Recrudescence in 21 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A 16-year-old boy with a two-year history of recurrent attacks of myalgia, muscle cramps without weakness, and myoglobinuria was shown to have a deficiency in muscle carnitine palmityltransferase." | 7.65 | Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency. ( Herman, J; Nadler, HL, 1977) |
| "Objective- Stroke is a heterogeneous disease with diverse causes, which affect the risk of recurrence." | 5.48 | Medium-Chain Acylcarnitines Are Associated With Cardioembolic Stroke and Stroke Recurrence. ( Jo, G; Oh, K; Seo, WK; Shin, MJ, 2018) |
| " The rising hyperbilirubinemia and transaminitis rapidly and permanently reversed using the amino-acid derivative L-carnitine." | 3.83 | L-Carnitine for Treatment of Pegasparaginase-Induced Hepatotoxicity. ( Alshiekh-Nasany, R; Douer, D, 2016) |
| "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) |
| "A 16-year-old boy with a two-year history of recurrent attacks of myalgia, muscle cramps without weakness, and myoglobinuria was shown to have a deficiency in muscle carnitine palmityltransferase." | 3.65 | Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency. ( Herman, J; Nadler, HL, 1977) |
| "Objective- Stroke is a heterogeneous disease with diverse causes, which affect the risk of recurrence." | 1.48 | Medium-Chain Acylcarnitines Are Associated With Cardioembolic Stroke and Stroke Recurrence. ( Jo, G; Oh, K; Seo, WK; Shin, MJ, 2018) |
| "Carnitine is a carrier for the transport of long-chain fatty acids from the cytoplasmic to the mitochondrial space." | 1.26 | [Carnitine deficiency myopathy (author's transl)]. ( Engel, AG; Imbach, P; Jerusalem, F; Lämmli, J; Sengupta, C, 1980) |
| "The clinical diagnosis of recurrent Reye's syndrome can be made only after a systemic exclusion of other diagnostic possibilities." | 1.26 | Recurrent Reye's syndrome. ( McCabe, ER; Pichichero, ME, 1978) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (23.81) | 18.7374 |
| 1990's | 6 (28.57) | 18.2507 |
| 2000's | 2 (9.52) | 29.6817 |
| 2010's | 8 (38.10) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Seo, WK | 1 |
| Jo, G | 1 |
| Shin, MJ | 1 |
| Oh, K | 1 |
| Phowthongkum, P | 1 |
| Suphapeetiporn, K | 1 |
| Shotelersuk, V | 1 |
| Hanai, S | 1 |
| Iwata, M | 1 |
| Terasawa, T | 1 |
| Vissing, CR | 1 |
| Duno, M | 1 |
| Olesen, JH | 1 |
| Rafiq, J | 1 |
| Risom, L | 1 |
| Christensen, E | 1 |
| Wibrand, F | 1 |
| Vissing, J | 1 |
| Shang, R | 1 |
| Sun, Z | 1 |
| Li, H | 1 |
| Alshiekh-Nasany, R | 1 |
| Douer, D | 1 |
| Qian, GL | 1 |
| Hong, F | 1 |
| Tong, F | 1 |
| Fu, HD | 1 |
| Liu, AM | 1 |
| Yamamoto, Y | 1 |
| Matsui, N | 1 |
| Hiramatsu, Y | 1 |
| Miyazaki, Y | 1 |
| Nodera, H | 1 |
| Izumi, Y | 1 |
| Takashima, H | 1 |
| Kaji, R | 1 |
| Ogundare, O | 1 |
| Jumma, O | 1 |
| Turnbull, DM | 1 |
| Woywodt, A | 1 |
| Hou, JW | 1 |
| Jerusalem, F | 1 |
| Engel, AG | 1 |
| Sengupta, C | 1 |
| Imbach, P | 1 |
| Lämmli, J | 1 |
| Moore, R | 1 |
| Glasgow, JF | 1 |
| Bingham, MA | 1 |
| Dodge, JA | 1 |
| Pollitt, RJ | 1 |
| Olpin, SE | 1 |
| Middleton, B | 1 |
| Carpenter, K | 1 |
| Carrasco Marina, LL | 1 |
| Ramos Lizana, J | 1 |
| Vázquez López, M | 1 |
| Garrote de Marcos, JM | 1 |
| Arregui Sierra, A | 1 |
| Bornstein, B | 1 |
| Arenas, J | 1 |
| Straussberg, R | 1 |
| Harel, L | 1 |
| Varsano, I | 1 |
| Elpeleg, ON | 1 |
| Shamir, R | 1 |
| Amir, J | 1 |
| Törel Ergür, A | 1 |
| Tanzer, F | 1 |
| Cetinkaya, O | 1 |
| Eirís, J | 1 |
| Ribes, A | 1 |
| Fernández-Prieto, R | 1 |
| Rodríguez-García, J | 1 |
| Rodríguez-Segade, S | 1 |
| Castro-Gago, M | 1 |
| Patten, BM | 1 |
| Wood, JM | 1 |
| Harati, Y | 1 |
| Hefferan, P | 1 |
| Howell, RR | 1 |
| Dusheiko, G | 1 |
| Kew, MC | 1 |
| Joffe, BI | 1 |
| Lewin, JR | 1 |
| Mantagos, S | 1 |
| Tanaka, K | 1 |
| Pichichero, ME | 1 |
| McCabe, ER | 1 |
| Herman, J | 1 |
| Nadler, HL | 1 |
| Dionisi Vici, C | 1 |
| Burlina, AB | 1 |
| Bertini, E | 1 |
| Bachmann, C | 1 |
| Mazziotta, MR | 1 |
| Zacchello, F | 1 |
| Sabetta, G | 1 |
| Hale, DE | 1 |
3 reviews available for carnitine and Recrudescence
| Article | Year |
|---|---|
Effective dosing of L-carnitine in the secondary prevention of cardiovascular disease: a systematic review and meta-analysis.
Topics: Administration, Oral; Cardiovascular Agents; Cardiovascular Diseases; Carnitine; Chi-Square Distribu | 2014 |
Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.
Topics: Amino Acid Metabolism, Inborn Errors; Biopsy, Needle; Brain Diseases, Metabolic; Carnitine; Child, P | 2016 |
[Recurrent myoglobinuria in a girl due to carnitine palmitoyltransferase deficiency].
Topics: Administration, Oral; Adult; Carnitine; Carnitine O-Palmitoyltransferase; Female; Humans; Myoglobinu | 1996 |
18 other studies available for carnitine and Recrudescence
| Article | Year |
|---|---|
Medium-Chain Acylcarnitines Are Associated With Cardioembolic Stroke and Stroke Recurrence.
Topics: Aged; Biomarkers; Brain Ischemia; Carnitine; Chromatography, Liquid; Female; Humans; Male; Metabolom | 2018 |
Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists.
Topics: Adult; Anti-Bacterial Agents; Carnitine; Carnitine O-Palmitoyltransferase; Escherichia coli Infectio | 2019 |
Relapsing Hypoglycemia Associated with Hypocarnitinemia Following Treatment with Cefcapene Pivoxil in an Elderly Man.
Topics: Administration, Oral; Aged, 80 and over; Blood Glucose; Cardiomyopathies; Carnitine; Cephalosporins; | 2019 |
Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene.
Topics: Adult; Carnitine; DNA, Mitochondrial; Electron Transport Complex IV; Humans; Male; Mutation; Myoglob | 2013 |
L-Carnitine for Treatment of Pegasparaginase-Induced Hepatotoxicity.
Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Carnit | 2016 |
Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease.
Topics: Biomarkers; Cardiomyopathies; Carnitine; Charcot-Marie-Tooth Disease; Diagnosis, Differential; Disea | 2017 |
Searching for the needle in the Haystacks.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Biopsy; Carnitine; Creatine Kinase; Creatinine; Hi | 2009 |
Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy.
Topics: Cardiomyopathy, Dilated; Carnitine; Child; Female; Humans; Recurrence; Reye Syndrome | 2002 |
[Carnitine deficiency myopathy (author's transl)].
Topics: Biopsy; Carnitine; Electromyography; Humans; Male; Middle Aged; Muscles; Muscular Diseases; Paralysi | 1980 |
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; Female; Gastrointestinal Diseases; Hu | 1993 |
Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Carnitine; Child; Diet; Fatty Acid Desaturases; Fe | 1997 |
Serum free carnitine levels in children with recurrent pulmonary infections.
Topics: Carnitine; Case-Control Studies; Child; Female; Humans; Lung Diseases; Male; Recurrence; Respiratory | 1997 |
[3-hydroxy-3-methylglutaric aciduria and recurrent Reye-like syndrome].
Topics: Acidosis; Adolescent; Apnea; Carnitine; Coma; Diagnosis, Differential; Fatty Liver; Female; Fibrobla | 1998 |
Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency.
Topics: Acyltransferases; Adult; Animals; Carnitine; Carnitine O-Palmitoyltransferase; Cell Membrane; Humans | 1979 |
Recurrent hypoglycemia associated with glutaric aciduria type II in an adult.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Carnitine; Fatty Acid Desaturases; Fatty Acids, Noneste | 1979 |
Recurrent Reye's syndrome.
Topics: Adolescent; Carnitine; Diagnosis, Differential; Female; Humans; Ornithine Carbamoyltransferase; Recu | 1978 |
Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
Topics: Acyltransferases; Adolescent; Carnitine; Carnitine O-Palmitoyltransferase; Humans; Male; Muscles; My | 1977 |
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Biopsy; Carnitine; Child; Combined Modality Therapy; Dietary Fats; | 1991 |