carnitine has been researched along with Cardiomyopathy, Hypertrophic Obstructive in 21 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Brugada syndrome is an autosomal dominant trait with right bundle branch block and ST elevation." | 2.43 | Pathogenesis of cardiac conduction disorders in children genetic and histopathologic aspects. ( Barness, LA; Gilbert-Barness, E, 2006) |
| "L-Carnitine treatment led to gradual improvement in exercise tolerance and cognitive performance; plasma and tissue carnitine levels returned to normal, and echocardiographic evidence of left ventricular hypertrophy disappeared." | 1.30 | Myoadenylate deaminase deficiency, hypertrophic cardiomyopathy and gigantism syndrome. ( Bittner, RE; Gross, M; Marx, M; Skyllouriotis, ML; Skyllouriotis, P; Wimmer, M, 1997) |
| "Carnitine is an essential cofactor for the beta-oxidation of fats." | 1.27 | Plasma carnitine concentrations in cardiomyopathy patients. ( Shug, AL; Tripp, ME, 1984) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (28.57) | 18.7374 |
| 1990's | 8 (38.10) | 18.2507 |
| 2000's | 6 (28.57) | 29.6817 |
| 2010's | 1 (4.76) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kishimoto, S | 1 |
| Suda, K | 1 |
| Yoshimoto, H | 1 |
| Teramachi, Y | 1 |
| Nishino, H | 1 |
| Koteda, Y | 1 |
| Itoh, S | 1 |
| Kudo, Y | 1 |
| Iemura, M | 1 |
| Matsuishi, T | 1 |
| Wasant, P | 1 |
| Matsumoto, I | 1 |
| Naylor, E | 1 |
| Liammongkolkul, S | 1 |
| Takahashi, R | 2 |
| Okumura, K | 2 |
| Asai, T | 2 |
| Hirai, T | 1 |
| Murakami, H | 2 |
| Murakami, R | 2 |
| Numaguchi, Y | 2 |
| Matsui, H | 2 |
| Ito, M | 1 |
| Murohara, T | 2 |
| Gilbert-Barness, E | 1 |
| Barness, LA | 1 |
| Tripp, ME | 1 |
| Shug, AL | 1 |
| Ferro, M | 1 |
| Crivello, R | 1 |
| Gianotti, A | 1 |
| Conti, M | 1 |
| Skyllouriotis, ML | 2 |
| Marx, M | 2 |
| Bittner, RE | 1 |
| Skyllouriotis, P | 2 |
| Gross, M | 1 |
| Wimmer, M | 2 |
| Bittner, R | 1 |
| Scholte, HR | 1 |
| Van Coster, RN | 1 |
| de Jonge, PC | 1 |
| Poorthuis, BJ | 1 |
| Jeneson, JA | 1 |
| Andresen, BS | 1 |
| Gregersen, N | 1 |
| de Klerk, JB | 1 |
| Busch, HF | 1 |
| Nakamura, T | 2 |
| Sugihara, H | 2 |
| Kinoshita, N | 2 |
| Ito, K | 1 |
| Adachi, Y | 1 |
| Hirasaki, S | 1 |
| Matsuo, A | 1 |
| Azuma, A | 2 |
| Kodo, N | 1 |
| Nakagawa, M | 2 |
| Alizad, A | 1 |
| Seward, JB | 1 |
| Yoneyama, S | 1 |
| Duncan, WJ | 1 |
| Tyrrell, MJ | 1 |
| Bharadwaj, BB | 1 |
| Bautista, J | 1 |
| Rafel, E | 1 |
| Martinez, A | 1 |
| Sainz, I | 1 |
| Herrera, J | 1 |
| Segura, L | 1 |
| Chinchon, I | 1 |
| Stanley, CA | 1 |
| Treem, WR | 1 |
| Hale, DE | 1 |
| Coates, PM | 1 |
| Coratelli, P | 1 |
| Buongiorno, E | 1 |
| Petrarulo, F | 1 |
| Corciulo, R | 1 |
| Giannattasio, M | 1 |
| Passavanti, G | 1 |
| Antonelli, G | 1 |
| Caforio, AL | 1 |
| Rossi, B | 1 |
| Risaliti, R | 1 |
| Siciliano, G | 1 |
| Marchetti, A | 1 |
| Angelini, C | 1 |
| Crea, F | 1 |
| Mariani, M | 1 |
| Muratorio, A | 1 |
| Ino, T | 1 |
| Sherwood, WG | 1 |
| Benson, LN | 1 |
| Wilson, GJ | 1 |
| Freedom, RM | 1 |
| Rowe, RD | 1 |
| Conte, A | 1 |
| Hess, OM | 1 |
| Maire, R | 1 |
| Gautschi, K | 1 |
| Brogli, S | 1 |
| Knaus, U | 1 |
| Krayenbühl, HP | 1 |
| Rabinovitch, MA | 1 |
| Kalff, V | 1 |
| Allen, R | 1 |
| Rosenthal, A | 1 |
| Albers, J | 1 |
| Das, SK | 1 |
| Pitt, B | 1 |
| Swanson, DP | 1 |
| Mangner, T | 1 |
| Rogers, WL | 1 |
3 reviews available for carnitine and Cardiomyopathy, Hypertrophic Obstructive
| Article | Year |
|---|---|
Pathogenesis of cardiac conduction disorders in children genetic and histopathologic aspects.
Topics: Arrhythmias, Cardiac; Cardiomyopathy, Hypertrophic; Carnitine; Female; Heart Block; Heart Conduction | 2006 |
[Treatment of hypertrophic cardiomyopathy with a combination of carnitine and beta blockaders. Review of the literature. Description of a clinical case and long-term follow up].
Topics: Adrenergic beta-Antagonists; Cardiomyopathy, Hypertrophic; Carnitine; Drug Therapy, Combination; Hum | 1993 |
Echocardiographic features of genetic diseases: part 1. Cardiomyopathy.
Topics: Arrhythmogenic Right Ventricular Dysplasia; Beckwith-Wiedemann Syndrome; Cardiomyopathies; Cardiomyo | 2000 |
18 other studies available for carnitine and Cardiomyopathy, Hypertrophic Obstructive
| Article | Year |
|---|---|
Thirty-year follow-up of carnitine supplementation in two siblings with hypertrophic cardiomyopathy caused by primary systemic carnitine deficiency.
Topics: Adult; Cardiomyopathies; Cardiomyopathy, Hypertrophic; Carnitine; Dietary Supplements; Follow-Up Stu | 2012 |
Mitochondrial fatty acid oxidation disorders in Thai infants: a report of 3 cases.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathy, Hypertrophic; Carnitine; Fatal Outcome; Fatty Acid | 2002 |
Dietary fish oil attenuates cardiac hypertrophy in lipotoxic cardiomyopathy due to systemic carnitine deficiency.
Topics: Animals; Blood Glucose; Cardiomyopathy, Hypertrophic; Carnitine; Cell Membrane; Dietary Fats, Unsatu | 2005 |
Combined therapy with PPARalpha agonist and L-carnitine rescues lipotoxic cardiomyopathy due to systemic carnitine deficiency.
Topics: Adenosine Triphosphate; Animals; Cardiomyopathy, Hypertrophic; Carnitine; Diglycerides; Drug Therapy | 2006 |
Plasma carnitine concentrations in cardiomyopathy patients.
Topics: Adolescent; Adult; Cardiomyopathies; Cardiomyopathy, Dilated; Cardiomyopathy, Hypertrophic; Carnitin | 1984 |
Myoadenylate deaminase deficiency, hypertrophic cardiomyopathy and gigantism syndrome.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Adult; AMP Deaminase; Biopsy; Cardiomyopathy, Hypertr | 1997 |
Nemaline myopathy and cardiomyopathy.
Topics: Acyl-CoA Dehydrogenase; Biopsy; Cardiomyopathy, Hypertrophic; Carnitine; Child, Preschool; Diet, Fat | 1999 |
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Acyl-CoA Dehydrogenases; Adolescent; Adult; Cardiomyopathy, Hype | 1999 |
Serum carnitine concentrations in patients with idiopathic hypertrophic cardiomyopathy: relationship with impaired myocardial fatty acid metabolism.
Topics: Adolescent; Adult; Aged; Biomarkers; Cardiomyopathy, Hypertrophic; Carnitine; Fatty Acids; Fatty Aci | 1999 |
Can serum carnitine levels distinguish hypertrophic cardiomyopathy from hypertensive hearts?
Topics: Adult; Aged; Analysis of Variance; Cardiomyopathy, Hypertrophic; Carnitine; Diagnosis, Differential; | 2000 |
Disopyramide as a negative inotrope in obstructive cardiomyopathy in children.
Topics: Cardiomyopathy, Hypertrophic; Carnitine; Child; Disopyramide; Ductus Arteriosus, Patent; Echocardiog | 1991 |
Familial hypertrophic cardiomyopathy and muscle carnitine deficiency.
Topics: Adolescent; Adult; Aged; Biopsy; Cardiomyopathy, Hypertrophic; Carnitine; Child; Female; Humans; Mal | 1990 |
A genetic defect in carnitine transport causing primary carnitine deficiency.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Biological Transport; Cardiomyopathy, Hy | 1990 |
Pathogenetic aspects of uremic cardiomyopathy.
Topics: Adult; Aged; Calcium; Cardiomyopathy, Hypertrophic; Carnitine; Echocardiography; Female; Humans; Iro | 1989 |
Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: evidence of subclinical myogenic myopathy.
Topics: Adult; Cardiomyopathy, Dilated; Cardiomyopathy, Hypertrophic; Carnitine; Electrocardiography; Electr | 1989 |
Cardiac manifestations in disorders of fat and carnitine metabolism in infancy.
Topics: Biopsy; Cardiac Catheterization; Cardiomyopathy, Hypertrophic; Carnitine; Echocardiography; Electroc | 1988 |
[Clinical significance of serum carnitine in the course and prognosis of dilated cardiomyopathy].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Cardiomyopathy, Alcoholic; Cardiomyopathy, Dilated; Card | 1987 |
omega-123I-hexadecanoic acid metabolic probe of cardiomyopathy.
Topics: Adolescent; Adult; Aged; Alcoholism; Atrial Fibrillation; Cardiomyopathies; Cardiomyopathy, Dilated; | 1985 |