carnitine has been researched along with Endocardial Fibroelastosis in 4 studies
Endocardial Fibroelastosis: A condition characterized by the thickening of ENDOCARDIUM due to proliferation of fibrous and elastic tissue, usually in the left ventricle leading to impaired cardiac function (CARDIOMYOPATHY, RESTRICTIVE). It is most commonly seen in young children and rarely in adults. It is often associated with congenital heart anomalies (HEART DEFECTS CONGENITAL;) INFECTION; or gene mutation. Defects in the tafazzin protein, encoded by TAZ gene, result in a form of autosomal dominant familial endocardial fibroelastosis.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Endocardial fibroelastosis (EFE) has previously been shown to be associated with tissue carnitine deficiency, although the basis for the carnitine deficiency has not been documented." | 7.69 | Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter. ( Bennett, MJ; Hale, DE; Pollitt, RJ; Stanley, CA; Variend, S, 1996) |
| "Endocardial fibroelastosis (EFE) has previously been shown to be associated with tissue carnitine deficiency, although the basis for the carnitine deficiency has not been documented." | 3.69 | Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter. ( Bennett, MJ; Hale, DE; Pollitt, RJ; Stanley, CA; Variend, S, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tripp, ME | 1 |
| Katcher, ML | 1 |
| Peters, HA | 1 |
| Gilbert, EF | 1 |
| Arya, S | 1 |
| Hodach, RJ | 1 |
| Shug, AL | 1 |
| Bennett, MJ | 1 |
| Hale, DE | 1 |
| Pollitt, RJ | 1 |
| Stanley, CA | 1 |
| Variend, S | 1 |
| Hanukoglu, A | 1 |
| Fried, D | 1 |
| Somekh, E | 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 |
4 other studies available for carnitine and Endocardial Fibroelastosis
| Article | Year |
|---|---|
Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy.
Topics: Administration, Oral; Carnitine; Child; Endocardial Fibroelastosis; Female; Humans; Infant; Infant, | 1981 |
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter.
Topics: Cardiomyopathy, Dilated; Carnitine; Cell Membrane; Endocardial Fibroelastosis; Female; Fibroblasts; | 1996 |
Inheritance of familial primary endocardial fibroelastosis.
Topics: Carnitine; Digoxin; Endocardial Fibroelastosis; Female; HLA Antigens; Humans; Infant; Infant, Newbor | 1986 |
omega-123I-hexadecanoic acid metabolic probe of cardiomyopathy.
Topics: Adolescent; Adult; Aged; Alcoholism; Atrial Fibrillation; Cardiomyopathies; Cardiomyopathy, Dilated; | 1985 |