carnitine has been researched along with Atrophy in 15 studies
Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Therefore, the overlapping syndrome of chronic progressive external ophthalmoplegia in the MELAS syndrome is considered in this case." | 5.29 | CPEO and carnitine deficiency overlapping in MELAS syndrome. ( Chen, HL; Chuang, YH; Hsu, CC; Huang, HL; Jong, HJ; Lee, HC; Pang, CY; Shen, YY; Tsai, JL; Wei, YH, 1995) |
| " In addition to the typical findings of Norman-Roberts syndrome, case 1 had atrial septal defect, corpus callosum agenesis, intracranial widespread calcification and case 2 had bilateral macular cherry-red spot, persistent foramen ovale, increased blood level of C6 hexanoylcarnitine, cavum septum pellucidum vergae anomaly and cerebellar atrophy." | 3.72 | Report of two Turkish infants with Norman-Roberts syndrome. ( Caksen, H; Cinal, A; Fryns, JP; Kirimi, E; Odabaş, D; Tuncer, O; Unal, O; Uner, A, 2004) |
| "These data on disease progression will be useful in future studies using the canine model for therapeutic intervention studies." | 1.72 | Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis. ( Coates, JR; Jensen, CA; Katz, ML; Kick, GR; Meiman, EJ, 2022) |
| "Neurodevelopmental delay and encephalopathy are complications of both HIV and GA1." | 1.48 | Favourable outcome in a child with symptomatic diagnosis of Glutaric aciduria type 1 despite vertical HIV infection and minor head trauma. ( Ackermann, C; Cotton, MF; Dobbels, EFM; Laughton, B; Springer, PE; Thomas, A, 2018) |
| "Therefore, the overlapping syndrome of chronic progressive external ophthalmoplegia in the MELAS syndrome is considered in this case." | 1.29 | CPEO and carnitine deficiency overlapping in MELAS syndrome. ( Chen, HL; Chuang, YH; Hsu, CC; Huang, HL; Jong, HJ; Lee, HC; Pang, CY; Shen, YY; Tsai, JL; Wei, YH, 1995) |
| "Carnitine levels were found to be reduced in all patients at diagnosis." | 1.29 | Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. ( Athanassopoulos, S; Burlina, AB; Christensen, E; de Klerk, JB; Duran, M; Hoffmann, GF; Lehnert, W; Leonard, JV; Monavari, AA; Müller, E; Muntau, AC; Naughten, ER; Plecko-Starting, B; Superti-Furga, A; Zschocke, J, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (13.33) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 7 (46.67) | 29.6817 |
| 2010's | 3 (20.00) | 24.3611 |
| 2020's | 1 (6.67) | 2.80 |
| Authors | Studies |
|---|---|
| Meiman, EJ | 1 |
| Kick, GR | 1 |
| Jensen, CA | 1 |
| Coates, JR | 1 |
| Katz, ML | 1 |
| Thomas, A | 1 |
| Dobbels, EFM | 1 |
| Springer, PE | 1 |
| Ackermann, C | 1 |
| Cotton, MF | 1 |
| Laughton, B | 1 |
| Mahfoud, A | 1 |
| Domínguez, CL | 1 |
| Rashed, M | 1 |
| Durán, M | 2 |
| Rodríguez, T | 1 |
| Rodríguez, D | 1 |
| Landa, V | 1 |
| Schiff, M | 1 |
| Bénit, P | 1 |
| El-Khoury, R | 1 |
| Schlemmer, D | 1 |
| Benoist, JF | 1 |
| Rustin, P | 1 |
| Sonne, S | 1 |
| Shekhawat, PS | 2 |
| Matern, D | 2 |
| Ganapathy, V | 2 |
| Ignatowicz, L | 1 |
| Kölker, S | 2 |
| Hoffmann, GF | 3 |
| Schor, DS | 1 |
| Feyh, P | 1 |
| Wagner, L | 1 |
| Jeffrey, I | 1 |
| Pourfarzam, M | 1 |
| Okun, JG | 1 |
| Zschocke, J | 3 |
| Baric, I | 1 |
| Bain, MD | 1 |
| Jakobs, C | 1 |
| Chalmers, RA | 1 |
| Caksen, H | 1 |
| Tuncer, O | 1 |
| Kirimi, E | 1 |
| Fryns, JP | 1 |
| Uner, A | 1 |
| Unal, O | 1 |
| Cinal, A | 1 |
| Odabaş, D | 1 |
| Külkens, S | 1 |
| Harting, I | 1 |
| Sauer, S | 1 |
| Gruber, S | 1 |
| Bodamer, OA | 1 |
| Oglesbee, D | 1 |
| Freedenberg, D | 1 |
| Kramer, KA | 1 |
| Anderson, BD | 1 |
| Hahn, SH | 1 |
| Spasov, AA | 1 |
| Iezhitsa, IN | 1 |
| Pisarev, VB | 1 |
| Snigur, GL | 1 |
| Kravchenko, MS | 1 |
| Srinivas, SR | 1 |
| Bennett, MJ | 1 |
| Boriack, R | 1 |
| George, V | 1 |
| Xu, H | 1 |
| Prasad, PD | 1 |
| Roon, P | 1 |
| Hsu, CC | 1 |
| Chuang, YH | 1 |
| Tsai, JL | 1 |
| Jong, HJ | 1 |
| Shen, YY | 1 |
| Huang, HL | 1 |
| Chen, HL | 1 |
| Lee, HC | 1 |
| Pang, CY | 1 |
| Wei, YH | 1 |
| Athanassopoulos, S | 1 |
| Burlina, AB | 1 |
| de Klerk, JB | 1 |
| Lehnert, W | 1 |
| Leonard, JV | 1 |
| Monavari, AA | 1 |
| Müller, E | 1 |
| Muntau, AC | 1 |
| Naughten, ER | 1 |
| Plecko-Starting, B | 1 |
| Superti-Furga, A | 1 |
| Christensen, E | 1 |
| Medvedev, DI | 1 |
| Babichenko, II | 1 |
| Kravtsova, AI | 1 |
| Eremina, IZ | 1 |
| Markesbery, WR | 1 |
| McQuillen, MP | 1 |
| Procopis, PG | 1 |
| Harrison, AR | 1 |
| Engel, AG | 1 |
15 other studies available for carnitine and Atrophy
| Article | Year |
|---|---|
Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis.
Topics: Animals; Atrophy; Carnitine; Disease Progression; Dogs; Homozygote; Nervous System Diseases; Neurona | 2022 |
Favourable outcome in a child with symptomatic diagnosis of Glutaric aciduria type 1 despite vertical HIV infection and minor head trauma.
Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Brain; Brain Diseases; Brain Diseases, Metabolic; Car | 2018 |
[D-2-hydroxyglutaric aciduria. Report of two cases].
Topics: Anticonvulsants; Atrophy; Brain; Brain Diseases, Metabolic, Inborn; Carnitine; Child, Preschool; Con | 2009 |
Mouse studies to shape clinical trials for mitochondrial diseases: high fat diet in Harlequin mice.
Topics: Animals; Atrophy; Carnitine; Cattle; Cell Death; Cell Respiration; Cerebellum; Clinical Trials as To | 2011 |
Carnitine deficiency in OCTN2-/- newborn mice leads to a severe gut and immune phenotype with widespread atrophy, apoptosis and a pro-inflammatory response.
Topics: Animals; Apoptosis; Atrophy; Bone Morphogenetic Proteins; Carnitine; Cytokines; Down-Regulation; Ent | 2012 |
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.
Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Anal | 2003 |
Report of two Turkish infants with Norman-Roberts syndrome.
Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Atrophy; Brain; Carnitine; Cell Movement; Cerebellum | 2004 |
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency.
Topics: Age of Onset; Aged; Atrophy; Brain Diseases, Metabolic, Inborn; Carnitine; Cerebral Cortex; Cognitio | 2005 |
Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis.
Topics: Acidosis, Lactic; Atrophy; Biopsy; Blotting, Western; Carnitine; Central Nervous System Cysts; Cereb | 2006 |
[Changes in myocardium, skeletal muscle and liver of rats fed carnitine-deficient diet and treated with carnitine optical isomers].
Topics: Animals; Atrophy; Carnitine; Diet; Fatty Liver; Liver; Male; Muscle, Skeletal; Myocardium; Rats; Ste | 2006 |
Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) mice.
Topics: Amino Acid Transport Systems; Animals; Atrophy; Carnitine; Colon; Crohn Disease; Disease Models, Ani | 2007 |
CPEO and carnitine deficiency overlapping in MELAS syndrome.
Topics: Adult; Atrophy; Biopsy; Brain; Carnitine; Cerebral Cortex; DNA, Mitochondrial; Female; Humans; MELAS | 1995 |
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Atrophy; Brain; Brain Diseases, Metabolic; Carniti | 1996 |
[Ultrastructural characteristics of the cerebellar cortex in the postnatal development of animals with protein-calorie malnutrition and in subsequent rehabilitation].
Topics: Age Factors; Animals; Atrophy; Carnitine; Caseins; Cerebellar Cortex; Dietary Proteins; Hypertrophy; | 1989 |
Muscle carnitine deficiency. Association with lipid myopathy, vacuolar neuropathy, and vacuolated leukocytes.
Topics: Atrophy; Biological Transport; Carnitine; Electromyography; Female; Humans; Leukocytes; Lipid Metabo | 1974 |