Page last updated: 2024-10-16

carnitine and Atrophy

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.

Research Excerpts

ExcerptRelevanceReference
"Therefore, the overlapping syndrome of chronic progressive external ophthalmoplegia in the MELAS syndrome is considered in this case."5.29CPEO 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."3.72Report 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."1.72Characterization 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."1.48Favourable 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."1.29CPEO 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."1.29Clinical 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)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19902 (13.33)18.7374
1990's2 (13.33)18.2507
2000's7 (46.67)29.6817
2010's3 (20.00)24.3611
2020's1 (6.67)2.80

Authors

AuthorsStudies
Meiman, EJ1
Kick, GR1
Jensen, CA1
Coates, JR1
Katz, ML1
Thomas, A1
Dobbels, EFM1
Springer, PE1
Ackermann, C1
Cotton, MF1
Laughton, B1
Mahfoud, A1
Domínguez, CL1
Rashed, M1
Durán, M2
Rodríguez, T1
Rodríguez, D1
Landa, V1
Schiff, M1
Bénit, P1
El-Khoury, R1
Schlemmer, D1
Benoist, JF1
Rustin, P1
Sonne, S1
Shekhawat, PS2
Matern, D2
Ganapathy, V2
Ignatowicz, L1
Kölker, S2
Hoffmann, GF3
Schor, DS1
Feyh, P1
Wagner, L1
Jeffrey, I1
Pourfarzam, M1
Okun, JG1
Zschocke, J3
Baric, I1
Bain, MD1
Jakobs, C1
Chalmers, RA1
Caksen, H1
Tuncer, O1
Kirimi, E1
Fryns, JP1
Uner, A1
Unal, O1
Cinal, A1
Odabaş, D1
Külkens, S1
Harting, I1
Sauer, S1
Gruber, S1
Bodamer, OA1
Oglesbee, D1
Freedenberg, D1
Kramer, KA1
Anderson, BD1
Hahn, SH1
Spasov, AA1
Iezhitsa, IN1
Pisarev, VB1
Snigur, GL1
Kravchenko, MS1
Srinivas, SR1
Bennett, MJ1
Boriack, R1
George, V1
Xu, H1
Prasad, PD1
Roon, P1
Hsu, CC1
Chuang, YH1
Tsai, JL1
Jong, HJ1
Shen, YY1
Huang, HL1
Chen, HL1
Lee, HC1
Pang, CY1
Wei, YH1
Athanassopoulos, S1
Burlina, AB1
de Klerk, JB1
Lehnert, W1
Leonard, JV1
Monavari, AA1
Müller, E1
Muntau, AC1
Naughten, ER1
Plecko-Starting, B1
Superti-Furga, A1
Christensen, E1
Medvedev, DI1
Babichenko, II1
Kravtsova, AI1
Eremina, IZ1
Markesbery, WR1
McQuillen, MP1
Procopis, PG1
Harrison, AR1
Engel, AG1

Other Studies

15 other studies available for carnitine and Atrophy

ArticleYear
Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis.
    Developmental neurobiology, 2022, Volume: 82, Issue:4

    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.
    Metabolic brain disease, 2018, Volume: 33, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Brain; Brain Diseases; Brain Diseases, Metabolic; Car

2018
[D-2-hydroxyglutaric aciduria. Report of two cases].
    Investigacion clinica, 2009, Volume: 50, Issue:3

    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.
    PloS one, 2011, Volume: 6, Issue:12

    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.
    PloS one, 2012, Volume: 7, Issue:10

    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.
    Neuropediatrics, 2003, Volume: 34, Issue:5

    Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Anal

2003
Report of two Turkish infants with Norman-Roberts syndrome.
    Genetic counseling (Geneva, Switzerland), 2004, Volume: 15, Issue:1

    Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Atrophy; Brain; Carnitine; Cell Movement; Cerebellum

2004
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency.
    Neurology, 2005, Jun-28, Volume: 64, Issue:12

    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.
    Pediatric neurology, 2006, Volume: 35, Issue:4

    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].
    Morfologiia (Saint Petersburg, Russia), 2006, Volume: 129, Issue:3

    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.
    Molecular genetics and metabolism, 2007, Volume: 92, Issue:4

    Topics: Amino Acid Transport Systems; Animals; Atrophy; Carnitine; Colon; Crohn Disease; Disease Models, Ani

2007
CPEO and carnitine deficiency overlapping in MELAS syndrome.
    Acta neurologica Scandinavica, 1995, Volume: 92, Issue:3

    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.
    Neuropediatrics, 1996, Volume: 27, Issue:3

    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].
    Arkhiv anatomii, gistologii i embriologii, 1989, Volume: 97, Issue:10

    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.
    Archives of neurology, 1974, Volume: 31, Issue:5

    Topics: Atrophy; Biological Transport; Carnitine; Electromyography; Female; Humans; Leukocytes; Lipid Metabo

1974