phenylalanine and Mitochondrial Diseases

phenylalanine has been researched along with Mitochondrial Diseases in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Al Asmari, A; AlHashem, A; Aljadhai, YI; Almannai, M; Alsaman, AS; Alwadei, AH; Benini, R; Dai, H; El-Hattab, AW; Faqeih, EA; Grange, DK; Katsonis, P; Lichtarge, O; Lines, MA; Mahmoud, A; Saleh, MA; Tabarki, B; Wang, J; Wong, LC1
Hargreaves, I; Kyprianou, N; Lee, P; Murphy, E1
Blakely, EL; Carter, JE; de Silva, RN; Kartsounis, LD; O'Donovan, DG; Swalwell, H; Taylor, RW; Turnbull, DM; Young, TM1
Hosoki, K; Saitoh, S; Sudo, A; Takeichi, N1
Briddon, A; Hargreaves, IP; Heales, SJ; Land, JM; Lee, PJ1
Guerrero, JM; Martínez-Cruz, F; Osuna, C1
Hargreaves, IP1

Reviews

1 review(s) available for phenylalanine and Mitochondrial Diseases

ArticleYear
Coenzyme Q10 in phenylketonuria and mevalonic aciduria.
    Mitochondrion, 2007, Volume: 7 Suppl

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Antioxidants; Coenzymes; Humans; Hydroxymethylglutaryl CoA Reductases; Metabolic Networks and Pathways; Mevalonic Acid; Mitochondrial Diseases; Models, Biological; Oxidative Stress; Phenylalanine; Phenylketonurias; Ubiquinone

2007

Trials

1 trial(s) available for phenylalanine and Mitochondrial Diseases

ArticleYear
Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome-c reductase activity in phenylketonuric patients.
    Journal of inherited metabolic disease, 2002, Volume: 25, Issue:8

    Topics: Adolescent; Adult; Chromatography, High Pressure Liquid; Citrate (si)-Synthase; Coenzymes; Female; Humans; Hydroxymethylglutaryl CoA Reductases; Male; Middle Aged; Mitochondrial Diseases; Monocytes; Phenylalanine; Phenylketonurias; Succinate Cytochrome c Oxidoreductase; Ubiquinone

2002

Other Studies

5 other study(ies) available for phenylalanine and Mitochondrial Diseases

ArticleYear
FARS2 deficiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance.
    Molecular genetics and metabolism, 2018, Volume: 125, Issue:3

    Topics: Adolescent; Adult; Amino Acyl-tRNA Synthetases; Child; Child, Preschool; Female; Gene Deletion; Humans; Male; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Paraplegia; Phenylalanine; Phenylalanine-tRNA Ligase; Protein Isoforms; Structure-Activity Relationship; Young Adult

2018
Assessment of mitochondrial respiratory chain function in hyperphenylalaninaemia.
    Journal of inherited metabolic disease, 2009, Volume: 32, Issue:2

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Cell Line, Tumor; Cells, Cultured; Culture Media; Electron Transport; Female; Humans; Lactic Acid; Male; Middle Aged; Mitochondrial Diseases; Phenylalanine; Phenylketonurias; Pyruvic Acid; Tremor; Tyrosine; Ubiquinone; Young Adult

2009
Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity.
    Archives of neurology, 2010, Volume: 67, Issue:11

    Topics: Atrophy; Brain; Dementia; Disease Progression; Female; Humans; Magnetic Resonance Imaging; Middle Aged; Mitochondrial Diseases; Muscle Rigidity; Mutation; Neurodegenerative Diseases; Neuropsychological Tests; Phenylalanine; RNA, Transfer

2010
Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.
    The Journal of laryngology and otology, 2011, Volume: 125, Issue:12

    Topics: Audiometry, Pure-Tone; Brain; Child; Cochlear Implantation; Electron Transport Complex III; Epilepsy, Generalized; Female; Genome, Mitochondrial; Growth Disorders; Hearing Loss, Sensorineural; Humans; Hypertrichosis; Lactates; Magnetic Resonance Imaging; Mitochondria; Mitochondrial Diseases; Phenylalanine; Point Mutation; RNA, Transfer; Treatment Outcome

2011
Mitochondrial damage induced by fetal hyperphenylalaninemia in the rat brain and liver: its prevention by melatonin, Vitamin E, and Vitamin C.
    Neuroscience letters, 2006, Jan-09, Volume: 392, Issue:1-2

    Topics: Aldehydes; Animals; Animals, Newborn; Ascorbic Acid; Disease Models, Animal; Drug Interactions; Female; Male; Malondialdehyde; Melatonin; Mitochondrial Diseases; Phenethylamines; Phenylalanine; Phenylketonurias; Pregnancy; Prenatal Exposure Delayed Effects; Rats; Rats, Wistar; Time Factors; Vitamin A

2006