phenylalanine and Alcaptonuria

phenylalanine has been researched along with Alcaptonuria in 18 studies

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-19907 (38.89)18.7374
1990's3 (16.67)18.2507
2000's1 (5.56)29.6817
2010's2 (11.11)24.3611
2020's5 (27.78)2.80

Authors

AuthorsStudies
Arslan Gulten, Z; Arslan, N; Aydogan, A; Bahceci, H; Eroglu Erkmen, S; Karalar Pekuz, OK; Ozturk, T; Teke Kisa, P; Uysal, S; Yuce Inel, T1
Arnoux, JB; Bou-Gharios, G; Davison, AS; Gallagher, JA; Hughes, AT; Imrich, R; M, K; Milan, AM; Norman, BP; Olsson, B; Ranganath, LR; Rudebeck, M1
Bou-Gharios, G; Gallagher, JA; Hughes, AT; Hughes, JH; Jarvis, JC; Judd, S; Milan, AM; Ranganath, LR; Sutherland, H; Wilson, PJM1
Arnoux, JB; Braconi, D; Bygott, H; Davison, AS; Fitzgerald, R; Gallagher, JA; Genovese, F; Glasova, H; Hughes, AT; Hughes, JH; Imrich, R; Jarvis, JC; Khedr, M; Laan, D; Le Quan Sang, KH; Luangrath, E; Mankowitz, L; Milan, AM; Norman, BP; Olsson, B; Psarelli, EE; Ranganath, LR; Rhodes, NP; Rudebeck, M; Santucci, A; Shweihdi, E; Sireau, N; Stančík, R; van Kan, C; Zatkova, A1
Cooper, MS; Davison, AS; Deutz, NEP; Fitzgerald, R; Gallagher, JA; Ghane, P; Hughes, AT; Jarvis, JC; Khedr, M; Markinson, L; Milan, AM; Norman, BP; Psarelli, EE; Ranganath, LR; Sutherland, H1
Cox, TF; Davison, AS; Gallagher, JA; Hughes, AT; Khedr, M; Milan, AM; Psarelli, EE; Ranganath, LR; Rhodes, NP; Rovensky, J1
Arnoux, JB; Brassier, A; de Lonlay, P; Dubois, S; Grisel, C; Job-Deslandre, C; Le Quan Sang, KH; Ranganath, L; Servais, A; Sireau, N; Wippf, J1
CLAYTON, BE1
Kotwal, MR; Rinchhen, CZ1
Scazzocchio, C1
Dom, K; Pittevils, T1
Takita, H1
Peñalva, MA1
Angsusingha, K; Punnakanta, L; Tuchinda, C1
Fahlén, M; Lindstedt, G; Rosén, KG1
Balda, BR; Lukacs, I1
Adolphsen, P; Lenz, H; Siegenthaler, W; Zimmermann, KG1
Borud, O; Gjessing, LR1

Reviews

6 review(s) available for phenylalanine and Alcaptonuria

ArticleYear
Efficacy of Phenylalanine- and Tyrosine-Restricted Diet in Alkaptonuria Patients on Nitisinone Treatment: Case Series and Review of Literature.
    Annals of nutrition & metabolism, 2022, Volume: 78, Issue:1

    Topics: Adult; Alkaptonuria; Cyclohexanones; Diet; Dietary Proteins; Female; Humans; Male; Middle Aged; Nitrobenzoates; Phenylalanine; Tyrosine

2022
Old treatments for new insights and strategies: proposed management in adults and children with alkaptonuria.
    Journal of inherited metabolic disease, 2015, Volume: 38, Issue:5

    Topics: Adult; Age Factors; Alkaptonuria; Antioxidants; Child; Cyclohexanones; Humans; Nitrobenzoates; Ochronosis; Phenylalanine; Tyrosine

2015
Ochronotic arthropathy: the black hip. Case report and review of the literature.
    Acta orthopaedica Belgica, 1997, Volume: 63, Issue:2

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Cartilage, Articular; Follow-Up Studies; Hip Joint; Hip Prosthesis; Humans; Male; Middle Aged; Ochronosis; Osteoarthritis; Phenylalanine; Tyrosine

1997
[Alkaptonuria (homogentisic aciduria)].
    Ryoikibetsu shokogun shirizu, 1998, Issue:18 Pt 1

    Topics: Alkaptonuria; Arthritis; Diagnosis, Differential; Dioxygenases; Homogentisate 1,2-Dioxygenase; Homogentisic Acid; Humans; Ochronosis; Oxygenases; Phenylalanine; Tyrosine

1998
A fungal perspective on human inborn errors of metabolism: alkaptonuria and beyond.
    Fungal genetics and biology : FG & B, 2001, Volume: 34, Issue:1

    Topics: Alkaptonuria; Animals; Aspergillus nidulans; Genes, Fungal; Humans; Metabolism, Inborn Errors; Models, Chemical; Mutation; Phenylalanine; Tyrosine

2001
[Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
    Zeitschrift fur Haut- und Geschlechtskrankheiten, 1968, Dec-01, Volume: 43, Issue:23

    Topics: Albinism; Alkaptonuria; Anemia, Sickle Cell; Chromosomes; Hartnup Disease; Humans; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Models, Chemical; Molecular Biology; Phenylalanine; Phenylketonurias; Porphyrias; Skin Diseases; Tyrosine

1968

Trials

1 trial(s) available for phenylalanine and Alcaptonuria

ArticleYear
Quantification of the flux of tyrosine pathway metabolites during nitisinone treatment of Alkaptonuria.
    Scientific reports, 2019, 07-11, Volume: 9, Issue:1

    Topics: Adult; Alkaptonuria; Cyclohexanones; Female; Homogentisic Acid; Humans; Male; Middle Aged; Nitrobenzoates; Phenylalanine; Pigments, Biological; Tandem Mass Spectrometry; Tyrosine

2019

Other Studies

11 other study(ies) available for phenylalanine and Alcaptonuria

ArticleYear
Determinants of tyrosinaemia during nitisinone therapy in alkaptonuria.
    Scientific reports, 2022, 09-27, Volume: 12, Issue:1

    Topics: Alkaptonuria; Brain Diseases, Metabolic, Inborn; Cyclohexanones; Homogentisic Acid; Humans; Nitrobenzoates; Phenylalanine; Phenylpropionates; Tyrosine; Tyrosinemias

2022
Dietary restriction of tyrosine and phenylalanine lowers tyrosinemia associated with nitisinone therapy of alkaptonuria.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:2

    Topics: Alkaptonuria; Animals; Cyclohexanones; Diet, Protein-Restricted; Female; Humans; Male; Mice; Nitrobenzoates; Phenylalanine; Tyrosine; Tyrosinemias

2020
Homogentisic acid is not only eliminated by glomerular filtration and tubular secretion but also produced in the kidney in alkaptonuria.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:4

    Topics: Adult; Alkaptonuria; Case-Control Studies; Creatinine; Female; Glomerular Filtration Rate; Homogentisic Acid; Humans; Kidney; Linear Models; Male; Middle Aged; Ochronosis; Phenylalanine; Sex Factors; Tyrosine

2020
Nitisinone causes acquired tyrosinosis in alkaptonuria.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:5

    Topics: Adult; Aged; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Animals; Cyclohexanones; Female; Humans; Male; Mice; Mice, Inbred BALB C; Middle Aged; Nitrobenzoates; Phenylalanine; Tyrosine; Young Adult

2020
Symposium on metabolic diseases of the eye, Biochemical remarks on amino acid metabolism.
    Proceedings of the Royal Society of Medicine, 1963, Volume: 56

    Topics: Alkaptonuria; Amino Acids; Humans; Metabolic Diseases; Phenylalanine; Proteins; Tyrosine

1963
Alkaptonuria.
    Journal of the Indian Medical Association, 1983, Jan-01, Volume: 80, Issue:1

    Topics: Alkaptonuria; Dietary Proteins; Humans; Male; Middle Aged; Phenylalanine; Tyrosine

1983
Alkaptonuria: from humans to moulds and back.
    Trends in genetics : TIG, 1997, Volume: 13, Issue:4

    Topics: Alkaptonuria; Aspergillus nidulans; Dioxygenases; History, 20th Century; Homogentisate 1,2-Dioxygenase; Humans; Oxygenases; Phenylalanine; Tyrosine

1997
Intermittent alcaptonuria.
    Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1975, Volume: 58, Issue:5

    Topics: Alkaptonuria; Child; Homogentisic Acid; Humans; Male; Oxygenases; Phenylalanine; Tyrosine

1975
[Case of joint pain, dark colored tissue and darkened urine].
    Lakartidningen, 1975, Mar-19, Volume: 72, Issue:12

    Topics: Alkaptonuria; Female; Humans; Middle Aged; Phenylalanine

1975
[Alkaptonuria and ochronosis].
    Deutsche medizinische Wochenschrift (1946), 1972, Feb-18, Volume: 97, Issue:7

    Topics: Alkaptonuria; Chemical Phenomena; Chemistry; Diagnosis, Differential; Female; Germany, West; Homogentisic Acid; Humans; Male; Middle Aged; Ochronosis; Phenols; Phenylalanine; Radiography; Sex Factors; Spinal Diseases; Tyrosine

1972
Studies on urinary phenolic compounds in man. IV. O-Tyrosine and its metabolites.
    Scandinavian journal of clinical and laboratory investigation, 1966, Volume: 18, Issue:2

    Topics: Alkaptonuria; Humans; In Vitro Techniques; Lactates; Male; Phenylacetates; Phenylalanine; Tyramine; Tyrosine

1966