phenylalanine and Cystinuria

phenylalanine has been researched along with Cystinuria in 15 studies

Research

Studies (15)

Timeframe	Studies, this research(%)	All Research%
pre-1990	14 (93.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (6.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Böhles, H; Buxmann, H; Eggermann, T; Lorenz, D; Merz, E; Schlößer, RL; Sewell, AC	1
BORLAND, JL; LYNCH, HJ; MCCARTHY, CF; OWEN, EE; TYOR, MP	1
Lee, ML; Toke, DA; Wang, TR	1
Arakawa, T; Chikaoka, H; Katsushima, N; Kobayashi, M; Minagawa, A; Saito, TG; Shioji, R	1
Brown, DA; Connelly, J; Francis, I; Hill, G; Masters, P; McFarlane, J; Pitt, D; Raby, J; Tucker, RG; Wilcken, B	1
Minami, R; Olek, K; Wardenbach, P	1
Gundalakh, AI; Mel'k, MV; Shcheglova, SA; Volkova, ZA	1
Reavey, PC; Yadav, GC	1
Levy, HL	1
Silk, DB	1
Brown, DA; Gaha, TJ; McLeay, AC; Smith, A; Wilcken, B	1
Lohrenz, FN; Tewksbury, DA	1
Bunting, R; Diamond, S; Hansen, S; Perry, TL; Tischler, B; Weppler, VC	1
Mawer, GE; Nixon, E	1
Juul, P	1

Reviews

2 review(s) available for phenylalanine and Cystinuria

Article	Year
Genetic screening. Advances in human genetics, 1973, Volume: 4 Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine	1973
Progress report. Peptide absorption in man. Gut, 1974, Volume: 15, Issue:6 Topics: Amino Acids; Betaine; Biological Transport, Active; Cystinuria; Dietary Proteins; Gelatin; Glycine; Hartnup Disease; Humans; Hydrolysis; Intestinal Absorption; Intestinal Mucosa; Kinetics; Methionine; Milk Proteins; Models, Biological; Nutritional Physiological Phenomena; Peptides; Phenylalanine; Structure-Activity Relationship	1974

Article

Year

Genetic screening.

Advances in human genetics, 1973, Volume: 4

Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine

1973

Progress report. Peptide absorption in man.

Gut, 1974, Volume: 15, Issue:6

Topics: Amino Acids; Betaine; Biological Transport, Active; Cystinuria; Dietary Proteins; Gelatin; Glycine; Hartnup Disease; Humans; Hydrolysis; Intestinal Absorption; Intestinal Mucosa; Kinetics; Methionine; Milk Proteins; Models, Biological; Nutritional Physiological Phenomena; Peptides; Phenylalanine; Structure-Activity Relationship

1974

Other Studies

13 other study(ies) available for phenylalanine and Cystinuria

Article	Year
Cystinuria in a girl presenting with a hyperechogenic colon detected by prenatal ultrasonography and a new SLC3A1 gene mutation (p.Phe278Ser). Ultraschall in der Medizin (Stuttgart, Germany : 1980), 2014, Volume: 35, Issue:5 Topics: Adult; Alleles; Amino Acid Substitution; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Colon; Consanguinity; Cystinuria; DNA Mutational Analysis; Exons; Female; Homozygote; Humans; Infant; Infant, Newborn; Kidney; Kidney Calculi; Phenylalanine; Pregnancy; Pregnancy Trimester, Third; Serine; Ultrasonography, Prenatal	2014
DEFECTIVE UPTAKE OF BASIC AMINO ACIDS AND L-CYSTINE BY INTESTINAL MUCOSA OF PATIENTS WITH CYSTINURIA. The Journal of clinical investigation, 1964, Volume: 43 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Basic; Arginine; Carbon Isotopes; Cystine; Cystinuria; Duodenum; Humans; Intestinal Absorption; Intestinal Mucosa; Leucine; Lysine; Mucous Membrane; Ornithine; Phenylalanine	1964
A rapid semi-quantitative determination of phenylalanine, glycine and cystine from urine and phenylalanine from serum. Jinrui idengaku zasshi. The Japanese journal of human genetics, 1983, Volume: 28, Issue:4 Topics: Chromatography, Thin Layer; Cystinuria; Fluorescamine; Glycine; Humans; Phenylalanine; Spiro Compounds; Staining and Labeling	1983
Higher excretion of urinary bound amino acids in infants: probably related to protein-anabolic effect of growth hormone. The Tohoku journal of experimental medicine, 1982, Volume: 137, Issue:1 Topics: Aging; Alanine; Amino Acids; Arginine; Child; Child, Preschool; Cystine; Cystinuria; Glycine; Growth Hormone; Histidine; Humans; Infant; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Proteins; Valine	1982
Genetic screening of the newborn in Australia. Results for 1978. The Medical journal of Australia, 1979, Sep-08, Volume: 2, Issue:5 Topics: Australia; Blood Stains; Congenital Hypothyroidism; Cystinuria; Female; Fetal Blood; Genetic Testing; Histidine; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Male; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias	1979
Phenylketonuria in a patient with cystinuria. Humangenetik, 1975, Aug-25, Volume: 28, Issue:4 Topics: Adolescent; Amino Acids; Cystine; Cystinuria; Genes, Recessive; Heterozygote; Homozygote; Humans; Male; Pedigree; Phenylalanine; Phenylketonurias	1975
[Some indices of nitrogen metabolism in patients with viral hepatitis]. Terapevticheskii arkhiv, 1975, Volume: 47, Issue:8 Topics: Adolescent; Adult; Alanine; Ammonia; Asparagine; Chronic Disease; Cysteine; Cystinuria; Glutamates; Glycine; Hepatitis A; Humans; Isoleucine; Leucine; Methionine; Middle Aged; Nitrogen; Phenylalanine; Serine; Threonine; Urea; Valine	1975
Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital. Journal of inherited metabolic disease, 1988, Volume: 11, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Citrulline; Cystinuria; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Kuwait; Male; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1988
Screening for metabolic diseases in New South Wales. The Medical journal of Australia, 1973, Jun-09, Volume: 1, Issue:23 Topics: Australia; Biological Assay; Chromatography, Paper; Cystathionine; Cystinuria; Female; Hartnup Disease; Homocystinuria; Humans; Infant, Newborn; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Seasons	1973
Circadian ythm of human urinary amino acid excretion in fed and fasted states. Metabolism: clinical and experimental, 1970, Volume: 19, Issue:5 Topics: 17-Hydroxycorticosteroids; Adult; Alanine; Amino Acids; Asparagine; Circadian Rhythm; Cystinuria; Fasting; Feeding Behavior; Glutamates; Glutamine; Glycine; Humans; Male; Middle Aged; Phenylalanine; Serine; Threonine; Tyrosine; Valine	1970
Unrecognized maternal biochemical disease: an uncommon cause of mental retardation in children. Journal of mental deficiency research, 1970, Volume: 14, Issue:1 Topics: Child; Cystinuria; Female; Glycine; Humans; Infant, Newborn; Intellectual Disability; Lysine; Metabolic Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Proline; Tyrosine	1970
The net absorption of the amino acid constituents of a protein meal in normal and cystinuric subjects. Clinical science, 1969, Volume: 36, Issue:3 Topics: Adult; Amino Acids; Arginine; Cystine; Cystinuria; Dietary Proteins; Female; Glycols; Humans; Indicators and Reagents; Intestinal Absorption; Lysine; Male; Phenylalanine; Tyrosine	1969
Quantitative measurement of individual free amino acids in urine by means of high voltage paper electrophoresis. Investigations of a group of mentally retarded patients. Scandinavian journal of clinical and laboratory investigation, 1966, Volume: 18, Issue:6 Topics: Adolescent; Adult; Aged; Amino Acids; Chromatography, Ion Exchange; Cystinuria; Electrophoresis; Female; Humans; Intellectual Disability; Male; Middle Aged; Phenylalanine; Phenylketonurias	1966