histidine has been researched along with Metabolic Diseases in 20 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 19 (95.00) | 18.7374 |
1990's | 1 (5.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
FREYCON, MT | 1 |
GHADIMI, H; HUNTER, A; PARTINGTON, MW | 1 |
LA DU, BN; ZANNONI, VG | 1 |
CANBY, JP; HOWELL, RR; JACOBY, GA; LADU, BN; SEEGMILLER, JE; SOBER, EK; ZANNONI, VG; ZIEGLER, LK | 1 |
ARAKAWA, T; HAYASHI, T; KUDO, Z; MIZUNO, T; OHARA, K; TADA, K | 1 |
SAMUELS, S | 1 |
COFFEY, VP | 1 |
GIOVANNINI, M; TERZOLI, S | 1 |
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
RYDER, RJ | 1 |
HOLTON, JB | 1 |
Krüger, M; Menne, F; Otte, HJ; Winterhoff, D | 1 |
Davidow, B; Goldberg, D; Grossi, M; Grover, R; Shahidi, S; Wethers, D | 1 |
Bronzert, DA; Henkin, RI; Patten, BM; Re, PK | 1 |
Glanzmann, C; Horst, W; Lütolf, UM; Renk, IW | 1 |
Granić, P; Rajić, Z; Vranić, L | 1 |
Lutz, P | 1 |
Bremer, HJ; Przyrembel, H | 1 |
Charlas, J; Fournet, JP; Meyer, B; Nodot, A; Saint-Martin, J; Schaison, G; Vialatte, J | 1 |
Menkès, G | 1 |
1 review(s) available for histidine and Metabolic Diseases
Article | Year |
---|---|
[Transitory disorders of amino acid metabolism. Practical viewpoints].
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Ascorbic Acid; Cystathionine; Diagnosis, Differential; Histidine; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Infant, Premature, Diseases; Male; Metabolic Diseases; Methionine; Milk Proteins; Phenylalanine; Rats; Testicular Diseases; Time Factors; Tyrosine | 1973 |
19 other study(ies) available for histidine and Metabolic Diseases
Article | Year |
---|---|
[Histidinemia].
Topics: Amino Acid Metabolism, Inborn Errors; Histidine; Histidine Ammonia-Lyase; Humans; Intellectual Disability; Metabolic Diseases | 1962 |
Inborn error of histidine metabolism.
Topics: Histidine; Medical Records; Metabolic Diseases | 1962 |
Determination of histidine alpha-deaminase in human stratum corneum and its absence in histidinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Epidermis; Histidine; Histidine Ammonia-Lyase; Humans; Intellectual Disability; Lyases; Metabolic Diseases; Skin | 1963 |
CLINICAL AND BIOCHEMICAL STUDIES ON TWO CASES OF HISTIDINEMIA.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Child; Deficiency Diseases; Diagnosis, Differential; Genetics; Histidine; Histidine Ammonia-Lyase; Humans; Intellectual Disability; Liver; Metabolic Diseases; Phenylketonurias; Spectrophotometry; Speech Disorders; Urine | 1963 |
"HYPERFOLIC-ACIDEMIA WITH FORMIMINOGLUTAMIC-ACIDURIA FOLLOWING HISTIDINE LOADING". SUGGESTED FOR A CASE OF CONGENITAL DEFICIENCY IN FORMIMINOTRANSFERASE.
Topics: Blood; Folic Acid; Glutamate Formimidoyltransferase; Glutamates; Histidine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Metabolism; Metabolism, Inborn Errors; Urine | 1963 |
HIGH-RESOLUTION SCREENING OF AMINO-ACIDURIAS.
Topics: Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Electrophoresis; Histidine; Humans; Indicators and Reagents; Lead Poisoning; Maple Syrup Urine Disease; Mass Screening; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Urine | 1964 |
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
[CONSIDERATIONS ON A CASE OF MENTAL DEFICIENCY WITH ABNORMALITIES OF HISTIDINE METABOLISM].
Topics: Child; Histidine; Humans; Intellectual Disability; Language; Metabolic Diseases; Proteins; Speech Disorders | 1964 |
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine | 1964 |
AN EVALUATION OF THE MEASUREMENT OF URINARY FORMIMINOGLUTAMIC ACID EXCRETION AS AN INDICATION OF DISTURBED FOLIC ACID METABOLISM.
Topics: Anemia; Anemia, Macrocytic; Anticonvulsants; Celiac Disease; Female; FIGLU Test; Folic Acid; Folic Acid Antagonists; Folic Acid Deficiency; Formiminoglutamic Acid; Histidine; Humans; Intestinal Diseases; Intestine, Small; Intestines; Liver Diseases; Metabolic Diseases; Neoplasms; Postoperative Complications; Pregnancy; Sprue, Tropical; Vitamin B 12 | 1964 |
SKIN L-HISTIDINE AMMONIA-LYASE ACTIVITY IN THE FAMILY OF A CHILD WITH HISTIDINAEMIA.
Topics: Amino Acid Metabolism, Inborn Errors; Chemistry Techniques, Analytical; Child; Clinical Enzyme Tests; Genetics, Medical; Histidine; Histidine Ammonia-Lyase; Humans; Intellectual Disability; Lyases; Metabolic Diseases; Skin | 1965 |
[Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].
Topics: Galactokinase; Galactosemias; Germany, West; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Maple Syrup Urine Disease; Mass Screening; Metabolic Diseases; Phenylketonurias | 1979 |
Evaluation of the expanded newborn screening program in New York City.
Topics: Adenosine Deaminase; Anemia, Sickle Cell; Costs and Cost Analysis; Counseling; Galactosemias; Hemoglobinopathies; Histidine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Legislation, Medical; Mass Screening; Metabolic Diseases; New York; New York City; Organization and Administration; Phenylketonurias | 1978 |
A syndrome of acute zinc loss. Cerebellar dysfunction, mental changes, anorexia, and taste and smell dysfunction.
Topics: Adult; Anorexia; Cerebellar Diseases; Child; Female; Histidine; Humans; Mental Disorders; Metabolic Diseases; Middle Aged; Olfaction Disorders; Scleroderma, Systemic; Syndrome; Taste Disorders; Zinc | 1975 |
[Exhalation diagnosis with C14 tagged compounds, methods and results].
Topics: Bile Acids and Salts; Carbon Radioisotopes; Citric Acid Cycle; Fatty Acids; Histidine; Humans; Metabolic Diseases; Radiotherapy; Triglycerides; Uridine Monophosphate | 1975 |
Basic amino acid in the pathogenesis of caries.
Topics: Adolescent; Amino Acids; Arginine; Child; Chromatography, Ion Exchange; Dental Caries; Female; Histidine; Humans; Male; Metabolic Diseases; Methylhistidines; Saliva | 1991 |
[Diagnostic methods for the detection of amino acid metabolism disorders].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Bacillus subtilis; Blood Protein Electrophoresis; Chemistry, Clinical; Chromatography; Clinical Enzyme Tests; Colorimetry; Fluorometry; Histidine; Humans; Leucine; Mass Screening; Metabolic Diseases; Methionine; Methods; Microbial Sensitivity Tests; Organization and Administration; Phenylalanine; Phenylketonurias; Tyrosine | 1973 |
[External pancreatic insufficiency with chronic granulopenia. A further case with osseous abnormalities].
Topics: Agranulocytosis; Body Weight; Bone Diseases; Bone Marrow Examination; Female; Femur; Histidine; Humans; Infant, Newborn; Leukocyte Count; Male; Metabolic Diseases; Muscle Contraction; Pancreas; Pancreatic Diseases; Pancreatic Extracts; Pancreatic Juice; Pregnancy; Psychomotor Disorders | 1969 |
[The "reequilibration" test and its use in the treatment of certain forms of cancer and other afflictions].
Topics: Adenosine Triphosphate; Asparagine; Betaine; Choline; Creatine; Cysteine; Deficiency Diseases; Electrophoresis; Elements; Glutamates; Histidine; Humans; Metabolic Diseases; Methionine; Neoplasms; Quaternary Ammonium Compounds | 1966 |