histidine has been researched along with Amino Acid Transport Disorder, Neutral in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 25 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Ersser, RS; Seakins, JW | 1 |
| Frimpter, GW | 1 |
| Asatoor, AM; Navab, F | 1 |
| Ampola, MG | 1 |
| Levy, HL | 2 |
| Kroll, S; Toussaint, W; Zebisch, P | 2 |
| Tomaszewski, L | 1 |
| Antener, I; Bartelheimer, HK; Grüttner, R; Rybak, C | 1 |
| Ampola, MG; Efron, ML | 1 |
| Menne, F | 1 |
| Buravina, TA; Iur'eva, EA; Koroleva, IA; Lebedev, VP; Mukhina, IuG | 1 |
| Milne, MD | 1 |
| Rostenberg, A; Solomon, LM | 1 |
| Cheng, B; Lloyd, JK; Matthews, DM; Seakins, JW; Tarlow, MJ; Thomas, AJ | 2 |
| Barois, A; Caldera, R; Escourolle, R; Goulon, M; Grosbuis, S; Nouailhat, F | 1 |
| Asatoor, AM; Bandoh, JK; Lant, AF; Milne, MD; Navab, F | 2 |
| Sjaastad, O | 1 |
| Halvorsen, S; Sjaastad, O | 1 |
| Ashurst, PJ | 1 |
| Halvorsen, S; Hygstedt, O; Jagenburg, R; Sjaastad, O | 1 |
7 review(s) available for histidine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
Phenylketonuria and other disorders of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1973 |
Genetic screening.
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 |
Neonatal screening for inborn errors of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Assay; Chromatography, Paper; Evaluation Studies as Topic; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Mass Screening; Methionine; Methods; Phenylalanine; Phenylketonurias; Pregnancy; Tyrosine | 1974 |
The aminoacidurias.
Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine | 1967 |
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine | 1968 |
[Primary and secondary hyperaminoaciduria in children (review of the literature)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biological Transport, Active; Cystinuria; Fanconi Syndrome; Glycine; Glycosuria, Renal; Hartnup Disease; Histidine; Humans; Infant, Newborn; Kidney Diseases; Kidney Tubules; Maple Syrup Urine Disease; Phenylketonurias; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Sodium | 1970 |
Transport of amino acids and peptides in the gut and the kidney.
Topics: Adult; Alanine; Amino Acids; Animals; Biological Transport, Active; Digestive System; Glycine; Hartnup Disease; Histidine; Humans; Hydrolysis; Intestinal Absorption; Kidney; Kidney Tubules; Leucine; Lysine; Methionine; Peptides; Phenylalanine; Proteins; Rats; Serine; Threonine; Tryptophan; Valine | 1971 |
18 other study(ies) available for histidine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.
Topics: Amino Acids; Hartnup Disease; Histidine; Humans; Infant, Newborn; Intestinal Absorption; Kidney Function Tests; Lysine; Male; Nicotinic Acids; Phenylalanine; Tyrosine | 1967 |
Sulfur amino acids, hyperglycinemia, and certain possibly benign conditions.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Cystathionine; Diagnosis, Differential; Disulfides; Glycine; Hartnup Disease; Histidine; Histidine Ammonia-Lyase; Homocystinuria; Humans; Methionine; Proline; Sulfites | 1976 |
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
Topics: Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Australia; Cystinuria; Ethnicity; Europe; Galactosemias; Genetics, Population; Hartnup Disease; Histidine; Homocystinuria; Humans; Inbreeding; Infant, Newborn; Israel; Japan; Maple Syrup Urine Disease; Mass Screening; New Zealand; North America; Phenylketonurias; Tyrosine | 1975 |
Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease.
Topics: Adult; Alanine; Amino Acids; Chromatography, Paper; Dipeptides; Female; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Intestine, Small; Niacinamide; Phenylalanine; Radiography; Tryptophan | 1970 |
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |
[The inborn errors of metabolism of amino acids].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chemical Phenomena; Chemistry; Cystinuria; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Sarcosine; Tyrosine; Valine | 1973 |
[Hartnup disease (author's transl)].
Topics: Adolescent; Amino Acids; Child; Feces; Female; Hartnup Disease; Hippurates; Histidine; Humans; Malabsorption Syndromes; Nicotinic Acids; Pyridoxine; Renal Aminoacidurias; Tryptophan; Tyrosine | 1973 |
Infantile eczema and systemic disease.
Topics: Acrodermatitis; Agammaglobulinemia; Ataxia Telangiectasia; Child; Dermatitis, Atopic; Eczema; Gastrointestinal Diseases; Glutens; Hartnup Disease; Histidine; Humans; Infant; Lymphatic Diseases; Mucopolysaccharidoses; Phenylketonurias; Wiskott-Aldrich Syndrome | 1968 |
Absorption of amino acids and peptides in a child with a variant of Hartnup disease and coexistent coeliac disease.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biopsy; Celiac Disease; Dipeptides; Glycine; Hartnup Disease; Histidine; Humans; Infant; Intestinal Absorption; Intestine, Small; Jejunum; Male; Peptides; Tyrosine | 1972 |
[Endogenous pellagra without hyperaminoaciduria].
Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography, Paper; Diagnosis, Differential; Electroencephalography; Glutamates; Glutamine; Hartnup Disease; Histidine; Humans; Lysine; Male; Pellagra; Serine; Skin Manifestations; Threonine | 1969 |
Absorption of amino acids and the dipeptide, carnosine, from the gut in normal subjects and a case of Hartnup disease.
Topics: Alanine; Amino Acids; Dipeptides; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Phenylalanine | 1969 |
Intestinal absorption of carnosine and its constituent amino acids in man.
Topics: Alanine; Dipeptides; Hartnup Disease; Histidine; Humans; Intestinal Absorption | 1970 |
Intestinal absorption and biopsy transport of peptides and amino acids in Hartnup disease.
Topics: Amino Acids; Biological Transport; Biopsy; Body Fluids; Celiac Disease; Dipeptides; Glycine; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Jejunum; Peptides; Tyrosine | 1970 |
N-acetylhistaminuria in dystrophia myotonica.
Topics: Amino Acids; Feces; Hartnup Disease; Histamine; Histidine; Humans; Hydrogen-Ion Concentration; Intestinal Mucosa; Malabsorption Syndromes; Myotonic Dystrophy; Pancreatitis | 1968 |
Histaminuria in Hartnup disease.
Topics: Adolescent; Feces; Female; Hartnup Disease; Histamine; Histidine; Humans; Intestine, Small; Malabsorption Syndromes; Male | 1968 |
Hydroa vacciniforme occurring in association with Hartnup disease.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Paper; Erythema; Hartnup Disease; Histidine; Humans; Hydroa Vacciniforme; Indoles; Male; Photosensitivity Disorders | 1969 |
Cellular transport of L-histidine in Hartnup disease.
Topics: Adolescent; Adult; Age Factors; Amino Acids; Biological Transport; Chromatography, Paper; Feces; Female; Hartnup Disease; Histidine; Humans; Injections, Intravenous; Male; Tritium | 1969 |