glycine has been researched along with Infant, Newborn, Diseases in 37 studies
Infant, Newborn, Diseases: Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Two substitutions for glycine in the triple-helical domain were found in type I procollagen synthesized by skin fibroblasts from two probands with lethal osteogenesis imperfecta." | 7.68 | Substitutions for glycine alpha 1-637 and glycine alpha 2-694 of type I procollagen in lethal osteogenesis imperfecta. The conformational strain on the triple helix introduced by a glycine substitution can be transmitted along the helix. ( Constantinou, CD; Prockop, DJ; Tsuneyoshi, T; Westerhausen, A, 1991) |
| "Two substitutions for glycine in the triple-helical domain were found in type I procollagen synthesized by skin fibroblasts from two probands with lethal osteogenesis imperfecta." | 3.68 | Substitutions for glycine alpha 1-637 and glycine alpha 2-694 of type I procollagen in lethal osteogenesis imperfecta. The conformational strain on the triple helix introduced by a glycine substitution can be transmitted along the helix. ( Constantinou, CD; Prockop, DJ; Tsuneyoshi, T; Westerhausen, A, 1991) |
| "Three Finnish infants with a severe neonatal-onset-type of nonketotic hyperglycinemia were treated with strychnine nitrate in a daily dosage of 0." | 1.26 | Failure of strychnine treatment during the neonatal period in three Finnish children with nonketotic hyperglycinemia. ( Koivisto, M; Saukkonen, AL; Similä, S; von Wendt, L, 1980) |
| "In a newborn twin with haemolytic anaemia an unstable fetal haemoglobin was found to be the cause." | 1.25 | A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine. ( Deacon-Smith, RA; Kamuzora, H; Lee-Potter, JP; Lehmann, H; Simpkiss, MJ, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 35 (94.59) | 18.7374 |
| 1990's | 1 (2.70) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (2.70) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mayr, JA | 1 |
| Zimmermann, FA | 1 |
| Fauth, C | 1 |
| Bergheim, C | 1 |
| Meierhofer, D | 1 |
| Radmayr, D | 1 |
| Zschocke, J | 1 |
| Koch, J | 1 |
| Sperl, W | 1 |
| TADA, K | 1 |
| YOSHIDA, T | 1 |
| MORIKAWA, T | 1 |
| MINAKAWA, A | 1 |
| WADA, Y | 1 |
| ANDO, T | 3 |
| SHIMURA, K | 1 |
| HILLMAN, DA | 1 |
| SCRIVER, CR | 2 |
| PEDVIS, S | 1 |
| SHRAGOVITCH, I | 1 |
| SCHREIER, K | 1 |
| MUELLER, W | 1 |
| Agamanolis, DP | 1 |
| Potter, JL | 1 |
| Herrick, MK | 1 |
| Sternberger, NH | 1 |
| Purkiss, P | 1 |
| Chalmers, RA | 1 |
| Borud, O | 1 |
| Del Valle, JA | 1 |
| Merinero, B | 1 |
| Garciá, MJ | 1 |
| Ugarte, M | 1 |
| Omeñaca, F | 1 |
| Neustadt, G | 1 |
| Aicardi, J | 1 |
| Schultz, K | 2 |
| Mestyán, J | 2 |
| Soltész, G | 2 |
| Klujber, L | 1 |
| Dóber, I | 1 |
| Von Wendt, L | 3 |
| Similä, S | 3 |
| Saukkonen, AL | 3 |
| Koivisto, M | 2 |
| Kouvalainen, K | 1 |
| Hartikainen-Sorri, AL | 1 |
| Kääpä, P | 1 |
| Baumgartner, ER | 1 |
| Bachmann, C | 2 |
| Brechbühler, T | 2 |
| Wick, H | 2 |
| Gebre-Medhin, M | 1 |
| Larsson, U | 1 |
| Lindblad, BS | 1 |
| Zetterström, R | 1 |
| Steinmann, B | 1 |
| Gitzelmann, R | 1 |
| Brun, A | 1 |
| Börjeson, M | 1 |
| Hultberg, B | 1 |
| Sjöblad, S | 1 |
| Akesson, H | 1 |
| Litwin, E | 1 |
| Slager, UT | 1 |
| Berggren, RL | 1 |
| Marubayashi, S | 1 |
| Speilberg, SP | 1 |
| Lucky, AW | 1 |
| Schulman, JD | 1 |
| Kramer, LI | 1 |
| Hefner, L | 1 |
| Goodman, SI | 1 |
| Lee-Potter, JP | 1 |
| Deacon-Smith, RA | 1 |
| Simpkiss, MJ | 1 |
| Kamuzora, H | 1 |
| Lehmann, H | 1 |
| Sherman, JO | 1 |
| Hamly, CA | 1 |
| Khachadurina, AK | 1 |
| Horváth, M | 1 |
| Tsuneyoshi, T | 1 |
| Westerhausen, A | 1 |
| Constantinou, CD | 1 |
| Prockop, DJ | 1 |
| Eldjarn, L | 1 |
| Jellum, E | 1 |
| Stokke, O | 1 |
| Martin, JJ | 1 |
| Schlote, W | 1 |
| Koepp, P | 1 |
| de Groot, CJ | 1 |
| Grüttner, R | 1 |
| Rybak, C | 1 |
| Krieger, I | 1 |
| Hart, ZH | 1 |
| Thalhammer, O | 1 |
| Scheibenreiter, S | 1 |
| Schön, R | 1 |
| Knoll, E | 1 |
| Schmierer, G | 1 |
| Mihatsch, MJ | 1 |
| Baumgartner, RE | 1 |
| Bühler, UK | 1 |
| Olafsson, A | 1 |
| Ohnacker, H | 1 |
| Frazier, PD | 1 |
| Summer, GK | 1 |
| Raven, EJ | 1 |
| Baumgartner, R | 1 |
| Nyhan, WL | 2 |
| Cook, RC | 1 |
| Rickham, PP | 1 |
| Broyer, M | 1 |
| Berger, R | 1 |
| Rushton, DI | 1 |
| Diezel, PB | 1 |
| Martin, K | 1 |
1 review available for glycine and Infant, Newborn, Diseases
| Article | Year |
|---|---|
[Myoclonias as a manifestation of degenerative disorders of the central nervous system in childhood].
Topics: Adolescent; Age Factors; Brain Diseases; Cerebellar Diseases; Ceroid; Child; Child, Preschool; Diagn | 1982 |
36 other studies available for glycine and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation.
Topics: Abnormalities, Multiple; Acidosis, Lactic; Amino Acid Sequence; Base Sequence; Chromosomes, Human, P | 2011 |
IDIOPATHIC HYPERGLYCINEMIA (THE FIRST CASE IN JAPAN).
Topics: Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Chromatography; Epidemiology; Glycine | 1963 |
NEONATAL FAMILIAL PRIMARY HYPERPARATHYROIDISM.
Topics: Calcium; Calcium, Dietary; Electrocardiography; Genetics, Medical; Glycine; Humans; Hydroxyproline; | 1964 |
[IDIOPATHIC HYPERGLYCINEMIA (GLYCINOSIS)].
Topics: Amino Acid Metabolism, Inborn Errors; Blood Protein Disorders; Chromosome Aberrations; Diagnosis, Di | 1964 |
Membrane transport in disorders of imino-acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Hydroxyproline; Infant; Infant, Newbo | 1967 |
The neuropathology of glycine encephalopathy: a report of five cases with immunohistochemical and ultrastructural observations.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Female; Glial Fibrillary Aci | 1982 |
Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Diamino; Child; Child, Preschool; Cr | 1980 |
Leukocyte propionyl-CoA carboxylase deficiency in a patient with ketotic hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Female; Glycine; Humans; Infant, Newbor | 1980 |
Metabolic effects of septicaemia in newborn and young infants with particular reference to the plasma free amino acids.
Topics: Alanine; Amino Acids; Amino Acids, Branched-Chain; Bacterial Infections; Escherichia coli Infections | 1980 |
Prenatal brain damage in nonketotic hyperglycinemia.
Topics: Brain Damage, Chronic; Electroencephalography; Female; Fetus; Glycine; Humans; Infant, Newborn; Infa | 1981 |
Failure of strychnine treatment during the neonatal period in three Finnish children with nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Exchange Transfusion, Whole Blood; Female; Glycine; Humans; In | 1980 |
Sodium valproate, pregnancy, and neonatal hyperglycinaemia.
Topics: Adult; Epilepsy; Female; Glycine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Pregnancy; Pre | 1979 |
Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism.
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Coenzyme A; Female; Fi | 1975 |
Subclinical protein-energy malnutrition in under-privileged Ethiopian mothers and their newborn infants.
Topics: Adolescent; Adult; Developing Countries; Ethiopia; Female; Fetal Blood; Glycine; Humans; Infant, New | 1978 |
Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemia.
Topics: Diseases in Twins; Electroencephalography; Female; Glycine; Humans; Infant, Newborn; Infant, Newborn | 1979 |
Neonatal non-ketotic hyperglycinemia: a clinical, biochemical and neuropathological study including electronmicroscopic findings.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Cerebral Hemorrhage; Female; Glycine; Humans; Infant, N | 1979 |
Nonketotic hyperglycinemia: report of a case and review of the clinical, chemical, and pathological changes.
Topics: Amino Acids; Brain; Female; Glycine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Nerve Fiber | 1977 |
Letter: Failure of Leucovorin therapy in nonketotic hyperglycinemia.
Topics: Glycine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucovorin | 1976 |
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.
Topics: Amino Acid Sequence; Anemia, Hemolytic; Diseases in Twins; Fetal Hemoglobin; Glycine; Hemoglobins, A | 1975 |
Use of an oral elemental diet in infants with severe intractable diarrhea.
Topics: Acid-Base Equilibrium; Administration, Oral; Alanine Transaminase; Amino Acids; Blood Urea Nitrogen; | 1975 |
Hyperaminoacidemia due to the accumulation of gluconeogenic amino acid precursors in hypoglycemic small-for-gestational age infants.
Topics: Alanine; Amino Acids; Birth Weight; Female; Gestational Age; Gluconeogenesis; Glycine; Humans; Hypog | 1975 |
Substitutions for glycine alpha 1-637 and glycine alpha 2-694 of type I procollagen in lethal osteogenesis imperfecta. The conformational strain on the triple helix introduced by a glycine substitution can be transmitted along the helix.
Topics: Alleles; Base Sequence; DNA; Electrophoresis, Polyacrylamide Gel; Female; Genes, Lethal; Glycine; Ho | 1991 |
Application of gas chromatography-mass spectrometry in routine and research in clinical chemistry.
Topics: Acidosis; Adult; Body Fluids; Carbon Dioxide; Chemistry, Clinical; Chromatography, Gas; Clinical Lab | 1974 |
Neuropathological study of aminoacidurias.
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Central Nervous System; Cystathionine; Female; Gl | 1972 |
Clinical finding and therapeutic problems in non-ketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbon Radioisotopes; Diet Therapy; Glycine; Humans; Hypotensi | 1973 |
Valine-sensitive nonketotic hyperglycinemia. Case report.
Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Benzoates; Brain Diseases; Brain Stem; C | 1974 |
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
Topics: Amino Acid Metabolism, Inborn Errors; Austria; Child, Preschool; Chromatography, Thin Layer; Diet Th | 1972 |
[Non-ketotic hyperglycinemia: peracute course in neonatal period].
Topics: Acute Disease; Amino Acids; Biopsy; Brain; Cerebellum; Fatty Liver; Glycine; Hiccup; Humans; Infant, | 1971 |
An automated fluorometric method for analysis of glycine in biological fluids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Autoanalysis; Chemistry, Clinical; Chrom | 1971 |
[Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
Topics: Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Infant; Infant, Newborn; Infant, Newb | 1969 |
Nonketotic hyperglycinemia.
Topics: Agranulocytosis; Amino Acid Metabolism, Inborn Errors; Benzoates; Body Weight; Carbon Isotopes; Diet | 1969 |
Neonatal intestinal obstruction due to milk curds.
Topics: Adult; Animals; Female; Gelatin; Glucose; Glycine; Humans; Infant; Infant Nutritional Physiological | 1969 |
A simple screening method for detecting isovalerylglycine in urine patients with isovaleric acidemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Thin Lay | 1970 |
[Glycinosis (hyperglycinemia)].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child Development; Child, Preschool; Ch | 1968 |
Spongy degeneration of the white matter of the central nervous system associated with hyperglycinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Central Nervous System; Central Nervous System Diseases; Femal | 1968 |
[Hyperglycinemia (glycinosis) with familial idiopathic hyperglycinuria. 1st observation in Germany].
Topics: Amino Acid Metabolism, Inborn Errors; Central Nervous System Diseases; Cerebral Cortex; Cytoplasm; F | 1966 |