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aspartic acid and Carbohydrate Metabolism, Inborn Error

aspartic acid has been researched along with Carbohydrate Metabolism, Inborn Error in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19907 (70.00)18.7374
1990's1 (10.00)18.2507
2000's2 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rohr, A; Stephani, U; van Baalen, A1
Allen, KN; Dai, J; Dunaway-Mariano, D; Lu, Z; Silvaggi, NR; Zhang, C1
Engelke, UF; Feikema, W; Jakobs, C; Pouwels, PJ; Struys, EA; Valk, J; van der Knaap, MS; Verhoeven, NM; Wevers, RA1
Collart, M; Humbel, R1
Konttinen, A; Palo, J; Savolainen, H; Somer, H1
Lee, TY; Onisawa, J1
Palo, J; Savolainen, H1
Kretchmer, N1
Autio, S1
Arstila, A; Autio, S; Palo, J; Riekkinen, P1

Reviews

2 review(s) available for aspartic acid and Carbohydrate Metabolism, Inborn Error

ArticleYear
Developmental biochemistry--a relevant endeavor. Borden Award address.
    Pediatrics, 1970, Volume: 46, Issue:2

    Topics: Alanine Transaminase; Animals; Aspartic Acid; Carbamates; Carbohydrate Metabolism, Inborn Errors; Cetacea; Chick Embryo; Galactosidases; Glucose; Glycoside Hydrolases; Growth; Intestinal Mucosa; Intestine, Small; Ligases; Pyrimidines; Rats; Transferases; Tyrosine Transaminase

1970
Aspartylglycosaminuria. Analysis of thirty-four patients.
    Journal of mental deficiency research, 1972, Volume: 1, Issue:0

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Birth Order; Birth Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Electrocardiography; Electroencephalography; Female; Finland; Geography; Glucosamine; Humans; Infant; Intellectual Disability; Intelligence Tests; Life Expectancy; Male; Pedigree; Socioeconomic Factors

1972

Other Studies

8 other study(ies) available for aspartic acid and Carbohydrate Metabolism, Inborn Error

ArticleYear
Increased brain lactate during stroke-like episode in a patient with congenital disorder of glycosylation type Ia.
    Brain & development, 2009, Volume: 31, Issue:2

    Topics: Acidosis, Lactic; Aspartic Acid; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Female; Fever; Glycoproteins; Glycosylation; Humans; Lactic Acid; Magnetic Resonance Spectroscopy; Mutation; Paresis; Phosphotransferases (Phosphomutases); Stroke

2009
The X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1a.
    The Journal of biological chemistry, 2006, May-26, Volume: 281, Issue:21

    Topics: Amino Acid Sequence; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Cloning, Molecular; Crystallography, X-Ray; Humans; Hydrolases; Magnesium; Models, Chemical; Models, Molecular; Molecular Conformation; Molecular Sequence Data; Phosphotransferases (Phosphomutases); Protein Isoforms

2006
Leukoencephalopathy associated with a disturbance in the metabolism of polyols.
    Annals of neurology, 1999, Volume: 46, Issue:6

    Topics: Adolescent; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Choline; Creatine; Demyelinating Diseases; Humans; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Parietal Lobe; Ribitol; Sugar Alcohols

1999
Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography.
    Clinica chimica acta; international journal of clinical chemistry, 1975, Apr-16, Volume: 60, Issue:2

    Topics: Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glucosamine; Glycoproteins; Humans; Mannose; Methods; Oligosaccharides; Time Factors

1975
Studies on N-aspartyl-beta-glucosaminidase in aspartylglycosaminuria.
    Clinica chimica acta; international journal of clinical chemistry, 1975, Apr-16, Volume: 60, Issue:2

    Topics: Animals; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Cell Nucleus; Chromatography, Agarose; Hexosamines; Hexosaminidases; Humans; Intellectual Disability; Liver; Lysosomes; Mitochondria, Liver; Rats; Subcellular Fractions

1975
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
    Biochemical medicine, 1970, Volume: 3, Issue:5

    Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glutamates; Glycine; Glycosaminoglycans; Humans; Hypertrichosis; Joint Diseases; Male; Mucopolysaccharidosis I; Retinitis Pigmentosa; Serine; Uronic Acids

1970
Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 36, Issue:2

    Topics: Amidohydrolases; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Chromatography, Thin Layer; Electrophoresis; Glucosamine; Glucuronidase; Glycopeptides; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Hydrogen-Ion Concentration; Lysosomes; Neuraminic Acids; Peptides

1972
Biochemical and fine structural studies on brain and liver biopsies in aspartylglucosaminuria.
    Neurology, 1971, Volume: 21, Issue:12

    Topics: Acetamides; Adult; Amino Acids; Aspartic Acid; Biopsy; Brain; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Chromatography; Female; Glycopeptides; Glycoside Hydrolases; Glycosides; Glycosuria; Hexosaminidases; Hexoses; Histocytochemistry; Humans; Liver; Lysosomes; Male; Microscopy, Electron; Neuroglia; Neurons

1971