n-acetylneuraminic acid and Deficiency, Mental

n-acetylneuraminic acid has been researched along with Deficiency, Mental in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19904 (44.44)18.7374
1990's4 (44.44)18.2507
2000's1 (11.11)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
ARONSON, SM; SAIFER, A; VOLK, BW1
Halverson, GR; Hurlet-Jensen, A; Lee, AH; Reid, ME; Reiss, RF; Øyen, R1
Barabino, A; Borrone, C; Di Rocco, M; Gandullia, P; Gatti, R; Picco, P1
Iwakiri, N; Ohba, N; Sameshima, M; Uehara, F; Yanagita, T1
Braga, AC; Ferreira, H; Gahl, WA; Gomes, L; Huizing, M; Krasnewich, DM; Martins, E; Pinto, R; Sa Miranda, MC; Seppala, R1
Beemer, FA; Hu, P; Janse, HC; Jennekens, FG; Kleijer, WJ; Mancini, GM; van Diggelen, OP; Verheijen, FW1
Aula, P; Koskela, SL; Raivio, KO; Renlund, M1
Finne, J; Haltia, M; Palmgren, K; Palo, J; Rauvala, H1
Autio-Harmainen, H; Linna, SL; Ruokonen, A; Similä, S; Väyrynen, M; von Wendt, L1

Other Studies

9 other study(ies) available for n-acetylneuraminic acid and Deficiency, Mental

ArticleYear
Neuraminic (sialic) acid studies of biological fluids in amaurotic family idiocy and related disorders.
    A.M.A. journal of diseases of children, 1959, Volume: 97, Issue:5, Part 2

    Topics: Amino Acids; Body Fluids; Feces; Intellectual Disability; N-Acetylneuraminic Acid; Neuronal Ceroid-Lipofuscinoses; Tay-Sachs Disease

1959
Altered glycosylation leads to Tr polyagglutination.
    Transfusion, 2004, Volume: 44, Issue:11

    Topics: Anemia, Hemolytic; Bernard-Soulier Syndrome; Blood; Electrophoresis, Polyacrylamide Gel; Erythrocytes; Fetal Blood; Glycosylation; Hemagglutination; Hematologic Diseases; Humans; Infant, Newborn; Intellectual Disability; Lectins; Male; Mitral Valve Insufficiency; N-Acetylneuraminic Acid; Neutropenia

2004
Report on two patients with Costello syndrome and sialuria.
    American journal of medical genetics, 1993, Nov-15, Volume: 47, Issue:7

    Topics: Abnormalities, Multiple; Child, Preschool; Face; Feeding and Eating Disorders; Female; Growth Disorders; Humans; Intellectual Disability; Limb Deformities, Congenital; Male; N-Acetylneuraminic Acid; Nose Neoplasms; Papilloma; Sialic Acids; Skin Abnormalities; Syndrome

1993
Lectin-histochemical study of O-linked glycoconjugates in dysplastic retina of Norrie disease.
    Japanese journal of ophthalmology, 1996, Volume: 40, Issue:2

    Topics: Acetylglucosamine; Antigens, Tumor-Associated, Carbohydrate; Eye Abnormalities; Female; Glycoconjugates; Histocytochemistry; Humans; Immunoenzyme Techniques; Infant; Intellectual Disability; Lectins; N-Acetylneuraminic Acid; Peanut Agglutinin; Polysaccharides; Retina; Retinal Dysplasia; Wheat Germ Agglutinins

1996
Sialuria in a Portuguese girl: clinical, biochemical, and molecular characteristics.
    Molecular genetics and metabolism, 1999, Volume: 67, Issue:2

    Topics: Abnormalities, Multiple; Carbohydrate Epimerases; Cells, Cultured; Child; Cytidine Monophosphate N-Acetylneuraminic Acid; Escherichia coli Proteins; Female; Fibroblasts; Humans; Intellectual Disability; Metabolism, Inborn Errors; N-Acetylneuraminic Acid; Point Mutation; Sialic Acids; Subcellular Fractions

1999
Salla disease variant in a Dutch patient. Potential value of polymorphonuclear leucocytes for heterozygote detection.
    European journal of pediatrics, 1992, Volume: 151, Issue:8

    Topics: Ataxia; Child, Preschool; Chorionic Villi; Fibroblasts; Genetic Carrier Screening; Humans; Intellectual Disability; Lysosomal Storage Diseases; Male; N-Acetylneuraminic Acid; Neutrophils; Prenatal Diagnosis; Sialic Acids; Skin

1992
Screening of inherited oligosaccharidurias among mentally retarded patients in northern Finland.
    Journal of mental deficiency research, 1986, Volume: 30 ( Pt 4)

    Topics: Adolescent; Adult; Aspartylglucosylaminase; Chromatography, Thin Layer; Female; Finland; Humans; Intellectual Disability; Male; Mass Screening; Metabolism, Inborn Errors; N-Acetylneuraminic Acid; Sialic Acids

1986
Hyperexcretion of free N-acetylneuraminic acid--a novel type of sialuria.
    Clinica chimica acta; international journal of clinical chemistry, 1985, Feb-15, Volume: 145, Issue:3

    Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Epilepsy, Tonic-Clonic; Female; Humans; Intellectual Disability; N-Acetylneuraminic Acid; Sialic Acids

1985
Finnish type of sialic acid storage disease with sialuria (Salla disease): the occurrence and diagnostic significance of cytoplasmic vacuoles in blood lymphocytes.
    Journal of mental deficiency research, 1985, Volume: 29 ( Pt 2)

    Topics: Adolescent; Adult; Aged; Brain Diseases, Metabolic; Child; Child, Preschool; Cytoplasm; Female; Humans; Intellectual Disability; Lymphocytes; Lysosomes; Male; Middle Aged; N-Acetylneuraminic Acid; Organoids; Sialic Acids; Vacuoles

1985