Page last updated: 2024-08-17

nad and Deficiency, Mental

nad has been researched along with Deficiency, Mental in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19905 (62.50)18.7374
1990's1 (12.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's2 (25.00)2.80

Authors

AuthorsStudies
Bartsch, U; Donnelly, NA; Eaton, C; Hall, J; Hall, JH; Jones, MW; Marston, H; Moulding, HA; Owen, MJ; van den Bree, MBM1
Ayuso, C; Banfi, S; Bedoni, N; Brunetti-Pierri, N; Cappuccio, G; Corton, M; Di Rocco, M; Filocamo, M; Lanza, F; Lualdi, S; Morana, G; Nigro, V; Pinelli, M; Quinodoz, M; Rivolta, C; Simonelli, F; Superti-Furga, A; Testa, F; Torella, A1
SAIFER, A; SCHNECK, L; VOLK, BW; WALLACE, BJ1
Jaffé, ER1
Hayek, G; Jacomelli, G; Micheli, V; Pescaglini, M; Pompucci, G; Rocchigiani, M; Sestini, S1
Lingam, S; Simmonds, HA; Webster, DR; Wilson, J1
Fischer, JC; Gabreëls, FJ; Janssen, AJ; Renier, WO; Ruitenbeek, W; Sengers, RC; Stadhouders, AM; ter Laak, HJ; Trijbels, JM; Veerkamp, JH1
Astedt, B; Barthelmai, W; Neuvians, D; Vetrella, M1

Reviews

1 review(s) available for nad and Deficiency, Mental

ArticleYear
Methaemoglobinaemia.
    Clinics in haematology, 1981, Volume: 10, Issue:1

    Topics: Ascorbic Acid; Cytochrome-B(5) Reductase; Erythrocytes; Glutathione; Hemoglobins; Humans; Intellectual Disability; Methemoglobin; Methemoglobinemia; Metmyoglobin; NAD; NADP; Oxidation-Reduction

1981

Other Studies

7 other study(ies) available for nad and Deficiency, Mental

ArticleYear
Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms.
    eLife, 2022, 08-30, Volume: 11

    Topics: Adolescent; Autism Spectrum Disorder; Cross-Sectional Studies; DiGeorge Syndrome; Electroencephalography; Humans; Intellectual Disability; NAD; Sleep

2022
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs.
    Human molecular genetics, 2020, 08-03, Volume: 29, Issue:13

    Topics: Adolescent; Animals; Child; Child, Preschool; Disease Models, Animal; Exons; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Infant; Intellectual Disability; Leber Congenital Amaurosis; Male; Mice; Mutation; NAD; Nicotinamide-Nucleotide Adenylyltransferase; Osteochondrodysplasias; Pedigree; Retinal Degeneration

2020
LATE INFANTILE AMAUROTIC IDIOCY. ULTRAMICROSCOPIC AND HISTOCHEMICAL STUDIES ON A CASE.
    Archives of pathology, 1964, Volume: 78

    Topics: Acid Phosphatase; Biopsy; Cerebral Cortex; Chromatography; Diagnosis, Differential; Electrons; Histocytochemistry; Humans; Infant; Intellectual Disability; L-Lactate Dehydrogenase; Lipidoses; Lipids; Malate Dehydrogenase; Microscopy; Microscopy, Electron; NAD; NADP; Neuroglia; Pathology; Tay-Sachs Disease

1964
Altered pyridine metabolism in the erythrocytes of a mentally retarded infant with partial HPRT deficiency.
    Advances in experimental medicine and biology, 1994, Volume: 370

    Topics: Adenine; Carbon Radioisotopes; Child; Erythrocytes; Humans; Hypoxanthine; Hypoxanthine Phosphoribosyltransferase; Hypoxanthines; Infant; Intellectual Disability; Male; NAD; NADP; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines; Radioisotope Dilution Technique; Reference Values; Ribonucleotides

1994
An inborn error of purine metabolism, deafness and neurodevelopmental abnormality.
    Neuropediatrics, 1985, Volume: 16, Issue:2

    Topics: Deafness; Erythrocytes; Female; Guanosine Triphosphate; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; NAD; Purine-Pyrimidine Metabolism, Inborn Errors; Ribose-Phosphate Pyrophosphokinase; Syndrome; Uric Acid; X Chromosome

1985
A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.
    European journal of pediatrics, 1986, Volume: 144, Issue:5

    Topics: Acidosis; Adenosine Triphosphate; Brain Diseases; Epilepsy; Humans; Infant; Intellectual Disability; Lactates; Male; Mitochondria, Muscle; Muscle Spasticity; Myoclonus; NAD; Nystagmus, Pathologic; Oxidation-Reduction; Pyruvates; Ubiquinone

1986
Activity of NADH- and NADPH-dependent methemoglobin reductases in erythrocytes from fetal to adult age. A parallel assessment.
    Klinische Wochenschrift, 1971, Sep-01, Volume: 49, Issue:17

    Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Erythrocytes; Female; Fetus; Gestational Age; Humans; Infant; Infant, Newborn; Infant, Premature; Intellectual Disability; Methemoglobin; Methemoglobinemia; NAD; NADP; Oxidoreductases; Pregnancy

1971