nad has been researched along with Deficiency, Mental in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (62.50) | 18.7374 |
1990's | 1 (12.50) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 2 (25.00) | 2.80 |
Authors | Studies |
---|---|
Bartsch, U; Donnelly, NA; Eaton, C; Hall, J; Hall, JH; Jones, MW; Marston, H; Moulding, HA; Owen, MJ; van den Bree, MBM | 1 |
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, A | 1 |
SAIFER, A; SCHNECK, L; VOLK, BW; WALLACE, BJ | 1 |
Jaffé, ER | 1 |
Hayek, G; Jacomelli, G; Micheli, V; Pescaglini, M; Pompucci, G; Rocchigiani, M; Sestini, S | 1 |
Lingam, S; Simmonds, HA; Webster, DR; Wilson, J | 1 |
Fischer, JC; Gabreëls, FJ; Janssen, AJ; Renier, WO; Ruitenbeek, W; Sengers, RC; Stadhouders, AM; ter Laak, HJ; Trijbels, JM; Veerkamp, JH | 1 |
Astedt, B; Barthelmai, W; Neuvians, D; Vetrella, M | 1 |
1 review(s) available for nad and Deficiency, Mental
Article | Year |
---|---|
Methaemoglobinaemia.
Topics: Ascorbic Acid; Cytochrome-B(5) Reductase; Erythrocytes; Glutathione; Hemoglobins; Humans; Intellectual Disability; Methemoglobin; Methemoglobinemia; Metmyoglobin; NAD; NADP; Oxidation-Reduction | 1981 |
7 other study(ies) available for nad and Deficiency, Mental
Article | Year |
---|---|
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.
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.
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.
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.
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.
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.
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.
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 |