sulfur has been researched along with Deficiency, Mental in 22 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 10 (45.45) | 18.7374 |
1990's | 7 (31.82) | 18.2507 |
2000's | 4 (18.18) | 29.6817 |
2010's | 1 (4.55) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cao, Y; Liang, Z; Liu, L; Su, H; Yang, XC; Zheng, Y; Zhou, YK | 1 |
Hansen, S; MacDougall, L; Perry, TL; Warrington, PD | 1 |
Carter, DM; Kirsch, N; Lucky, AW; Lucky, PA | 1 |
Atherton, DJ; Crounse, RG; Jorizzo, JL; Wells, RS | 1 |
Hersh, JH; Hordinsky, MK; Hyzer, R; Joyce, MR; Klein, LR; Paller, A; Tsai, MY; Zax, RH | 1 |
Gentner, NE; Marcoux, D; McCuaig, C; Rasmussen, JE; Werner, MM | 1 |
Armier, J; Benoit, A; Marionnet, C; Quilliet, X; Sarasin, A; Stary, A | 1 |
Alapetite, C; Benoit, A; Moustacchi, E; Sarasin, A | 1 |
Botzi, C; Bracun, R; Focke, M; Götz, M; Hemmer, W; Jarisch, R; Killian, W; Wolf-Abdolvahab, S | 1 |
Calvieri, S; Giustini, S; Richetta, A; Rossi, A | 1 |
Alaibac, M; Fortina, AB; Peserico, A; Piaserico, S | 1 |
Boltshauser, E; Toelle, SP; Valsangiacomo, E | 1 |
Wood, RD | 1 |
Itin, PH; Pittelkow, MR | 1 |
Arlett, CF; Broughton, BC; Green, S; Harcourt, SA; Lehmann, AR; Malcolm, A; Natarajan, AT; Stefanini, M; Steingrimsdottir, H; Taylor, R | 1 |
Giorgi, R; Lagomarsini, P; Nuzzo, F; Stefanini, M | 1 |
Crawhall, JC; Purkiss, P; Stanbury, JB | 1 |
Baillehache-Sigod, N | 1 |
Jackson, CE; Watson, JH; Weiss, L | 1 |
Bir, K; Crawhall, JC; Purkiss, P; Stanbury, JB | 1 |
Pollitt, RJ; Stonier, PD | 1 |
Feres, M; Figueiredo, LC; Salvador, SL | 1 |
2 review(s) available for sulfur and Deficiency, Mental
Article | Year |
---|---|
PIBI(D)S: clinical and molecular characterization of a new case.
Topics: Child; Dwarfism; Hair; Humans; Ichthyosis; Intellectual Disability; Male; Photosensitivity Disorders; Sulfur; Syndrome | 2001 |
Human diseases associated with defective DNA excision repair.
Topics: Cockayne Syndrome; DNA Damage; DNA Repair; Hair Diseases; Humans; Intellectual Disability; Skin Neoplasms; Sulfur; Xeroderma Pigmentosum | 1991 |
20 other study(ies) available for sulfur and Deficiency, Mental
Article | Year |
---|---|
A homozygous G insertion in MPLKIP leads to TTDN1 with the hypergonadotropic hypogonadism symptom.
Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Base Sequence; Exons; Female; Gene Expression; Genes, Recessive; Hair; Homozygote; Humans; Hypogonadism; Intellectual Disability; Male; Mutagenesis, Insertional; Pedigree; Phenotype; Protein Interaction Mapping; Sulfur; Trichothiodystrophy Syndromes | 2018 |
Sulfur-containing amino acids in the plasma and urine of homocystinurics.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Homocysteine; Homocystine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Iodoacetates; Methionine; Sulfoxides; Sulfur; Ultraviolet Rays | 1967 |
Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure.
Topics: Adolescent; Dwarfism; Hair; Hair Diseases; Hearing Loss, Sensorineural; Humans; Hypogonadism; Intellectual Disability; Male; Photosensitivity Disorders; Sulfur; Syndrome | 1984 |
Ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature (IBIDS syndrome).
Topics: Child; Growth Disorders; Hair; Humans; Ichthyosis; Infertility, Male; Intellectual Disability; Male; Sulfur; Syndrome | 1982 |
Trichothiodystrophy and associated anomalies: a variant of SIBIDS or new symptom complex?
Topics: Growth Disorders; Hair Diseases; Humans; Ichthyosis; Infant, Newborn; Infertility, Male; Intellectual Disability; Male; Microscopy, Polarization; Osteosclerosis; Phenotype; Sulfur; Tomography, X-Ray Computed | 1993 |
Trichothiodystrophy associated with photosensitivity, gonadal failure, and striking osteosclerosis.
Topics: Adult; Age Determination by Skeleton; Body Height; Child, Preschool; Face; Hair; Humans; Hypogonadism; Ichthyosis; Intellectual Disability; Male; Osteosclerosis; Photosensitivity Disorders; Sexual Maturation; Sulfur; Syndrome | 1993 |
Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
Topics: Cell Line, Transformed; Colony-Forming Units Assay; DNA Helicases; DNA Repair; DNA-Binding Proteins; Fibroblasts; Genetic Complementation Test; Hair Diseases; Humans; Intellectual Disability; Metabolism, Inborn Errors; Mutagenesis; Photosensitivity Disorders; Protein Biosynthesis; Proteins; Recombinant Fusion Proteins; Sulfur; Transcription Factors; Transfection; Ultraviolet Rays; Xeroderma Pigmentosum; Xeroderma Pigmentosum Group D Protein | 1996 |
The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy.
Topics: Cells, Cultured; DNA Damage; DNA Repair; Electrophoresis; Female; Fetus; Hair Diseases; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Microscopy, Fluorescence; Pregnancy; Prenatal Diagnosis; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1997 |
Diagnosis of trichothiodystrophy in 2 siblings.
Topics: Ataxia; Child; Consanguinity; Cystine; Dermatitis, Atopic; Dysarthria; Epilepsy; Female; Finger Joint; Genes, Recessive; Growth Disorders; Hair; Humans; Intellectual Disability; Joint Instability; Male; Microscopy, Electron, Scanning; Microscopy, Polarization; Muscle Spasticity; Strabismus; Sulfur | 1997 |
What's new in trichothiodystrophy.
Topics: Hair; Humans; Infertility; Intellectual Disability; Sulfur; Syndrome | 2001 |
Trichothiodystrophy with severe cardiac and neurological involvement in two sisters.
Topics: Cardiomyopathies; DNA Repair; Echocardiography; Female; Genes, Recessive; Hair; Hair Diseases; Heart Defects, Congenital; Humans; Infant, Newborn; Intellectual Disability; Magnetic Resonance Imaging; Neurocutaneous Syndromes; Nuclear Family; Sulfur | 2001 |
Trichothiodystrophy with chronic neutropenia and mild mental retardation.
Topics: Child; Chronic Disease; Female; Hair; Hair Diseases; Humans; Intellectual Disability; Neutropenia; Skin Diseases; Sulfur | 1991 |
Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
Topics: Cell Survival; Child; Cockayne Syndrome; DNA; DNA Repair; Hair Diseases; Humans; Intellectual Disability; Male; RNA; Sister Chromatid Exchange; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1988 |
Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
Topics: Cell Fusion; Cells, Cultured; DNA Repair; Fibroblasts; Genetic Complementation Test; Hair Diseases; Humans; Intellectual Disability; Photosensitivity Disorders; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1987 |
Metabolism of sulfur-containing amino acids in a patient excreting -mercaptolactate-cysteine disulfide.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Cysteine; Cystine; Disulfides; Humans; Intellectual Disability; Lactates; Male; Methionine; Sulfur; Sulfur Isotopes; Taurine; Time Factors | 1973 |
[Use of Soufrane as preventive treatment of respiratory insufficiency in patients with mental retardation].
Topics: Anti-Infective Agents, Local; Humans; Intellectual Disability; Respiratory Insufficiency; Respiratory Tract Infections; Sulfur | 1973 |
"Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred.
Topics: Abnormalities, Multiple; Activation Analysis; Adult; Ceruloplasmin; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Consanguinity; Copper; Ethnicity; Female; Genes, Recessive; Growth Disorders; Hair; Humans; Indiana; Infertility; Intellectual Disability; Karyotyping; Male; Microscopy, Electron, Scanning; Microscopy, Polarization; Pedigree; Skin Diseases; Sulfur; Syndrome | 1974 |
Sulfur amino acids as precursors of beta-mercaptolactate-cysteine disulfide in human subjects.
Topics: Adult; Anilides; Cysteine; Diet; Dietary Proteins; Disulfides; Electrophoresis; Female; Humans; Intellectual Disability; Lactates; Male; Metabolism; Methionine; Models, Biological; Neomycin; Phthalic Acids; Pyridoxine; Sulfates; Sulfathiazoles; Sulfur; Taurine; Thiosulfates | 1971 |
Proteins of normal hair and of cystine-deficient hair from mentally retarded siblings.
Topics: Acrylates; Amino Acids; Animals; Chromatography, DEAE-Cellulose; Cystine; Electrophoresis; Female; Gels; Hair; Humans; Hydrolysis; Intellectual Disability; Isoelectric Focusing; Molecular Weight; Optical Rotatory Dispersion; Proteins; Sheep; Sulfur; Tritium; Wool | 1971 |
Halitosis and periodontal disease in subjects with mental disabilities.
Topics: Adolescent; Adult; Benzoylarginine-2-Naphthylamide; Case-Control Studies; Dental Plaque; Down Syndrome; Female; Halitosis; Humans; Intellectual Disability; Male; Periodontal Diseases; Persons with Mental Disabilities; Sulfur Compounds; Tongue | 2005 |