Page last updated: 2024-08-23

sulfur and Deficiency, Mental

sulfur has been researched along with Deficiency, Mental in 22 studies

Research

Studies (22)

TimeframeStudies, this research(%)All Research%
pre-199010 (45.45)18.7374
1990's7 (31.82)18.2507
2000's4 (18.18)29.6817
2010's1 (4.55)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cao, Y; Liang, Z; Liu, L; Su, H; Yang, XC; Zheng, Y; Zhou, YK1
Hansen, S; MacDougall, L; Perry, TL; Warrington, PD1
Carter, DM; Kirsch, N; Lucky, AW; Lucky, PA1
Atherton, DJ; Crounse, RG; Jorizzo, JL; Wells, RS1
Hersh, JH; Hordinsky, MK; Hyzer, R; Joyce, MR; Klein, LR; Paller, A; Tsai, MY; Zax, RH1
Gentner, NE; Marcoux, D; McCuaig, C; Rasmussen, JE; Werner, MM1
Armier, J; Benoit, A; Marionnet, C; Quilliet, X; Sarasin, A; Stary, A1
Alapetite, C; Benoit, A; Moustacchi, E; Sarasin, A1
Botzi, C; Bracun, R; Focke, M; Götz, M; Hemmer, W; Jarisch, R; Killian, W; Wolf-Abdolvahab, S1
Calvieri, S; Giustini, S; Richetta, A; Rossi, A1
Alaibac, M; Fortina, AB; Peserico, A; Piaserico, S1
Boltshauser, E; Toelle, SP; Valsangiacomo, E1
Wood, RD1
Itin, PH; Pittelkow, MR1
Arlett, CF; Broughton, BC; Green, S; Harcourt, SA; Lehmann, AR; Malcolm, A; Natarajan, AT; Stefanini, M; Steingrimsdottir, H; Taylor, R1
Giorgi, R; Lagomarsini, P; Nuzzo, F; Stefanini, M1
Crawhall, JC; Purkiss, P; Stanbury, JB1
Baillehache-Sigod, N1
Jackson, CE; Watson, JH; Weiss, L1
Bir, K; Crawhall, JC; Purkiss, P; Stanbury, JB1
Pollitt, RJ; Stonier, PD1
Feres, M; Figueiredo, LC; Salvador, SL1

Reviews

2 review(s) available for sulfur and Deficiency, Mental

ArticleYear
PIBI(D)S: clinical and molecular characterization of a new case.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2001, Volume: 15, Issue:1

    Topics: Child; Dwarfism; Hair; Humans; Ichthyosis; Intellectual Disability; Male; Photosensitivity Disorders; Sulfur; Syndrome

2001
Human diseases associated with defective DNA excision repair.
    Journal of the Royal College of Physicians of London, 1991, Volume: 25, Issue:4

    Topics: Cockayne Syndrome; DNA Damage; DNA Repair; Hair Diseases; Humans; Intellectual Disability; Skin Neoplasms; Sulfur; Xeroderma Pigmentosum

1991

Other Studies

20 other study(ies) available for sulfur and Deficiency, Mental

ArticleYear
A homozygous G insertion in MPLKIP leads to TTDN1 with the hypergonadotropic hypogonadism symptom.
    BMC medical genetics, 2018, 12-31, Volume: 19, Issue:Suppl 1

    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.
    Clinica chimica acta; international journal of clinical chemistry, 1967, Volume: 15, Issue:3

    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.
    Journal of the American Academy of Dermatology, 1984, Volume: 11, Issue:2 Pt 2

    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).
    The British journal of dermatology, 1982, Volume: 106, Issue:6

    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?
    Pediatric dermatology, 1993, Volume: 10, Issue:2

    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.
    Journal of the American Academy of Dermatology, 1993, Volume: 28, Issue:5 Pt 2

    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.
    Cancer research, 1996, Dec-01, Volume: 56, Issue:23

    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.
    The Journal of investigative dermatology, 1997, Volume: 108, Issue:2

    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.
    Dermatology (Basel, Switzerland), 1997, Volume: 194, Issue:1

    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.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2001, Volume: 15, Issue:1

    Topics: Hair; Humans; Infertility; Intellectual Disability; Sulfur; Syndrome

2001
Trichothiodystrophy with severe cardiac and neurological involvement in two sisters.
    European journal of pediatrics, 2001, Volume: 160, Issue:12

    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.
    Journal of the American Academy of Dermatology, 1991, Volume: 24, Issue:2 Pt 2

    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.
    Cancer research, 1988, Nov-01, Volume: 48, Issue:21

    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.
    Mutation research, 1987, Volume: 191, Issue:2

    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.
    Biochemical medicine, 1973, Volume: 7, Issue:1

    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].
    Revue de neuropsychiatrie infantile et d'hygiene mentale de l'enfance, 1973, Volume: 21, Issue:6

    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.
    Pediatrics, 1974, Volume: 54, Issue:2

    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.
    Biochemical medicine, 1971, Volume: 5, Issue:2

    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.
    The Biochemical journal, 1971, Volume: 122, Issue:4

    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.
    Oral diseases, 2005, Volume: 11 Suppl 1

    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