sulfur has been researched along with Syndrome in 26 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 17 (65.38) | 18.7374 |
1990's | 4 (15.38) | 18.2507 |
2000's | 5 (19.23) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
COTTE, L; MARIN, A | 1 |
DiGiovanna, JJ; Kraemer, KH; Liang, C; Menefee, E; Morris, A; Price, VH; Schiffmann, R | 1 |
Carter, DM; Kirsch, N; Lucky, AW; Lucky, PA | 1 |
Graves, DS; Stadalnik, RC | 1 |
Atherton, DJ; Crounse, RG; Jorizzo, JL; Wells, RS | 1 |
Hubbard, AM; Starshak, RJ; Sty, JR | 1 |
Lieberman, LM; Polcyn, RE; Rao, BK; Shore, RM | 1 |
Ehrlich, CP; Hurwitz, RA; Papanicolaou, N; Richards, P; Treves, S | 1 |
Donati, RM; Fletcher, JW; Lin, MS | 1 |
Gentner, NE; Marcoux, D; McCuaig, C; Rasmussen, JE; Werner, MM | 1 |
Itin, PH; Pittelkow, MR; Sarasin, A | 1 |
Calvieri, S; Giustini, S; Richetta, A; Rossi, A | 1 |
Alaibac, M; Fortina, AB; Peserico, A; Piaserico, S | 1 |
Makita, Y | 1 |
Abdel-Dayam, HM; Elkousy, AM; Leslie, EV; Panaro, VA | 1 |
Haines, JE; Larson, SM; Yeung, WC | 1 |
Neish, AS; Pober, BR; Shapira, SK | 1 |
Hamm, H; Traupe, H | 1 |
al-Ismaily, SI; al-Sumry, HS; Harper, RB; Hidiroglou, M; Ivan, M | 1 |
Bat, P; Blanc, A; Poissonnier, M | 1 |
Crovato, F; Rebora, A | 1 |
Arlett, CF; Borrone, C; Cordone, G; Crovato, F; Lagomarsini, P; Marinoni, S; Nuzzo, F; Stefanini, M; Trevisan, G | 1 |
Baden, HP; Goldsmith, LA; Matz, MH; Parrish, JA | 1 |
Bonte, FJ; Parkey, RW | 1 |
Barron, KD; Cox, JF; Koeppen, AH | 1 |
Jackson, CE; Watson, JH; Weiss, L | 1 |
4 review(s) available for sulfur and Syndrome
Article | Year |
---|---|
Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
Topics: Animals; DNA Damage; DNA Helicases; DNA-Binding Proteins; Face; Gene Expression Regulation; Hair; Humans; Mice; Mice, Knockout; Point Mutation; Proteins; Skin Diseases; Sulfur; Syndrome; Transcription Factors; Ultraviolet Rays; Xeroderma Pigmentosum Group D Protein | 2001 |
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 |
[Trichothiodystrophy].
Topics: Growth Disorders; Hair; Humans; Ichthyosis; Sulfur; Syndrome | 2001 |
[What is new in genetically-induced hair diseases?].
Topics: Ectodermal Dysplasia; Genetic Carrier Screening; Hair Diseases; Humans; Ichthyosis, X-Linked; Sulfur; Syndrome | 1990 |
22 other study(ies) available for sulfur and Syndrome
Article | Year |
---|---|
[Late appearing epilepsy following an acute intoxication with anoxemic syndrome].
Topics: Dementia; Epilepsy; Humans; Hypoxia, Brain; Occupational Diseases; Psychotic Disorders; Sulfur; Syndrome | 1961 |
Characterization of tiger-tail banding and hair shaft abnormalities in trichothiodystrophy.
Topics: Cystine; Darier Disease; DNA Repair; Ectodermal Dysplasia; Hair; Hair Diseases; Humans; Hyperkeratosis, Epidermolytic; Ichthyosis; Microscopy, Polarization; Photosensitivity Disorders; Sensitivity and Specificity; Sulfur; Syndrome; Xeroderma Pigmentosum | 2005 |
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 |
Anatomic and functional asplenia--absence of the splenic image during 99mTc-sulfur colloid scintigraphy.
Topics: Colloids; Female; Heart Defects, Congenital; Humans; Infant, Newborn; Radionuclide Imaging; Spleen; Splenic Diseases; Sulfur; Syndrome; Technetium; Technetium Tc 99m Sulfur Colloid | 1982 |
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 |
Radionuclide hepatobiliary imaging in congenital biliary tract ectasia (Caroli disease).
Topics: Adolescent; Bile Duct Diseases; Bile Ducts, Intrahepatic; Child; Child, Preschool; Humans; Imino Acids; Infant; Organotechnetium Compounds; Radionuclide Imaging; Sulfur; Syndrome; Technetium; Technetium Tc 99m Diethyl-iminodiacetic Acid; Technetium Tc 99m Sulfur Colloid; Tomography, X-Ray Computed; Ultrasonography | 1982 |
Dual radiopharmaceutical imaging in congenital asplenia syndrome.
Topics: Erythrocyte Inclusions; Female; Heart Defects, Congenital; Humans; Imino Acids; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Male; Middle Aged; Organotechnetium Compounds; Radionuclide Imaging; Spleen; Sulfur; Syndrome; Technetium; Technetium Tc 99m Sulfur Colloid | 1982 |
Splenic scintigraphy using Tc-99m-labeled heat-denatured red blood cells in pediatric patients: concise communication.
Topics: Abdominal Injuries; Adolescent; Child, Preschool; Erythrocytes; Female; Humans; Infant; Infant, Newborn; Isotope Labeling; Male; Purpura, Thrombocytopenic; Radionuclide Imaging; Reagent Kits, Diagnostic; Spleen; Sulfur; Syndrome; Technetium; Technetium Tc 99m Sulfur Colloid | 1982 |
Local colloid trapping in the liver in the inferior vena cava syndrome.
Topics: Collateral Circulation; Colloids; Constriction, Pathologic; Humans; Injections, Intravenous; Leg; Liver; Male; Middle Aged; Radionuclide Imaging; Sulfur; Syndrome; Technetium; Umbilical Veins; Vascular Diseases; Vena Cava, Inferior; Vena Cava, Superior | 1981 |
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 |
What's new in trichothiodystrophy.
Topics: Hair; Humans; Infertility; Intellectual Disability; Sulfur; Syndrome | 2001 |
Experience with 111-In-chloride scanning in patients with focal defects on 99-mTc-sulfur colloid liver scans.
Topics: Adolescent; Alcoholism; Carcinoma, Hepatocellular; Chlorides; Diagnosis, Differential; Fatty Liver; Female; Humans; Indium; Liver Cirrhosis; Liver Neoplasms; Lymphoma, Large B-Cell, Diffuse; Male; Middle Aged; Neoplasm Metastasis; Radioisotopes; Radionuclide Imaging; Sulfur; Syndrome; Technetium | 1975 |
Diagnosis of posterolateral congenital diaphragmatic (Bochdalek) hernia by liver scintigram: case report.
Topics: Colloids; Hernia, Diaphragmatic; Hernias, Diaphragmatic, Congenital; Humans; Infant, Newborn; Liver Diseases; Male; Radionuclide Imaging; Sulfur; Syndrome; Technetium | 1976 |
Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.
Topics: Argininosuccinic Acid; Child; Child, Preschool; Consanguinity; Copper; Deafness; Developmental Disabilities; Female; Growth Disorders; Hair; Humans; Male; Sulfur; Syndrome | 1992 |
Copper deficiency and posterior paralysis (Shalal) in small ruminants in the Sultanate of Oman.
Topics: Animal Feed; Animals; Ataxia; Copper; Goat Diseases; Goats; Iron; Liver; Oman; Paralysis; Rumen; Sheep; Sheep Diseases; Sulfur; Syndrome | 1990 |
[Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].
Topics: Abnormalities, Multiple; Child; Female; Genetic Counseling; Hair; Hair Diseases; Humans; Sulfur; Syndrome | 1988 |
Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.
Topics: Hair Diseases; Humans; Photosensitivity Disorders; Sulfur; Syndrome; Xeroderma Pigmentosum | 1988 |
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity.
Topics: Cells, Cultured; Child; Child, Preschool; Chromosomes, Human, 13-15; DNA Damage; DNA Replication; Female; Hair; Hair Diseases; Humans; Mutation; Photosensitivity Disorders; Sulfur; Syndrome; Ultraviolet Rays; Xeroderma Pigmentosum | 1986 |
Studies of the density and the properties of the hair in a new inherited syndrome of hypotrichosis.
Topics: Age Factors; Alopecia; Child; Color; Electrophoresis; Electrophoresis, Polyacrylamide Gel; Epidermal Cyst; Female; Fetal Diseases; Follow-Up Studies; Hair; Humans; Miliaria; Pedigree; Pregnancy; Proteins; Sulfur; Syndrome | 1972 |
Scintigraphic demonstration of abdominal wall collateral venous blood pool in cirrhosis.
Topics: Abdominal Muscles; Alcoholism; Collateral Circulation; Colloids; Fatty Liver; Female; Humans; Hypertension, Portal; Liver Cirrhosis; Middle Aged; Radionuclide Imaging; Sulfur; Syndrome; Technetium | 1973 |
Foix-Alajouanine syndrome.
Topics: Aged; Blood Vessels; Calcium; Histocytochemistry; Humans; Ischemia; Male; Microscopy, Electron, Scanning; Myelitis; Necrosis; Paraplegia; Phosphorus; Spinal Cord; Sulfur; Syndrome | 1974 |
"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 |