Compounds > trolamine salicylate
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trolamine salicylate and Dwarfism

trolamine salicylate has been researched along with Dwarfism in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19903 (33.33)18.7374
1990's1 (11.11)18.2507
2000's1 (11.11)29.6817
2010's4 (44.44)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, L; Dong, Z; Lu, W; Ma, X; Ni, J; Shi, J; Wang, D; Wang, J; Wang, W; Xiao, Y; Yang, L; Zhang, C1
Dudek, M; Meng, QJ1
Cui, LR; Gehrke, T; Guenther, D; Haasper, C; Jakobs, O; Kendoff, D; Omar, M; Schmidl, S1
Acland, GM; Aguirre, GD; Goldstein, O; Guyon, R; Johnson, J; Kukekova, A; Kuznetsova, TN; Pearce-Kelling, SE1
BROWN, CH; MICHENER, WM; TURNBULL, RB1
De Fine, M; Palmonari, M; Tassinari, E; Toni, A; Traina, F1
Bianco, P; Birkedal-Hansen, H; Caterina, J; Holmbeck, K; Kromer, M; Kuznetsov, SA; Mankani, M; Pidoux, I; Poole, AR; Robey, PG; Ward, JM; Yamada, S1
Bhat, RV; Krishnamachari, KA1
Lorber, J1

Other Studies

9 other study(ies) available for trolamine salicylate and Dwarfism

ArticleYear
Pathogenic gene screening in 91 Chinese patients with short stature of unknown etiology with a targeted next-generation sequencing panel.
    BMC medical genetics, 2018, 12-12, Volume: 19, Issue:1

    Topics: Adolescent; Aggrecans; Arthritis; Asian People; Cartilage Oligomeric Matrix Protein; Child; Child, Preschool; Collagen Type II; Connective Tissue Diseases; Dwarfism; Female; Gene Expression; Genetic Testing; Hearing Loss, Sensorineural; High-Throughput Nucleotide Sequencing; Homeodomain Proteins; Humans; Male; Mutation; Noonan Syndrome; Osteochondrodysplasias; Protein Tyrosine Phosphatase, Non-Receptor Type 11; Retinal Detachment; SOS1 Protein; Transcription Factors

2018
Running on time: the role of circadian clocks in the musculoskeletal system.
    The Biochemical journal, 2014, Oct-01, Volume: 463, Issue:1

    Topics: Animals; Arthritis; Calcinosis; Cartilage; Circadian Rhythm; Dwarfism; Humans; Locomotion; Mice; Muscle, Skeletal; Tendons

2014
Total knee arthroplasty in patients with skeletal dysplasia.
    Archives of orthopaedic and trauma surgery, 2015, Volume: 135, Issue:8

    Topics: Aged; Arthritis; Arthroplasty, Replacement, Knee; Disability Evaluation; Dwarfism; Female; Follow-Up Studies; Humans; Knee Prosthesis; Male; Reoperation

2015
COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia.
    Mammalian genome : official journal of the International Mammalian Genome Society, 2010, Volume: 21, Issue:7-8

    Topics: Animals; Animals, Newborn; Arthritis; Base Sequence; Cataract; Collagen Type IX; Collagen Type XI; Connective Tissue Diseases; Craniofacial Abnormalities; Dog Diseases; Dogs; Dwarfism; Eye Diseases, Hereditary; Female; Genes, Recessive; Genetic Association Studies; Hearing Loss, Sensorineural; Humans; Male; Molecular Sequence Data; Mutation; Osteochondrodysplasias; Pedigree; Retinal Detachment

2010
ULCERATIVE COLITIS IN CHILDREN. II. MEDICAL AND SURGICAL THERAPY.
    American journal of diseases of children (1960), 1964, Volume: 108

    Topics: Adolescent; Adrenocorticotropic Hormone; Arthritis; Child; Chloramphenicol; Colitis; Colitis, Ulcerative; Drug Therapy; Dwarfism; Humans; Ileostomy; Infant; Intestinal Perforation; Megacolon; Methylprednisolone; Prednisone; Pyoderma; Sulfasalazine; Sulfathiazoles; Surgical Procedures, Operative; Toxicology

1964
Total hip arthroplasty in dwarfism. A case report.
    La Chirurgia degli organi di movimento, 2008, Volume: 92, Issue:1

    Topics: Aged; Arthritis; Arthroplasty, Replacement, Hip; Dwarfism; Female; Hip Joint; Humans

2008
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover.
    Cell, 1999, Oct-01, Volume: 99, Issue:1

    Topics: Animals; Arthritis; Body Constitution; Bone Development; Bone Diseases, Metabolic; Bone Resorption; Cachexia; Cartilage; Collagen; Connective Tissue Diseases; Disease Models, Animal; Dwarfism; Fibrosis; Growth Plate; Hyalin; Matrix Metalloproteinase 14; Matrix Metalloproteinases; Matrix Metalloproteinases, Membrane-Associated; Metalloendopeptidases; Mice; Mice, Knockout; Osteoblasts; Skin; Skull; Stromal Cells; Synovial Membrane

1999
Endemic familial arthritis of Malnad--an epidemiological study.
    The Indian journal of medical research, 1977, Volume: 66, Issue:5

    Topics: Adolescent; Adult; Arthritis; Child; Child, Preschool; Dwarfism; Female; Humans; India; Infant; Male; Middle Aged; Pedigree

1977
Syndrome for diagnosis: dwarfing, persistently open fontanelle; recurrent meningitis; recurrent subdural effusions with temporary alternate-sided hemiplegia; high-tone deafness; visual defect with pseudopapilloedema; slowing intellectual development; recu
    Proceedings of the Royal Society of Medicine, 1973, Volume: 66, Issue:11

    Topics: Anemia, Hypochromic; Arthritis; Child; Collagen Diseases; Deafness; Dwarfism; Erythema; Hemiplegia; Humans; Hyperopia; Intelligence; Lipidoses; Male; Meningitis, Pneumococcal; Papilledema; Skull; Splenomegaly; Syndrome

1973