Page last updated: 2024-08-22

trolamine salicylate and Congenital Hand Deformities

trolamine salicylate has been researched along with Congenital Hand Deformities in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19902 (25.00)18.7374
1990's0 (0.00)18.2507
2000's1 (12.50)29.6817
2010's3 (37.50)24.3611
2020's2 (25.00)2.80

Authors

AuthorsStudies
Alkaiyat, A; Fatouleh, M; Iriqat, S; Safieh, MA1
Hagen, M; Karempelis, P; Morrell, N; Roby, BB1
Brogan, P; Compeyrot-Lacassagne, S; Dias, C; Klein, N; Melo Gomes, S; Omoyinmi, E; Sebire, NJ1
Moran, R; Shen, M; Tomecki, KJ; Yao, Q1
Ellis, CV; Kulber, DA1
LENOCH, F; WEISSER, L1
Amor, DJ; Bateman, JF; Gardner, RJ; Lamandé, SR; Savarirayan, R; Tudball, C1
Arturi, A; Babini, JC; Babini, SM; Cocco, JA; de la Sota, M; Marcos, JC; Morteo, OG1

Reviews

1 review(s) available for trolamine salicylate and Congenital Hand Deformities

ArticleYear
Acellular dermal matrices in hand reconstruction.
    Plastic and reconstructive surgery, 2012, Volume: 130, Issue:5 Suppl 2

    Topics: Acellular Dermis; Adult; Arthritis; Biological Dressings; Burns; Carpometacarpal Joints; Child; Collagen; Contracture; Cross-Sectional Studies; Dupuytren Contracture; Hand; Hand Deformities, Acquired; Hand Deformities, Congenital; Hand Injuries; Humans; Ligaments; Neuralgia; Plastic Surgery Procedures; Prospective Studies; Retrospective Studies; Skin, Artificial; Surgical Flaps

2012

Other Studies

7 other study(ies) available for trolamine salicylate and Congenital Hand Deformities

ArticleYear
Blau syndrome: a case report from Palestine.
    Pediatric rheumatology online journal, 2021, Aug-31, Volume: 19, Issue:1

    Topics: Adolescent; Antirheumatic Agents; Arthritis; Arthritis, Juvenile; Diagnosis, Differential; Female; Hand Deformities, Congenital; Humans; Medical History Taking; Methotrexate; Nod2 Signaling Adaptor Protein; Patient Care Management; Pedigree; Sarcoidosis; Steroids; Synovitis; Tomography, Optical Coherence; Uveitis

2021
Associated syndromes in patients with Pierre Robin Sequence.
    International journal of pediatric otorhinolaryngology, 2020, Volume: 131

    Topics: 22q11 Deletion Syndrome; Adolescent; Arthritis; Arthrogryposis; Child; Child, Preschool; Chromosome Disorders; Cleft Palate; Clubfoot; Connective Tissue Diseases; De Lange Syndrome; Duane Retraction Syndrome; Female; Hand Deformities, Congenital; Hearing Loss, Sensorineural; Heart Defects, Congenital; Humans; Hypoventilation; Infant; Infant, Newborn; Intellectual Disability; Male; Mandibulofacial Dysostosis; Mobius Syndrome; Muscle Hypotonia; Pierre Robin Syndrome; Retinal Detachment; Retrospective Studies; Sleep Apnea, Central

2020
Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome.
    Pediatrics, 2019, Volume: 144, Issue:1

    Topics: Abnormalities, Multiple; Anti-Inflammatory Agents, Non-Steroidal; Arthritis; Child; Codon, Nonsense; Diagnosis, Differential; DNA-Binding Proteins; Etanercept; Face; Facies; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Hypotrichosis; Intellectual Disability; Male; Methotrexate; Micrognathism; Neck; Transcription Factors

2019
Granulomatous disease associated with NOD2 sequence variants and familial camptodactyly: An intermediate form of NOD2-associated diseases?
    Seminars in arthritis and rheumatism, 2015, Volume: 45, Issue:3

    Topics: Arthritis; Dermatitis; Female; Genotype; Granulomatous Disease, Chronic; Hand Deformities, Congenital; Humans; Middle Aged; Mutation; Nod2 Signaling Adaptor Protein; Pedigree; Phenotype

2015
[Osteolysis in chronic polyarthritis; digiti telescopiti, main en lorgnette].
    Bratislavske lekarske listy, 1952, Volume: 32, Issue:1-2

    Topics: Arthritis; Arthritis, Rheumatoid; Chronic Disease; Hand Deformities, Congenital; Humans; Osteolysis

1952
Familial digital arthropathy-brachydactyly.
    American journal of medical genetics, 2002, Mar-15, Volume: 108, Issue:3

    Topics: Arthritis; Family Health; Female; Finger Joint; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Male; Pedigree

2002
Tendinous laxity and Jaccoud's syndrome in patients with systemic lupus erythematosus. Possible role of secondary hyperparathyroidism.
    The Journal of rheumatology, 1989, Volume: 16, Issue:4

    Topics: Adolescent; Adult; Arthritis; Calcium; Child; Creatinine; Female; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Hyperparathyroidism, Secondary; Joint Instability; Knee Joint; Lupus Erythematosus, Systemic; Male; Middle Aged; Parathyroid Hormone; Phosphorus; Tendons; Uric Acid

1989