Compounds > trolamine salicylate

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trolamine salicylate and Autosomal Chromosome Disorders

trolamine salicylate has been researched along with Autosomal Chromosome Disorders in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (10.00)	18.7374
1990's	5 (50.00)	18.2507
2000's	2 (20.00)	29.6817
2010's	1 (10.00)	24.3611
2020's	1 (10.00)	2.80

Authors

Authors	Studies
Hagen, M; Karempelis, P; Morrell, N; Roby, BB	1
De Marchi, M; Furlan, A; Gava, A; Peserico, A; Podswiadek, M; Punzi, L; Valente, M	1
Fathalla, BM; Safi, KH	1
Altschuler, EL; Kast, RE	1
Harrod, MJ; Menter, MA; Morris, LF; Silverman, AK	1
Conard, K; Ihnat, DH; McIlvain-Simpson, G; Scott, CI; Singsen, BH	1
Arsenault, TM; Lindor, NM; McEvoy, MT; Seidman, CE; Solomon, H	1
Puéchal, X	1
Boone, RA; Fitchett, M; Flint, J; Hilton-Jones, D; Horsley, SW; Huson, S; Kearney, L; Knight, SJ; Nixon, J	1
Buchanan, JG; McLachlan, EM; North, JD; Richmond, DE; Scott, PJ; Smith, F	1

Reviews

1 review(s) available for trolamine salicylate and Autosomal Chromosome Disorders

Article	Year
Methotrexate and reproduction in men: case report and recommendations. Journal of the American Academy of Dermatology, 1993, Volume: 29, Issue:5 Pt 2 Topics: Adult; Arthritis; Chromosome Aberrations; Chromosome Disorders; Genetic Counseling; Humans; Male; Methotrexate; Mutation; Psoriasis; Spermatogenesis	1993

Other Studies

9 other study(ies) available for trolamine salicylate and Autosomal Chromosome Disorders

Article	Year
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
Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review. Autoimmunity reviews, 2009, Volume: 8, Issue:3 Topics: Anti-Inflammatory Agents, Non-Steroidal; Arthritis; Carrier Proteins; Chromosome Disorders; Crohn Disease; Exanthema; Female; Follow-Up Studies; Genes, Dominant; Genetic Predisposition to Disease; Humans; Intracellular Signaling Peptides and Proteins; Italy; Male; Mutation, Missense; Nod2 Signaling Adaptor Protein; Pedigree; Polymorphism, Genetic; Syndrome; Time Factors; Uveitis	2009
Inflammatory and noninflammatory arthropathy in patients with 18q deletion syndrome. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 2012, Volume: 18, Issue:1 Topics: Anti-Inflammatory Agents; Antirheumatic Agents; Arthritis; Child; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Drug Therapy, Combination; Female; Humans; Magnetic Resonance Imaging; Methotrexate; Naproxen; Prednisone; Synovitis	2012
Bupropion for Blau syndrome. Medical hypotheses, 2004, Volume: 62, Issue:2 Topics: Arthritis; Bupropion; Carrier Proteins; Chromosome Disorders; Crohn Disease; Dopamine Uptake Inhibitors; Granulomatous Disease, Chronic; Intracellular Signaling Peptides and Proteins; Nod2 Signaling Adaptor Protein; Syndrome; Treatment Outcome	2004
Inflammatory arthropathies in children with chromosomal abnormalities. The Journal of rheumatology, 1993, Volume: 20, Issue:4 Topics: Adolescent; Arthritis; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 2; Chromosomes, Human, Pair 5; Humans; Male; Pedigree; Radiography; Trisomy	1993
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndrome. Mayo Clinic proceedings, 1997, Volume: 72, Issue:7 Topics: Acne Vulgaris; Adult; Arthritis; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Humans; Leg Ulcer; Male; Pedigree; Pyoderma Gangrenosum; Suppuration; Syndrome	1997
Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists? Revue du rhumatisme (English ed.), 1997, Volume: 64, Issue:10 Topics: Animals; Arthritis; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 6; Genetic Linkage; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; HLA Antigens; Humans; Membrane Proteins; Mutation; Pedigree; Phenotype; Rheumatology	1997
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements. Journal of medical genetics, 1998, Volume: 35, Issue:9 Topics: Adult; Arthritis; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Female; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Keratosis; Muscular Atrophy, Spinal; Telomere; Translocation, Genetic	1998
A chromosome translocation in association with periarteritis nodosa and macroglobulinemia. The American journal of medicine, 1967, Volume: 42, Issue:6 Topics: Anemia; Arthritis; Blood Proteins; Chlorambucil; Chromosome Aberrations; Chromosome Disorders; Diaphragm; Electrophoresis; gamma-Globulins; Humans; Immunoelectrophoresis; Jejunum; Karyotyping; Male; Middle Aged; Pancreas; Polyarteritis Nodosa; Rheumatoid Factor; Ultracentrifugation; Waldenstrom Macroglobulinemia	1967