trolamine salicylate has been researched along with Genetic Diseases, Inborn in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (30.77) | 18.7374 |
| 1990's | 3 (23.08) | 18.2507 |
| 2000's | 4 (30.77) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ni, X; Shi, T | 1 |
| Pastores, GM | 1 |
| Kambe, N; Kanazawa, N; Nishikomori, R | 1 |
| Haase, H; Overbeck, S; Rink, L | 1 |
| Bodmer, WF | 1 |
| Dausset, J | 1 |
| Berthelot, JM; David, A; Maugars, Y; Pascal, O; Prost, A; Robillard, N; Stalder, JF | 1 |
| Agudelo, CA; Stern, MA; Tanglao, EC | 1 |
| Bouchard, TJ; Hodges, JS; Michalowicz, BS; Pihlstrom, BL | 1 |
| Cyranoski, D | 1 |
| Colman, RW; Wong, PY | 1 |
| Seegmiller, JE | 1 |
4 review(s) available for trolamine salicylate and Genetic Diseases, Inborn
| Article | Year |
|---|---|
The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders.
Topics: Arthritis; Cell Wall; Crohn Disease; Cytosol; Genetic Diseases, Inborn; Granuloma; Humans; Immune System; Inflammation; Intracellular Signaling Peptides and Proteins; Models, Biological; Monocytes; Mutation; Mutation, Missense; Nod2 Signaling Adaptor Protein; Peptidoglycan; Protein Structure, Tertiary; Sarcoidosis; Skin; Syndrome; Uveitis | 2005 |
Zinc supplementation for the treatment or prevention of disease: current status and future perspectives.
Topics: Arthritis; Diabetes Mellitus; Diarrhea; Dietary Supplements; Genetic Diseases, Inborn; Humans; Immune System Diseases; Infections; Skin Diseases; Trace Elements; Vaccination; Zinc | 2008 |
Participation of Hageman factor dependent pathways in human disease states.
Topics: Angioedema; Arthritis; Blood Coagulation Disorders; Coronary Disease; Cystic Fibrosis; Dengue; Disseminated Intravascular Coagulation; Factor XII; Factor XII Deficiency; Genetic Diseases, Inborn; Graft Rejection; Humans; Hyperlipidemias; Hypersensitivity; Kidney Transplantation; Kininogens; Liver Cirrhosis; Malignant Carcinoid Syndrome; Metabolic Diseases; Molecular Weight; Nephrotic Syndrome; Polycythemia Vera; Postgastrectomy Syndromes; Prekallikrein; Shock, Septic; Transfusion Reaction; Transplantation, Homologous; Typhoid Fever | 1977 |
Genetic and molecular basis of human hereditary diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Arthritis; Brain Diseases; Genetic Diseases, Inborn; Glycogen Storage Disease; Gout; Histidine; Humans; Metabolism, Inborn Errors; Mutation; Nutrition Disorders; Phenylketonurias; Tyrosine | 1967 |
9 other study(ies) available for trolamine salicylate and Genetic Diseases, Inborn
| Article | Year |
|---|---|
The challenge and promise of rare disease diagnosis in China.
Topics: Arthritis; Bardet-Biedl Syndrome; China; Genetic Diseases, Inborn; Humans; Rare Diseases; Rhabdomyosarcoma; Sarcoidosis; Synovitis; Uveitis | 2017 |
Synovium, synergy and serendipity.
Topics: Arthritis; Cell Adhesion Molecules; Disease Susceptibility; Genetic Diseases, Inborn; Genome-Wide Association Study; GPI-Linked Proteins; Health Resources; Humans; Hyaluronoglucosaminidase; Synovial Membrane | 2011 |
The HLA system and disease. The Oliver Sharpey Lecture 1979.
Topics: Adult; Arthritis; Asian People; Autoimmune Diseases; Celiac Disease; Child; Diabetes Mellitus; Genes, MHC Class II; Genetic Diseases, Inborn; Graves Disease; Hemochromatosis; Hepatitis; HLA Antigens; Humans; Multiple Sclerosis; Myasthenia Gravis; Psoriasis; White People | 1980 |
[Disease-proneness].
Topics: Alleles; Arthritis; Bacterial Infections; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Histocompatibility Antigens Class II; HLA Antigens; Humans; Metabolic Diseases; Spondylitis, Ankylosing | 1980 |
Autosomal dominant Muckle-Wells syndrome associated with cystinuria, ichthyosis, and aphthosis in a four-generation family.
Topics: Adolescent; Adult; Amyloidosis; Arthritis; Cystinuria; Female; Genes, Dominant; Genetic Diseases, Inborn; Hearing Loss, Sensorineural; Humans; Ichthyosis; Male; Middle Aged; Pedigree; Stomatitis, Aphthous; Syndrome; Urticaria | 1994 |
Pediatric and heritable disorders.
Topics: Adult; Arthritis; Child; Chronic Disease; Connective Tissue Diseases; Genetic Diseases, Inborn; Humans; Lyme Disease; Pain; Rheumatic Diseases; Virus Diseases | 1994 |
Case report: arthropathy as the presenting symptom in hereditary hemochromatosis.
Topics: Alcoholism; Arthritis; Back Pain; Bone and Bones; Genetic Diseases, Inborn; Hemochromatosis; Humans; Iron; Male; Middle Aged; Radiology | 1996 |
No heritability of temporomandibular joint signs and symptoms.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Analysis of Variance; Arthritis; Bruxism; Chi-Square Distribution; Diseases in Twins; Genetic Diseases, Inborn; Habits; Humans; Middle Aged; Minnesota; Odds Ratio; Surveys and Questionnaires; Temporomandibular Joint Disorders | 2000 |
Japan speeds up mission to unravel genetic diseases.
Topics: Academies and Institutes; Arthritis; Asthma; Biotechnology; Genetic Diseases, Inborn; Genetics, Medical; Humans; Japan; Polymorphism, Single Nucleotide | 2001 |