Page last updated: 2024-08-22

trolamine salicylate and Adult Premature Aging Syndrome

trolamine salicylate has been researched along with Adult Premature Aging Syndrome in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kuroda, M; Mitani, Y; Niida, Y; Okumura, A; Yokoi, A	1
Jablonska, S	1

Other Studies

2 other study(ies) available for trolamine salicylate and Adult Premature Aging Syndrome

Article	Year
Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis. Molecular genetics and metabolism, 2012, Volume: 107, Issue:3 Topics: Arthritis; Base Sequence; Biological Assay; Child, Preschool; Coffin-Lowry Syndrome; Collagen Type II; Connective Tissue Diseases; DNA Restriction Enzymes; Electrophoresis, Polyacrylamide Gel; Exodeoxyribonucleases; Exons; Hearing Loss, Sensorineural; Humans; Infant; Male; Middle Aged; Molecular Sequence Data; Mutation; Nucleic Acid Heteroduplexes; RecQ Helicases; Reproducibility of Results; Retinal Detachment; Ribosomal Protein S6 Kinases, 90-kDa; Sensitivity and Specificity; Silver Staining; Werner Syndrome; Werner Syndrome Helicase	2012
[Pseudoscleroderma]. Medizinische Klinik, 1967, Jul-28, Volume: 62, Issue:30 Topics: Arteriosclerosis; Arthritis; Dermatomyositis; Diagnosis, Differential; Humans; Hypopituitarism; Porphyrias; Raynaud Disease; Scleredema Adultorum; Scleroderma, Systemic; Skin Diseases; Tryptophan; Werner Syndrome	1967

Article

Year

Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis.

Molecular genetics and metabolism, 2012, Volume: 107, Issue:3

Topics: Arthritis; Base Sequence; Biological Assay; Child, Preschool; Coffin-Lowry Syndrome; Collagen Type II; Connective Tissue Diseases; DNA Restriction Enzymes; Electrophoresis, Polyacrylamide Gel; Exodeoxyribonucleases; Exons; Hearing Loss, Sensorineural; Humans; Infant; Male; Middle Aged; Molecular Sequence Data; Mutation; Nucleic Acid Heteroduplexes; RecQ Helicases; Reproducibility of Results; Retinal Detachment; Ribosomal Protein S6 Kinases, 90-kDa; Sensitivity and Specificity; Silver Staining; Werner Syndrome; Werner Syndrome Helicase

2012

[Pseudoscleroderma].

Medizinische Klinik, 1967, Jul-28, Volume: 62, Issue:30

Topics: Arteriosclerosis; Arthritis; Dermatomyositis; Diagnosis, Differential; Humans; Hypopituitarism; Porphyrias; Raynaud Disease; Scleredema Adultorum; Scleroderma, Systemic; Skin Diseases; Tryptophan; Werner Syndrome

1967