dehydroepiandrosterone sulfate and Dwarfism

dehydroepiandrosterone sulfate has been researched along with Dwarfism in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chang, G; Ding, Y; Li, G; Li, J; Li, N; Shen, Y; Wang, J; Wang, X; Xu, Y; Yao, R; Yu, T	1
Bilguvar, K; Evliyaoğlu, O; Gül, E; Günel, M; Kolb, L; Tüysüz, B; Yılmaz, S	1
Baron, J; Bernstein, DB; Cutler, GB; Leschek, EW; Rose, SR; Troendle, JF; Yanovski, JA	1

Trials

1 trial(s) available for dehydroepiandrosterone sulfate and Dwarfism

Article	Year
Effect of growth hormone treatment on testicular function, puberty, and adrenarche in boys with non-growth hormone-deficient short stature: a randomized, double-blind, placebo-controlled trial. The Journal of pediatrics, 2001, Volume: 138, Issue:3 Topics: Adolescent; Age of Onset; Analysis of Variance; Child; Dehydroepiandrosterone Sulfate; Double-Blind Method; Dwarfism; Human Growth Hormone; Humans; Male; Puberty; Survival Analysis; Testis; Testosterone	2001

Article

Year

Effect of growth hormone treatment on testicular function, puberty, and adrenarche in boys with non-growth hormone-deficient short stature: a randomized, double-blind, placebo-controlled trial.

The Journal of pediatrics, 2001, Volume: 138, Issue:3

Topics: Adolescent; Age of Onset; Analysis of Variance; Child; Dehydroepiandrosterone Sulfate; Double-Blind Method; Dwarfism; Human Growth Hormone; Humans; Male; Puberty; Survival Analysis; Testis; Testosterone

2001

Other Studies

2 other study(ies) available for dehydroepiandrosterone sulfate and Dwarfism

Article	Year
Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature. American journal of medical genetics. Part A, 2017, Volume: 173, Issue:12 Topics: Adolescent; Asian People; Dehydroepiandrosterone Sulfate; Dwarfism; Fatty Liver; Glycerolphosphate Dehydrogenase; HEK293 Cells; High-Throughput Nucleotide Sequencing; Humans; Insulin Resistance; Male; Mutation; Obesity; Phenotype; RNA Splice Sites; RNA Splicing; Sequence Analysis, DNA; Skin Abnormalities	2017
Spondyloepimetaphyseal dysplasia Pakistani type: expansion of the phenotype. American journal of medical genetics. Part A, 2013, Volume: 161A, Issue:6 Topics: Abnormalities, Multiple; Adolescent; Adult; Calcification, Physiologic; Codon, Nonsense; Consanguinity; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Dwarfism; Female; Genotype; Growth Disorders; Homozygote; Humans; Male; Multienzyme Complexes; Musculoskeletal Abnormalities; Osteochondrodysplasias; Pedigree; Phenotype; Radiography; Sequence Analysis, DNA; Sulfate Adenylyltransferase; Turkey	2013

Article

Year

Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature.

American journal of medical genetics. Part A, 2017, Volume: 173, Issue:12

Topics: Adolescent; Asian People; Dehydroepiandrosterone Sulfate; Dwarfism; Fatty Liver; Glycerolphosphate Dehydrogenase; HEK293 Cells; High-Throughput Nucleotide Sequencing; Humans; Insulin Resistance; Male; Mutation; Obesity; Phenotype; RNA Splice Sites; RNA Splicing; Sequence Analysis, DNA; Skin Abnormalities

2017

Spondyloepimetaphyseal dysplasia Pakistani type: expansion of the phenotype.

American journal of medical genetics. Part A, 2013, Volume: 161A, Issue:6

Topics: Abnormalities, Multiple; Adolescent; Adult; Calcification, Physiologic; Codon, Nonsense; Consanguinity; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Dwarfism; Female; Genotype; Growth Disorders; Homozygote; Humans; Male; Multienzyme Complexes; Musculoskeletal Abnormalities; Osteochondrodysplasias; Pedigree; Phenotype; Radiography; Sequence Analysis, DNA; Sulfate Adenylyltransferase; Turkey

2013