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About 142 results

ALLMedicine™ 11-deoxycortisol Center

Research & Reviews  71 results

Storage stability of five steroids and in dried blood spots for newborn screening and r...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259505
PloS One; Grecsó N, Zádori A et. al.

May 29th, 2020 - Congenital adrenal hyperplasia (CAH) is a severe inherited disorder of cortisol biosynthesis that is potentially lethal or can seriously affect quality of life. For the first time, we aimed to assess the stability of 21-deoxycortisol (21Deox), 11-...

Residual Corticosteroid Production in Autoimmune Addison Disease.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274491
The Journal of Clinical Endocrinology and Metabolism; Sævik ÅB, Åkerman AK et. al.

May 11th, 2020 - Contrary to current dogma, growing evidence suggests that some patients with autoimmune Addison disease (AAD) produce corticosteroids even years after diagnosis. To determine frequencies and clinical features of residual corticosteroid production ...

Mass spectrometry-based steroid profiling in primary bilateral macronodular adrenocorti...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354003
Endocrine-related Cancer; Hannah-Shmouni F, Berthon A et. al.

Apr 29th, 2020 - Biochemical characterization of primary bilateral macronodular adrenocortical hyperplasia (PBMAH) by distinct plasma steroid profiles and its putative correlation to disease has not been previously studied. LC-MS/MS-based steroid profiling of 16 p...

Androgen Reduction in Congenital Adrenal Hyperplasia, Phase 1
https://clinicaltrials.gov/ct2/show/NCT02574910

Mar 18th, 2020 - Congenital adrenal hyperplasia (CAH) is an inherited inability to synthesize cortisol in the adrenal gland. More than 90% of cases are cause by deficiency of steroid 21-hydroxylase (CYP21, also termed CYP21A2, P450c21), which is a cytochrome P450 ...

Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency: An Update on Genetic A...
https://doi.org/10.1055/a-1108-1419
Experimental and Clinical Endocrinology & Diabetes : Offi... Carvalho B, Marques CJ et. al.

Mar 4th, 2020 - Congenital Adrenal Hyperplasia is a group of genetic autosomal recessive disorders that affects adrenal steroidogenesis in the adrenal cortex. One of the most common defects associated with Congenital Adrenal Hyperplasia is the deficiency of 21-hy...

see more →

Clinicaltrials.gov  71 results

Storage stability of five steroids and in dried blood spots for newborn screening and r...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259505
PloS One; Grecsó N, Zádori A et. al.

May 29th, 2020 - Congenital adrenal hyperplasia (CAH) is a severe inherited disorder of cortisol biosynthesis that is potentially lethal or can seriously affect quality of life. For the first time, we aimed to assess the stability of 21-deoxycortisol (21Deox), 11-...

Residual Corticosteroid Production in Autoimmune Addison Disease.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274491
The Journal of Clinical Endocrinology and Metabolism; Sævik ÅB, Åkerman AK et. al.

May 11th, 2020 - Contrary to current dogma, growing evidence suggests that some patients with autoimmune Addison disease (AAD) produce corticosteroids even years after diagnosis. To determine frequencies and clinical features of residual corticosteroid production ...

Mass spectrometry-based steroid profiling in primary bilateral macronodular adrenocorti...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354003
Endocrine-related Cancer; Hannah-Shmouni F, Berthon A et. al.

Apr 29th, 2020 - Biochemical characterization of primary bilateral macronodular adrenocortical hyperplasia (PBMAH) by distinct plasma steroid profiles and its putative correlation to disease has not been previously studied. LC-MS/MS-based steroid profiling of 16 p...

Androgen Reduction in Congenital Adrenal Hyperplasia, Phase 1
https://clinicaltrials.gov/ct2/show/NCT02574910

Mar 18th, 2020 - Congenital adrenal hyperplasia (CAH) is an inherited inability to synthesize cortisol in the adrenal gland. More than 90% of cases are cause by deficiency of steroid 21-hydroxylase (CYP21, also termed CYP21A2, P450c21), which is a cytochrome P450 ...

Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency: An Update on Genetic A...
https://doi.org/10.1055/a-1108-1419
Experimental and Clinical Endocrinology & Diabetes : Offi... Carvalho B, Marques CJ et. al.

Mar 4th, 2020 - Congenital Adrenal Hyperplasia is a group of genetic autosomal recessive disorders that affects adrenal steroidogenesis in the adrenal cortex. One of the most common defects associated with Congenital Adrenal Hyperplasia is the deficiency of 21-hy...

see more →