Page last updated: 2024-08-23

pregnanolone and Deficiency, Mental

pregnanolone has been researched along with Deficiency, Mental 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	0 (0.00)	29.6817
2010's	2 (66.67)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Samanta, D	1
Bertini, ES; Biagini, G; Cusmai, R; Gecz, J; Giannone, G; Lucchi, C; Rustichelli, C; Specchio, N; Terracciano, A; Trivisano, M; Ubertini, GM; Vigevano, F	1
Berkovic, SF; Buchanan, G; Corbett, M; Depienne, C; Douglas, E; Gecz, J; Guerrini, R; Haan, E; Hynes, K; Kumar, R; Leach, D; Marini, C; Mcmahon, J; Moller, RS; Nguyen, LS; Pham, DH; Ranieri, E; Sadleir, L; Scheffer, IE; Shard, C; Shoubridge, C; Specchio, N; Tan, C; Thomas, PQ	1

Reviews

1 review(s) available for pregnanolone and Deficiency, Mental

Article	Year
PCDH19-Related Epilepsy Syndrome: A Comprehensive Clinical Review. Pediatric neurology, 2020, Volume: 105 Topics: Animals; Behavioral Symptoms; Cadherins; Epileptic Syndromes; Humans; Intellectual Disability; Pregnanolone; Protocadherins	2020

Other Studies

2 other study(ies) available for pregnanolone and Deficiency, Mental

Article	Year
Reduced steroidogenesis in patients with PCDH19-female limited epilepsy. Epilepsia, 2017, Volume: 58, Issue:6 Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenocorticotropic Hormone; Adrenogenital Syndrome; Cadherins; Case-Control Studies; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy; Estradiol; Female; Genetic Diseases, X-Linked; Gonadal Steroid Hormones; Humans; Hydrocortisone; Intellectual Disability; Pregnanolone; Pregnenolone; Progesterone; Prospective Studies; Protocadherins; Puberty, Precocious; Reference Values	2017
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency. Human molecular genetics, 2015, Sep-15, Volume: 24, Issue:18 Topics: 3-Hydroxysteroid Dehydrogenases; Adolescent; Adult; Age of Onset; Aldo-Keto Reductase Family 1 Member C3; Cadherins; Child; Child, Preschool; Cluster Analysis; Epilepsy; Female; Fibroblasts; Gene Expression Profiling; Gene Expression Regulation; Gene Regulatory Networks; Humans; Hydroxyprostaglandin Dehydrogenases; Infant; Infant, Newborn; Intellectual Disability; Middle Aged; Mutation; Phenotype; Pregnanolone; Protocadherins; Reproducibility of Results; Signal Transduction; Young Adult	2015

Article

Year

Reduced steroidogenesis in patients with PCDH19-female limited epilepsy.

Epilepsia, 2017, Volume: 58, Issue:6

Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenocorticotropic Hormone; Adrenogenital Syndrome; Cadherins; Case-Control Studies; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy; Estradiol; Female; Genetic Diseases, X-Linked; Gonadal Steroid Hormones; Humans; Hydrocortisone; Intellectual Disability; Pregnanolone; Pregnenolone; Progesterone; Prospective Studies; Protocadherins; Puberty, Precocious; Reference Values

2017

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.

Human molecular genetics, 2015, Sep-15, Volume: 24, Issue:18

Topics: 3-Hydroxysteroid Dehydrogenases; Adolescent; Adult; Age of Onset; Aldo-Keto Reductase Family 1 Member C3; Cadherins; Child; Child, Preschool; Cluster Analysis; Epilepsy; Female; Fibroblasts; Gene Expression Profiling; Gene Expression Regulation; Gene Regulatory Networks; Humans; Hydroxyprostaglandin Dehydrogenases; Infant; Infant, Newborn; Intellectual Disability; Middle Aged; Mutation; Phenotype; Pregnanolone; Protocadherins; Reproducibility of Results; Signal Transduction; Young Adult

2015