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Page 1
Premenstrual disorders: Premenstrual syndrome and premenstrual dysphoric disorder.
Takeda T. Takeda T. J Obstet Gynaecol Res. 2023 Feb;49(2):510-518. doi: 10.1111/jog.15484. Epub 2022 Nov 1. J Obstet Gynaecol Res. 2023. PMID: 36317488 Review.
Recently, the term premenstrual disorders (PMDs), which includes premenstrual syndrome and premenstrual dysphoric disorder as a continuum, has been proposed. ...In this review, I would like to outline the latest information and problems in the etiology, diagnosis, and trea …
Recently, the term premenstrual disorders (PMDs), which includes premenstrual syndrome and premenstrual dysphoric disorder as a conti …
Premenstrual disorders and PMDD - a review.
Cary E, Simpson P. Cary E, et al. Best Pract Res Clin Endocrinol Metab. 2024 Jan;38(1):101858. doi: 10.1016/j.beem.2023.101858. Epub 2023 Dec 28. Best Pract Res Clin Endocrinol Metab. 2024. PMID: 38182436 Free article. Review.
Defining, diagnosing and managing premenstrual disorders (PMDs) remains a challenge both for general practitioners and specialists. Yet these disorders are common and can have an enormous impact on women. ...The aim of this chapter is to give some clarity to this area, pro …
Defining, diagnosing and managing premenstrual disorders (PMDs) remains a challenge both for general practitioners and specialists. Y …
Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group.
Mancuso M, Papadopoulou MT, Ng YS, Ardissone A, Bellusci M, Bertini E, Di Vito L, Evangelista T, Fons C, Hikmat O, Horvath R, Klopstock T, Kornblum C, Lamperti C, Licchetta L, Molnar MJ, Varhaug KN, O'Callaghan M, Pressler RM, Schiff M, Servidei S, Szabo N, Gorman GS, Cross JH, Rahman S. Mancuso M, et al. Eur J Neurol. 2024 Jul;31(7):e16275. doi: 10.1111/ene.16275. Epub 2024 Apr 4. Eur J Neurol. 2024. PMID: 38576261 Free PMC article.
BACKGROUND AND PURPOSE: Primary mitochondrial diseases (PMDs) are common inborn errors of energy metabolism, with an estimated prevalence of one in 4300. ...
BACKGROUND AND PURPOSE: Primary mitochondrial diseases (PMDs) are common inborn errors of energy metabolism, with an estimated preval …
Primary mitochondrial diseases.
Pizzamiglio C, Hanna MG, Pitceathly RDS. Pizzamiglio C, et al. Handb Clin Neurol. 2024;204:53-76. doi: 10.1016/B978-0-323-99209-1.00004-1. Handb Clin Neurol. 2024. PMID: 39322395 Review.
Primary mitochondrial diseases (PMDs) are a heterogeneous group of hereditary disorders characterized by an impairment of the mitochondrial respiratory chain. ...In this chapter, PMDs associated with white matter involvement are outlined, including details of clinic …
Primary mitochondrial diseases (PMDs) are a heterogeneous group of hereditary disorders characterized by an impairment of the mitocho …
Gene therapy for mitochondrial disorders.
Keshavan N, Minczuk M, Viscomi C, Rahman S. Keshavan N, et al. J Inherit Metab Dis. 2024 Jan;47(1):145-175. doi: 10.1002/jimd.12699. Epub 2024 Jan 3. J Inherit Metab Dis. 2024. PMID: 38171948 Free article. Review.
In this review, we detail the current state of application of gene therapy to primary mitochondrial disorders (PMDs). Recombinant adeno-associated virus-based (rAAV) gene replacement approaches for nuclear gene disorders have been undertaken successfully in more than ten p …
In this review, we detail the current state of application of gene therapy to primary mitochondrial disorders (PMDs). Recombinant ade …
Ectopic expression of DNMT3L in human trophoblast stem cells restores features of the placental methylome.
Lea G, Doria-Borrell P, Ferrero-Micó A, Varma A, Simon C, Anderson H, Biggins L, De Clercq K, Andrews S, Niakan KK, Gahurova L, McGovern N, Pérez-García V, Hanna CW. Lea G, et al. Cell Stem Cell. 2025 Feb 6;32(2):276-292.e9. doi: 10.1016/j.stem.2024.12.007. Epub 2025 Jan 8. Cell Stem Cell. 2025. PMID: 39788122 Free article.
The placental DNA methylation landscape is unique, with widespread partially methylated domains (PMDs). The placental "methylome" is conserved across mammals, a shared feature of many cancers, and extensively studied for links with pregnancy complications. ...Remarkably, w …
The placental DNA methylation landscape is unique, with widespread partially methylated domains (PMDs). The placental "methylome" is …
A Phenotypical Male With a Uterus.
Tansupswatdikul P, Chainapapong K, Snabboon T. Tansupswatdikul P, et al. J Obstet Gynaecol Can. 2023 Sep;45(9):629-630. doi: 10.1016/j.jogc.2021.01.010. Epub 2021 Jun 29. J Obstet Gynaecol Can. 2023. PMID: 35589520 No abstract available.
Validity and reliability of the Polish Maladaptive Daydreaming Scale (PMDS-16) and its short form (PMDS-5).
Pietkiewicz IJ, Hełka AM, Barłóg M, Tomalski R. Pietkiewicz IJ, et al. Clin Psychol Psychother. 2023 Jul-Aug;30(4):882-897. doi: 10.1002/cpp.2844. Epub 2023 Mar 10. Clin Psychol Psychother. 2023. PMID: 36809856
This study tests psychometric properties of the Polish version of the Maladaptive Daydreaming Scale (PMDS-16) and a short 5-item version derived from it (PMDS-5), and their capacity to screen for MD. ...Maladaptive daydreamers also had lower quality of life in the p …
This study tests psychometric properties of the Polish version of the Maladaptive Daydreaming Scale (PMDS-16) and a short 5-item vers …
Persistent Mullerian duct syndrome (PMDS) presenting as bilateral cryptorchidism and left-sided inguinal hernia.
Adke S, Khot CI, Thakkar H. Adke S, et al. BMJ Case Rep. 2024 Jul 23;17(7):e259784. doi: 10.1136/bcr-2024-259784. BMJ Case Rep. 2024. PMID: 39043463
PMDS (persistent Mullerian duct syndrome) is a rare disorder of sex development characterised by the presence of Mullerian duct remnants in a phenotypically male individual with a 46XY karyotype. ...They help to non-invasively localise the gonad …
PMDS (persistent Mullerian duct syndrome) is a rare disorder of sex development characterised by the pres …
Primary Mitochondrial Disorders in the Neonate.
Starosta RT, Shinawi M. Starosta RT, et al. Neoreviews. 2022 Dec 1;23(12):e796-e812. doi: 10.1542/neo.23-12-e796. Neoreviews. 2022. PMID: 36450643 Review.
PMDs are caused by pathogenic variants in nuclear and mitochondrial genes, resulting in distinct modes of inheritance. ...We discuss common PMDs that can present in the neonate, including general, nonsyndromic presentations as well as specific syndromic disorders. . …
PMDs are caused by pathogenic variants in nuclear and mitochondrial genes, resulting in distinct modes of inheritance. ...We discuss …
153 results