Results 31 to 40 of about 160,312 (281)

Sterilisation and intellectually disabled people in New Zealand—still on the agenda? [PDF]

open access: yes, 2012
Support through care and protection within a medical framework, rather than through the idea of independence within the least restrictive environment, continues to guide service provision for intellectually disabled people in the sexuality area.
Hamilton, Carol
core   +2 more sources

Endometrial Epithelial Lactate Deficiency Drives CD8+ T‐Cells Dysregulation in Unexplained Recurrent Implantation Failure

open access: yesAdvanced Science, EarlyView.
Unexplained recurrent implantation failure (RIF) represents a significant clinical challenge. Our results demonstrate that reduced lactate production in the RIF endometrium impairs the suppression of cytotoxic CD8+ T‑cells, allowing their proliferation and thereby disrupting the local immune balance essential for successful embryo implantation.
Yuanlin He   +18 more
wiley   +1 more source

The Extent to Which Menstruation-Related Issues Are Included in Graduate-Level Public Health Curricula

open access: yesFrontiers in Public Health, 2020
Objectives: Menstruation is increasingly recognized as an issue in domestic and global public health. Public health graduates of U.S. schools of public health must have adequate competencies to address menstruation and its implications for health and ...
Marni Sommer   +3 more
doaj   +1 more source

A Critique of Advertisements for Female Hygiene Products: A Silent Crisis in America [PDF]

open access: yes, 2019
Female hygiene advertisements can be ambiguous due to the intimate nature of menstruation. This can result in a lack of information and invoke the need to hide signals of menstruation.
Schulte, Laura
core   +1 more source

Why Ganymede Faints and the Duke of York Weeps: Passion Plays in Shakespeare [PDF]

open access: yes, 2017
This article revisits contemporary critical debates surrounding the presence of cross-dressed boys as women on the early modern stage – in particular the question of whether or to what extent boy-actors could or should be said to represent ‘women’ or ...
Sujata Iyengar
core   +1 more source

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT GCNT2‐related cataracts is a disorder characterized by bilateral congenital cataracts (CC) of various types (with or without the adult i blood phenotype) and is caused by biallelic variants in GCNT2, which has 3 major isoforms, differentiated by alternative splicing of the first exon (known as exon 1A, B, and C).
Audrey O'Neill   +5 more
wiley   +1 more source

Menstruation-related recurrent psychotic disorder: a case report [PDF]

open access: yesDüşünen Adam Psikiyatri ve Nörolojik Bilimler Dergisi, 2010
Changes of mental status that are related to menstrual cycles causes significant mental problems. As an accepted disorder “premenstrual syndrome” do not cover all cases that are in literature.
Hasan Turan Karatepe   +3 more
doaj  

Hubungan Pengetahuan Remaja Putri Terhadap Perilaku Penatalaksanaan Vulvahygiene Saat Menstruasi Pada Siswi Kelas X Dan Xi Di Sma Xaverius 2 Palembang 2017 [PDF]

open access: yes, 2017
Background: At the time of menstruation is very necessary self care to keep and maintain the hygiene during the menstruation, especially the vulva hygiene.
Anisa, Putri
core  

Studi Pengetahuan Tentang Menstruasi Dengan Upaya Penanganan Dismenore Pada Mahasiswa Pendidikan Biologi [PDF]

open access: yes, 2016
. Dysmenorrhea is a condition of pain during menstruation experienced by women. There are heavy and light of menstruation pain, knowledge of menstruation disorder will determine of the dysmenorrhea holding efforts.
Bahri, S. (Syamsul)   +2 more
core   +2 more sources

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young   +6 more
wiley   +1 more source

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