295 research outputs found
For over 60 years, the U.S has promoted family planning programs to protect its own interests in the developing world rather than to promote women’s empowerment
After the end of World War II, American fears of growing populations in the developing world led to efforts to control this population through the use of targeted foreign aid. Denise M. Horn looks at the history of U.S. efforts to protect American security and interests by encouraging population control. She argues that while the language of ‘population control’ has now shifted to that of ‘family planning’, US policy in this area in less developed countries is still geared towards population reduction rather than the empowerment of women
Chapter 9 Continuums of Violence
"This handbook provides a comprehensive overview of feminist approaches to questions of violence, justice, and peace.
The volume argues that critical feminist thinking is necessary to analyse core peace and conflict issues and is fundamental to thinking about solutions to global problems and promoting peaceful conflict transformation. Contributions to the volume consider questions at the intersection of feminism, gender, peace, justice, and violence through interdisciplinary perspectives. The handbook engages with multiple feminisms, diverse policy concerns, and works with diverse theoretical and methodological contributions.
The volume covers the gendered nature of five major themes:
• Methodologies and genealogies (including theories, concepts, histories, methodologies)
• Politics, power, and violence (including the ways in which violence is created, maintained, and reproduced, and the gendered dynamics of its instantiations)
• Institutional and societal interventions to promote peace (including those by national, regional, and international organisations, and civil society or informal groups/bodies)
• Bodies, sexualities, and health (including sexual health, biopolitics, sexual orientation)
• Global inequalities (including climate change, aid, global political economy).
This handbook will be of great interest to students of peace and conflict studies, security studies, feminist studies, gender studies, international relations, and politics.
Differential diagnosis of syndromic craniosynostosis: a case series
Purpose: Syndromic craniosynostosis is a rare genetic disease caused by premature fusion of one or multiple cranial sutures combined with malformations of other organs. The aim of this publication is to investigate sonographic signs of different syndromic craniosynostoses and associated malformations to facilitate a precise and early diagnosis.
Methods: We identified in the period of 2000-2019 thirteen cases with a prenatal suspected diagnosis of syndromic craniosynostosis at our department. We analyzed the ultrasound findings, MRI scans, genetic results as well as the mode of delivery, and postnatal procedures.
Results: Eight children were diagnosed with Apert Syndrome, two with Saethre Chotzen syndrome, one with Crouzon syndrome, and one with Greig cephalopolysyndactyly syndrome. One child had a mutation p.(Pro253Leu) in the FGFR2 gene. We identified characteristic changes of the head shape as well as typical associated malformations.
Conclusion: Second trimester diagnosis of syndromic craniosynostosis is feasible based on the identified sonographic signs. In case of a suspected diagnosis a genetic, neonatal as well as surgical counseling is recommended. We also recommend to offer a fetal MRI. The delivery should be planned in a perinatal center
The 70 Percent Solution Summary Report
This summary report offers a different vision of how educators, employers, parents, and all those who care about the development of young people should understand and address life after high school. The report finds that students and all Americans need better and more informed choices for the next step after high school, and at every stage of their careers, as they seek the knowledge and skills that will help them succeed in the workplace and meet their economic necessities. It calls upon parents, students, policymakers, and educators to recognize the realities and opportunities of the changing new economy for people of different educational backgrounds -- and to support the increasing importance of lifelong learning to the success of so many Americans
The 70 Percent Solution: Five Principles for Helping Young People Make Decisions During and After High School
This report offers a different vision of how educators, employers, parents, and all those who care about the development of young people should understand and address life after high school. The report finds that students and all Americans need better and more informed choices for the next step after high school, and at every stage of their careers, as they seek the knowledge and skills that will help them succeed in the workplace and meet their economic necessities. It calls upon parents, students, policymakers, and educators to recognize the realities and opportunities of the changing new economy for people of different educational backgrounds -- and to support the increasing importance of lifelong learning to the success of so many Americans
Comparision of Membrane Interactions of Acylated and Non-Acylated Lactoferricins by Solid-State NMR Spectroscopy and Molecular Dynamics Simulations
Kagami‐Ogata syndrome: an important differential diagnosis to Beckwith‐Wiedemann syndrome
We report the case of a fetus with sonographic characteristics of Beckwith-Wiedemann syndrome (BWS). A 30-year-old gravida 2 para 1 was referred to our fetal medicine unit with an omphalocele. Fetal macrosomia, organomegaly, and polyhydramnios but no macroglossia were detected and BWS was suspected. Genetic testing for BWS did not confirm the suspected diagnosis as the karyotype was normal. Symptomatic polyhydramnios led to repeated amnioreductions. At 35 + 5 weeks of gestation, a female neonate of 3660 g was delivered with APGAR scores of 6/7/8, after 1/5/10 min, respectively. The abnormal shape of the thorax, facial dysmorphism, need for ventilation, and generalized muscular hypotonia led to the suspicion of Kagami-Ogata syndrome (KOS), which was confirmed by genetic testing. KOS in our patient was caused by a large deletion in the MEG3-region on chromosome 14q32 affecting the maternal allele. In this report, we highlight the notion that when sonographic signs suggestive of BWS such as macrosomia, polyhydramnios, and omphalocele are present and genetic testing does not confirm the suspected diagnosis, KOS should be tested for
The Effects of Fire Fighting and On-Scene Rehabilitation on Hemostatis
Fire fighting is a dangerous occupation – in part because firefighters are called upon to perform strenuous physical activity in hot, hostile environments. Each year, approximately 100 firefighters lose their lives in the line of duty and tens of thousands are injured. Over the past 15 years, approximately 45% of line of duty deaths have been attributed to heart attacks and another 650-1,000 firefighters suffer non-fatal heart attacks in the line of duty each year. From 1990 to 2004, the total number of fireground injuries has declined, yet during this same period, the number of cases related to the leading cause of injury - overexertion/strain – remained relatively constant.
It is well recognized that fire fighting leads to increased cardiovascular and thermal strain. However, the time course of recovery from fire fighting is not well documented, despite the fact that a large percentage of fire fighting fatalities occur after fire fighting activity. Furthermore, on scene rehabilitation (OSR) has been broadly recommended to mitigate the cardiovascular and thermal strain associated with performing strenuous
fire fighting activity, yet the efficacy of different rehabilitation interventions has not been
documented.
Twenty-five firefighters were recruited to participate in a “within-subjects, repeated measures” study designed to describe the acute effects of fire fighting on a broad array of physiological and psychological measures and several key cardiovascular
variables. This study provided the first detailed documentation of the time course of recovery during 2½ hours post-fire fighting. Additionally, we compared two OSR strategies (standard and enhanced) to determine their effectiveness.published or submitted for publicationnot peer reviewe
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome
Background Floating-Harbor syndrome is a rare autosomal dominant short stature
syndrome with retarded speech development, intellectual disability and
dysmorphic facial features. Recently dominant mutations almost exclusively
located in exon 34 of the Snf2-related CREBBP activator protein gene were
identified to cause FHS. Methods Here we report the genetic analysis of 5
patients fulfilling the diagnostic criteria of FHS obtained by Sanger
sequencing. All of them presented with short stature, speech delay as well as
psychomotor delay and typical facial dysmorphism. Three patients showed a good
response to growth hormone treatment. Results Two patients demonstrate novel,
heterozygous de novo frameshift mutations in exon 34 (c.7396delA and
c.7218dupT) leading to premature stop mutations in SRCAP (p.Val2466Tyrfs*9 and
p.Gln2407Serfs*36, respectively). In two further patients we found already
known SRCAP mutations in exon 34, c.7330C > T and c.7303C > T, respectively,
which also lead to premature stop codons: p.Arg2444* and p.Arg2435*. In one
patient, we identified a novel de novo stop mutation in exon 33 (c.6985C > T,
p.Arg2329*) demonstrating that not all FHS cases are caused by mutations in
exon 34 of SRCAP. Conclusions Our data confirm a mutational hot spot in the
final exon of SRCAP in the majority of FHS patients but also show that exon 33
of this gene can be affected
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