Results 111 to 120 of about 4,505,520 (333)
Abstract Research‐Practice Partnerships seek to close the research‐practice gap through developing collaborative, authentic partnerships between researchers and community members. Our team has leveraged Research‐Practice Ambassadors to support socially just and equitable partnership processes in schools.
Danielle R. Hatchimonji +8 more
wiley +1 more source
The current status of oral reading in professional literature [PDF]
Thesis (M.A.)--Boston ...
Fortier, Gerard L., Stanley, Dorothy B.
core +1 more source
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle +26 more
wiley +1 more source
Walter J. Ong, S.J.: A retrospective [PDF]
Communication Research Trends usually charts current communication research, introducing its readers to recent developments across the range of inquiry into communication.
Soukup, Paul A.
core +1 more source
ABSTRACT DEAF1‐associated neurodevelopmental disorder (DAND) is a neurodevelopmental spectrum disorder caused by two methods of inheritance: the autosomal dominant intellectual disability syndrome (Vulto‐van Silfout‐de Vries syndrome (VSVS), OMIM #615828), and the autosomal recessive Neurodevelopmental disorder with hypotonia and impaired expressive ...
Kylie Katz, Philip Jensik, Milen Velinov
wiley +1 more source
Differing instructional needs for children of similar reading achievement grades two, four, and six [PDF]
Thesis (Ed.M.)--Boston ...
Baumann, Mayvis L +10 more
core +1 more source
Longitudinal Behavior Phenotype Hallmarks in RNU4‐2 Syndrome: Implications for Clinical Management
ABSTRACT Pathogenic variants in the non‐coding spliceosomal gene RNU4‐2 underlie ReNU syndrome, one of the most prevalent monogenic causes of neurodevelopmental disorders, accounting for ~0.4% of cases. Despite increasing recognition, little is known about the longitudinal behavioral and neuropsychiatric phenotype of affected individuals. We report two
Paola Francesca Ajmone +8 more
wiley +1 more source
Friends of Musselman Library Newsletter Spring 2005
Table of Contents: From the Director: “Forever Free” Abraham Lincoln Exhibit (Robin Wagner, Christina Ericson Hansen ’92, Gabor Boritt); Fortenbaugh Internship Expands (Julia Grover ’06, Anne Kennedy ’05); Bontanicals Brighten Browsing Room (Jim Ramos ...
Musselman Library,
core
‘Turkeys Cannot Vote for Christmas’: Why Epistemic Disobedience in an Anti‐Black World Matters
ABSTRACT Never in the history of global coloniality has the idea of epistemic disobedience been as important as in the 21st century. This is not only because the struggle for decolonisation has shifted from physical confrontation between the coloniser and the colonised into a battle of ideas but also because the former has deployed the idea of ...
Morgan Ndlovu
wiley +1 more source
Introduction: It is not only hormonal changes but also natural phenomena such as puberty, pregnancy and menopause that predispose women to many disease conditions. The aim of this study was to compare the prevalence of oral symptoms between premenopausal
N Sinaie +3 more
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