Results 131 to 140 of about 981,328 (290)
Suspicion of Motives Predicts Minorities' Responses to Positive Feedback in Interracial Interactions. [PDF]
, 2016 Strong social and legal norms in the United States discourage the overt expression of bias against ethnic and racial minorities, increasing the attributional ambiguity of Whites' positive behavior to ethnic minorities. Minorities who suspect that Whites'
Kunstman, Jonathan W +5 more
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The objective of this study is to describe outcomes of rapid exome (rES) and rapid genome sequencing (rGS) in an inpatient setting. This is a retrospective cohort of inpatients with rES or rGS during their hospitalization between April 2016 and November 2023.
Cecilia M. Kessler +5 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Substantial data supports the use of rapid exome and genome sequencing (rES/rGS) in Neonatal Intensive Care Units (NICU), but fewer studies have examined the impact of rES/rGS in other pediatric critical care units. We evaluated the impact on diagnostic yield and time to diagnosis following a single‐center hospital policy change allowing ...
Alexandra C. Keefe +22 more
wiley +1 more source
The troubling legal and political uncertainty facing Catalonia [PDF]
, 2018 There is still no end in sight to the political uncertainty in Catalonia. As Javier García Oliva writes, the issue has raised questions over processes of constitutional reform in Spain.
García Oliva, Javier
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Wilson disease (WD) is an autosomal recessive disorder of copper metabolism caused by ATP7B mutations. Diagnosis is usually straightforward in symptomatic patients, but can be challenging in children and adolescents with mild liver disease, borderline urinary copper excretion, or inconclusive genetic findings.
Emanuele Nicastro +10 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Chakravarti v Advertiser Newspapers: Lessons for journalists [PDF]
, 1999 The lower courts are now interpreting the High Court\u27s judgement in Chakravarti v Advertiser Newspaper Ltd, which was handed down in May 1998. As the lower courts grapple with the decision, journalists must still produce reports of complex legal ...
Breit, Rhonda
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi +6 more
wiley +1 more source
La impugnación jurisdiccional de las relaciones de puestos de trabajo
Revista Vasca de Administración Pública, 2013 It is analyzed the legal regime of the lists of job positions and specially its regime of judicial review before the administrative courts. The Supreme Court¿s case law has proclaimed the assimilation of those instruments of organization to the category ...
Miguel Ángel Ruiz López
doaj +1 more source
Willful Infringement and the Evidentiary Value of Opinion Letters After Knorr–Bremse v. Dana [PDF]
, 2005 Recently, the Federal Circuit in Knorr-Bremse v. Dana overruled almost twenty years of precedent by striking down the adverse inference doctrine, which had created a negative presumption against any alleged patent infringer for failing to obtain and ...
Stowell, Joshua
core +1 more source