Results 131 to 140 of about 4,594 (256)
Problemy Wczesnej Edukacji, 2016 Migration, as a global phenomenon has a long history also in the Slovak Republic. Most of the migrants come, or are passing through its territory legally. There are still cases of illegal migration, too.
Monika Mačkinová, Agnieszka Nowicka
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Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos +5 more
wiley +1 more source
Taking care of the unaccompanied foreign minors starting from the housing
In Italy the subject of the rights of unaccompanied foreign minors (UAMs) is not an easy one. UAMs are increasingly becoming “victims of collateral damage” due to the risks of urban marginalization (Bauman 2011).
Tumminelli G., D'Amico V.
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Ethics in Age Estimation of Unaccompanied Minors
, 2012 Children absconding from countries of conflict and war are often not able to document their age. When an age is given, it is frequently untraceable or poorly documented and therefore questioned by immigration authorities.
Thevissen, Patrick +3 more
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Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Oxysterols (cholestane‐3β,5α,6β‐triol and 7‐ketocholesterol) and N‐palmitoyl‐O‐phosphocholineserine (PPCS) are sensitive biomarkers for Niemann‐Pick disease type C (NPC) screening. However, false‐positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or ...
Maria Makrygianni +19 more
wiley +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
International migration of unaccompanied minors to Czech Republic and their integration into the majority society [PDF]
, 2015 The bachelor thesis outlines some background context regarding the phenomenon of unaccompanied minors in Czech Republic. Czech Republic belongs to the group of transit countries, through which unaccompanied minors travel to reach their destination ...
Cojocaru Zahorková, Vanda
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, 2021 The purpose of these reports is to analyse and assess the integration context and integration services provided to unaccompanied minors via semi-structured interviews with stakeholders in countries of project partners.
Universitat Autònoma de Barcelona. Departament d'Antropologia Social i Cultural +2 more
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
, 2020 Unaccompanied minors from Central America and Mexico have endeavored treacherous journeys to enter the United States for many decades. In recent years, there has been an influx of unaccompanied minors fleeing their native country and arriving at the ...
Duarte, Crystal
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