Results 131 to 140 of about 10,185,945 (317)
A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain Edema
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives SLC4A4 encodes electrogenic sodium bicarbonate cotransporter NBCe1, prominently expressed in kidney and brain. Recessive loss‐of‐function variants in SLC4A4 cause proximal renal tubular acidosis, no brain edema. In the brain, NBCe1 is expressed by astrocytes, where it regulates pH and mediates astrocyte volume changes.
Quinty Bisseling +16 more
wiley +1 more source
Translating for children beyond stereotypes / Traduire pour la jeunesse au-delà des stéréotypes
Strenae, 2021 Susan Pickford
doaj +1 more source
Literatura infantil contemporânea: o passado (revestido) bate à porta
Estudos de Literatura Brasileira Contemporânea, 2010 Contemporary children's literature has revealed a tendency to upgrade speeches of the past by means of creating scenarios, which show conflicts situated within a distant time from the contemporary reader.
Flávia Brocchetto Ramos +1 more
doaj
StrenaeIllustrated novel for young readers, Le chant du troll, by Pierre Bottero and Gilles Francescano, tells the journey of a young girl, Léna, who gradually leaves the world of the living to enter a different realm.
Florie Maurin
doaj +1 more source
Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi +8 more
wiley +1 more source
Introduction : le texte de jeunesse au risque de l’école
Strenae, 2021 Hélène Weis
doaj +1 more source
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Dementia Incidence in Individuals With Parkinson's Disease in the Framingham Heart Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Limited information exists on incident dementia in individuals with Parkinson's disease (PD) in US community‐based samples. We examined cognitive statuses and PD diagnoses of 183 individuals in the Framingham Heart Study (FHS) to establish incident dementia, mortality rates, associations with sex, age at PD onset, and education level.
Joshi Dookhy +11 more
wiley +1 more source
What\u27s New on Jane\u27s Bookshelf? [PDF]
, 2011 When I’m not teaching, I’m scouring bookstores and websites for interesting new releases in children’s and young adult literature. My dogs don’t even bark anymore when the UPS man shows up at the front door with a box of books; he’s sort of become part ...
Leeth, Jane
core +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background X‐linked adrenoleukodystrophy (X‐ALD) is a neurometabolic disorder caused by pathogenic variants in ABCD1, leading to slowly progressive spinal cord disease in nearly all affected men. Sensitive biomarkers to quantify disease severity and predict progression are needed for clinical care and trial design.
Eda G. Kabak +4 more
wiley +1 more source