Results 91 to 100 of about 1,607 (262)
Enfances, Familles, GénérationsResearch Framework : In Quebec, a child conceived through a surrogate pregnancy has initially as parents the woman who gave birth to him and the man (or one of the men) who instigated the parental project.
Kévin Lavoie +2 more
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Mémoire et filiation dans La Nuit d’obsidienne et Retour à Satyah de François Emmanuel
Studia Romanica Posnaniensia, 2016 François Emmanuel, renown Belgian contemporary writer and practicing psychotherapist, has so far published more than fifteen novels which are all focused on recurring and obsessive questions about memory, heritage and unknown past.
Ewa Grabowska
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SPG4 and Dementia: Expanding the Clinical Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Reconocimiento de Paternidad: Tópicos y Cuestiones Civiles
Revista Chilena de Derecho, 2007 En el presente texto se pretende: 1. Brindar una justificación de la figura del reconocimiento. 2. Investigar su ámbito de operatividad en los contextos, los procedimientos de la filiación y los contextos de la misma. 3.
Eduardo Gandulfo R
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Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +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
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background and Purpose White matter hyperintensities (WMH) are a core neuroimaging marker of cerebral small vessel disease (CSVD). Sleep apnoea (SA) is a recognized vascular risk factor, but its associations with regional WMH burden, short‐interval WMH change and cognitive performance in population‐based cohorts remain incompletely defined. We
Peng Cheng +4 more
wiley +1 more source
مجلة الآداب و العلوم الإجتماعيةÀ la lumière d’un héritage littéraire maghrébin fortement marqué par des dynamiques filiales problématiques, la présente contribution se propose d’examiner la redéfinition de la figure paternelle dans Et si mon père avait une âme d’enfant de Fateh ...
سهيلة بوشافة
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Voix Plurielles, 2016 En partant du double mouvement rhizomatique de la « déterritorialisation » et de la « reterritorialisation », cet article se propose d’étudier la conception dynamique de l’identité dans Le procès-verbal de Jean-Marie Gustave Le Clézio (1963).
Abdoulaye Diouf
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Revisiting Schistosoma mansoni Micro-Exon Gene (MEG) Protein Family: A Tour into Conserved Motifs and Annotation. [PDF]
Biomolecules, 2023 Nedvědová Š +4 more
europepmc +1 more source