Results 21 to 30 of about 469 (142)

Les archives sans repos: enjeux d’une édition électronique

Digital Studies, 2019
In 1970, Gabrielle Roy published Windflower (La Rivière sans repos), a short novel preceded by three short stories “Nouvelles Esquimaudes.” Conserved in the Gabrielle Roy collection of Library and Archives Canada, the archives contain a myriad of ...
Jacinthe Martel, Nathanaël Pono
doaj   +2 more sources

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source

Faibles concentrations cellulaires du lait et sensibilité aux mammites des ruminants laitiers

INRAE Productions Animales, 2018
La concentration en cellules du lait (CCS) est un indicateur indirect d’une infection mammaire très utilisé en épidémiologie, mais aussi un prédicteur de la sensibilité aux infections mammaires utile pour la sélection génétique d’animaux plus résistants
Pascal RAINARD, Gilles FOUCRAS, Didier BOICHARD, Rachel RUPP   +3 more
doaj   +1 more source

Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll, Yves Alembik, Marie‐Paule Roth   +2 more
wiley   +1 more source

Multiobjective Simulation–Optimization of Crop Allocation and Water Resources in Canal Command Areas Using Genetic Algorithms

Irrigation and Drainage, EarlyView.
ABSTRACT This study develops an integrated simulation–optimization framework for sustainable crop allocation and water resource management in the Bargarh Canal Command (BCC), eastern India. Efficient irrigation allocation remains a critical challenge due to competing demands, groundwater–surface water interactions and environmental constraints ...
Priyanka Mohapatra, J. C. Paul, Sushree Sangita Dash   +2 more
wiley   +1 more source

Crítica genética e literatura comparada: para uma metodologia do in-between

Manuscrítica, 2014
Tradução do artigo "Critique génétique et littérature comparée: d’une fausse impasse dans la théorie littéraire contemporaine".
Erica Durante, Natalia Oliveira
doaj  

Continuous Intrajejunal Levodopa–Carbidopa Infusion in Parkinson's Disease Associated with 22q11.2 Deletion Syndrome: A Case Series

Movement Disorders Clinical Practice, EarlyView.
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a multisystem genetic disorder associated with a significantly increased risk of early‐onset Parkinson's disease (EOPD). Management is challenging because psychiatric and cognitive comorbidities often limit advanced therapies such as deep brain stimulation (DBS). Cases We report 2 patients with
Valle Victor Andrés, Jardel Amory, Hopes Lucie, Clément Guillemette, Lambert Laetitia, Becker Aurélie, Dexheimer Mylène, Bonnet Céline, Frismand Solène, Renaud Mathilde, Puisieux Salomé   +10 more
wiley   +1 more source

H. W. Gabler, Text Genetics in Literary Modernism and Other Essays, OpenBook Publishers (2018)

Umanistica Digitale, 2019
Text Genetics in Literary Modernism is the title of the recent collection of essays from Hans Walter Gabler, published by OpenBook Publishers in 2018. The book shows, through sixteen stimulating contributions, the research itinerary of a scholar, critic ...
Carolina Rossi
doaj   +1 more source

Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia

Movement Disorders, EarlyView.
Abstract Background Pathogenic variants within the unique N‐terminal inactivation particle of FGF13 isoform A (FGF13A) have so far been associated only with an X‐linked dominant epileptic encephalopathy (DEE). Objective The aim was to expand the clinical and molecular spectrum of FGF13A‐related disorder.
Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli, Elisabeth Bosch, Xueqin Lin, Adeline Trauffler, Roseline Caumes, Andrew E. Fry, Clementine Fort, Gaelle Gauthe, Regina Trollmann, Thomas Wirth, Mathieu Anheim, Aurélie Méneret, Emmanuel Roze, Jean‐Madeleine de Sainte Agathe, Hailan He, Eleni Panagiotakaki, Gaëtan Lesca, André Reis, Diane Doummar, Thomas Smol, Georgia Vasileiou   +22 more
wiley   +1 more source

Machiavelli in Vasari

Laboratoire Italien, 2007
La philologie des dernières décennies a cherché de nouvelles voies, éloignées du modèle lachmannien et a fait naître des propositions visant à abandonner le modèle génétique et la préférence pour « la dernière volonté de l’auteur».
Enrico Mattioda
doaj   +1 more source