Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Thiébaut-Noël Willig"'
Autor:
Thiébaut-Noël Willig, Jean-Paul Blanc, Rémy Assathiany, Claire Bilbault, Laurent Raffier, Andreas Werner
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Introduction and aimsThe organization of healthcare pathways for neurodevelopmental disorders (NDD) relies on different levels of expertise depending on the complexity of these disorders. NDDs affect between 8% and 15% of children. Historically, nati
Externí odkaz:
https://doaj.org/article/85ef0315ff164e62a1573320b3bd842b
Autor:
Stéphanie Pinel-Jacquemin, Amalia Martinez, Maud Martinasso, Valerie Katkoff, Thiébaut-Noël Willig, Chantal Zaouche Gaudron
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
BackgroundFamilies with young children have faced serious challenges during the first lockdown as a result of the COVID-19 pandemic. In addition to remote working, parents have had to monitor their children’s schoolwork and manage their daily lives
Externí odkaz:
https://doaj.org/article/5521c993ce2347ccb29bde0574e07c23
Autor:
Thiébaut-Noël Willig, Vincent Henry, Jean-Claude Netter, Patrick Contis, Cécile Castro-Gutierrez, Claire Oget-Gendre, Christophe Bonnier, Emilie Cabarrou, Laurent Raffier, Agnès Kabantchenko
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Introduction: Access in France to early diagnosis and care for the most severe, but infrequent, Neurodevelopmental Disorders (NDD), autism spectrum disorder and global developmental delay, in children aged 0–7 was improved through measures implemen
Externí odkaz:
https://doaj.org/article/6dd9460bb5284489815a7a764b2c8232
Autor:
Catherine Billard, Camille Jung, Arnold Munnich, Sahawanatou Gassama, Monique Touzin, Anne Mirassou, Thiébaut-Noël Willig
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Learning disabilities (LDs) are a major public health issue, affecting cognitive functions and academic performance for 8% of children. If LDs are not detected early and addressed through appropriate interventions, they have a heavy impac
Externí odkaz:
https://doaj.org/article/527b7820bb5b4c1d92b0f94f1b29b224
Publikováno v:
Current Opinion in Hematology. 7:85-94
Diamond Blackfan anemia is a rare congenital hypoplastic anemia that usually presents early in infancy. Congenital anomalies, in particular of the head and upper limbs, are present in about 25% of reported patients. The disease is characterized by a
Autor:
Anne Filipe, Josette Guichard, Jean-Pierre Cartron, Catherine Pasquier, Cécile Kaplan, J Breton-Gorius, Rosella Mollicone, Marie-Anne Gougerot-Pocidalo, Najet Debili, Jean-Paul Dommergues, Narla Mohandas, Carole Elbim, F Mielot, Gil Tchernia, Vincent Mignotte, Thiébaut-Noël Willig
Publikováno v:
Blood. 97:826-828
A new megathrombocytopenic syndrome with giant platelets in peripheral blood and severe thrombocytopenia was diagnosed in a 4-month-old boy. His clinical course included repeated hemorrhagic incidents leading to death at age 37 months. Bone marrow ul
Publikováno v:
Current opinion in pediatrics. 13(1)
Diamond-Blackfan Anemia (DBA) is a rare, congenital hypoplastic anemia often diagnosed early in infancy. A moderate to severe aregenerative anemia is found in association with erythroblastopenia in an otherwise normocellular bone marrow. In 40% of th
Autor:
Luanne L. Peters, David J. Anstee, J. Aura Gimm, Narla Mohandas, Stephen F. Parsons, Michael J. A. Tanner, Thiébaut-Noël Willig, Joel Anne Chasis, Frances A. Spring, Gloria Lee
Publikováno v:
Blood. 97(1)
Lutheran blood group glycoproteins (Lu gps) are receptors for the extracellular matrix protein, laminin. Studies suggest that Lu gps may contribute to vaso-occlusion in sickle cell disease and it has recently been shown that sickle cells adhere to la
Autor:
Hope H. Punnett, Niklas Dahl, Sarah E. Ball, Gil Tchernia, Thiébaut-Noël Willig, D. Tentler, Irma Dianzani, Ugo Ramenghi, Emanuela Garelli, Frank E. Shafer, Göran Elinder, Andy Goringe, Nancy F. Olivieri, Holger Cario, Elizabeth Smibert, Peter Gustavsson, Rudolf A. Pfeiffer, Anders Glomstein, Natalia Draptchinskaia
Diamond-Blackfan anemia (DBA) is a rare pure red-cell hypoplasia of unknown etiology and pathogenesis. A major DBA locus has previously been localized to chromosome 19q13.2. Samples from additional families have been collected to identify key recombi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6170455d6e9f3971b102ea06cb8adc4c
https://europepmc.org/articles/PMC1377548/
https://europepmc.org/articles/PMC1377548/
Publikováno v:
Current opinion in hematology. 5(2)
Diamond-Blackfan anemia, although rare, has been the focus of much attention with respect to both its clinical features and the characterization of the in vitro erythroid defect. Despite this, its pathophysiology is still unclear, and the treatment o