Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Agnès Liprandi"'
Publikováno v:
CYTOPATHOLOGY
CYTOPATHOLOGY, 2022, 33 (5), pp.633-635. ⟨10.1111/cyt.13156⟩
CYTOPATHOLOGY, 2022, 33 (5), pp.633-635. ⟨10.1111/cyt.13156⟩
International audience
Autor:
Annie Laquerrière, Dominique Bonneau, Fabien Guimiot, Françoise Menez, Bettina Bessières, Nicole Bigi, Agnès Liprandi, C. Bouchet, Dominique Figarella-Branger, Tania Attié-Bitach, Elisabeth Alanio, Dominique Gaillard, Stéphane Triau, Catherine Fallet-Bianco, Anne-Lise Delezoide, Madeleine Joubert, Martine Bucourt, Marie-José Perez, Pascale Marcorelles, Sophie Delahaye, Patricia Blanchet, Fanny Pelluard, Bernard Gasser, Maryse Bonnières, Louise Devisme, Sophie Patrier, Nicole Laurent, Marie Gonzales, Dominique Carles, Anne Bazin, Philippe Loget, B. Clarisse, Jelena Martinovic, Férechté Encha-Razavi, Sandrine Vuillaumier-Barrot, Caroline Rouleau, Nathalie Seta
Publikováno v:
Brain. 135:469-482
Cobblestone lissencephaly represents a peculiar brain malformation with characteristic radiological anomalies, defined as cortical dysplasia combined with dysmyelination, dysplastic cerebellum with cysts and brainstem hypoplasia. Cortical dysplasia r
Autor:
Agnès Liprandi, Georges Leonetti, Christophe Bartoli, A. Sanvoisin, Béma Coulibaly, Marie-Dominique Piercecchi-Marti
Publikováno v:
Pediatrics International. 51:428-431
Autor:
Fabienne Giuliano, Agnès Liprandi, Catherine Fallet-Bianco, Dominique Figarella-Branger, Marie Soulier, Béma Coulibaly, Bernard Benoit, Carla Fernandez, Sabine Sigaudy
Publikováno v:
Acta Neuropathologica. 115:151-156
Acrocallosal syndrome (ACS) is an autosomal recessive disorder characterized by craniofacial dysmorphism, agenesis or hypoplasia of the corpus callosum, duplication of the phalanges of the hallux, more rarely the thumbs, post-axial polydactyly, synda
Autor:
J. E. Morice, Agnès Liprandi, C. Fredouille, Katty Delbecque, Piercecchi-Marti, M. Gonzales, Dominique Figarella-Branger
Publikováno v:
Annales de Pathologie. 26:60-65
Our findings on hearts of trisomic 21 fetuses of a new minor cardiac anomaly, belonging to the atrioventricular septal defect (AVSD) spectrum and the improved performances of the fetal ultrasound screening lend us to propose a new section, complement
Autor:
Patricia Garcia-Meric, Farid Boubred, Valérie Lacroze, Alina Rizzotti, Agnès Liprandi, Maria Vendemmia, Umberto Simeoni
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 18:137-140
Sartans are selective type 1 angiotensin II receptor-antagonists that are used in the treatment of arterial hypertension. Few reports are available concerning the use of sartans during pregnancy. We report two cases of adverse fetal outcome in hypert
Autor:
Jean Francçois Pellissier, Dominique Figarella-Branger, Gilberte Monti, Corinne Bouvier-Labit, Agnès Liprandi
Publikováno v:
Journal of Neuro-Oncology. 60:127-134
CD44, a family of cell surface glycoproteins involved in cell–cell and cell–extracellular matrix adhesion, is widely expressed in the white matter of the normal brain and in astrocytic gliomas under its standard form (CD44s also called CD44H). On
Autor:
Béma Coulibaly, Jean-François Pellissier, Christophe Bartoli, Georges Leonetti, Marie-Dominique Piercecchi-Marti, Agnès Liprandi
Publikováno v:
Journal of Applied Toxicology. 30:378-380
Lethal injection of potassium chloride (KCl) can be used as a method of either suicide or homicide. As biological tests are still inadequate to differentiate endogenous from exogenous potassium, at the scene of death the cause can only be suspected.
Local expression of monocyte chemoattractant protein-1 (MCP-1) in idiopathic inflammatory myopathies
Autor:
Hubert Lepidi, Jean-François Pellissier, Dominique Figarella-Branger, Agnès Liprandi, C. Bartoli
Publikováno v:
Acta Neuropathologica. 97:642-648
The idiopathic inflammatory myopathies (IIM), including dermatomyositis (DM), polymyositis (PM), and inclusion body myositis (IBM), are a group of autoimmune diseases characterized by the recruitment of lymphocytes and monocytes to the site of affect
Autor:
Marie Soulier, Corinne Bouvier, K. Chaumoitre, Elise Barel, Claude D'Ercole, Béma Coulibaly, Agnès Liprandi
Publikováno v:
Prenatal Diagnosis. 28:773-775