Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Sandrine Bouillot"'
Autor:
Bernard George, Annie Laquerrière, Christian Sainte-Rose, Homa Adle-Biassette, Stéphanie Bolle, Stéphanie Puget, Laetitia Maillot, Gaëlle Pierron, Laurent Coffinet, Edouard Gimbert, Henri Sevestre, Pascale Varlet, M. Zerah, Marc Polivka, Schahrazed Bouazza, Arnault Tauziède-Espariat, Claire Alapetite, Julien Masliah-Planchon, Franck Monnien, Kevin Beccaria, Guillaume Gauchotte, Sandrine Bouillot-Eimer, Dominic Thompson
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 77:207-215
Pediatric chordomas are rare malignant neoplasms, and few data are available for optimizing therapeutic strategies and outcome. This study aimed at evaluating how best to manage them and to identify prognostic factors. This multicentric retrospective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b88ffe82a4e6598f970051e5c3c919c
https://doi.org/10.1093/jnen/nlx118
https://doi.org/10.1093/jnen/nlx118
Autor:
Guillaume Osterstock, Anne-Cécile Meunier, Nicola Romanò, Hugues Loiseau, Marie-Noelle Mathieu, Pierre Fontanaud, Eric Baccino, Philippe Osterstock, Valérie Rigau, Norbert Chauvet, Anne Barlier, Sandrine Bouillot-Eimer, Patrice Mollard, Nathalie Coutry, Evelyne Galibert
Publikováno v:
Journal of Neuroendocrinology
Journal of Neuroendocrinology, Wiley, 2016, 28 (2), pp.12352. ⟨10.1111/jne.12352⟩
Journal of Neuroendocrinology, Wiley, 2016, 28 (2), pp.12352. ⟨10.1111/jne.12352⟩
Although growth hormone (GH)- and prolactin (PRL)-secreting pituitary adenomas are considered benign, in many patients, tumour growth and/or invasion constitute a particular challenge. In other tumours, progression relies in part on dysfunction of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8409f8f7df2715d6ee67a82683b20c01
https://pubmed.ncbi.nlm.nih.gov/26686489
https://pubmed.ncbi.nlm.nih.gov/26686489
Autor:
Alain Lagueny, Claude Vital, Sandrine Bouillot-Eimer, Xavier Ferrer, Anne Vital, Christiane Brechenmacher
Publikováno v:
Journal of the Peripheral Nervous System. 9:232-241
We performed a retrospective study of 35 peripheral nerve biopsies (PNBs) with amyloid deposits in the endoneurium. In every case, nerve lesions were studied on paraffin-embedded fragments (PEFs) and by ultrastructural examination (USE). In addition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad222c0a108dbecde8736636af31d32
https://doi.org/10.1111/j.1085-9489.2004.09405.x
https://doi.org/10.1111/j.1085-9489.2004.09405.x
Autor:
Gilles Carnac, Catherine Bisbal, Claude Desnuelle, Sandrine Bouillot, Dalila Laoudj-Chenivesse, Gérald Hugon, Anne Fernandez, Yegor S. Vassetzky
Publikováno v:
Journal of Molecular Medicine. 83:216-224
Facioscapulohumeral muscular dystrophy (FSHD), an autosomal dominant neuromuscular disorder, has been causally related to deletion of tandemly arrayed 3.3 kb repeats (D4Z4) on chromosome 4q35. Although increased expression of several 4q35 genes has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b537624149ba3292284a33831af69f8
https://doi.org/10.1007/s00109-004-0583-7
https://doi.org/10.1007/s00109-004-0583-7
Publikováno v:
Journal of the Peripheral Nervous System. 8:1-7
Ultrastructural immunolabeling of peripheral nervous system components is an important tool to study the relation between structure and function. Owing to the scarcity of certain antigens and the dense structure of the peripheral nerve, a pre-embeddi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0bf0107b5bb72a14998fbe2c9976984
https://doi.org/10.1046/j.1529-8027.2003.03001.x
https://doi.org/10.1046/j.1529-8027.2003.03001.x
Autor:
Alain Lagueny, J M Orgogozo, B Bloch, D Vincent, Anne Vital, Xavier Ferrer, C Vita, Marie-Laure Martin-Negrier, Sandrine Bouillot, Coquet M
Publikováno v:
Journal of the Peripheral Nervous System. 7:213-220
Forty-three cases of peripheral neuropathy (PN) have been reported in the literature with a proven mitochondria (mt) DNA mutation, and 21 had a peripheral nerve biopsy (PNB). We studied 8 patients, 1 of whom had severe sensory PN, 3 mild PN, and 4 su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c0903d90ad5751d2166389d051d20d2
https://doi.org/10.1046/j.1529-8027.2002.02027.x
https://doi.org/10.1046/j.1529-8027.2002.02027.x
Publikováno v:
Ultrastructural Pathology. 26:9-13
In 1969, Fardeau and Engel described polygonal organelles containing crystalline-like structures located in the Schwann cell cytoplasm of unmyelinated fibers. Such inclusions were reported in various conditions, mainly with axonal lesions. They were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73a021ad7ec45ee160f12ac9c5f64551
https://doi.org/10.1080/01913120252934279
https://doi.org/10.1080/01913120252934279
Autor:
Joël Dehais, Pierre Germain, Gabriel Etienne, L. Malterre, Hadja Rakatonovao, Bernard Bannwarth, Sandrine Bouillot, Chantal Dumoulin, Thierry Schaeverbeke
Publikováno v:
Revue du Rhumatisme. 68:451-453
Resume Les manifestations thrombotiques liees aux emboles de cristaux de cholesterol sont habituellement accompagnees de signes cutanes. Nous rapportons l’observation d’une myosite isolee du mollet chez un homme de 58 ans, originale par l’absen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98ae51d283db8477f007f6130778fdd0
https://doi.org/10.1016/s1169-8330(01)00009-6
https://doi.org/10.1016/s1169-8330(01)00009-6
Autor:
Chantal Dumoulin, Thierry Schaeverbeke, Bernard Bannwart, Pierre Germain, Sandrine Bouillot, Hadja Rakatonovao, L. Malterre, Joël Dehais, Gabriel Etienne
Publikováno v:
Joint Bone Spine. 68:267-269
Cholesterol crystal embolization usually produces characteristic skin lesions. We report a case responsible for myositis of the calf without suggestive skin lesions. The outcome in this 58-year-old patient was spontaneously favorable. Cholesterol cry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9fe22f248b682f8f83ed6bba00a6bf
https://doi.org/10.1016/s1297-319x(01)00250-0
https://doi.org/10.1016/s1297-319x(01)00250-0
Autor:
Martin Krahn, Adolfo Lopez De Munain, Nathalie Streichenberger, Rafaëlle Bernard, Christophe Pécheux, Hervé Testard, José L. Pena-Segura, Eugenia Yoldi, Ana Cabello, Norma B. Romero, Juan J. Poza, Sandrine Bouillot-Eimer, Xavier Ferrer, Maria Goicoechea, Federico Garcia-Bragado, France Leturcq, J. Andoni Urtizberea, Nicolas Lévy
Publikováno v:
Annals of neurology. 59(6)
Objective Eosinophilic myositis (EM) constitutes a rare pathological entity characterized by eosinophilic infiltration of skeletal muscles, usually associated with parasite infections, systemic disorders, or the intake of drugs or L-tryptophan. The e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2b897bd24a835cc44979d0f70765953
https://pubmed.ncbi.nlm.nih.gov/16718709
https://pubmed.ncbi.nlm.nih.gov/16718709