| Year |
Citation |
Score |
| 2017 |
Laquerriere A, Maillard C, Cavallin M, Chapon F, Marguet F, Molin A, Sigaudy S, Blouet M, Benoist G, Fernandez C, Poirier K, Chelly J, Thomas S, Bahi-Buisson N. Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations. Journal of Neuropathology and Experimental Neurology. 76: 195-205. PMID 28395088 DOI: 10.1093/Jnen/Nlw124 |
0.324 |
|
| 2014 |
Jiguet Jiglaire C, Baeza-Kallee N, Denicolaï E, Barets D, Metellus P, Padovani L, Chinot O, Figarella-Branger D, Fernandez C. Ex vivo cultures of glioblastoma in three-dimensional hydrogel maintain the original tumor growth behavior and are suitable for preclinical drug and radiation sensitivity screening. Experimental Cell Research. 321: 99-108. PMID 24355810 DOI: 10.1016/J.Yexcr.2013.12.010 |
0.735 |
|
| 2013 |
Mercurio S, Padovani L, Colin C, Carré M, Tchoghandjian A, Scavarda D, Lambert S, Baeza-Kallee N, Fernandez C, Chappé C, André N, Figarella-Branger D. Evidence for new targets and synergistic effect of metronomic celecoxib/fluvastatin combination in pilocytic astrocytoma. Acta Neuropathologica Communications. 1: 17. PMID 24252689 DOI: 10.1186/2051-5960-1-17 |
0.729 |
|
| 2013 |
Adle-Biassette H, Saugier-Veber P, Fallet-Bianco C, Delezoide AL, Razavi F, Drouot N, Bazin A, Beaufrère AM, Bessières B, Blesson S, Bucourt M, Carles D, Devisme L, Dijoud F, Fabre B, ... Fernandez C, et al. Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases. Acta Neuropathologica. 126: 427-42. PMID 23820807 DOI: 10.1007/S00401-013-1146-1 |
0.33 |
|
| 2013 |
Broucqsault N, Morere J, Gaillard MC, Dumonceaux J, Torrents J, Salort-Campana E, Maues De Paula A, Bartoli M, Fernandez C, Chesnais AL, Ferreboeuf M, Sarda L, Dufour H, Desnuelle C, Attarian S, et al. Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy. Human Molecular Genetics. 22: 4206-14. PMID 23777630 DOI: 10.1093/Hmg/Ddt272 |
0.315 |
|
| 2013 |
Dabadie A, Fernandez C, Gorincour G, Panuel M, Petit P. A rare case of a calcified glomus tumour in the thigh of an adolescent. Pediatric Radiology. 43: 1045-8. PMID 23417232 DOI: 10.1007/S00247-013-2640-2 |
0.337 |
|
| 2013 |
Fernandez C, Bardin N, De Paula AM, Salort-Campana E, Benyamine A, Franques J, Schleinitz N, Weiller PJ, Pouget J, Pellissier JF, Figarella-Branger D. Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosis. Medicine. 92: 15-24. PMID 23269233 DOI: 10.1097/Md.0B013E31827Ebba1 |
0.478 |
|
| 2012 |
Padovani L, Colin C, Fernandez C, Maues de Paula A, Mercurio S, Scavarda D, Frassineti F, Adélaïde J, Loundou A, Intagliata D, Bouvier C, Lena G, Birnbaum D, Girard N, Figarella-Branger D. Search for distinctive markers in DNT and cortical grade II glioma in children: same clinicopathological and molecular entities? Current Topics in Medicinal Chemistry. 12: 1683-92. PMID 22978341 DOI: 10.2174/156802612803531450 |
0.749 |
|
| 2012 |
Kadri M, Fabre A, Coze C, Daniel L, Petit P, Sigaudy S, Pinson S, Bouvier C, Delarue A, Fernandez C. Vasoactive intestinal polypeptide-secreting diffuse ganglioneuromatosis affecting the small intestine and the colon in an infant: An exceptional inaugural manifestation of NF1 | Ganglioneuromatose iléo-colique diffuse avec hypersécrétion de peptide vaso-intestinal chez un nourrisson: Une manifestation inaugurale exceptionnelle d'une NF1 Annales De Pathologie. 32: 58-64. PMID 22325315 DOI: 10.1016/J.Annpat.2011.10.007 |
0.665 |
|
| 2012 |
Campana-Salort E, Franques J, Attarian S, Verschueren A, Maues de Paula A, Eymard B, Fernandez C, Suominen T, Penttilä S, Richard P, Monnier N, Lehtokari V, Wallgren-Pettersson C, Figarella-Branger D, Levy N, et al. Myopathies distales : à propos d’une étude rétrospective Revue Neurologique. 168: S15. DOI: 10.1016/S0035-3787(12)70029-2 |
0.433 |
|
| 2011 |
Coulibaly B, Piercecchi-Marti MD, Fernandez C, Wasier AP, Viard L, Fraisse A, Figarella-Branger D, Leonetti G, Camboulives J, Paut O. [A rare cause of sudden cardiac failure: histiocytoid cardiomyopathy]. Annales De Pathologie. 31: 93-7. PMID 21601113 DOI: 10.1016/J.Annpat.2011.02.010 |
0.702 |
|
| 2011 |
El Ayachi I, Fernandez C, Baeza N, De Paula AM, Pesheva P, Figarella-Branger D. Spatiotemporal distribution of tenascin-R in the developing human cerebral cortex parallels neuronal migration. The Journal of Comparative Neurology. 519: 2379-89. PMID 21456020 DOI: 10.1002/Cne.22632 |
0.439 |
|
| 2011 |
Coulibaly B, Bouvier C, Paula AM, Fernandez C, Dufour H, Figarella-Branger D. [Pituitary melanocytoma mimicking an adenoma]. Annales De Pathologie. 31: 50-2. PMID 21349390 DOI: 10.1016/J.Annpat.2010.09.007 |
0.749 |
|
| 2010 |
Uro-Soste E, Fernandez C, Authier FJ, Bassez G, Butori C, Chapon F, Delisle MB, Dubourg O, Feasson L, Gherardi R, Lacroix C, Laquerriere A, Letournel F, Magy L, Maisonobe T, et al. [Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l'Association française contre les myopathies]. Revue Neurologique. 166: 477-85. PMID 20626090 DOI: 10.1016/J.Neurol.2010.03.015 |
0.412 |
|
| 2010 |
Coulibaly B, Sigaudy S, Girard N, Popovici C, Missirian C, Heckenroth H, Tasei AM, Fernandez C. Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum. European Journal of Medical Genetics. 53: 318-21. PMID 20624500 DOI: 10.1016/J.Ejmg.2010.07.005 |
0.654 |
|
| 2010 |
De Paula AM, André N, Fernandez C, Coulibaly B, Scavarda D, Lena G, Bouvier C. Solitary, extracutaneous, skull-based juvenile xanthogranuloma. Pediatric Blood & Cancer. 55: 380-2. PMID 20582967 DOI: 10.1002/Pbc.22534 |
0.739 |
|
| 2010 |
Fernandez C, Halbert C, De Paula AM, Lacroze V, Froissart R, Figarella-Branger D, Chabrol B, Pellissier JF. Non-lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations. Muscle & Nerve. 41: 269-71. PMID 19813197 DOI: 10.1002/Mus.21499 |
0.439 |
|
| 2010 |
Fernandez C, Halbert C, Paula AMd, Figarella-Branger D, Chabrol B, Pellissier J-. Dystrophies musculaires liées au gène DMD : myopathie de Duchenne, myopathie de Becker, formes féminine et atypiques Emc - Neurologie. 7: 1-15. DOI: 10.1016/S0246-0378(10)43869-5 |
0.411 |
|
| 2009 |
Coulibaly B, Fernandez C, Reynaud-Gaubert M, D'Journo X, Doddoli C, Taséi AM. [Alveolar microlithiasis with severe interstitial fibrosis leading to lung transplantation]. Annales De Pathologie. 29: 241-4. PMID 19619834 DOI: 10.1016/J.Annpat.2009.02.015 |
0.65 |
|
| 2009 |
De Paula AM, Franques J, Fernandez C, Monnier N, Lunardi J, Pellissier JF, Figarella-Branger D, Pouget J. A TPM3 mutation causing cap myopathy. Neuromuscular Disorders : Nmd. 19: 685-8. PMID 19553118 DOI: 10.1016/J.Nmd.2009.06.365 |
0.491 |
|
| 2009 |
Tchoghandjian A, Fernandez C, Colin C, El Ayachi I, Voutsinos-Porche B, Fina F, Scavarda D, Piercecchi-Marti MD, Intagliata D, Ouafik L, Fraslon-Vanhulle C, Figarella-Branger D. Pilocytic astrocytoma of the optic pathway: a tumour deriving from radial glia cells with a specific gene signature. Brain : a Journal of Neurology. 132: 1523-35. PMID 19336457 DOI: 10.1093/Brain/Awp048 |
0.773 |
|
| 2009 |
Coulibaly B, Le Hémon A, Sorbier C, George L, Blanc JL, Fernandez C. [Ameloblastic carcinoma: primary or secondary?]. Annales De Pathologie. 29: 28-31. PMID 19233091 DOI: 10.1016/J.Annpat.2008.09.049 |
0.666 |
|
| 2009 |
Salas S, de Pinieux G, Gomez-Brouchet A, Larrousserie F, Leroy X, Aubert S, Decouvelaere AV, Giorgi R, Fernandez C, Bouvier C. Ezrin immunohistochemical expression in cartilaginous tumours: a useful tool for differential diagnosis between chondroblastic osteosarcoma and chondrosarcoma. Virchows Archiv : An International Journal of Pathology. 454: 81-7. PMID 19050913 DOI: 10.1007/S00428-008-0692-8 |
0.6 |
|
| 2009 |
Krahn M, Béroud C, Labelle V, Nguyen K, Bernard R, Bassez G, Figarella-Branger D, Fernandez C, Bouvenot J, Richard I, Ollagnon-Roman E, Bevilacqua JA, Salvo E, Attarian S, Chapon F, et al. Analysis of the DYSF mutational spectrum in a large cohort of patients. Human Mutation. 30: E345-75. PMID 18853459 DOI: 10.1002/Humu.20910 |
0.458 |
|
| 2009 |
Franques J, Campana-Salort E, Attarian S, Verschueren A, Fernandez C, Paula AMd, Figarella-Branger D, Pouget J. G.P.5.01 Retrospective study of 29 cases of distal myopathies Neuromuscular Disorders. 19: 567-568. DOI: 10.1016/J.Nmd.2009.06.079 |
0.432 |
|
| 2008 |
Coulibalya B, Liprandia A, Le Hémon A, Fernandez C, Hardwigsen J, Berthet B, Bouvier C. [Desmoplastic small round-cell tumor: two cases of diffuse abdominopelvic infiltration]. Gastroenterologie Clinique Et Biologique. 32: 278-81. PMID 18663785 DOI: 10.1016/J.Gcb.2008.01.023 |
0.602 |
|
| 2008 |
Figarella-Branger D, Colin C, Coulibaly B, Quilichini B, Maues De Paula A, Fernandez C, Bouvier C. [Histological and molecular classification of gliomas]. Revue Neurologique. 164: 505-15. PMID 18565348 DOI: 10.1016/J.Neurol.2008.03.011 |
0.759 |
|
| 2008 |
Bouvier C, Paula AMD, Fernandez C, Quilichini B, Scavarda D, Gentet JC, Figarella-Branger D. Atypical teratoid/rhabdoid tumour: 7-year event-free survival with gross total resection and radiotherapy in a 7-year-old boy. Childs Nervous System. 24: 143-147. PMID 17968559 DOI: 10.1007/S00381-007-0438-Y |
0.667 |
|
| 2008 |
Fernandez C, Soulier M, Coulibaly B, Liprandi A, Benoit B, Giuliano F, Sigaudy S, Figarella-Branger D, Fallet-Bianco C. Acrocallosal syndrome in fetus: focus on additional brain abnormalities. Acta Neuropathologica. 115: 151-6. PMID 17593378 DOI: 10.1007/S00401-007-0249-Y |
0.715 |
|
| 2008 |
Fernandez C, Maues De Paula A, Figarella-Branger D, Chabrol B, Pouget J, Pellissier J. Intérêt de la biopsie musculaire dans l’exploration des hyperCKémies chroniques isolées Revue Du Rhumatisme. 75: 126-129. DOI: 10.1016/J.Rhum.2007.11.002 |
0.414 |
|
| 2007 |
Figarella-Branger D, Metellus P, Barrié M, Maues de Paula A, Fernandez C, Polivka M, Vital A, Labrousse F, Vignaud JM, Laquerrière A, Rousselet MC, Lacroix C, Saikali S, Chapon F, Gontier MF, et al. [Intracranial ependymomas in adult patients. Diagnosis and histological prognostic factors]. Neuro-Chirurgie. 53: 76-84. PMID 17445840 DOI: 10.1016/J.Neuchi.2006.11.007 |
0.525 |
|
| 2007 |
Colin C, Virard I, Baeza N, Tchoghandjian A, Fernandez C, Bouvier C, Calisti A, Tong S, Durbec P, Figarella-Branger D. Relevance of combinatorial profiles of intermediate filaments and transcription factors for glioma histogenesis. Neuropathology and Applied Neurobiology. 33: 431-9. PMID 17442061 DOI: 10.1111/J.1365-2990.2007.00829.X |
0.745 |
|
| 2007 |
Cantagrel V, Lossi AM, Lisgo S, Missirian C, Borges A, Philip N, Fernandez C, Cardoso C, Figarella-Branger D, Moncla A, Lindsay S, Dobyns WB, Villard L. Truncation of NHEJ1 in a patient with polymicrogyria. Human Mutation. 28: 356-64. PMID 17191205 DOI: 10.1002/Humu.20450 |
0.505 |
|
| 2007 |
Figarella-Branger D, Fernandez C, Maues de Paula A, Pellissier J. Pièges diagnostiques dans les myopathies inflammatoires Revue Neurologique. 163: 217. DOI: 10.1016/S0035-3787(07)90912-1 |
0.402 |
|
| 2006 |
Fernandez C, Maues de Paula A, Colin C, Quilichini B, Bouvier-Labit C, Girard N, Scavarda D, Lena G, Figarella-Branger D. Thalamic gliomas in children: an extensive clinical, neuroradiological and pathological study of 14 cases. Child's Nervous System : Chns : Official Journal of the International Society For Pediatric Neurosurgery. 22: 1603-10. PMID 16951965 DOI: 10.1007/S00381-006-0184-6 |
0.684 |
|
| 2006 |
Fernandez C, De Paula AM, Figarella-Branger D, Krahn M, Giorgi R, Chabrol B, Monfort MF, Pouget J, Pellissier JF. Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia Neurology. 66: 1585-1587. PMID 16717227 DOI: 10.1212/01.Wnl.0000216144.69630.6E |
0.455 |
|
| 2006 |
Guerroui N, Mattei J, Bendahan D, Fernandez C, Figarella-Branger D, Levy N, Pellissier J, Cozzone P, Roudier J, Guis S. Trois classes d'hypolipémiants pourvoyeuses de myalgies chez un patient Revue Du Rhumatisme. 73: 1102-1103. DOI: 10.1016/J.Rhum.2006.10.200 |
0.401 |
|
| 2005 |
Fernandez C, Figarella-Branger D, Meyronet D, Cassote E, Tong S, Pellissier JF. Electron microscopy in neuromuscular disorders. Ultrastructural Pathology. 29: 437-50. PMID 16316944 DOI: 10.1080/01913120500323175 |
0.453 |
|
| 2005 |
Fogliarini C, Chaumoitre K, Chapon F, Fernandez C, Lévrier O, Figarella-Branger D, Girard N. Assessment of cortical maturation with prenatal MRI. Part I: Normal cortical maturation. European Radiology. 15: 1671-85. PMID 15856237 DOI: 10.1007/S00330-005-2782-1 |
0.463 |
|
| 2005 |
Fogliarini C, Chaumoitre K, Chapon F, Fernandez C, Lévrier O, Figarella-Branger D, Girard N. Assessment of cortical maturation with prenatal MRI: part II: abnormalities of cortical maturation. European Radiology. 15: 1781-9. PMID 15843935 DOI: 10.1016/J.Clinimag.2005.12.003 |
0.455 |
|
| 2005 |
Fogliarini C, Chaumoitre K, Chapon F, Fernandez C, Lévrier O, Figarella-Branger D, Girard N. Assessment of cortical maturation with prenatal MRI:Part I. Normal cortical maturation Clinical Imaging. 30: 146. DOI: 10.1016/J.Clinimag.2005.12.002 |
0.463 |
|
| 2003 |
Civatte M, Schleinitz N, Krammer PH, Fernandez C, Guis S, Veit V, Pouget J, Harlé JR, Pellissier JF, Figarella-Branger D. Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM). Neuropathology and Applied Neurobiology. 29: 546-552. PMID 14636161 DOI: 10.1046/J.1365-2990.2003.00471.X |
0.463 |
|
| 2003 |
Fernandez C, Figarella-Branger D, Girard N, Bouvier-Labit C, Gouvernet J, Paz Paredes A, Lena G. Pilocytic astrocytomas in children: prognostic factors--a retrospective study of 80 cases. Neurosurgery. 53: 544-53; discussion 5. PMID 12943571 DOI: 10.1227/01.Neu.0000079330.01541.6E |
0.498 |
|
| 2003 |
Figarella-Branger D, Pouget J, Bernard R, Krahn M, Fernandez C, Lévy N, Pellissier JF. Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene Neurology. 61: 562-564. PMID 12939441 DOI: 10.1212/01.Wnl.0000076486.57572.5C |
0.487 |
|
| 2003 |
Bouvier C, Bartoli C, Aguirre-Cruz L, Virard I, Colin C, Fernandez C, Gouvernet J, Figarella-Branger D. Shared oligodendrocyte lineage gene expression in gliomas and oligodendrocyte progenitor cells. Journal of Neurosurgery. 99: 344-50. PMID 12924709 DOI: 10.3171/Jns.2003.99.2.0344 |
0.751 |
|
| 2003 |
Fernandez C, Girard N, Paz Paredes A, Bouvier-Labit C, Lena G, Figarella-Branger D. The usefulness of MR imaging in the diagnosis of dysembryoplastic neuroepithelial tumor in children: a study of 14 cases. Ajnr. American Journal of Neuroradiology. 24: 829-34. PMID 12748079 |
0.421 |
|
| 2001 |
Fernandez C, Figarella-Branger D, Alla P, Harlé JR, Pellissier JF. Colchicine myopathy: a vacuolar myopathy with selective type I muscle fiber involvement. An immunohistochemical and electron microscopic study of two cases. Acta Neuropathologica. 103: 100-6. PMID 11810174 DOI: 10.1007/S004010100434 |
0.462 |
|
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