C. Fernandez

发表

Assessment of cortical maturation with prenatal MRI: part II: abnormalities of cortical maturation.

D. Figarella-Branger, N. Girard, O. Lévrier, 2006, European radiology.

Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations

F. Chapon, A. Laquérriere, J. Chelly, 2017, Journal of neuropathology and experimental neurology.

HMGA2-NFIB fusion in a pediatric intramuscular lipoma: a novel case of NFIB alteration in a large deep-seated adipocytic tumor.

F. Pedeutour, A. Pierron, Frédérique Keslair, 2009, Cancer genetics and cytogenetics.

Pilocytic Astrocytomas in Children: Prognostic Factors—A Retrospective Study of 80 Cases

D. Figarella-Branger, N. Girard, J. Gouvernet, 2003, Neurosurgery.

BBS 10 mutations are frequent in “ Meckel ” type cystic kidneys

Marie-Pierre, Sophie, R. Bouvier, 2018 .

BBS10 mutations are common in ‘Meckel’-type cystic kidneys

R. Salomon, M. Gubler, R. Bouvier, 2010, Journal of Medical Genetics.

Electron Microscopy in Neuromuscular Disorders

D. Figarella-Branger, D. Meyronet, J. Pellissier, 2005, Ultrastructural pathology.

Truncation of NHEJ1 in a patient with polymicrogyria

N. Philip, D. Figarella-Branger, S. Lindsay, 2007, Human mutation.

Analysis of the DYSF mutational spectrum in a large cohort of patients

C. Béroud, D. Figarella-Branger, F. Chapon, 2009, Human mutation.

Assessment of cortical maturation with prenatal MRI. Part I: normal cortical maturation

Nadine Girard, Carla Fernandez, D. Figarella-Branger, 2005, European Radiology.

Assessment of cortical maturation with prenatal MRI

Nadine Girard, Carla Fernandez, D. Figarella-Branger, 2005, European Radiology.

Spatiotemporal distribution of tenascin‐R in the developing human cerebral cortex parallels neuronal migration

D. Figarella-Branger, A. D. de Paula, N. Baeza, 2011, The Journal of comparative neurology.

Pilocytic astrocytoma of the optic pathway: a tumour deriving from radial glia cells with a specific gene signature.

D. Figarella-Branger, C. Colin, L. Ouafik, 2009, Brain : a journal of neurology.

A TPM3 mutation causing cap myopathy

D. Figarella-Branger, J. Pouget, N. Monnier, 2009, Neuromuscular Disorders.

Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.

J. L. Siles, José Miguel Lezana Rosales, C. P. Milla, 2018 .

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.

O. Chinot, D. Figarella-Branger, P. Metellus, 2014, Experimental cell research.

Acrocallosal syndrome in fetus: focus on additional brain abnormalities

C. Fallet-Bianco, D. Figarella-Branger, F. Giuliano, 2007, Acta Neuropathologica.

Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.

N. Girard, A. Tasei, B. Coulibaly, 2010, European journal of medical genetics.

Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases

N. Drouot, C. Fallet-Bianco, P. Gressens, 2013, Acta Neuropathologica.

Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.

L. Shaffer, S. Canún, O. Mutchinick, 1998, American journal of medical genetics.

Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy.

F. Magdinier, N. Lévy, H. Dufour, 2013, Human molecular genetics.

The usefulness of MR imaging in the diagnosis of dysembryoplastic neuroepithelial tumor in children: a study of 14 cases.

D. Figarella-Branger, N. Girard, C. Fernandez, 2003, AJNR. American journal of neuroradiology.

Thalamic gliomas in children: an extensive clinical, neuroradiological and pathological study of 14 cases

D. Figarella-Branger, N. Girard, C. Colin, 2006, Child's Nervous System.

Non‐lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations

D. Figarella-Branger, R. Froissart, A. D. de Paula, 2009, Muscle & nerve.

Correlation of Clinicoserologic and Pathologic Classifications of Inflammatory Myopathies

D. Figarella-Branger, J. Pouget, J. Franques, 2013, Medicine.

Assessment of cortical maturation with prenatal MRI:Part I. Normal cortical maturation

Nadine Girard, Kathia Chaumoitre, Carla Fernandez, 2005 .

Evidence for new targets and synergistic effect of metronomic celecoxib/fluvastatin combination in pilocytic astrocytoma

N. André, D. Figarella-Branger, M. Carré, 2013, Acta neuropathologica communications.

Shared oligodendrocyte lineage gene expression in gliomas and oligodendrocyte progenitor cells.

D. Figarella-Branger, C. Colin, C. Bouvier, 2003, Journal of neurosurgery.

Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia

D. Figarella-Branger, J. Pouget, M. Krahn, 2006, Neurology.

Pituicytomas, a mis-diagnosed benign tumor of the neurohypophysis: report of three cases

D. Figarella-Branger, H. Dufour, J. Pellissier, 2002, Acta Neuropathologica.

Spatiotemporal distribution of tenascin‐R in the developing human cerebral cortex parallels neuronal migration

D. Figarella-Branger, A. D. de Paula, N. Baeza, 2011, The Journal of comparative neurology.

Atypical teratoid/rhabdoid tumour: 7-year event-free survival with gross total resection and radiotherapy in a 7-year-old boy

D. Figarella-Branger, A. M. Paula, C. Bouvier, 2007, Child's Nervous System.