C. Soler

发表

Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase 2 trial PNET HR+5.

N. André, D. Figarella-Branger, L. Guerrini-Rousseau, 2020, Neuro-oncology.

Double minute chromosomes harboring MDM2 amplification in a pediatric atypical lipomatous tumor

F. Burel-Vandenbos, F. Pedeutour, L. Bianchini, 2019, Genes, chromosomes & cancer.

Subdural hematomas of the posterior fossa in normal-weight newborns. Report of two cases.

C. Principe, D. Rodríguez, F. Muñoz, 1984, Journal of neurosurgery.

Tandem high-dose chemotherapy with stem cell rescue followed by risk-adapted radiation in children with high-risk cerebral primitive neuroectodermal tumor: Results of the prospective SFCE-trial PNET HR+5.

N. André, D. Frappaz, C. Berger, 2014 .

[Kimura's disease of the lymph node. Histology, immunohistochemistry, and differential diagnosis].

A. Deville, P. Hofman, J. Michiels, 1998, Annales de pathologie.

Nephrogenic adenofibroma in a young child.

C. Turc‐Carel, P. Chevallier, J. Michiels, 2000, Pathology, research and practice.

Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients

O. Delattre, F. Giuliano, F. Bourdeaut, 2018, European Journal of Human Genetics.

Severe interaction between methotrexate and a macrolide-like antibiotic.

G. Milano, P. Jambou, E. Cassuto‐Viguier, 1993, Journal of the National Cancer Institute.

Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients

O. Delattre, F. Giuliano, F. Bourdeaut, 2018, European Journal of Human Genetics.

The PRINTO evidence-based proposal for glucocorticoids tapering/discontinuation in new onset juvenile dermatomyositis patients

A. Martini, A. Pistorio, M. Fischbach, 2019, Pediatric Rheumatology.

Clinical and Laboratory Manifestations of Congenital Dyserythropoietic Anemia Type I in a Cohort of French Children

G. Leverger, T. Leblanc, B. Bader-Meunier, 2005, Journal of pediatric hematology/oncology.

Thirteen cystic fibrosis patients, 12 compound heterozygous and one homozygous for the missense mutation G85E: a pancreatic sufficiency/insufficiency mutation with variable clinical presentation.

X. Estivill, G. Antiñolo, T. Casals, 1996, Journal of medical genetics.

Conventional Dose Intensive Immunochemo therapy Regimen in an Adult Patient with Very Late Relapse of Burkitt's Lymphoma

F. Peyrade, A. Thyss, A. Italiano, 2007, Journal of chemotherapy.

Urinary excretion of methylated catecholamine metabolites in a child with neuroblastoma maturing into ganglioneuroma.

M. Candito, S. Bekri, A. Thyss, 1996, Medical and pediatric oncology.

SAT0596 Thoracic involvement at diagnosis drives a differentiated clinical presentation of sarcoidosis: analysis of 1245 patients (SARCOGEAS-SEMI)

M. Penadés, B. Kostov, X. Bosch, 2018 .

[Solid and pseudopapillary tumor of the pancreas: immunohistochemical and ultrastructural study of 2 pediatric cases].

J. Valla, P. Bedossa, V. Hofman, 2000, Annales de pathologie.