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Alexandre Vasiljevic

Showing results (91-100 of 132) with videos related to

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The American Journal of Surgical Pathology|March 19, 2015
Chordoid gliomas of the third ventricle share TTF-1 expression with organum vasculosum of the lamina terminalisFranck Bielle, Chiara Villa, Marine Giry, et al.
Acta Neuropathologica|November 17, 2010
Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosisPhilippe Metellus, Bema Coulibaly, Carole Colin, et al.
Birth Defects Research|July 9, 2024
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicismEmmanuelle Pannier, Abel Sekri, Nathalie Roux, et al.
European Journal of Medical Genetics|February 19, 2013
Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasiaDelphine Rocas, Eudeline Alix, Jessica Michel, et al.
Frontiers in Oncology|March 15, 2021
Specific and Sensitive Diagnosis of <i>BCOR</i>-ITD in Various Cancers by Digital PCRDoriane Barets, Romain Appay, Marie Heinisch, et al.
Human Molecular Genetics|August 23, 2013
DUX4 and DUX4 downstream target genes are expressed in fetal FSHD musclesMaxime Ferreboeuf, Virginie Mariot, Bettina Bessières, et al.
European Journal of Endocrinology|August 19, 2024
BRAF and MEK inhibitor targeted therapy in papillary craniopharyngiomas: a cohort studyDario De Alcubierre, Grigorios Gkasdaris, Margaux Mordrel, et al.
European Journal of Cancer (Oxford, England : 1990)|June 6, 2022
Immune contexture of paediatric cancersMeghna Das Thakur, Carl J Franz, Laura Brennan, et al.
Virchows Archiv : an International Journal of Pathology|June 22, 2024
PIT-EASY survey: validation of the European Pituitary Pathology Group proposal for reporting pituitary neuroendocrine tumorsMaria Francesca Birtolo, Anne Jouinot, Alexandre Vasiljevic, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 23, 2020
Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genesGeoffroy Delplancq, Georges Tarris, Antonio Vitobello, et al.
Pageof 14

Showing results (91-100 of 132) with videos related to

Sort By:
Pageof 14
The American Journal of Surgical Pathology|March 19, 2015
Chordoid gliomas of the third ventricle share TTF-1 expression with organum vasculosum of the lamina terminalisFranck Bielle, Chiara Villa, Marine Giry, et al.
Acta Neuropathologica|November 17, 2010
Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosisPhilippe Metellus, Bema Coulibaly, Carole Colin, et al.
Birth Defects Research|July 9, 2024
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicismEmmanuelle Pannier, Abel Sekri, Nathalie Roux, et al.
European Journal of Medical Genetics|February 19, 2013
Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasiaDelphine Rocas, Eudeline Alix, Jessica Michel, et al.
Frontiers in Oncology|March 15, 2021
Specific and Sensitive Diagnosis of <i>BCOR</i>-ITD in Various Cancers by Digital PCRDoriane Barets, Romain Appay, Marie Heinisch, et al.
Human Molecular Genetics|August 23, 2013
DUX4 and DUX4 downstream target genes are expressed in fetal FSHD musclesMaxime Ferreboeuf, Virginie Mariot, Bettina Bessières, et al.
European Journal of Endocrinology|August 19, 2024
BRAF and MEK inhibitor targeted therapy in papillary craniopharyngiomas: a cohort studyDario De Alcubierre, Grigorios Gkasdaris, Margaux Mordrel, et al.
European Journal of Cancer (Oxford, England : 1990)|June 6, 2022
Immune contexture of paediatric cancersMeghna Das Thakur, Carl J Franz, Laura Brennan, et al.
Virchows Archiv : an International Journal of Pathology|June 22, 2024
PIT-EASY survey: validation of the European Pituitary Pathology Group proposal for reporting pituitary neuroendocrine tumorsMaria Francesca Birtolo, Anne Jouinot, Alexandre Vasiljevic, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 23, 2020
Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genesGeoffroy Delplancq, Georges Tarris, Antonio Vitobello, et al.
Pageof 14