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Jean Donadieu

Showing results (51-60 of 174) with videos related to

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Pediatric Blood & Cancer|July 1, 2010
Juvenile xanthogranuloma with hematological dysfunction treated with 2CDA-AraCPascale Blouin, Marion Yvert, Flavie Arbion, et al.
Journal of Clinical Immunology|March 23, 2019
Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic NeutropeniaJulie Seguier, Vincent Barlogis, Laure Croisille, et al.
Plos One|April 17, 2012
B-RAF mutant alleles associated with Langerhans cell histiocytosis, a granulomatous pediatric diseaseTakeshi Satoh, Alexander Smith, Aurelien Sarde, et al.
British Journal of Haematology|July 27, 2021
A circulating subset of BRAF<sup>V600E</sup> -positive cells in infants with high-risk Langerhans cell histiocytosis treated with BRAF inhibitorsRita Poch, Solenne Le Louet, Zofia Hélias-Rodzewicz, et al.
Chest|November 1, 2019
Lung Involvement in Destombes-Rosai-Dorfman Disease: Clinical and Radiological Features and Response to the MEK Inhibitor CobimetinibQuentin Moyon, Samia Boussouar, Philippe Maksud, et al.
Molecular Cancer|July 7, 2017
New somatic BRAF splicing mutation in Langerhans cell histiocytosisSébastien Héritier, Zofia Hélias-Rodzewicz, Rikhia Chakraborty, et al.
Blood|February 14, 2004
Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia RegisterChristine Bellanné-Chantelot, Séverine Clauin, Thierry Leblanc, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 27, 2022
Eye movement abnormalities in neurodegenerative langerhans cell histiocytosisLila Autier, Bertrand Gaymard, Eléonore Bayen, et al.
Neurology|September 5, 2020
Central nervous system involvement in Erdheim-Chester disease: An observational cohort studyFleur Cohen Aubart, Ahmed Idbaih, Damien Galanaud, et al.
Human Mutation|May 15, 2012
Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activityFlavia Guillem, Caroline Kannengiesser, Claire Oudin, et al.
Pageof 18

Showing results (51-60 of 174) with videos related to

Sort By:
Pageof 18
Pediatric Blood & Cancer|July 1, 2010
Juvenile xanthogranuloma with hematological dysfunction treated with 2CDA-AraCPascale Blouin, Marion Yvert, Flavie Arbion, et al.
Journal of Clinical Immunology|March 23, 2019
Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic NeutropeniaJulie Seguier, Vincent Barlogis, Laure Croisille, et al.
Plos One|April 17, 2012
B-RAF mutant alleles associated with Langerhans cell histiocytosis, a granulomatous pediatric diseaseTakeshi Satoh, Alexander Smith, Aurelien Sarde, et al.
British Journal of Haematology|July 27, 2021
A circulating subset of BRAF<sup>V600E</sup> -positive cells in infants with high-risk Langerhans cell histiocytosis treated with BRAF inhibitorsRita Poch, Solenne Le Louet, Zofia Hélias-Rodzewicz, et al.
Chest|November 1, 2019
Lung Involvement in Destombes-Rosai-Dorfman Disease: Clinical and Radiological Features and Response to the MEK Inhibitor CobimetinibQuentin Moyon, Samia Boussouar, Philippe Maksud, et al.
Molecular Cancer|July 7, 2017
New somatic BRAF splicing mutation in Langerhans cell histiocytosisSébastien Héritier, Zofia Hélias-Rodzewicz, Rikhia Chakraborty, et al.
Blood|February 14, 2004
Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia RegisterChristine Bellanné-Chantelot, Séverine Clauin, Thierry Leblanc, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 27, 2022
Eye movement abnormalities in neurodegenerative langerhans cell histiocytosisLila Autier, Bertrand Gaymard, Eléonore Bayen, et al.
Neurology|September 5, 2020
Central nervous system involvement in Erdheim-Chester disease: An observational cohort studyFleur Cohen Aubart, Ahmed Idbaih, Damien Galanaud, et al.
Human Mutation|May 15, 2012
Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activityFlavia Guillem, Caroline Kannengiesser, Claire Oudin, et al.
Pageof 18