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Emilie Castermans

Showing results (1-10 of 22) with videos related to

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Respiratory Medicine Case Reports|April 10, 2026
Painful large traumatic intercostal pulmonary herniaEmilie Castermans, Apostolos C Agrafiotis, Marie Bruyneel
Sleep Medicine|June 5, 2026
Pharmacological and non-pharmacological treatments for chronic insomnia in perimenopausal and postmenopausal women: a systematic review and meta-analysisMarie Bruyneel, Serge Rozenberg, Christina Sanida, et al.
Stem Cells (Dayton, Ohio)|April 15, 2006
Despite inhibition of hematopoietic progenitor cell growth in vitro, the tyrosine kinase inhibitor imatinib does not impair engraftment of human CD133+ cells into NOD/SCIDbeta2mNull miceLaurence Pirson, Frédéric Baron, Nathalie Meuris, et al.
Clinical Kidney Journal|April 9, 2015
Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosisOriane Hanssen, Emilie Castermans, Christophe Bovy, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Pituitary|June 12, 2016
Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screeningRuth Mangupli, Liliya Rostomyan, Emilie Castermans, et al.
Molecular Pharmacology|February 25, 2006
Raloxifene-induced myeloma cell apoptosis: a study of nuclear factor-kappaB inhibition and gene expression signatureSabine Olivier, Pierre Close, Emilie Castermans, et al.
Transplantation|December 23, 2003
T-cell reconstitution after unmanipulated, CD8-depleted or CD34-selected nonmyeloablative peripheral blood stem-cell transplantationFrédéric Baron, Nicole Schaaf-Lafontaine, Stéphanie Humblet-Baron, et al.
Familial Cancer|February 14, 2014
Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expressionMaria Chiara Zatelli, Federico Tagliati, Mauro Di Ruvo, et al.
Endocrine Connections|March 2, 2019
AIP and MEN1 mutations and AIP immunohistochemistry in pituitary adenomas in a tertiary referral centerAdrian F Daly, David A Cano, Eva Venegas-Moreno, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Respiratory Medicine Case Reports|April 10, 2026
Painful large traumatic intercostal pulmonary herniaEmilie Castermans, Apostolos C Agrafiotis, Marie Bruyneel
Sleep Medicine|June 5, 2026
Pharmacological and non-pharmacological treatments for chronic insomnia in perimenopausal and postmenopausal women: a systematic review and meta-analysisMarie Bruyneel, Serge Rozenberg, Christina Sanida, et al.
Stem Cells (Dayton, Ohio)|April 15, 2006
Despite inhibition of hematopoietic progenitor cell growth in vitro, the tyrosine kinase inhibitor imatinib does not impair engraftment of human CD133+ cells into NOD/SCIDbeta2mNull miceLaurence Pirson, Frédéric Baron, Nathalie Meuris, et al.
Clinical Kidney Journal|April 9, 2015
Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosisOriane Hanssen, Emilie Castermans, Christophe Bovy, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Pituitary|June 12, 2016
Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screeningRuth Mangupli, Liliya Rostomyan, Emilie Castermans, et al.
Molecular Pharmacology|February 25, 2006
Raloxifene-induced myeloma cell apoptosis: a study of nuclear factor-kappaB inhibition and gene expression signatureSabine Olivier, Pierre Close, Emilie Castermans, et al.
Transplantation|December 23, 2003
T-cell reconstitution after unmanipulated, CD8-depleted or CD34-selected nonmyeloablative peripheral blood stem-cell transplantationFrédéric Baron, Nicole Schaaf-Lafontaine, Stéphanie Humblet-Baron, et al.
Familial Cancer|February 14, 2014
Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expressionMaria Chiara Zatelli, Federico Tagliati, Mauro Di Ruvo, et al.
Endocrine Connections|March 2, 2019
AIP and MEN1 mutations and AIP immunohistochemistry in pituitary adenomas in a tertiary referral centerAdrian F Daly, David A Cano, Eva Venegas-Moreno, et al.
Pageof 3