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Contact Dermatitis
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June 4, 2009
Allergic contact dermatitis from fragrance components in specific topical pharmaceutical products in Belgium
Andrea Nardelli, Ellen D'Hooghe, Jacques Drieghe, et al.
Journal of Medical Ethics
|
September 28, 2011
A fair share for the orphans: ethical guidelines for a fair distribution of resources within the bounds of the 10-year-old European Orphan Drug Regulation
Wim Pinxten, Yvonne Denier, Marc Dooms, et al.
Orphanet Journal of Rare Diseases
|
May 6, 2019
Information needs of physicians regarding the diagnosis of rare diseases: a questionnaire-based study in Belgium
Liese Vandeborne, Eline van Overbeeke, Marc Dooms, et al.
European Journal of Medical Genetics
|
October 7, 2024
Lessons learned from the RE(ACT) conference on medical devices for rare diseases
Anneliene H Jonker, Tim Buckinx, Lucia Pannese, et al.
Frontiers in Pediatrics
|
September 20, 2021
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era
Evelien De Sutter, Birte Coopmans, Femke Vanendert, et al.
Personalized Medicine
|
May 2, 2018
Noninvasive prenatal testing: a survey of young (future) parents in Flanders
Pascal Borry, Maddalena Favaretto, Ann Batthyany, et al.
Frontiers in Medicine
|
October 27, 2018
Patient Involvement in the Lifecycle of Medicines According to Belgian Stakeholders: The Gap Between Theory and Practice
Rosanne Janssens, Eline van Overbeeke, Lotte Verswijvel, et al.
Frontiers in Pharmacology
|
December 13, 2019
Reimbursement Status and Recommendations Related to Orphan Drugs in European Countries
Ewa Stawowczyk, Krzysztof Piotr Malinowski, Paweł Kawalec, et al.
EMBO Molecular Medicine
|
June 27, 2023
Targeting shared molecular etiologies to accelerate drug development for rare diseases
Galliano Zanello, Macarena Garrido-Estepa, Ana Crespo, et al.
Frontiers in Pharmacology
|
December 4, 2024
Clinical and non-clinical aspects of reimbursement policy for orphan drugs in selected European countries
Szczepan Jakubowski, Przemysław Holko, Rafał Nowak, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Contact Dermatitis
|
June 4, 2009
Allergic contact dermatitis from fragrance components in specific topical pharmaceutical products in Belgium
Andrea Nardelli, Ellen D'Hooghe, Jacques Drieghe, et al.
Journal of Medical Ethics
|
September 28, 2011
A fair share for the orphans: ethical guidelines for a fair distribution of resources within the bounds of the 10-year-old European Orphan Drug Regulation
Wim Pinxten, Yvonne Denier, Marc Dooms, et al.
Orphanet Journal of Rare Diseases
|
May 6, 2019
Information needs of physicians regarding the diagnosis of rare diseases: a questionnaire-based study in Belgium
Liese Vandeborne, Eline van Overbeeke, Marc Dooms, et al.
European Journal of Medical Genetics
|
October 7, 2024
Lessons learned from the RE(ACT) conference on medical devices for rare diseases
Anneliene H Jonker, Tim Buckinx, Lucia Pannese, et al.
Frontiers in Pediatrics
|
September 20, 2021
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era
Evelien De Sutter, Birte Coopmans, Femke Vanendert, et al.
Personalized Medicine
|
May 2, 2018
Noninvasive prenatal testing: a survey of young (future) parents in Flanders
Pascal Borry, Maddalena Favaretto, Ann Batthyany, et al.
Frontiers in Medicine
|
October 27, 2018
Patient Involvement in the Lifecycle of Medicines According to Belgian Stakeholders: The Gap Between Theory and Practice
Rosanne Janssens, Eline van Overbeeke, Lotte Verswijvel, et al.
Frontiers in Pharmacology
|
December 13, 2019
Reimbursement Status and Recommendations Related to Orphan Drugs in European Countries
Ewa Stawowczyk, Krzysztof Piotr Malinowski, Paweł Kawalec, et al.
EMBO Molecular Medicine
|
June 27, 2023
Targeting shared molecular etiologies to accelerate drug development for rare diseases
Galliano Zanello, Macarena Garrido-Estepa, Ana Crespo, et al.
Frontiers in Pharmacology
|
December 4, 2024
Clinical and non-clinical aspects of reimbursement policy for orphan drugs in selected European countries
Szczepan Jakubowski, Przemysław Holko, Rafał Nowak, et al.
Page
of 3