Search research articles
Contact Us
Filters
Showing results (191-200 of 219) with videos related to
Page
of 22
Sort By:
European Journal of Radiology
|
July 9, 2023
Intramuscular capillary-type hemangioma: Diagnosis, treatment, and outcomes. A French multicentric retrospective study of 66 cases
Jordan Orly, Annouk Bisdorff, Antoine Fraissenon, et al.
Journal of the American Society of Nephrology : JASN
|
July 12, 2018
ABCC6 Deficiency Promotes Development of Randall Plaque
Emmanuel Letavernier, Gilles Kauffenstein, Léa Huguet, et al.
Contact Dermatitis
|
June 19, 2010
Fragrance allergy: assessing the safety of washed fabrics
David A Basketter, Annick Pons-Guiraud, Arian van Asten, et al.
Trials
|
May 4, 2016
Dedicated call center (SOS-HAE) for hereditary angioedema attacks: study protocol for a randomised controlled trial
Nicolas Javaud, Olivier Fain, Isabelle Durand-Zaleski, et al.
BMC Medical Education
|
October 1, 2024
Learning curves of novice residents on cataract surgery simulator: the E3CAPS pedagogic study
Jean-Baptiste Ducloyer, Alexandra Poinas, Léa Duchesne, et al.
European Journal of Pediatrics
|
July 11, 2023
Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational study
Sophie Leducq, Annabel Maruani, Christine Bodemer, et al.
Bone Research
|
January 26, 2022
Theobroma cacao improves bone growth by modulating defective ciliogenesis in a mouse model of achondroplasia
Ludovic Martin, Nabil Kaci, Catherine Benoist-Lasselin, et al.
Annals of Emergency Medicine
|
March 6, 2018
Specialist Advice Support for Management of Severe Hereditary Angioedema Attacks: A Multicenter Cluster-Randomized Controlled Trial
Nicolas Javaud, Olivier Fain, Isabelle Durand-Zaleski, et al.
Acta Dermato-Venereologica
|
November 8, 2017
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE
Annabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, et al.
Human Mutation
|
June 1, 2010
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype
Eric Pasmant, Audrey Sabbagh, Gill Spurlock, et al.
Page
of 22
Search research articles
Search
Showing results (191-200 of 219) with videos related to
Sort By:
Page
of 22
European Journal of Radiology
|
July 9, 2023
Intramuscular capillary-type hemangioma: Diagnosis, treatment, and outcomes. A French multicentric retrospective study of 66 cases
Jordan Orly, Annouk Bisdorff, Antoine Fraissenon, et al.
Journal of the American Society of Nephrology : JASN
|
July 12, 2018
ABCC6 Deficiency Promotes Development of Randall Plaque
Emmanuel Letavernier, Gilles Kauffenstein, Léa Huguet, et al.
Contact Dermatitis
|
June 19, 2010
Fragrance allergy: assessing the safety of washed fabrics
David A Basketter, Annick Pons-Guiraud, Arian van Asten, et al.
Trials
|
May 4, 2016
Dedicated call center (SOS-HAE) for hereditary angioedema attacks: study protocol for a randomised controlled trial
Nicolas Javaud, Olivier Fain, Isabelle Durand-Zaleski, et al.
BMC Medical Education
|
October 1, 2024
Learning curves of novice residents on cataract surgery simulator: the E3CAPS pedagogic study
Jean-Baptiste Ducloyer, Alexandra Poinas, Léa Duchesne, et al.
European Journal of Pediatrics
|
July 11, 2023
Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational study
Sophie Leducq, Annabel Maruani, Christine Bodemer, et al.
Bone Research
|
January 26, 2022
Theobroma cacao improves bone growth by modulating defective ciliogenesis in a mouse model of achondroplasia
Ludovic Martin, Nabil Kaci, Catherine Benoist-Lasselin, et al.
Annals of Emergency Medicine
|
March 6, 2018
Specialist Advice Support for Management of Severe Hereditary Angioedema Attacks: A Multicenter Cluster-Randomized Controlled Trial
Nicolas Javaud, Olivier Fain, Isabelle Durand-Zaleski, et al.
Acta Dermato-Venereologica
|
November 8, 2017
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE
Annabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, et al.
Human Mutation
|
June 1, 2010
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype
Eric Pasmant, Audrey Sabbagh, Gill Spurlock, et al.
Page
of 22