Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Peter S Mortimer

Showing results (61-70 of 73) with videos related to

Pageof 8
Sort By:
Circulation Research|February 16, 2013
Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedemaKristiana Gordon, Dörte Schulte, Glen Brice, et al.
JCI Insight|September 12, 2023
Erythematous capillary-lymphatic malformations mimicking blood vascular anomaliesRené Hägerling, Malou Van Zanten, Rose Yinghan Behncke, et al.
JCI Insight|August 18, 2017
VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformationsRené Hägerling, Dominik Drees, Aaron Scherzinger, et al.
Plos One|October 13, 2022
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohortDionysios Grigoriadis, Ege Sackey, Katie Riches, et al.
The New England Journal of Medicine|May 3, 2013
Penicillin to prevent recurrent leg cellulitisKim S Thomas, Angela M Crook, Andrew J Nunn, et al.
Nature Communications|September 4, 2015
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisElisavet Fotiou, Silvia Martin-Almedina, Michael A Simpson, et al.
Nature Communications|April 28, 2019
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisElisavet Fotiou, Silvia Martin-Almedina, Michael A Simpson, et al.
Nature Genetics|September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutationsGabriela E Jones, Pia Ostergaard, Anthony T Moore, et al.
The Journal of Clinical Investigation|July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalisSilvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Circulation Research|February 16, 2013
Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedemaKristiana Gordon, Dörte Schulte, Glen Brice, et al.
JCI Insight|September 12, 2023
Erythematous capillary-lymphatic malformations mimicking blood vascular anomaliesRené Hägerling, Malou Van Zanten, Rose Yinghan Behncke, et al.
JCI Insight|August 18, 2017
VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformationsRené Hägerling, Dominik Drees, Aaron Scherzinger, et al.
Plos One|October 13, 2022
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohortDionysios Grigoriadis, Ege Sackey, Katie Riches, et al.
The New England Journal of Medicine|May 3, 2013
Penicillin to prevent recurrent leg cellulitisKim S Thomas, Angela M Crook, Andrew J Nunn, et al.
Nature Communications|September 4, 2015
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisElisavet Fotiou, Silvia Martin-Almedina, Michael A Simpson, et al.
Nature Communications|April 28, 2019
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisElisavet Fotiou, Silvia Martin-Almedina, Michael A Simpson, et al.
Nature Genetics|September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutationsGabriela E Jones, Pia Ostergaard, Anthony T Moore, et al.
The Journal of Clinical Investigation|July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalisSilvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
Pageof 8