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

Mette Ramsing

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Case Reports in Dermatology|October 30, 2023
Majocchi's Granuloma - The Great Mimicker: A Case ReportJakob Lillemoen Drivenes, Mette Ramsing, Anette Bygum
Case Reports in Dermatology|October 17, 2017
Successful Topical Treatment of Pigmented Purpuric Lichenoid Dermatitis of Gougerot-Blum in a Young Patient: A Case Report and Summary of the Most Common Pigmented Purpuric DermatosesJeyanthini Risikesan, Mette Sommerlund, Mette Ramsing, et al.
Dermatology Reports|November 12, 2014
Elastosis Perforans Serpiginosa in a patient with Down syndrome treated with imiquimod 5% creamPernille Axél Gregersen, Birgitte Stausbøl-Grøn, Mette Ramsing, et al.
American Journal of Medical Genetics. Part A|November 21, 2013
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variabilityMaria Rasmussen, Mette Ramsing, Olav Bjørn Petersen, et al.
NDT Plus|June 29, 2017
Two cases of nephrogenic systemic fibrosis after exposure to the macrocyclic compound gadobutrolTina Rask Elmholdt, Bettina Jørgensen, Mette Ramsing, et al.
Clinical Case Reports|May 5, 2017
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarrayHeidi Kristine Støve, Naja Becher, Vibike Gjørup, et al.
Physiological Reports|August 13, 2015
The development of hepatic stellate cells in normal and abnormal human fetuses - an immunohistochemical studyChristine K C Loo, Tamara N Pereira, Katarzyna N Pozniak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 13, 2016
Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndromeChristine K C Loo, Tamara N Pereira, Mette Ramsing, et al.
Stem Cell Research|July 22, 2017
Constitutive transgene expression of Stem Cell Antigen-1 in the hair follicle alters the sensitivity to tumor formation and progressionRikke Christensen, David M Owens, Annette C Füchtbauer, et al.
Clinical Case Reports|October 22, 2020
Idiopathic hypereosinophilic syndrome: A rare diagnosis in childrenKristine Appel Uldall Pallesen, Troels Herlin, Mette Holm, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Case Reports in Dermatology|October 30, 2023
Majocchi's Granuloma - The Great Mimicker: A Case ReportJakob Lillemoen Drivenes, Mette Ramsing, Anette Bygum
Case Reports in Dermatology|October 17, 2017
Successful Topical Treatment of Pigmented Purpuric Lichenoid Dermatitis of Gougerot-Blum in a Young Patient: A Case Report and Summary of the Most Common Pigmented Purpuric DermatosesJeyanthini Risikesan, Mette Sommerlund, Mette Ramsing, et al.
Dermatology Reports|November 12, 2014
Elastosis Perforans Serpiginosa in a patient with Down syndrome treated with imiquimod 5% creamPernille Axél Gregersen, Birgitte Stausbøl-Grøn, Mette Ramsing, et al.
American Journal of Medical Genetics. Part A|November 21, 2013
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variabilityMaria Rasmussen, Mette Ramsing, Olav Bjørn Petersen, et al.
NDT Plus|June 29, 2017
Two cases of nephrogenic systemic fibrosis after exposure to the macrocyclic compound gadobutrolTina Rask Elmholdt, Bettina Jørgensen, Mette Ramsing, et al.
Clinical Case Reports|May 5, 2017
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarrayHeidi Kristine Støve, Naja Becher, Vibike Gjørup, et al.
Physiological Reports|August 13, 2015
The development of hepatic stellate cells in normal and abnormal human fetuses - an immunohistochemical studyChristine K C Loo, Tamara N Pereira, Katarzyna N Pozniak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 13, 2016
Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndromeChristine K C Loo, Tamara N Pereira, Mette Ramsing, et al.
Stem Cell Research|July 22, 2017
Constitutive transgene expression of Stem Cell Antigen-1 in the hair follicle alters the sensitivity to tumor formation and progressionRikke Christensen, David M Owens, Annette C Füchtbauer, et al.
Clinical Case Reports|October 22, 2020
Idiopathic hypereosinophilic syndrome: A rare diagnosis in childrenKristine Appel Uldall Pallesen, Troels Herlin, Mette Holm, et al.
Pageof 2