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

Julia B Hennermann

Showing results (11-20 of 97) with videos related to

Pageof 10
Sort By:
Clinical Chemistry|October 1, 2008
Maple syrup urine disease: newborn screening fails to discriminate between classic and variant formsRalph Fingerhut, Eva Simon, Esther M Maier, et al.
Plos One|June 4, 2021
Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type CSusanne Hopf, Julia B Hennermann, Alexander K Schuster, et al.
Plos One|September 5, 2015
Eight-Year Follow-Up of Neuropsychiatric Symptoms and Brain Structural Changes in Fabry DiseaseIrene M Lelieveld, Anna Böttcher, Julia B Hennermann, et al.
Orphanet Journal of Rare Diseases|May 27, 2020
Saccadic reaction time and ocular findings in phenylketonuriaSusanne Hopf, Caroline Nowak, Julia B Hennermann, et al.
Journal of Inherited Metabolic Disease|February 13, 2019
Pharmacokinetics, pharmacodynamics, and safety of moss-aGalactosidase A in patients with Fabry diseaseJulia B Hennermann, Laila Arash-Kaps, György Fekete, et al.
Orphanet Journal of Rare Diseases|June 3, 2018
Retinal and optic nerve degeneration in α-mannosidosisJuliane Matlach, Thea Zindel, Yasmina Amraoui, et al.
Journal of Inherited Metabolic Disease|February 4, 2011
Features and outcome of galactokinase deficiency in children diagnosed by newborn screeningJulia B Hennermann, Peter Schadewaldt, Barbara Vetter, et al.
Orphanet Journal of Rare Diseases|September 8, 2019
The cardiovascular phenotype of adult patients with phenylketonuriaAline Azabdaftari, Markus van der Giet, Mirjam Schuchardt, et al.
Journal of Inherited Metabolic Disease|September 4, 2016
Treatment with pentosan polysulphate in patients with MPS I: results from an open label, randomized, monocentric phase II studyJulia B Hennermann, Seyfullah Gökce, Alexander Solyom, et al.
Journal of Inherited Metabolic Disease|October 18, 2011
Prediction of long-term outcome in glycine encephalopathy: a clinical surveyJulia B Hennermann, Jeanne-Marie Berger, Ulrike Grieben, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Clinical Chemistry|October 1, 2008
Maple syrup urine disease: newborn screening fails to discriminate between classic and variant formsRalph Fingerhut, Eva Simon, Esther M Maier, et al.
Plos One|June 4, 2021
Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type CSusanne Hopf, Julia B Hennermann, Alexander K Schuster, et al.
Plos One|September 5, 2015
Eight-Year Follow-Up of Neuropsychiatric Symptoms and Brain Structural Changes in Fabry DiseaseIrene M Lelieveld, Anna Böttcher, Julia B Hennermann, et al.
Orphanet Journal of Rare Diseases|May 27, 2020
Saccadic reaction time and ocular findings in phenylketonuriaSusanne Hopf, Caroline Nowak, Julia B Hennermann, et al.
Journal of Inherited Metabolic Disease|February 13, 2019
Pharmacokinetics, pharmacodynamics, and safety of moss-aGalactosidase A in patients with Fabry diseaseJulia B Hennermann, Laila Arash-Kaps, György Fekete, et al.
Orphanet Journal of Rare Diseases|June 3, 2018
Retinal and optic nerve degeneration in α-mannosidosisJuliane Matlach, Thea Zindel, Yasmina Amraoui, et al.
Journal of Inherited Metabolic Disease|February 4, 2011
Features and outcome of galactokinase deficiency in children diagnosed by newborn screeningJulia B Hennermann, Peter Schadewaldt, Barbara Vetter, et al.
Orphanet Journal of Rare Diseases|September 8, 2019
The cardiovascular phenotype of adult patients with phenylketonuriaAline Azabdaftari, Markus van der Giet, Mirjam Schuchardt, et al.
Journal of Inherited Metabolic Disease|September 4, 2016
Treatment with pentosan polysulphate in patients with MPS I: results from an open label, randomized, monocentric phase II studyJulia B Hennermann, Seyfullah Gökce, Alexander Solyom, et al.
Journal of Inherited Metabolic Disease|October 18, 2011
Prediction of long-term outcome in glycine encephalopathy: a clinical surveyJulia B Hennermann, Jeanne-Marie Berger, Ulrike Grieben, et al.
Pageof 10