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D Hendig

Showing results (1-10 of 6) with videos related to

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|March 5, 2015
[Pseudodominant inheritance of pseudoxanthoma elasticum]P Charbel Issa, M Gliem, F G Holz, et al.
Biochemical and Biophysical Research Communications|June 11, 2013
Human xylosyltransferase-I - a new marker for myofibroblast differentiation in skin fibrosisI Faust, C Roch, J Kuhn, et al.
Journal of Medical Genetics|March 31, 2006
Polymorphisms in the xylosyltransferase genes cause higher serum XT-I activity in patients with pseudoxanthoma elasticum (PXE) and are involved in a severe disease courseS Schön, V Schulz, C Prante, et al.
MMW Fortschritte Der Medizin|June 9, 2011
[Pseudoxanthoma elasticum--case report]Robert P Finger, D Hendig, C Götting, et al.
Clinical Genetics|November 15, 2017
Homozygous XYLT2 variants as a cause of spondyloocular syndromeM Umair, G Eckstein, G Rudolph, et al.
Transplantation Proceedings|April 14, 2019
Heart Transplantation in Systemic Sclerosis: New Impulses for Conventional Scleroderma Transplantation Regimen and Scleroderma Diagnostic Monitoring: 2 Case ReportsI Faust, J Weile, B Fujita, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|March 5, 2015
[Pseudodominant inheritance of pseudoxanthoma elasticum]P Charbel Issa, M Gliem, F G Holz, et al.
Biochemical and Biophysical Research Communications|June 11, 2013
Human xylosyltransferase-I - a new marker for myofibroblast differentiation in skin fibrosisI Faust, C Roch, J Kuhn, et al.
Journal of Medical Genetics|March 31, 2006
Polymorphisms in the xylosyltransferase genes cause higher serum XT-I activity in patients with pseudoxanthoma elasticum (PXE) and are involved in a severe disease courseS Schön, V Schulz, C Prante, et al.
MMW Fortschritte Der Medizin|June 9, 2011
[Pseudoxanthoma elasticum--case report]Robert P Finger, D Hendig, C Götting, et al.
Clinical Genetics|November 15, 2017
Homozygous XYLT2 variants as a cause of spondyloocular syndromeM Umair, G Eckstein, G Rudolph, et al.
Transplantation Proceedings|April 14, 2019
Heart Transplantation in Systemic Sclerosis: New Impulses for Conventional Scleroderma Transplantation Regimen and Scleroderma Diagnostic Monitoring: 2 Case ReportsI Faust, J Weile, B Fujita, et al.
Pageof 1