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Susanne Pitz

Showing results (51-60 of 87) with videos related to

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Deutsches Arzteblatt International|June 24, 2009
Quality of life and occupational disability in endocrine orbitopathyKatharina A Ponto, Susanne Pitz, Norbert Pfeiffer, et al.
Ophthalmology|June 21, 2011
Clinical relevance of thyroid-stimulating immunoglobulins in graves' ophthalmopathyKatharina A Ponto, Michael Kanitz, Paul D Olivo, et al.
Plos One|August 29, 2015
Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis PatientsJoanna Wasielica-Poslednik, Christina Butsch, Christina Lampe, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorderJennifer Haensel, Nicolai Kohlschmidt, Susanne Pitz, et al.
Orphanet Journal of Rare Diseases|November 16, 2019
A comprehensive monocentric ophthalmic study with Gaucher disease type 3 patients: vitreoretinal lesions, retinal atrophy and characterization of abnormal saccadesSusanne Hopf, Norbert Pfeiffer, Matthias Liesenfeld, et al.
Journal of Inherited Metabolic Disease|March 24, 2012
Clinical characteristics of adults with slowly progressing mucopolysaccharidosis VI: a case seriesAnke Thümler, Elke Miebach, Christina Lampe, et al.
Plos One|March 18, 2015
Ocular signs correlate well with disease severity and genotype in Fabry diseaseSusanne Pitz, Gisela Kalkum, Laila Arash, et al.
Plos One|June 28, 2019
Corneal topometric, aberrometric and biomechanical parameters in mucopolysaccharidosis patientsJoanna Wasielica-Poslednik, Alexander K Schuster, Giuseppe Politino, et al.
Deutsches Arzteblatt International|June 5, 2015
The prevalence of amblyopia in Germany: data from the prospective, population-based Gutenberg Health StudyHeike M Elflein, Susanne Fresenius, Julia Lamparter, et al.
Acta Ophthalmologica|December 6, 2011
Clinical guidelines for diagnosing and managing ocular manifestations in children with mucopolysaccharidosisKristina T Fahnehjelm, Jane L Ashworth, Susanne Pitz, et al.
Pageof 9

Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
Deutsches Arzteblatt International|June 24, 2009
Quality of life and occupational disability in endocrine orbitopathyKatharina A Ponto, Susanne Pitz, Norbert Pfeiffer, et al.
Ophthalmology|June 21, 2011
Clinical relevance of thyroid-stimulating immunoglobulins in graves' ophthalmopathyKatharina A Ponto, Michael Kanitz, Paul D Olivo, et al.
Plos One|August 29, 2015
Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis PatientsJoanna Wasielica-Poslednik, Christina Butsch, Christina Lampe, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorderJennifer Haensel, Nicolai Kohlschmidt, Susanne Pitz, et al.
Orphanet Journal of Rare Diseases|November 16, 2019
A comprehensive monocentric ophthalmic study with Gaucher disease type 3 patients: vitreoretinal lesions, retinal atrophy and characterization of abnormal saccadesSusanne Hopf, Norbert Pfeiffer, Matthias Liesenfeld, et al.
Journal of Inherited Metabolic Disease|March 24, 2012
Clinical characteristics of adults with slowly progressing mucopolysaccharidosis VI: a case seriesAnke Thümler, Elke Miebach, Christina Lampe, et al.
Plos One|March 18, 2015
Ocular signs correlate well with disease severity and genotype in Fabry diseaseSusanne Pitz, Gisela Kalkum, Laila Arash, et al.
Plos One|June 28, 2019
Corneal topometric, aberrometric and biomechanical parameters in mucopolysaccharidosis patientsJoanna Wasielica-Poslednik, Alexander K Schuster, Giuseppe Politino, et al.
Deutsches Arzteblatt International|June 5, 2015
The prevalence of amblyopia in Germany: data from the prospective, population-based Gutenberg Health StudyHeike M Elflein, Susanne Fresenius, Julia Lamparter, et al.
Acta Ophthalmologica|December 6, 2011
Clinical guidelines for diagnosing and managing ocular manifestations in children with mucopolysaccharidosisKristina T Fahnehjelm, Jane L Ashworth, Susanne Pitz, et al.
Pageof 9