Search research articles
Contact Us
Filters
Showing results (181-190 of 233) with videos related to
Page
of 24
Sort By:
European Journal of Pediatrics
|
November 1, 2011
The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensus
Joseph Muenzer, Olaf Bodamer, Barbara Burton, et al.
Journal of the American Society of Nephrology : JASN
|
April 10, 2009
Agalsidase alfa and kidney dysfunction in Fabry disease
Michael West, Kathy Nicholls, Atul Mehta, et al.
Clinical Nuclear Medicine
|
February 6, 2018
SPECT/CT With the PSMA Ligand 99mTc-MIP-1404 for Whole-Body Primary Staging of Patients With Prostate Cancer
Christian Schmidkonz, Michael Cordes, Michael Beck, et al.
Orphanet Journal of Rare Diseases
|
June 9, 2012
A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations
Andreas Herzog, Ralf Hartung, Arnold J J Reuser, et al.
Health and Quality of Life Outcomes
|
September 21, 2012
Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ)
Uma Ramaswami, Donald E Stull, Rossella Parini, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
May 5, 2018
<sup>68</sup>Ga-PSMA-11 PET/CT-derived metabolic parameters for determination of whole-body tumor burden and treatment response in prostate cancer
Christian Schmidkonz, Michael Cordes, Daniela Schmidt, et al.
Journal of Biomechanics
|
September 2, 2018
Effect of guided bone regeneration on bone quality surrounding dental implants
Trenton B Johnson, Ben Siderits, Seth Nye, et al.
Clinical Nuclear Medicine
|
June 20, 2018
Assessment of Treatment Response by 99mTc-MIP-1404 SPECT/CT: A Pilot Study in Patients With Metastatic Prostate Cancer
Christian Schmidkonz, Michael Cordes, Michael Beck, et al.
European Journal of Pediatrics
|
November 27, 2007
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
J Edmond Wraith, Maurizio Scarpa, Michael Beck, et al.
Human Mutation
|
May 28, 2009
GM1 gangliosidosis and Morquio B disease: expression analysis of missense mutations affecting the catalytic site of acid beta-galactosidase
Doris Hofer, Karl Paul, Katrin Fantur, et al.
Page
of 24
Search research articles
Search
Showing results (181-190 of 233) with videos related to
Sort By:
Page
of 24
European Journal of Pediatrics
|
November 1, 2011
The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensus
Joseph Muenzer, Olaf Bodamer, Barbara Burton, et al.
Journal of the American Society of Nephrology : JASN
|
April 10, 2009
Agalsidase alfa and kidney dysfunction in Fabry disease
Michael West, Kathy Nicholls, Atul Mehta, et al.
Clinical Nuclear Medicine
|
February 6, 2018
SPECT/CT With the PSMA Ligand 99mTc-MIP-1404 for Whole-Body Primary Staging of Patients With Prostate Cancer
Christian Schmidkonz, Michael Cordes, Michael Beck, et al.
Orphanet Journal of Rare Diseases
|
June 9, 2012
A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations
Andreas Herzog, Ralf Hartung, Arnold J J Reuser, et al.
Health and Quality of Life Outcomes
|
September 21, 2012
Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ)
Uma Ramaswami, Donald E Stull, Rossella Parini, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
May 5, 2018
<sup>68</sup>Ga-PSMA-11 PET/CT-derived metabolic parameters for determination of whole-body tumor burden and treatment response in prostate cancer
Christian Schmidkonz, Michael Cordes, Daniela Schmidt, et al.
Journal of Biomechanics
|
September 2, 2018
Effect of guided bone regeneration on bone quality surrounding dental implants
Trenton B Johnson, Ben Siderits, Seth Nye, et al.
Clinical Nuclear Medicine
|
June 20, 2018
Assessment of Treatment Response by 99mTc-MIP-1404 SPECT/CT: A Pilot Study in Patients With Metastatic Prostate Cancer
Christian Schmidkonz, Michael Cordes, Michael Beck, et al.
European Journal of Pediatrics
|
November 27, 2007
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
J Edmond Wraith, Maurizio Scarpa, Michael Beck, et al.
Human Mutation
|
May 28, 2009
GM1 gangliosidosis and Morquio B disease: expression analysis of missense mutations affecting the catalytic site of acid beta-galactosidase
Doris Hofer, Karl Paul, Katrin Fantur, et al.
Page
of 24