Хайлтын үр дүнгүүд - Joseph Muenzer
- 38-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Early initiation of enzyme replacement therapy for the mucopolysaccharidoses -н Joseph Muenzer
Хэвлэсэн 2013Revisão -
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Evaluation of the long-term treatment effects of intravenous idursulfase in patients with mucopolysaccharidosis II (MPS II) using statistical modeling: data from the Hunter Outcome... -н Joseph Muenzer, Jaco Botha, Paul Harmatz, Roberto Giugliani, Christoph Kampmann, Barbara K. Burton
Хэвлэсэн 2021Artigo -
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Impact of the COVID-19 pandemic on the standard of care for patients with lysosomal storage diseases: A survey of healthcare professionals in the Fabry, Gaucher, and Hunter Outcome... -н Deborah Elstein, Roberto Giugliani, Joseph Muenzer, Jörn Schenk, Ida Vanessa Döederlein Schwartz, Christina Anagnostopoulou
Хэвлэсэн 2021Artigo -
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Self-complementary adeno-associated virus serotype 2 vector: global distribution and broad dispersion of AAV-mediated transgene expression in mouse brain -н Haiyan Fu, Joseph Muenzer, R. Jude Samulski, George R. Breese, Jerillyn Sifford, Xinhua Zeng, Douglas M. McCarty
Хэвлэсэн 2003Artigo -
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Idursulfase treatment of Hunter syndrome in children younger than 6 years: Results from the Hunter Outcome Survey -н Joseph Muenzer, Michael Beck, Roberto Giugliani, Yasuyuki Suzuki, Anna Tylki‐Szymańska, Vassili Valayannopoulos, Ashok Vellodi, J. E. Wraith
Хэвлэсэн 2011Artigo -
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A charitable access program for patients with lysosomal storage disorders in underserved communities worldwide -н Atul Mehta, Uma Ramaswami, Joseph Muenzer, Roberto Giugliani, Kurt Ullrich, Tanya Collin-Histed, Zoya Panahloo, Hartmann Wellhoefer, Joel Frader
Хэвлэсэн 2021Artigo -
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Safety and Feasibility of High-pressure Transvenous Limb Perfusion With 0.9% Saline in Human Muscular Dystrophy -н Zheng Fan, Keith C. Kocis, Robert D. Valley, James F. Howard, Manisha Chopra, Hongyu An, Weili Lin, Joseph Muenzer, William J. Powers
Хэвлэсэн 2011Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Medicine
Internal medicine
Disease
Enzyme replacement therapy
Biology
Mucopolysaccharidosis
Hunter syndrome
Gene
Mucopolysaccharidosis type II
Pediatrics
Biochemistry
Genetics
Pathology
Surgery
Intensive care medicine
Lysosomal storage disease
Clinical trial
Mucopolysaccharidosis type I
Hurler syndrome
Mucopolysaccharidosis I
Chemistry
Endocrinology
Genetic enhancement
Genotype
Natural history
Newborn screening
Observational study
Phenotype
Psychiatry
Psychology