Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - Journal of neurology, 2013 - Springer
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
[PDF][PDF] Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - ethnicity, 2012 - academia.edu
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review.
A Toscano, B Schoser - Journal of Neurology, 2012 - europepmc.org
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
[PDF][PDF] Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - ethnicity, 2012 - researchgate.net
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
[PDF][PDF] Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - ethnicity, 2012 - nmfo.ru
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review.
A Toscano, B Schoser - Journal of Neurology, 2013 - search.ebscohost.com
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
[引用][C] Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - Journal of Neurology, 2012 - cir.nii.ac.jp
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review | CiNii
Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 …
Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 …
[PDF][PDF] Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - ethnicity, 2012 - nmfo.ru
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - Journal of neurology, 2013 - pubmed.ncbi.nlm.nih.gov
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review
A Toscano, B Schoser - Journal of Neurology, 2013 - infona.pl
Glycogen storage disease type 2/Pompe disease is a progressive muscle disorder with a
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …
wide range of phenotypic presentations, caused by an inherited deficiency of acid alpha …