Pompe disease: literature review and case series

M Dasouki, O Jawdat, O Almadhoun… - Neurologic …, 2014 - neurologic.theclinics.com
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the
lysosomal enzyme acid-a-glucosidase (GAA; EC 3.2. 1.20), leading to generalized …

[HTML][HTML] Pompe Disease: Literature Review and Case Series

M Dasouki, O Jawdat, O Almadhoun, M Pasnoor… - Neurologic …, 2014 - ncbi.nlm.nih.gov
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the
lysosomal enzyme acid-α-glucosidase (GAA, EC 3.2. 1.20), leading to generalized …

[PDF][PDF] Pompe Disease: Literature Review and Case Series

M Dasouki, O Jawdat, O Almadhoun, M Pasnoor… - researchgate.net
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the
lysosomal enzyme acid-α-glucosidase (GAA, EC 3.2. 1.20), leading to generalized …

Pompe disease: literature review and case series

M Dasouki, O Jawdat, O Almadhoun… - Neurologic …, 2014 - pubmed.ncbi.nlm.nih.gov
Pompe disease is a rare multi-systemic metabolic myopathy caused by autosomal recessive
mutations in the acidic alpha glucosidase (GAA) gene. Significant progress had been made …

Pompe disease: literature review and case series.

M Dasouki, O Jawdat, O Almadhoun, M Pasnoor… - Neurologic …, 2014 - europepmc.org
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the
lysosomal enzyme acid-α-glucosidase (GAA, EC 3.2. 1.20), leading to generalized …

[PDF][PDF] Pompe Disease

M Dasouki, O Jawdat, O Almadhoun, M Pasnoor… - Neurol Clin, 2014 - academia.edu
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the
lysosomal enzyme acid-a-glucosidase (GAA; EC 3.2. 1.20), leading to generalized …

[引用][C] Pompe Disease

M Dasouki, O Jawdat, O Almadhoun, M Pasnoor… - Neurologic Clinics, 2014 - cir.nii.ac.jp
Pompe Disease | 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 論文・データをさがす 大学図書館の本をさがす 日本の博士論文をさがす …

Pompe disease: literature review and case series

M Dasouki, O Jawdat, O Almadhoun… - Neurologic …, 2014 - pubmed.ncbi.nlm.nih.gov
Pompe disease is a rare multi-systemic metabolic myopathy caused by autosomal recessive
mutations in the acidic alpha glucosidase (GAA) gene. Significant progress had been made …