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Volumn 5, Issue 10, 2004, Pages 1101-1110

α-glucosidase (CHO) (genzyme)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; RECOMBINANT PROTEIN;

EID: 16644363403     PISSN: 14724472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (4)

References (70)
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    • 557380 Human acid α-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Bijvoet AG, Van Hirtum H, Kroos MA, Van de Kamp EH, Schoneveld O, Visser P, Brakenhoff JP, Weggeman M, van Corven EJ, Van der Ploeg AT, Reuser AJ HUM MOL GENET 1999 8 12 2145-2153
    • 557380 Human acid α-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Bijvoet AG, Van Hirtum H, Kroos MA, Van de Kamp EH, Schoneveld O, Visser P, Brakenhoff JP, Weggeman M, van Corven EJ, Van der Ploeg AT, Reuser AJ HUM MOL GENET 1999 8 12 2145-2153
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    • 557398 Isolation and characterization of a precursor form of lysosomal α-glucosidase from human urine. Oude Elferink RP, Brouwer-Kelder EM, Surya I, Strijland A, Kroos M, Reuser AJ, Tager JM EUR J BIOCHEM 1984 139 4 489-495
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    • 557402 Quantitation of Mr 46000 and Mr 300000 mannose 6-phosphate receptors in human cells and tissues. Wenk J, Hille A, von Figura K BIOCHEM INT 1991 23 4 723-732
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    • 557593 Acid maltase deficiency type II glycogenosis, Morphological and biochemical study of a childhood phenotype. Martin JJ, De Barsy T, De Schrijver, Leroy JG, Palladini G J NEUROL SCI 1976 30 1 155-166
    • 557593 Acid maltase deficiency (type II glycogenosis). Morphological and biochemical study of a childhood phenotype. Martin JJ, De Barsy T, De Schrijver, Leroy JG, Palladini G J NEUROL SCI 1976 30 1 155-166
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    • 557594 Pompe's disease: An inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle. Martin JJ, de Barsy T, van Hoof F, Palladini G ACTA NEUROPATHOL 1973 23 3 229-244
    • 557594 Pompe's disease: An inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle. Martin JJ, de Barsy T, van Hoof F, Palladini G ACTA NEUROPATHOL 1973 23 3 229-244
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    • 557598 Determination of acid α-glucosidase protein: Evaluation as a screening marker for Pompe disease and other lysosomal storage disorders. Umapathysivam K, Whittle AM, Ranieri E, Bindloss C, Ravenscroft EM, van Diggelen OP, Hopwood JJ, Meikle PJ CLIN CHEM 2000 46 9 1318-1325
    • 557598 Determination of acid α-glucosidase protein: Evaluation as a screening marker for Pompe disease and other lysosomal storage disorders. Umapathysivam K, Whittle AM, Ranieri E, Bindloss C, Ravenscroft EM, van Diggelen OP, Hopwood JJ, Meikle PJ CLIN CHEM 2000 46 9 1318-1325
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    • 557600 Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening. Li Y, Scott CR, Chamoles NA, Ghavami A, Pinto BM, Turecek F, Gelb MH CLIN CHEM 2004 doi:10.1373/ clinchem.2004.035907
    • 557600 Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening. Li Y, Scott CR, Chamoles NA, Ghavami A, Pinto BM, Turecek F, Gelb MH CLIN CHEM 2004 doi:10.1373/ clinchem.2004.035907
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    • 558193 CSFB Biotech Beat. Augustine ME, Troyer RL, Park MS, Biegert LR CREDIT SUISSE FIRST BOSTON 2004 July 19
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    • 558320 Genzyme Corporation. US BANCORP PIPER JAFFRAY INC 2004 August 25
    • 558320 Genzyme Corporation. US BANCORP PIPER JAFFRAY INC 2004 August 25


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.