SCOPUS 정보 검색 플랫폼

Volumn 65, Issue 1, 2012, Pages 100-102

When should we start enzyme replacement therapy for infantile pompe disease with severe cardiomyopathy?;¿cuándo deberíamos iniciar el tratamiento enzimático sustitutivo de la enfermedad de Pompe infantil con miocardiopatía severa?

(5) Bonilla Palomas, Juan L a Gámez López, Antonio L a Tejero Hernández, María A b Tejero Mateo, Ignacio b López López, Juana a

a Hospital San Juan de la Cruz (Spain)

b HOSPITAL UNIVERSITARIO REINA SOFÍA (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOMYOPATHY; DISEASE SEVERITY; ENZYME REPLACEMENT; GLYCOGEN STORAGE DISEASE TYPE 2; LETTER;

ALPHA-GLUCOSIDASES; CARDIOMYOPATHIES; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; ENZYME REPLACEMENT THERAPY; FEMALE; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; INFANT; INFANT, NEWBORN; MALE; PROGNOSIS;

EID: 84655162030 PISSN: 03008932 EISSN: 15792242 Source Type: Journal
DOI: 10.1016/j.recesp.2011.03.025 Document Type: Letter

Times cited : (3)

References (6)

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- Van Der Ploeg, A.T.¹ Reuser, A.J.²

2
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- Cardiomyopathy in Pompe's disease
- A. Fayssoil Cardiomyopathy in Pompe's disease Eur J Intern Med 19 2008 57 59
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- Fayssoil, A.¹

3
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- Early treatment with alglucosidase alpha prolongs long-term survival of infants with Pompe disease
- P.S. Kishnani, D. Corzo, N.D. Leslie, D. Gruskin, A. Van der Ploeg, and J.P. Clancy Early treatment with alglucosidase alpha prolongs long-term survival of infants with Pompe disease Pediatr Res 66 2009 329 335
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4
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- Ambulatory electrocardiogram analysis in infants treated with recombinant human acid α-glucosidase enzyme replacement therapy for Pompe disease
- DOI 10.1097/01.gim.0000217786.79173.a8, PII 0012581720060500000006
- A.L. Cook, P.S. Kishnani, M.P. Carboni, R.J. Kanter, Y.T. Chen, and A.K. Ansong Ambulatory electrocardiogram analysis in infants treated with recombinant human acid alpha-glucosidase enzyme replacement therapy for Pompe disease Genet Med 8 2006 313 317 (Pubitemid 44297319)
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- Cook, A.L.¹ Kishnani, P.S.² Carboni, M.P.³ Kanter, R.J.⁴ Chen, Y.T.⁵ Ansong, A.K.⁶ Kravitz, R.M.⁷ Rice, H.⁸ Li, J.S.⁹

5
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- Electrocardiographic response to enzyme replacement therapy for Pompe disease
- DOI 10.1097/01.gim.0000195896.04069.5f, PII 0012581720060500000003
- A.K. Ansong, J.S. Li, E. Nozik-Grayck, R. Ing, R.M. Kravitz, and S.F. Idriss Electrocardiographic response to enzyme replacement therapy for Pompe disease Genet Med 8 2006 297 301 (Pubitemid 44297316)
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- Ansong, A.K.¹ Li, J.S.² Nozik-Grayck, E.³ Ing, R.⁴ Kravitz, R.M.⁵ Idriss, S.F.⁶ Kanter, R.J.⁷ Rice, H.⁸ Chen, Y.T.⁹ Kishnani, P.S.¹⁰

6
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- Cardiac remodeling after enzyme replacement therapy with acid alpha-glucosidase for infants with Pompe disease
- J.C. Levine, P.S. Kishnani, Y.T. Chen, J.R. Herlong, and J.S. Li Cardiac remodeling after enzyme replacement therapy with acid alpha-glucosidase for infants with Pompe disease Pediatr Cardiol 29 2008 1033 1042
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- Levine, J.C.¹ Kishnani, P.S.² Chen, Y.T.³ Herlong, J.R.⁴ Li, J.S.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.