Hearing loss in Pompe disease revisited: results from a study of 24 children

By Capelle Carine   Goedegebure Andre   Homans Nienke   Hoeve Hans   Reuser Arnold   Ploeg Ans  

Journal of Inherited Metabolic Disease, Vol. 33, Iss. 5, 2010-10 ,pp. : 597-602

Springer Publishing Company

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Cardiac Remodeling After Enzyme Replacement Therapy with Acid α-Glucosidase for Infants with Pompe Disease

By Levine Jami   Kishnani Priya   Chen Y.   Herlong J.   Li Jennifer  

Pediatric Cardiology, Vol. 29, Iss. 6, 2008-11 ,pp. : 1033-1042

Springer Publishing Company

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Development of a disease-specific disability instrument for Pompe disease

By Haley Stephen M.   Fragala Maria A.   Aseltine Robert   Ni Pengsheng   Skrinar Alison M.  

Pediatric Rehabilitation, Vol. 6, Iss. 2, 2003-01 ,pp. : 77-84

Informa Healthcare

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Fractures in children with Pompe disease: a potentiallong-term complication

By Case Laura   Hanna Rabi   Frush Donald   Krishnamurthy Vidya   DeArmey Stephanie   Mackey Joanne   Boney Anne   Morgan Claire   Corzo Deyanira   Bouchard Susan   Weber Thomas   Chen Yuan-Tsong   Kishnani Priya  

Pediatric Radiology, Vol. 37, Iss. 5, 2007-05 ,pp. : 437-445

Springer Publishing Company

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A new fluorimetric enzyme assay for the diagnosis of Niemann–Pick A/B, with specificity of natural sphingomyelinase substrate

By Diggelen O.   Voznyi Ya.   Keulemans J.   Schoonderwoerd K.   Ledvinova J.   Mengel E.   Zschiesche M.   Santer R.   Harzer K.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 5, 2005-09 ,pp. : 733-741

Springer Publishing Company

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