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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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

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Isolated elevated serum transaminases leading to the diagnosis of asymptomatic Pompe disease

By Hoeksma Marieke   Boon Maartje   Niezen-Koning Klary   Overbeek-van Gils Lidy   Spronsen Francjan  

European Journal of Pediatrics, Vol. 166, Iss. 8, 2007-08 ,pp. : 871-874

Springer Publishing Company

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New GAA mutations in japanese patients with GSDII (pompe disease)

By Pipo J.R.   Feng J.-H.   Yamamoto T.   Ohsaki Y.   Nanba E.   Tsujino S.   Sakuragawa N.   Martiniuk F.   Ninomiya H.   Oka A.   Ohno K.  

Pediatric Neurology, Vol. 29, Iss. 4, 2003-10 ,pp. : 284-287

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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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