Two new mutations in the 3′ coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patient

By Parvari R.   Shen J.   Hershkovitz E.   Chen Y.T.   Moses S.W.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 2, 1998-04 ,pp. : 141-148

Springer Publishing Company

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Dietary dilemmas in the management of glycogen storage disease type I

By Bhattacharya Kaustuv  

Journal of Inherited Metabolic Disease, Vol. 34, Iss. 3, 2011-06 ,pp. : 621-629

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In search of proof-of-concept: gene therapy for glycogen storage disease type Ia

By Koeberl Dwight  

Journal of Inherited Metabolic Disease, Vol. 35, Iss. 4, 2012-07 ,pp. : 671-678

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Increased resting energy expenditure in glycogen storage disease type Ia

By Feillet F.   Bodamer O.A.F.   Leonard J.V.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 1, 1998-01 ,pp. : 80-81

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Clinical evaluation of a portable lactate meter in type I glycogen storage disease

By Saunders A.   Feldman H.   Correia C.   Weinstein D.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 5, 2005-09 ,pp. : 695-701

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