Neutrophil adherence receptor deficiency regressing with granulocyte-colony stimulating factor therapy in a case of glycogen storage disease type Ib

By Latger-Cannard Véronique   Marchand-Arvier Monique   Vidailhet Michel   Donadieu Jean   Vigneron Claude   Bordigoni Pierre  

European Journal of Pediatrics, Vol. 161, Iss. 2, 2002-02 ,pp. : 87-93

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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

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Absence of severe recurrent infections in glycogen storage disease type Ib with neutropenia and neutrophil dysfunction

By D’Eufemia P.   Finocchiaro R.   Celli M.   Zambrano A.   Tetti M.   Ferrucci V.   Lenti L.  

Journal of Inherited Metabolic Disease, Vol. 30, Iss. 1, 2007-02 ,pp. : 105-105

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Allelic heterogeneity of glycogen storage disease type Ib in French patients: A study of 11 cases

By Trioche P.   Petit F.   Francoual J.   Gajdos V.   Capel L.   Poüs C.   Labrune P.  

Journal of Inherited Metabolic Disease, Vol. 27, Iss. 5, 2004-01 ,pp. : 621-623

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Hepatocellular carcinoma in glycogen storage disease type Ia: A case series

By Franco L.   Krishnamurthy V.   Bali D.   Weinstein D.   Arn P.   Clary B.   Boney A.   Sullivan J.   Frush D.   Chen Y.-T.   Kishnani P.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 2, 2005-04 ,pp. : 153-162

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