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Unusual association of glycogen storage disease type I, nesidioblastosis and possible congenital hypopituitarism

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Journal of Inherited Metabolic Disease

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References

  • Baginski, E. S., Foà, P. P. and Zak, B. Glucose-6-phosphatase. In Bergmeyer, H. U. (ed.)Methods of Enzymatic Analysis, Academic Press, New York (1974), pp. 876–890

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  • Ansley-Green, A., Polak, J., Bloom, S., Gough, M., Keeling, J., Ashcroft, S., Turner, R. and Baum, J. Nesidioblastosis of the pancreas: definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia.Arch. Dis. Child. 56 (1981) 496–499

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Authors and Affiliations

  1. Clinica Pediatricá, Universitá di Pavia, IRCCS Policlinico S. Matteo, I-27100, Pavia, Italy

    M. Aricó, E. Bianchi, P. Zaninetti, D. Caselli, A. Colombo & M. C. Gasparoni

  2. Instituto di Anatomia Patologica, Universitá di Pavia, IRCCS Policlinico S. Matteo, I-27100, Pavia, Italy

    F. Sessa & P. Tenti

Authors
  1. M. Aricó
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  2. E. Bianchi
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  3. P. Zaninetti
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  4. D. Caselli
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  5. A. Colombo
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  6. M. C. Gasparoni
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  7. F. Sessa
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  8. P. Tenti
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Aricó, M., Bianchi, E., Zaninetti, P. et al. Unusual association of glycogen storage disease type I, nesidioblastosis and possible congenital hypopituitarism. J Inherit Metab Dis 10, 267–268 (1987). https://doi.org/10.1007/BF01800073

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  • DOI: https://doi.org/10.1007/BF01800073

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