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Enzyme replacement treatment in type 1 and type 3 Gaucher's disease
The development of intravenous enzyme-replacement treatment for Gaucher's disease has changed life expectancy in cases without neurological involvement (type 1). The effects in patients with… Expand
GENERALIZED FAMILIAL BRONCHOMALACIA
ABSTRACT. Agosti, E., De Filippi, G., Fior, R. and Chiussi, F. (Paediatric Clinic, University of Trieste, Departments of Radiology and Otorhinolaryngology, Istituto per I'Infanzia and Department of… Expand
Successful therapy of Niemann-Pick disease by implantation of human amniotic membrane.
- B. Scaggiante, A. Pineschi, M. Sustersich, M. Andolina, E. Agosti, D. Romeo
- 1 July 1987
In a patient with a lysosomal storage disorder, not involving the CNS, repeated implantations of human amniotic sheets have proved to provide a successful approach to enzyme replacement therapy.… Expand
1448C mutation linked to the Pv1.1- genotype in Italian patients with Gaucher disease.
Gaucher disease is the most common of the glycolipid storage diseases and is caused by an inherited deficiency of the enzyme glucocerebrosidase. It is a very heterogeneous disease and presents early… Expand
Myelopoiesis induction on human bone marrow precursor cells by a calf thymic derivative (thymomodulin): in vitro comparison with exogenous CSF
Electronic and dynamical effects from the unusual features of the Raman spectra of oligo and polythiophenes
Abstract A comprehensive search for structure/property correlations in the Raman spectra of oligo and polythiophenes is carried out for many homologous series of oligothiophenes (approximately 50… Expand
Aminohydroxypropylidene‐biphosphonate in the treatment of bone lesions in a case of Gaucher's disease type 3
- B. Bembi, E. Agosti, P. Boehm, G. Nassimbeni, M. Zanatta, L. Vidoni
- Acta paediatrica
- 1 January 1994
Bembi B, Agosti E, Boehm P, Nassimbeni G, Zanatta M, Vidoni L. Aminohydroxypropylidene‐biphosphonate in the treatment of bone lesions in a case of Gaucher's disease type 3. Acta Pædiatr… Expand
Treatment of sphingomyelinase deficiency by repeated implantations of amniotic epithelial cells.
- B. Bembi, M. Comelli, +7 authors D. Romeo
- American journal of medical genetics
- 1 November 1992
Five young patients with Niemann-Pick disease type B were treated with repeated implantations of amniotic epithelial cells, as a source of exogenous sphingomyelinase. This treatment abolished the… Expand
Repeated Implantations of Human Amniotic Epithelial Cells as a Curative Therapy of Niemann-Pick Disease
By a popular tradition, a baby delivered when still wrapped in the amniotic sac is destined for great luck throughout his or her life: people say that he or she was born with a caul. Besides its… Expand
[Mental patients in general practice. A diagnostic, sociological, and therapeutic study].