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E Miraglia

Showing results (1-10 of 101) with videos related to

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La Clinica Terapeutica|July 20, 2022
Juvenile xanthogranuloma in neurofibromatosis type 1. Prevalence and possible correlation with lymphoproliferative diseases: experience of a single center and review of the literatureE Miraglia, A Laghi, A Moramarco, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|September 4, 2018
Spot-beam effect in grazing atom-surface collisions: from quantum to classicalL Frisco, J E Miraglia, M S Gravielle
Haematologica|January 1, 1992
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosisA Iolascon, E Miraglia del Giudice, C Camaschella
La Clinica Terapeutica|December 20, 2014
Multiple painful papulo-nodular lesions: clinical pitfallC Cantisani, E Miraglia, S Giustini, et al.
Haematologica|May 21, 1998
Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infantE Miraglia del Giudice, S Perrotta, C Lombardi, et al.
La Clinica Terapeutica|February 22, 2019
A characteristic type of retinal microvascular abnormalities in a patient with Neurofibromatosis type 1A Moramarco, A Lambiase, F Mallone, et al.
Minerva Medica|September 29, 1979
[Incidence of cryoglobulinemia in a series of cases of chronic liver diseases]G Ruggiero, F Spadacenta, M Gargiulo, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 10, 2016
Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasiaA Rossi, E Miraglia, M C Fortuna, et al.
British Journal of Haematology|September 1, 1994
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosisE Miraglia del Giudice, A Iolascon, L Pinto, et al.
Dermatology Online Journal|August 23, 2014
Basal cell carcinomas in a young woman with Steinert's diseaseE Miraglia, C Cantisani, S Giustini, et al.
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
La Clinica Terapeutica|July 20, 2022
Juvenile xanthogranuloma in neurofibromatosis type 1. Prevalence and possible correlation with lymphoproliferative diseases: experience of a single center and review of the literatureE Miraglia, A Laghi, A Moramarco, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|September 4, 2018
Spot-beam effect in grazing atom-surface collisions: from quantum to classicalL Frisco, J E Miraglia, M S Gravielle
Haematologica|January 1, 1992
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosisA Iolascon, E Miraglia del Giudice, C Camaschella
La Clinica Terapeutica|December 20, 2014
Multiple painful papulo-nodular lesions: clinical pitfallC Cantisani, E Miraglia, S Giustini, et al.
Haematologica|May 21, 1998
Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infantE Miraglia del Giudice, S Perrotta, C Lombardi, et al.
La Clinica Terapeutica|February 22, 2019
A characteristic type of retinal microvascular abnormalities in a patient with Neurofibromatosis type 1A Moramarco, A Lambiase, F Mallone, et al.
Minerva Medica|September 29, 1979
[Incidence of cryoglobulinemia in a series of cases of chronic liver diseases]G Ruggiero, F Spadacenta, M Gargiulo, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 10, 2016
Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasiaA Rossi, E Miraglia, M C Fortuna, et al.
British Journal of Haematology|September 1, 1994
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosisE Miraglia del Giudice, A Iolascon, L Pinto, et al.
Dermatology Online Journal|August 23, 2014
Basal cell carcinomas in a young woman with Steinert's diseaseE Miraglia, C Cantisani, S Giustini, et al.
Pageof 11