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B Nobili

Showing results (21-30 of 52) with videos related to

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La Pediatria|March 31, 1978
[A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia]L Pinto, B Nobili, A Rossi, 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.
La Pediatria|December 31, 1978
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants]L Pinto, L Esposito, R Vitale, et al.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
La Pediatria|January 1, 1983
[Campylobacter enteritis: an emerging disease]L Pinto, I Alagia, P Imparato, et al.
Blood|September 25, 1999
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosisE M del Giudice, S Perrotta, B Nobili, et al.
La Pediatria|June 1, 1983
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family]B Nobili, A Iolascon, L Bello, et al.
Haematologica|May 1, 1997
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) alleleE Miraglia del Giudice, M Francese, R Polito, et al.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 16, 2002
Inadequate leptin level negatively affects body fat loss during a weight reduction programme for childhood obesitydel Giudice E Miraglia, N Santoro, A Marotta, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
La Pediatria|March 31, 1978
[A case of cutaneous mastocytosis associated with A-G dysgammaglobulinemia]L Pinto, B Nobili, A Rossi, 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.
La Pediatria|December 31, 1978
[Alpha thalassemia in Campania: results of a survey of 319 newborn infants]L Pinto, L Esposito, R Vitale, et al.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
La Pediatria|January 1, 1983
[Campylobacter enteritis: an emerging disease]L Pinto, I Alagia, P Imparato, et al.
Blood|September 25, 1999
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosisE M del Giudice, S Perrotta, B Nobili, et al.
La Pediatria|June 1, 1983
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family]B Nobili, A Iolascon, L Bello, et al.
Haematologica|May 1, 1997
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) alleleE Miraglia del Giudice, M Francese, R Polito, et al.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 16, 2002
Inadequate leptin level negatively affects body fat loss during a weight reduction programme for childhood obesitydel Giudice E Miraglia, N Santoro, A Marotta, et al.
Pageof 6