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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 spherocytosis
E 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 spherocytosis
S 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 spherocytosis
E 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) allele
E 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 phenotype
E 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 obesity
del Giudice E Miraglia, N Santoro, A Marotta, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 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 spherocytosis
E 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 spherocytosis
S 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 spherocytosis
E 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) allele
E 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 phenotype
E 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 obesity
del Giudice E Miraglia, N Santoro, A Marotta, et al.
Page
of 6