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Minerva Pediatrica
|
October 31, 1986
[Familial hypercholesterolemia. Study of low-density lipoprotein receptors. Treatment with plasmapheresis]
C Bellini, E Bonioli, G Ruffa, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor
E Bonioli, A DiStefano, A Palmieri, et al.
Lymphology
|
August 12, 2014
Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia
C Bellini, G Villa, G Sambuceti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1986
[Significance of the evaluation of C-peptide in children with type 1 diabetes mellitus]
E Gandullia, E Bonioli, R Monteverde, et al.
American Journal of Medical Genetics
|
December 18, 2001
Persistence of Müllerian derivatives and intestinal lymphangiectasis in two newborn brothers: confirmation of the Urioste syndrome
C Bellini, E Bonioli, N Josso, et al.
Lymphology
|
November 26, 2009
The role of lymphoscintigraphy in the diagnosis of lymphedema in Turner syndrome
C Bellini, E Di Battista, F Boccardo, et al.
American Journal of Medical Genetics
|
November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1
A E Lin, P H Birch, B R Korf, et al.
Lymphology
|
January 25, 2013
Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study
C Bellini, Z Ergaz, M Radicioni, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
Minerva Pediatrica
|
October 31, 1986
[Familial hypercholesterolemia. Study of low-density lipoprotein receptors. Treatment with plasmapheresis]
C Bellini, E Bonioli, G Ruffa, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor
E Bonioli, A DiStefano, A Palmieri, et al.
Lymphology
|
August 12, 2014
Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia
C Bellini, G Villa, G Sambuceti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1986
[Significance of the evaluation of C-peptide in children with type 1 diabetes mellitus]
E Gandullia, E Bonioli, R Monteverde, et al.
American Journal of Medical Genetics
|
December 18, 2001
Persistence of Müllerian derivatives and intestinal lymphangiectasis in two newborn brothers: confirmation of the Urioste syndrome
C Bellini, E Bonioli, N Josso, et al.
Lymphology
|
November 26, 2009
The role of lymphoscintigraphy in the diagnosis of lymphedema in Turner syndrome
C Bellini, E Di Battista, F Boccardo, et al.
American Journal of Medical Genetics
|
November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1
A E Lin, P H Birch, B R Korf, et al.
Lymphology
|
January 25, 2013
Congenital fetal and neonatal visceral chylous effusions: neonatal chylothorax and chylous ascites revisited. A multicenter retrospective study
C Bellini, Z Ergaz, M Radicioni, et al.
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of 9