引用次数
引用: 3,368
H-指数: 32
I10-指数 : 56
出版物: 195
Diet in the treatment of familial combined hyperlipidemia in children
P Giachino , L Occhiuto , E Rutto , O. Guardamagna
NMCD. NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES 305 -305
2003
Impaired lipid transport due to heterozygous hypobetalipoproteinemia.
E Bugianesi , C Allora , O. Guardamagna , R Bonardi
Journal of Inherited Metabolic Disease 161 -161
2002
Cholesteryl ester storage disese: experiences in pediatrics
A De Giorgi , I. Rabbone , P. Assandro , O. Guardamagna
GIORNALE ITALIANO DELL'ARTERIOSCLEROSI 3 47 -47
2011
Isolated Hyperlipoprotein(a) in children with familial cardiovascular events.
P. Assandro , O. Guardamagna , F. Abello
GIORNALE ITALIANO DELL'ARTERIOSCLEROSI 3 46 -46
2011
Selective Screening of genetic dyslipidemias in italian children.
G Mercadante , C Bondone , C Allora , O. Guardamagna
NMCD. NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES 77 -77
2004
Selective screening of genetic dislipemias in Italian children.
I Rabbone , C Allora , O. Guardamagna , G Mercadante
Atherosclerosis Supplements 77 -77
2002
Effects of lycopene supplementation on oxidative stess in children affected by primary dyslipidemia.
P. Cagliero , F. Abello , P. Assandro , C. Cena
GIORNALE ITALIANO DELL'ARTERIOSCLEROSI 3 46 -46
2011
Familial hypobetalipoproteinemia and liver steatosis.
E Bugianesi , O. Guardamagna , R Bonardi , Molini
Gut
2002
Familial Hypobetalipoproteinemia and liver steatosis.
C Allora , O. Guardamagna , Molini , I Rabbone
Digestive and Liver Disease
2003
Carotid artery intima-media thickness in children with primary dyslipidemia
B. Frigerio , D. Baldassarre , P. Cagliero , O. Guardamagna
GIORNALE ITALIANO DELL'ARTERIOSCLEROSI 5 ( 4) 74 -75
2014
Monitoring Treatment in Tetrahydrobiopterin Deficiency
M. Spada , T. Parrella , R. Ponzone , S. Ferraris
Pteridines 3 13 -15
7
1991
Prenatal Diagnosis of Dihydropteridine Reductase Deficiency in a Twin Pregnancy
O. Guardamagna , M. Spada , A. Ponzone , E. Viora
Pteridines 3 19 -21
1
1991
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype.
A. Ponzone , N. Blau , O. Guardamagna , G. B. Ferrero
Journal of Inherited Metabolic Disease 13 ( 3) 298 -300
18
1990
Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant protein.
R. G. H. Cotton , I. Jennings , G. Bracco , A. Ponzone
Journal of Inherited Metabolic Disease 9 ( 3) 239 -243
19
1986
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests
M. Spada , O. Guardamagna , D. Rabier , S.B. van der Meer
The Journal of Pediatrics 125 ( 2) 249 -251
21
1994
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuria
A. Niederwieser , H. Shintaku , Th. Hasler , H. Ch. Curtius
European Journal of Pediatrics 145 ( 3) 176 -178
33
1986
Genetic heterogeneity of patients with severe hypertriglyceridemia
C. Giacobbe , M.D. Di Taranto , M. Malamisura , R. Auricchio
Nutrition Metabolism and Cardiovascular Diseases 27 ( 1)
2017
Primary hyperlipidemias in children: effect of plant sterol supplementation on plasma lipids and markers of cholesterol synthesis and absorption
O. Guardamagna , F. Abello , V. Baracco , G. Federici
Acta Diabetologica 48 ( 2) 127 -133
67
2011
WO15-OR-4 A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL
T. Fasano , A.B. Cefalu' , E. Di Leo , D. Noto
Atherosclerosis Supplements 8 ( 1) 15 -16
2007
Prenatal Diagnosis of Atypical Phenylketonuria
N. Blau , A. Niederwieser , H. Ch. Curtius , L. Kierat
Journal of Inherited Metabolic Disease 12 ( 2) 295 -298
7
1989