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11
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma
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Changes of the main isoform of human apolipoprotein A-I following incubation of plasma

Ghisellini, M. ; Pecorari, M. ; Calandra, S.

Atherosclerosis, 1986-03, Vol.59 (3), p.247-256 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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12
Safety and efficacy assessment of plerixafor in patients with multiple myeloma proven or predicted to be poor mobilizers, including assessment of tumor cell mobilization
Safety and efficacy assessment of plerixafor in patients with multiple myeloma proven or predicted to be poor mobilizers, including assessment of tumor cell mobilization
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Safety and efficacy assessment of plerixafor in patients with multiple myeloma proven or predicted to be poor mobilizers, including assessment of tumor cell mobilization

TRICOT, G ; COTTLER-FOX, M. H ; CALANDRA, G

Bone marrow transplantation (Basingstoke), 2010-01, Vol.45 (1), p.63-68 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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13
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations
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Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations

Rabacchi, Claudio, PhD ; Bigazzi, Federico, PhD ; Puntoni, Mariarita, PhD ; Sbrana, Francesco, MD ; Sampietro, Tiziana, MD ; Tarugi, Patrizia, PhD ; Bertolini, Stefano, MD ; Calandra, Sebastiano, MD

Journal of clinical lipidology, 2016-07, Vol.10 (4), p.944-952.e1 [Periódico revisado por pares]

United States: Elsevier Inc

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14
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla )
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla )
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A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla )

Pisciotta, Livia, MD ; Vitali, Cecilia, PhD ; Favari, Elda, PhD ; Fossa, Paola, PhD ; Adorni, Maria Pia, PhD ; Leone, Daniela, PhD ; Artom, Nathan, MD ; Fresa, Raffaele, LabTech ; Calabresi, Laura, PhD ; Calandra, Sebastiano, MD ; Bertolini, Stefano, MD

Journal of clinical lipidology, 2015-11, Vol.9 (6), p.837-846 [Periódico revisado por pares]

United States: Elsevier Inc

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15
Increased Circulating Soluble Cd14 Is Associated With High Mortality In Gram-Negative Septic Shock
Increased Circulating Soluble Cd14 Is Associated With High Mortality In Gram-Negative Septic Shock
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Increased Circulating Soluble Cd14 Is Associated With High Mortality In Gram-Negative Septic Shock

Landmann, Regine ; Zimmerli, Werner ; Sansano, Sebastiano ; Link, Susanne ; Hahn, Alfred ; Glauser, Michel Pierre ; Calandra, Thierry

The Journal of infectious diseases, 1995-03, Vol.171 (3), p.639-644 [Periódico revisado por pares]

Chicago, IL: The University of Chicago Press

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16
A functional microsatellite of the macrophage migration inhibitory factor gene associated with meningococcal disease
A functional microsatellite of the macrophage migration inhibitory factor gene associated with meningococcal disease
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A functional microsatellite of the macrophage migration inhibitory factor gene associated with meningococcal disease

Renner, Pascal ; Roger, Thierry ; Bochud, Pierre‐Yves ; Sprong, Tom ; Sweep, Fred C. G. J. ; Bochud, Murielle ; Faust, Saul N. ; Haralambous, Elene ; Betts, Helen ; Chanson, Anne‐Laure ; Reymond, Marlies Knaup ; Mermel, Elliot ; Erard, Veronique ; Deuren, Marcel ; Read, Robert C. ; Levin, Michael ; Calandra, Thierry

The FASEB journal, 2012-02, Vol.26 (2), p.907-916 [Periódico revisado por pares]

United States

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17
Analysis of LDL Receptor Gene Mutations in Italian Patients With Homozygous Familial Hypercholesterolemia
Analysis of LDL Receptor Gene Mutations in Italian Patients With Homozygous Familial Hypercholesterolemia
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Analysis of LDL Receptor Gene Mutations in Italian Patients With Homozygous Familial Hypercholesterolemia

Bertolini, S ; Cassanelli, S ; Garuti, R ; Ghisellini, M ; Simone, M.L ; Rolleri, M ; Masturzo, P ; Calandra, S

Arteriosclerosis, thrombosis, and vascular biology, 1999-02, Vol.19 (2), p.408-418 [Periódico revisado por pares]

Philadelphia, PA: American Heart Association, Inc

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18
Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)
Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)
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Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)

Bertolini, S ; Simone, Ml ; Pes, Gm ; Ghisellini, M ; Rolleri, M ; Bellocchio, A ; Elicio, N ; Masturzo, P ; Calandra, S

Clinical genetics, 2000-02, Vol.57 (2), p.140-147 [Periódico revisado por pares]

Copenhagen: Munksgaard International Publishers

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19
Four novel mutations of sterol 27-hydroxylase gene in Italian patients with cerebrotendinous xanthomatosis
Four novel mutations of sterol 27-hydroxylase gene in Italian patients with cerebrotendinous xanthomatosis
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Four novel mutations of sterol 27-hydroxylase gene in Italian patients with cerebrotendinous xanthomatosis

Garuti, R ; Croce, M A ; Tiozzo, R ; Dotti, M T ; Federico, A ; Bertolini, S ; Calandra, S

Journal of lipid research, 1997-11, Vol.38 (11), p.2322-2334 [Periódico revisado por pares]

United States: Elsevier

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20
Tryptophan ? niacin pathway in scleroderma and in dermatomyositis
Tryptophan ? niacin pathway in scleroderma and in dermatomyositis
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Tryptophan ? niacin pathway in scleroderma and in dermatomyositis

Binazzi, Maurizio ; Calandra, Paolo

Archiv f r Dermatologische Forschung, 1973-03, Vol.246 (2), p.142-145 [Periódico revisado por pares]

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