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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
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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12
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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13
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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14
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
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A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease

Bertolini, S. ; Pisciotta, L. ; Seri, M. ; Cusano, R. ; Cantafora, A. ; Calabresi, L. ; Franceschini, G. ; Ravazzolo, R. ; Calandra, S.

Atherosclerosis, 2001-02, Vol.154 (3), p.599-605 [Periódico revisado por pares]

Ireland: Elsevier Ireland Ltd

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15
Keratoconus. I: Biochemical studies
Keratoconus. I: Biochemical studies
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Keratoconus. I: Biochemical studies

CRITCHFIELD, J. W ; CALANDRA, A. J ; NESBURN, A. B ; KENNEY, M. C

Experimental eye research, 1988-06, Vol.46 (6), p.953-963 [Periódico revisado por pares]

London: Elsevier

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16
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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17
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia
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A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia

Cassanelli, S. ; Bertolini, S. ; Rolleri, M. ; Stefano, F De ; Casarino, L. ; Elicio, N. ; Naselli, A. ; Calandra, S.

Clinical genetics, 1998-05, Vol.53 (5), p.391-395 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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18
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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19
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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20
Treatment of Gram-Negative Septic Shock with Human IgG Antibody to Escherichia coli J5: A Prospective, Double-Blind, Randomized Trial
Treatment of Gram-Negative Septic Shock with Human IgG Antibody to Escherichia coli J5: A Prospective, Double-Blind, Randomized Trial
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Treatment of Gram-Negative Septic Shock with Human IgG Antibody to Escherichia coli J5: A Prospective, Double-Blind, Randomized Trial

Calandra, Thierry ; Glauser, Michel P. ; Schellekens, Joop ; Verhoef, Jan

The Journal of infectious diseases, 1988-08, Vol.158 (2), p.312-319 [Periódico revisado por pares]

Chicago, IL: The University Chicago Press

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