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L Gargantini

Showing results (41-50 of 52) with videos related to

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British Journal of Haematology|February 14, 2002
A sequence of immuno-chemotherapy with Rituximab, mobilization of in vivo purged stem cells, high-dose chemotherapy and autotransplant is an effective and non-toxic treatment for advanced follicular and mantle cell lymphomaM Lazzarino, L Arcaini, P Bernasconi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2000
Etiology and age incidence of precocious puberty in girls: a multicentric studyM Cisternino, T Arrigo, A M Pasquino, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 11, 2012
Metabolic syndrome in adult patients with Prader-Willi syndromeG Grugni, A Crinò, G Bedogni, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2000
Etiology of central precocious puberty in males: the results of the Italian Study Group for Physiopathology of PubertyV De Sanctis, A Corrias, V Rizzo, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|January 22, 2010
Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesityP Brambilla, A Crinò, G Bedogni, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 18, 2008
Immunochemotherapy with in vivo purging and autotransplant induces long clinical and molecular remission in advanced relapsed and refractory follicular lymphomaL Arcaini, F Montanari, E P Alessandrino, et al.
Diabetologia|May 6, 2011
Permanent diabetes during the first year of life: multiple gene screening in 54 patientsL Russo, D Iafusco, S Brescianini, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|February 14, 2002
A sequence of immuno-chemotherapy with Rituximab, mobilization of in vivo purged stem cells, high-dose chemotherapy and autotransplant is an effective and non-toxic treatment for advanced follicular and mantle cell lymphomaM Lazzarino, L Arcaini, P Bernasconi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2000
Etiology and age incidence of precocious puberty in girls: a multicentric studyM Cisternino, T Arrigo, A M Pasquino, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 11, 2012
Metabolic syndrome in adult patients with Prader-Willi syndromeG Grugni, A Crinò, G Bedogni, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2000
Etiology of central precocious puberty in males: the results of the Italian Study Group for Physiopathology of PubertyV De Sanctis, A Corrias, V Rizzo, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|January 22, 2010
Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesityP Brambilla, A Crinò, G Bedogni, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 18, 2008
Immunochemotherapy with in vivo purging and autotransplant induces long clinical and molecular remission in advanced relapsed and refractory follicular lymphomaL Arcaini, F Montanari, E P Alessandrino, et al.
Diabetologia|May 6, 2011
Permanent diabetes during the first year of life: multiple gene screening in 54 patientsL Russo, D Iafusco, S Brescianini, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
Pageof 6