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A Corrias

Showing results (61-70 of 76) with videos related to

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Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
Journal of Medical Genetics|February 1, 1989
Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysisA Figus, R Lampis, M Devoto, et al.
Journal of Endocrinological Investigation|May 9, 2000
GH/IGF-I axis in Prader-Willi syndrome: evaluation of IGF-I levels and of the somatotroph responsiveness to various provocative stimuli. Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and DiabetologyA Corrias, J Bellone, L Beccaria, et al.
Diabetes|March 15, 2001
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseasesS DeFranco, S Bonissoni, F Cerutti, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
European Journal of Pediatrics|April 15, 2003
Hypogonadism and pubertal development in Prader-Willi syndromeA Crinò, R Schiaffini, P Ciampalini, et al.
Journal of Endocrinological Investigation|February 5, 2004
TSH receptor and Gs(alpha) genetic analysis in children with Down's syndrome and subclinical hypothyroidismM Tonacchera, A Perri, G De Marco, et al.
Clinical and Experimental Immunology|August 22, 2003
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseasesG Bona, S Defranco, A Chiocchetti, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, 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.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
Journal of Medical Genetics|February 1, 1989
Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysisA Figus, R Lampis, M Devoto, et al.
Journal of Endocrinological Investigation|May 9, 2000
GH/IGF-I axis in Prader-Willi syndrome: evaluation of IGF-I levels and of the somatotroph responsiveness to various provocative stimuli. Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and DiabetologyA Corrias, J Bellone, L Beccaria, et al.
Diabetes|March 15, 2001
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseasesS DeFranco, S Bonissoni, F Cerutti, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
European Journal of Pediatrics|April 15, 2003
Hypogonadism and pubertal development in Prader-Willi syndromeA Crinò, R Schiaffini, P Ciampalini, et al.
Journal of Endocrinological Investigation|February 5, 2004
TSH receptor and Gs(alpha) genetic analysis in children with Down's syndrome and subclinical hypothyroidismM Tonacchera, A Perri, G De Marco, et al.
Clinical and Experimental Immunology|August 22, 2003
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseasesG Bona, S Defranco, A Chiocchetti, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, 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.
Pageof 8