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Journal of Endocrinological Investigation
|
January 30, 2014
Subclinical hyperthyroidism when presenting as initial manifestation of juvenile Hashimoto's thyroiditis: first report on its natural history
T Aversa, M Valenzise, A Corrias, et al.
Journal of Endocrinological Investigation
|
May 10, 2006
Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development
T Arrigo, M Wasniewska, F De Luca, et al.
Journal of Endocrinological Investigation
|
February 6, 2014
Phenotypical and genotypical expression of Wolfram syndrome in 12 patients from a Sicilian district where this syndrome might not be so infrequent as generally expected
F Lombardo, G Salzano, C Di Bella, et al.
Hormone Research
|
December 7, 2007
Novel SHOX gene mutation in a short boy with Becker muscular dystrophy: double trouble in two adjacent genes
M F Messina, M Aguennouz, T Arrigo, et al.
Journal of Endocrinological Investigation
|
May 29, 2009
Novel mutation of CYP21A2 gene (N387K) affecting a non-conserved amino acid residue in exon 9
M Wasniewska, S Mirabelli, L Baldazzi, et al.
Journal of Endocrinological Investigation
|
July 12, 2002
Three-year prospective evaluation of glucose tolerance, beta-cell function and peripheral insulin sensitivity in non-diabetic patients with thalassemia major
M F Messina, F Lombardo, A Meo, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 10, 2015
Evans Syndrome: A case report
F Porcaro, M Valenzise, G Candela, et al.
Journal of Endocrinological Investigation
|
July 4, 2024
Association between osteocalcin and residual β-cell function in children and adolescents newly diagnosed with type 1 diabetes: a pivotal study
M Valenzise, B Bombaci, F Lombardo, et al.
Journal of Endocrinological Investigation
|
February 26, 2008
Subclinical hypothyroidism: the state of the art
T Arrigo, M Wasniewska, G Crisafulli, et al.
Journal of Endocrinological Investigation
|
February 24, 2007
TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism
L Santarpia, M Valenzise, G Di Pasquale, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
Journal of Endocrinological Investigation
|
January 30, 2014
Subclinical hyperthyroidism when presenting as initial manifestation of juvenile Hashimoto's thyroiditis: first report on its natural history
T Aversa, M Valenzise, A Corrias, et al.
Journal of Endocrinological Investigation
|
May 10, 2006
Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development
T Arrigo, M Wasniewska, F De Luca, et al.
Journal of Endocrinological Investigation
|
February 6, 2014
Phenotypical and genotypical expression of Wolfram syndrome in 12 patients from a Sicilian district where this syndrome might not be so infrequent as generally expected
F Lombardo, G Salzano, C Di Bella, et al.
Hormone Research
|
December 7, 2007
Novel SHOX gene mutation in a short boy with Becker muscular dystrophy: double trouble in two adjacent genes
M F Messina, M Aguennouz, T Arrigo, et al.
Journal of Endocrinological Investigation
|
May 29, 2009
Novel mutation of CYP21A2 gene (N387K) affecting a non-conserved amino acid residue in exon 9
M Wasniewska, S Mirabelli, L Baldazzi, et al.
Journal of Endocrinological Investigation
|
July 12, 2002
Three-year prospective evaluation of glucose tolerance, beta-cell function and peripheral insulin sensitivity in non-diabetic patients with thalassemia major
M F Messina, F Lombardo, A Meo, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 10, 2015
Evans Syndrome: A case report
F Porcaro, M Valenzise, G Candela, et al.
Journal of Endocrinological Investigation
|
July 4, 2024
Association between osteocalcin and residual β-cell function in children and adolescents newly diagnosed with type 1 diabetes: a pivotal study
M Valenzise, B Bombaci, F Lombardo, et al.
Journal of Endocrinological Investigation
|
February 26, 2008
Subclinical hypothyroidism: the state of the art
T Arrigo, M Wasniewska, G Crisafulli, et al.
Journal of Endocrinological Investigation
|
February 24, 2007
TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism
L Santarpia, M Valenzise, G Di Pasquale, et al.
Page
of 5