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Journal of Endocrinological Investigation
|
November 13, 2007
Novel nonsense mutation (W22X) in CYP21A2 gene causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl
L Di Pasquale, S Indovina, M Wasniewska, et al.
Clinical Nephrology
|
January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loading
L de Sanctis, G Bonetti, M Bruno, et al.
Hormone Research
|
July 15, 2000
Long-term results with growth hormone therapy in idiopathic hypopituitarism
S Bernasconi, T Arrigo, M Wasniewsk, et al.
Pathologica
|
August 16, 2011
Melanoma of the nipple. An additional case
V Mourmouras, M R Ambrosio, M Onorati, et al.
European Journal of Pediatrics
|
July 1, 1982
Thyroid function in children with cystic fibrosis
F De Luca, F Trimarchi, C Sferlazzas, et al.
European Journal of Pediatrics
|
July 1, 1990
Transient electrocardiographic changes suggesting myocardial ischaemia in newborn infants following tocolysis with beta-sympathomimetics
M Gemelli, F De Luca, R Manganaro, et al.
Archives of Biochemistry and Biophysics
|
October 1, 1982
25-hydroxy-26, 26,26,27,27,27-hexafluorovitamin D3: biological activity in the rat
Y Tanaka, D N Pahuja, J K Wichmann, et al.
European Journal of Endocrinology
|
June 1, 1996
Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis
D Cucinotta, T Arrigo, F De Luca, et al.
Journal of the Neurological Sciences
|
October 25, 2016
Corpus callosum microstructural changes associated with Kawashima Nintendo Brain Training in patients with multiple sclerosis
L De Giglio, N Upadhyay, F De Luca, et al.
Journal of Endocrinological Investigation
|
March 24, 2006
Testicular microlithiasis heralding mixed germ cell tumor of the testis in a boy
T Arrigo, M F Messina, M Valenzise, et al.
Page
of 35
Search research articles
Search
Showing results (251-260 of 350) with videos related to
Sort By:
Page
of 35
Journal of Endocrinological Investigation
|
November 13, 2007
Novel nonsense mutation (W22X) in CYP21A2 gene causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl
L Di Pasquale, S Indovina, M Wasniewska, et al.
Clinical Nephrology
|
January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loading
L de Sanctis, G Bonetti, M Bruno, et al.
Hormone Research
|
July 15, 2000
Long-term results with growth hormone therapy in idiopathic hypopituitarism
S Bernasconi, T Arrigo, M Wasniewsk, et al.
Pathologica
|
August 16, 2011
Melanoma of the nipple. An additional case
V Mourmouras, M R Ambrosio, M Onorati, et al.
European Journal of Pediatrics
|
July 1, 1982
Thyroid function in children with cystic fibrosis
F De Luca, F Trimarchi, C Sferlazzas, et al.
European Journal of Pediatrics
|
July 1, 1990
Transient electrocardiographic changes suggesting myocardial ischaemia in newborn infants following tocolysis with beta-sympathomimetics
M Gemelli, F De Luca, R Manganaro, et al.
Archives of Biochemistry and Biophysics
|
October 1, 1982
25-hydroxy-26, 26,26,27,27,27-hexafluorovitamin D3: biological activity in the rat
Y Tanaka, D N Pahuja, J K Wichmann, et al.
European Journal of Endocrinology
|
June 1, 1996
Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis
D Cucinotta, T Arrigo, F De Luca, et al.
Journal of the Neurological Sciences
|
October 25, 2016
Corpus callosum microstructural changes associated with Kawashima Nintendo Brain Training in patients with multiple sclerosis
L De Giglio, N Upadhyay, F De Luca, et al.
Journal of Endocrinological Investigation
|
March 24, 2006
Testicular microlithiasis heralding mixed germ cell tumor of the testis in a boy
T Arrigo, M F Messina, M Valenzise, et al.
Page
of 35