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Showing results (21-30 of 89) with videos related to
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Pediatric Dermatology
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July 8, 2000
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency
V Monafo, G L Marseglia, M Maghnie, et al.
Hormone Research
|
January 1, 1991
Hypopituitarism and stalk agenesis: a congenital syndrome worsened by breech delivery?
M Maghnie, D Larizza, F Triulzi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
January 11, 2001
Endoscopic approaches to the cranial base: perspectives and realities
D Locatelli, P Castelnuovo, L Santi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 1998
Dynamic endocrine testing and magnetic resonance imaging in the long-term follow-up of childhood langerhans cell histiocytosis
M Maghnie, G Bossi, C Klersy, et al.
AJNR. American Journal of Neuroradiology
|
September 1, 1992
MR of the hypothalamic-pituitary axis in Langerhans cell histiocytosis
M Maghnie, M Aricò, A Villa, et al.
Clinical Endocrinology
|
September 1, 1996
Dynamic MRI in the congenital agenesis of the neural pituitary stalk syndrome: the role of the vascular pituitary stalk in predicting residual anterior pituitary function
M Maghnie, E Genovese, A Villa, et al.
Acta Paediatrica Scandinavica
|
May 1, 1991
X-linked agammaglobulinemia and isolated growth hormone deficiency
V Monafo, M Maghnie, L Terracciano, et al.
European Journal of Pediatrics
|
June 1, 1995
Organ- and non-organ-specific auto-antibodies in children with hypopituitarism on growth hormone therapy
M Maghnie, R Lorini, L Vitali, et al.
European Journal of Pediatrics
|
February 1, 1991
Effects of short-term administration of human chorionic gonadotropin on immune functions in cryptorchid children
M Maghnie, A Valtorta, A Moretta, et al.
Clinical Endocrinology
|
January 1, 1994
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families
D Larizza, M Cuccia, M Martinetti, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 89) with videos related to
Sort By:
Page
of 9
Pediatric Dermatology
|
July 8, 2000
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency
V Monafo, G L Marseglia, M Maghnie, et al.
Hormone Research
|
January 1, 1991
Hypopituitarism and stalk agenesis: a congenital syndrome worsened by breech delivery?
M Maghnie, D Larizza, F Triulzi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
January 11, 2001
Endoscopic approaches to the cranial base: perspectives and realities
D Locatelli, P Castelnuovo, L Santi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 1998
Dynamic endocrine testing and magnetic resonance imaging in the long-term follow-up of childhood langerhans cell histiocytosis
M Maghnie, G Bossi, C Klersy, et al.
AJNR. American Journal of Neuroradiology
|
September 1, 1992
MR of the hypothalamic-pituitary axis in Langerhans cell histiocytosis
M Maghnie, M Aricò, A Villa, et al.
Clinical Endocrinology
|
September 1, 1996
Dynamic MRI in the congenital agenesis of the neural pituitary stalk syndrome: the role of the vascular pituitary stalk in predicting residual anterior pituitary function
M Maghnie, E Genovese, A Villa, et al.
Acta Paediatrica Scandinavica
|
May 1, 1991
X-linked agammaglobulinemia and isolated growth hormone deficiency
V Monafo, M Maghnie, L Terracciano, et al.
European Journal of Pediatrics
|
June 1, 1995
Organ- and non-organ-specific auto-antibodies in children with hypopituitarism on growth hormone therapy
M Maghnie, R Lorini, L Vitali, et al.
European Journal of Pediatrics
|
February 1, 1991
Effects of short-term administration of human chorionic gonadotropin on immune functions in cryptorchid children
M Maghnie, A Valtorta, A Moretta, et al.
Clinical Endocrinology
|
January 1, 1994
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families
D Larizza, M Cuccia, M Martinetti, et al.
Page
of 9