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M Maghnie

Showing results (21-30 of 89) with videos related to

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Pediatric Dermatology|July 8, 2000
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiencyV 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 realitiesD 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 histiocytosisM Maghnie, G Bossi, C Klersy, et al.
AJNR. American Journal of Neuroradiology|September 1, 1992
MR of the hypothalamic-pituitary axis in Langerhans cell histiocytosisM 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 functionM Maghnie, E Genovese, A Villa, et al.
Acta Paediatrica Scandinavica|May 1, 1991
X-linked agammaglobulinemia and isolated growth hormone deficiencyV 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 therapyM 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 childrenM 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 familiesD Larizza, M Cuccia, M Martinetti, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 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 deficiencyV 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 realitiesD 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 histiocytosisM Maghnie, G Bossi, C Klersy, et al.
AJNR. American Journal of Neuroradiology|September 1, 1992
MR of the hypothalamic-pituitary axis in Langerhans cell histiocytosisM 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 functionM Maghnie, E Genovese, A Villa, et al.
Acta Paediatrica Scandinavica|May 1, 1991
X-linked agammaglobulinemia and isolated growth hormone deficiencyV 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 therapyM 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 childrenM 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 familiesD Larizza, M Cuccia, M Martinetti, et al.
Pageof 9