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C Borrone

Showing results (51-60 of 89) with videos related to

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Journal of Medical Genetics|May 23, 1998
Spectrum of clinical features associated with interstitial chromosome 22q11 deletionsM Di Rocco, A Buocompagni, P Picco, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 1, 1993
Insulin like growth factor I (IGF1) in children with neural tube closure defects: a preliminary reportL Leveratto, P Picco, A Cama, et al.
Clinical and Experimental Rheumatology|May 1, 1996
Autoimmune thyroiditis developing into systemic lupus erythematosus in a 15-year-old girlP Picco, M Gattorno, A Buoncompagni, et al.
Human Genetics|October 1, 1979
Detection of carriers and prenatal diagnosis for fucosidosis in CalabriaP Durand, R Gatti, C Borrone, et al.
Clinical and Experimental Rheumatology|May 1, 1997
Erythema multiforme-like manifestations and arthritis in a 3-year-old child with leukocytoclastic vasculitisM Gattorno, P Picco, C Gambini, et al.
Quality Assurance in Health Care : the Official Journal of the International Society for Quality Assurance in Health Care|January 1, 1991
Discharge report accuracyU Rosati, L Minicucci, E Battistini, et al.
European Journal of Pediatrics|May 1, 1993
Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intoleranceM DiRocco, G Garibotto, G A Rossi, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Sjögren-Larsson syndrome: nuclear magnetic resonance imaging of the brain in a 4-year-old boyM Di Rocco, M Filocamo, P Tortori-Donati, et al.
Helvetica Paediatrica Acta|November 1, 1977
Sialidosis (mucolipidosis I)P Durand, R Gatti, S Cavalieri, et al.
Human Molecular Genetics|October 1, 1994
9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 geneC Carbonara, L Longa, E Grosso, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|May 23, 1998
Spectrum of clinical features associated with interstitial chromosome 22q11 deletionsM Di Rocco, A Buocompagni, P Picco, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 1, 1993
Insulin like growth factor I (IGF1) in children with neural tube closure defects: a preliminary reportL Leveratto, P Picco, A Cama, et al.
Clinical and Experimental Rheumatology|May 1, 1996
Autoimmune thyroiditis developing into systemic lupus erythematosus in a 15-year-old girlP Picco, M Gattorno, A Buoncompagni, et al.
Human Genetics|October 1, 1979
Detection of carriers and prenatal diagnosis for fucosidosis in CalabriaP Durand, R Gatti, C Borrone, et al.
Clinical and Experimental Rheumatology|May 1, 1997
Erythema multiforme-like manifestations and arthritis in a 3-year-old child with leukocytoclastic vasculitisM Gattorno, P Picco, C Gambini, et al.
Quality Assurance in Health Care : the Official Journal of the International Society for Quality Assurance in Health Care|January 1, 1991
Discharge report accuracyU Rosati, L Minicucci, E Battistini, et al.
European Journal of Pediatrics|May 1, 1993
Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intoleranceM DiRocco, G Garibotto, G A Rossi, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Sjögren-Larsson syndrome: nuclear magnetic resonance imaging of the brain in a 4-year-old boyM Di Rocco, M Filocamo, P Tortori-Donati, et al.
Helvetica Paediatrica Acta|November 1, 1977
Sialidosis (mucolipidosis I)P Durand, R Gatti, S Cavalieri, et al.
Human Molecular Genetics|October 1, 1994
9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 geneC Carbonara, L Longa, E Grosso, et al.
Pageof 9