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M DiRocco

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European Journal of Pediatrics|March 1, 1992
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancyP Picco, L Garibaldi, M Cotellessa, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type IaM Stroppiano, S Regis, M DiRocco, et al.
Neuropediatrics|November 7, 2007
Neuroimaging findings in malignant infantile osteopetrosis due to OSTM1 mutationsD Castellano Chiodo, M DiRocco, C Gandolfo, et al.
Human Reproduction (Oxford, England)|December 4, 2003
Testicular sperm extraction in azoospermic men submitted to bilateral orchidopexyL Negri, E Albani, M DiRocco, 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.
Neuropediatrics|May 7, 2010
Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe diseaseG Morana, R Biancheri, M Dirocco, et al.
The ISME Journal|October 17, 2015
Ectomycorrhizal fungal spore bank recovery after a severe forest fire: some like it hotSydney I Glassman, Carrie R Levine, Angela M DiRocco, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Journal of Inherited Metabolic Disease|January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromesA Spinazzola, F Invernizzi, F Carrara, et al.
Molecular Genetics and Metabolism|February 7, 2009
A randomized trial comparing the efficacy and safety of imiglucerase (Cerezyme) infusions every 4 weeks versus every 2 weeks in the maintenance therapy of adult patients with Gaucher disease type 1P S Kishnani, M DiRocco, P Kaplan, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Pediatrics|March 1, 1992
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancyP Picco, L Garibaldi, M Cotellessa, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type IaM Stroppiano, S Regis, M DiRocco, et al.
Neuropediatrics|November 7, 2007
Neuroimaging findings in malignant infantile osteopetrosis due to OSTM1 mutationsD Castellano Chiodo, M DiRocco, C Gandolfo, et al.
Human Reproduction (Oxford, England)|December 4, 2003
Testicular sperm extraction in azoospermic men submitted to bilateral orchidopexyL Negri, E Albani, M DiRocco, 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.
Neuropediatrics|May 7, 2010
Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe diseaseG Morana, R Biancheri, M Dirocco, et al.
The ISME Journal|October 17, 2015
Ectomycorrhizal fungal spore bank recovery after a severe forest fire: some like it hotSydney I Glassman, Carrie R Levine, Angela M DiRocco, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Journal of Inherited Metabolic Disease|January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromesA Spinazzola, F Invernizzi, F Carrara, et al.
Molecular Genetics and Metabolism|February 7, 2009
A randomized trial comparing the efficacy and safety of imiglucerase (Cerezyme) infusions every 4 weeks versus every 2 weeks in the maintenance therapy of adult patients with Gaucher disease type 1P S Kishnani, M DiRocco, P Kaplan, et al.
Pageof 2