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M Paradisi

Showing results (41-50 of 48) with videos related to

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Pathologica|September 1, 1993
[Erythema dischromicum perstans (ashy dermatosis). Report of two cases]M Paradisi, S Mostaccioli, G Celano, et al.
Cutis|July 6, 2000
Neonatal lupus erythematosusR Corona, C Angelo, M G Cacciaguerra, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2M Castori, S Morlino, M E Sana, et al.
International Journal of Immunopathology and Pharmacology|October 4, 2014
Human mesenchymal stem cells produce bioactive neurotrophic factors: source, individual variability and differentiation issuesM Paradisi, F Alviano, S Pirondi, et al.
Neuropathology and Applied Neurobiology|July 9, 2010
Ex vivo study of dentate gyrus neurogenesis in human pharmacoresistant temporal lobe epilepsyM Paradisi, M Fernández, G Del Vecchio, et al.
Neuropathology and Applied Neurobiology|October 20, 2011
Functional and molecular evidence of myelin- and neuroprotection by thyroid hormone administration in experimental allergic encephalomyelitisM L Dell'Acqua, L Lorenzini, G D'Intino, et al.
The Journal of Investigative Dermatology|March 12, 2002
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenitaA Terrinoni, F J Smith, B Didona, et al.
American Journal of Human Genetics|March 11, 2000
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mappingS Chavanas, C Garner, C Bodemer, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Pathologica|September 1, 1993
[Erythema dischromicum perstans (ashy dermatosis). Report of two cases]M Paradisi, S Mostaccioli, G Celano, et al.
Cutis|July 6, 2000
Neonatal lupus erythematosusR Corona, C Angelo, M G Cacciaguerra, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2M Castori, S Morlino, M E Sana, et al.
International Journal of Immunopathology and Pharmacology|October 4, 2014
Human mesenchymal stem cells produce bioactive neurotrophic factors: source, individual variability and differentiation issuesM Paradisi, F Alviano, S Pirondi, et al.
Neuropathology and Applied Neurobiology|July 9, 2010
Ex vivo study of dentate gyrus neurogenesis in human pharmacoresistant temporal lobe epilepsyM Paradisi, M Fernández, G Del Vecchio, et al.
Neuropathology and Applied Neurobiology|October 20, 2011
Functional and molecular evidence of myelin- and neuroprotection by thyroid hormone administration in experimental allergic encephalomyelitisM L Dell'Acqua, L Lorenzini, G D'Intino, et al.
The Journal of Investigative Dermatology|March 12, 2002
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenitaA Terrinoni, F J Smith, B Didona, et al.
American Journal of Human Genetics|March 11, 2000
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mappingS Chavanas, C Garner, C Bodemer, et al.
Pageof 5