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M Paradisi

Showing results (21-30 of 48) with videos related to

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The American Journal of Dermatopathology|August 1, 1988
Angiokeratoma corporis diffusum (Fabry's disease) with unusual features in a female patient. Light- and electron-microscopic investigationA Voglino, M Paradisi, G Dompé, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 2, 2009
Thyroid hormone induces glial lineage of primary neurospheres derived from non-pathological and pathological rat brain: implications for remyelination-enhancing therapiesM Fernández, M Paradisi, G Del Vecchio, et al.
Minerva Pediatrica|July 15, 2004
[Successful treatment of Norwegian scabies with ivermectin in a patient with recessive dystrophic epidermolysis bullosa]C Angelo, C Pedicelli, A Provini, et al.
Pediatric Dermatology|February 14, 2002
Association of piebaldism and neurofibromatosis type 1 in a girlC Angelo, G Cianchini, M G Grosso, et al.
Pediatric Dermatology|May 1, 1996
Epidermolysis bullosa of the Dowling-Meara type: clinical and ultrastructural findings in five patientsP Puddu, C Angelo, T Faraggiana, et al.
Minerva Pediatrica|May 1, 1997
[Ehlers-Danlos syndrome type I. Ultrastructural study]M Paradisi, L Giubilei, F Canzona, et al.
Histology and Histopathology|October 24, 2007
Skin homeostasis during inflammation: a role for nerve growth factorS Sivilia, M Paradisi, G D'Intino, et al.
Clinical and Experimental Dermatology|September 1, 1994
Dubowitz syndrome with keloidal lesionsM Paradisi, C Angelo, G Conti, et al.
Minerva Pediatrica|September 21, 2005
[PTPN11 gene mutation in LEOPARD syndrome]M Paradisi, C Pedicelli, A Ciasulli, et al.
The British Journal of Dermatology|July 17, 1998
180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotypeC Mazzanti, T Gobello, P Posteraro, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
The American Journal of Dermatopathology|August 1, 1988
Angiokeratoma corporis diffusum (Fabry's disease) with unusual features in a female patient. Light- and electron-microscopic investigationA Voglino, M Paradisi, G Dompé, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 2, 2009
Thyroid hormone induces glial lineage of primary neurospheres derived from non-pathological and pathological rat brain: implications for remyelination-enhancing therapiesM Fernández, M Paradisi, G Del Vecchio, et al.
Minerva Pediatrica|July 15, 2004
[Successful treatment of Norwegian scabies with ivermectin in a patient with recessive dystrophic epidermolysis bullosa]C Angelo, C Pedicelli, A Provini, et al.
Pediatric Dermatology|February 14, 2002
Association of piebaldism and neurofibromatosis type 1 in a girlC Angelo, G Cianchini, M G Grosso, et al.
Pediatric Dermatology|May 1, 1996
Epidermolysis bullosa of the Dowling-Meara type: clinical and ultrastructural findings in five patientsP Puddu, C Angelo, T Faraggiana, et al.
Minerva Pediatrica|May 1, 1997
[Ehlers-Danlos syndrome type I. Ultrastructural study]M Paradisi, L Giubilei, F Canzona, et al.
Histology and Histopathology|October 24, 2007
Skin homeostasis during inflammation: a role for nerve growth factorS Sivilia, M Paradisi, G D'Intino, et al.
Clinical and Experimental Dermatology|September 1, 1994
Dubowitz syndrome with keloidal lesionsM Paradisi, C Angelo, G Conti, et al.
Minerva Pediatrica|September 21, 2005
[PTPN11 gene mutation in LEOPARD syndrome]M Paradisi, C Pedicelli, A Ciasulli, et al.
The British Journal of Dermatology|July 17, 1998
180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotypeC Mazzanti, T Gobello, P Posteraro, et al.
Pageof 5