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F Facchetti

Showing results (131-140 of 164) with videos related to

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The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|February 27, 2008
Claudin-7 expression in human epithelial ovarian cancerR A Tassi, E Bignotti, M Falchetti, et al.
Lupus|May 26, 1999
Chilblain lupus erythematosus is associated with antibodies to SSA/RoF Franceschini, P Calzavara-Pinton, M Quinzanini, et al.
Archives of Dermatology|January 1, 1995
Angiokeratoma corporis diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disordersP G Calzavara-Pinton, M Colombi, A Carlino, et al.
Liver|February 1, 1989
Hepatocellular transferrin receptor expression in secondary siderosisR Sciot, P van Eyken, F Facchetti, et al.
Bone Marrow Transplantation|April 13, 2010
Risk of hepatitis B surface antigen seroreversion after allogeneic hematopoietic SCTM Viganò, C Vener, P Lampertico, et al.
Medicine|November 13, 2001
Cocaine-induced midline destructive lesions: clinical, radiographic, histopathologic, and serologic features and their differentiation from Wegener granulomatosisM Trimarchi, G Gregorini, F Facchetti, et al.
Cancer Gene Therapy|November 4, 2000
Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need for tight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndromeM G Sacco, M Ungari, E M Catò, et al.
The American Journal of Surgical Pathology|February 16, 1999
The spleen in the Wiskott-Aldrich syndrome: histopathologic abnormalities of the white pulp correlate with the clinical phenotype of the diseaseW Vermi, L Blanzuoli, M D Kraus, et al.
Journal of the American Academy of Dermatology|November 1, 1996
Defective expression of HLA class I and CD1a molecules in boy with Marfan-like phenotype and deep skin ulcersA Plebani, V Monafo, R Cattaneo, et al.
Pageof 17

Showing results (131-140 of 164) with videos related to

Sort By:
Pageof 17
The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|February 27, 2008
Claudin-7 expression in human epithelial ovarian cancerR A Tassi, E Bignotti, M Falchetti, et al.
Lupus|May 26, 1999
Chilblain lupus erythematosus is associated with antibodies to SSA/RoF Franceschini, P Calzavara-Pinton, M Quinzanini, et al.
Archives of Dermatology|January 1, 1995
Angiokeratoma corporis diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disordersP G Calzavara-Pinton, M Colombi, A Carlino, et al.
Liver|February 1, 1989
Hepatocellular transferrin receptor expression in secondary siderosisR Sciot, P van Eyken, F Facchetti, et al.
Bone Marrow Transplantation|April 13, 2010
Risk of hepatitis B surface antigen seroreversion after allogeneic hematopoietic SCTM Viganò, C Vener, P Lampertico, et al.
Medicine|November 13, 2001
Cocaine-induced midline destructive lesions: clinical, radiographic, histopathologic, and serologic features and their differentiation from Wegener granulomatosisM Trimarchi, G Gregorini, F Facchetti, et al.
Cancer Gene Therapy|November 4, 2000
Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need for tight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndromeM G Sacco, M Ungari, E M Catò, et al.
The American Journal of Surgical Pathology|February 16, 1999
The spleen in the Wiskott-Aldrich syndrome: histopathologic abnormalities of the white pulp correlate with the clinical phenotype of the diseaseW Vermi, L Blanzuoli, M D Kraus, et al.
Journal of the American Academy of Dermatology|November 1, 1996
Defective expression of HLA class I and CD1a molecules in boy with Marfan-like phenotype and deep skin ulcersA Plebani, V Monafo, R Cattaneo, et al.
Pageof 17