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Agustí Toll

Showing results (11-20 of 53) with videos related to

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The Journal of Investigative Dermatology|January 27, 2007
Fibroblast growth factor receptor 3 mutations in epidermal nevi and associated low grade bladder tumorsSilvia Hernández, Agustí Toll, Eulàlia Baselga, et al.
Pediatric Dermatology|August 3, 2005
Large atypical melanocytic nevi in recessive dystrophic epidermolysis bullosa: clinicopathological, ultrastructural, and dermoscopic studyFernando Gallardo, Agustí Toll, Josep Malvehy, et al.
Plos One|May 16, 2020
Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gelSonia Segura, Alejandra Gadea, Lara Nonell, et al.
The American Journal of Dermatopathology|May 17, 2013
Verruciform xanthoma developing in recessive dystrophic epidermolysis bullosa: A sheep in wolf's clothingLaia Curto-Barredo, Sonia Segura, Carlos Barranco, et al.
Dermatology (Basel, Switzerland)|February 3, 2009
Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutationsAgustí Toll, Elisabet Parera, Ana M Giménez-Arnau, et al.
Experimental Dermatology|February 17, 2010
Epidermal growth factor receptor gene numerical aberrations are frequent events in actinic keratoses and invasive cutaneous squamous cell carcinomasAgustí Toll, Rocío Salgado, Mireia Yébenes, et al.
Environmental Health Perspectives|February 12, 2002
Evaluation of urinary porphyrin excretion in neonates born to mothers exposed to airborne hexachlorobenzeneDolores Ozalla, Carmen Herrero, Núria Ribas-Fitó, et al.
Radiology Case Reports|July 17, 2020
Heinz-Lippmann disease as an underrecognized cause of chronic venous insufficiency-associated cutaneous ulcers: Clinical and imaging findingsAgustí Toll, Salvatore Marsico, Ivan Camilo Garcia Duitama, et al.
Genes, Chromosomes & Cancer|November 27, 2018
Transcriptome and cytogenetic profiling analysis of matched in situ/invasive cutaneous squamous cell carcinomas from immunocompetent patientsIrene García-Díez, Inmaculada Hernández-Muñoz, Eugenia Hernández-Ruiz, et al.
Human Pathology|November 30, 2010
Identification of t(17;22)(q22;q13) (COL1A1/PDGFB) in dermatofibrosarcoma protuberans by fluorescence in situ hybridization in paraffin-embedded tissue microarraysSonia Segura, Rocío Salgado, Agustí Toll, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Investigative Dermatology|January 27, 2007
Fibroblast growth factor receptor 3 mutations in epidermal nevi and associated low grade bladder tumorsSilvia Hernández, Agustí Toll, Eulàlia Baselga, et al.
Pediatric Dermatology|August 3, 2005
Large atypical melanocytic nevi in recessive dystrophic epidermolysis bullosa: clinicopathological, ultrastructural, and dermoscopic studyFernando Gallardo, Agustí Toll, Josep Malvehy, et al.
Plos One|May 16, 2020
Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gelSonia Segura, Alejandra Gadea, Lara Nonell, et al.
The American Journal of Dermatopathology|May 17, 2013
Verruciform xanthoma developing in recessive dystrophic epidermolysis bullosa: A sheep in wolf's clothingLaia Curto-Barredo, Sonia Segura, Carlos Barranco, et al.
Dermatology (Basel, Switzerland)|February 3, 2009
Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutationsAgustí Toll, Elisabet Parera, Ana M Giménez-Arnau, et al.
Experimental Dermatology|February 17, 2010
Epidermal growth factor receptor gene numerical aberrations are frequent events in actinic keratoses and invasive cutaneous squamous cell carcinomasAgustí Toll, Rocío Salgado, Mireia Yébenes, et al.
Environmental Health Perspectives|February 12, 2002
Evaluation of urinary porphyrin excretion in neonates born to mothers exposed to airborne hexachlorobenzeneDolores Ozalla, Carmen Herrero, Núria Ribas-Fitó, et al.
Radiology Case Reports|July 17, 2020
Heinz-Lippmann disease as an underrecognized cause of chronic venous insufficiency-associated cutaneous ulcers: Clinical and imaging findingsAgustí Toll, Salvatore Marsico, Ivan Camilo Garcia Duitama, et al.
Genes, Chromosomes & Cancer|November 27, 2018
Transcriptome and cytogenetic profiling analysis of matched in situ/invasive cutaneous squamous cell carcinomas from immunocompetent patientsIrene García-Díez, Inmaculada Hernández-Muñoz, Eugenia Hernández-Ruiz, et al.
Human Pathology|November 30, 2010
Identification of t(17;22)(q22;q13) (COL1A1/PDGFB) in dermatofibrosarcoma protuberans by fluorescence in situ hybridization in paraffin-embedded tissue microarraysSonia Segura, Rocío Salgado, Agustí Toll, et al.
Pageof 6