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Jorge Frank

Showing results (111-120 of 136) with videos related to

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International Journal of Dermatology|December 6, 2007
Erythema nodosum as an early sign of Crohn's diseaseJaap J A J van der Velden, Ariënne M W van Marion, Bernd Kremer, et al.
Journal of Dermatological Science|June 3, 2008
Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase geneSadhanna Badeloe, Reno S Bladergroen, Marcel F Jonkman, et al.
Healthcare (Basel, Switzerland)|January 11, 2024
German Porphyria Registry (PoReGer)-Background and SetupLea Gerischer, Mona Mainert, Nils Wohmann, et al.
The Journal of Investigative Dermatology|November 25, 2006
Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patientsMaurice A M van Steensel, Valerie L R M Verstraeten, Jorge Frank, et al.
Experimental Dermatology|February 19, 2010
Smoking but not homozygosity for CYP1A2 g-163A allelic variant leads to earlier disease onset in patients with sporadic porphyria cutanea tardaAntonio Fontanellas, María Martínez-Fresno, María Concepción Garrido-Astray, et al.
Experimental Dermatology|January 22, 2005
Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyriaJ Nico P de Villiers, Maritha J Kotze, Carel J van Heerden, et al.
Journal of Dermatological Science|January 12, 2022
Evolutionary distinct roles of γ-secretase subunit nicastrin in zebrafish and humansMatthias Andreas Hermasch, Helena Janning, Roshan Priyarangana Perera, et al.
Experimental Dermatology|January 22, 2005
Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyriaSusana Navarro, Pilar Del Hoyo, Yolanda Campos, et al.
The Journal of Investigative Dermatology|August 23, 2008
Functional analysis of FLT4 mutations associated with Nonne-Milroy lymphedemaValerie L R M Verstraeten, Wolfgang Holnthoner, Maurice A M van Steensel, et al.
Experimental Dermatology|March 18, 2011
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypesEugene A de Zwart-Storm, Rafael F M Rosa, Patricia E Martin, et al.
Pageof 14

Showing results (111-120 of 136) with videos related to

Sort By:
Pageof 14
International Journal of Dermatology|December 6, 2007
Erythema nodosum as an early sign of Crohn's diseaseJaap J A J van der Velden, Ariënne M W van Marion, Bernd Kremer, et al.
Journal of Dermatological Science|June 3, 2008
Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase geneSadhanna Badeloe, Reno S Bladergroen, Marcel F Jonkman, et al.
Healthcare (Basel, Switzerland)|January 11, 2024
German Porphyria Registry (PoReGer)-Background and SetupLea Gerischer, Mona Mainert, Nils Wohmann, et al.
The Journal of Investigative Dermatology|November 25, 2006
Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patientsMaurice A M van Steensel, Valerie L R M Verstraeten, Jorge Frank, et al.
Experimental Dermatology|February 19, 2010
Smoking but not homozygosity for CYP1A2 g-163A allelic variant leads to earlier disease onset in patients with sporadic porphyria cutanea tardaAntonio Fontanellas, María Martínez-Fresno, María Concepción Garrido-Astray, et al.
Experimental Dermatology|January 22, 2005
Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyriaJ Nico P de Villiers, Maritha J Kotze, Carel J van Heerden, et al.
Journal of Dermatological Science|January 12, 2022
Evolutionary distinct roles of γ-secretase subunit nicastrin in zebrafish and humansMatthias Andreas Hermasch, Helena Janning, Roshan Priyarangana Perera, et al.
Experimental Dermatology|January 22, 2005
Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyriaSusana Navarro, Pilar Del Hoyo, Yolanda Campos, et al.
The Journal of Investigative Dermatology|August 23, 2008
Functional analysis of FLT4 mutations associated with Nonne-Milroy lymphedemaValerie L R M Verstraeten, Wolfgang Holnthoner, Maurice A M van Steensel, et al.
Experimental Dermatology|March 18, 2011
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypesEugene A de Zwart-Storm, Rafael F M Rosa, Patricia E Martin, et al.
Pageof 14