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Rudolf Happle

Showing results (191-200 of 223) with videos related to

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Journal of the American Academy of Dermatology|February 15, 2011
Papular epidermal nevus with "skyline" basal cell layer (PENS)Antonio Torrelo, Isabel Colmenero, Leonard Kristal, et al.
European Journal of Dermatology : EJD|June 25, 2008
Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata"María del C Boente, Roxana Obeid, Raúl A Asial, et al.
Pigment Cell & Melanoma Research|August 18, 2018
Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2AMarc-Alexander Rauschendorf, Andreas D Zimmer, Astrid Laut, et al.
Acta Dermato-Venereologica|June 8, 2010
Phacomatosis pigmentokeratotica with nephroblastoma and juvenile hypertensionSimon Jacobelli, Stéphanie Leclerc-Mercier, Rémi Salomon, et al.
Pediatric Dermatology|May 27, 2005
Nevus psiloliparus and aplasia cutis: a further possible example of didymosisAntonio Torrelo, María del C Boente, Olga Nieto, et al.
The Journal of Investigative Dermatology|October 31, 2002
Interleukin-10-deficient mice are less susceptible to the induction of alopecia areataPia Freyschmidt-Paul, Kevin J McElwee, Rudolf Happle, et al.
The Journal of Investigative Dermatology|March 23, 2012
Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutationAndreas W Arnold, Dimitra Kiritsi, Rudolf Happle, et al.
Pediatric Dermatology|November 8, 2021
Conradi-Hünermann-Happle syndrome with minimal signsManuel Agud-Dios, Nelmar Valentina Ortiz Cabrera, Lucero Noguera-Morel, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|August 5, 2003
Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-affected skin from C3H/HeJ micePia Freyschmidt-Paul, Kevin J McElwee, Vladimir Botchkarev, et al.
Archives of Dermatology|May 20, 2009
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entityM Antonia González-Enseñat, Asunción Vicente, Pilar Poo, et al.
Pageof 23

Showing results (191-200 of 223) with videos related to

Sort By:
Pageof 23
Journal of the American Academy of Dermatology|February 15, 2011
Papular epidermal nevus with "skyline" basal cell layer (PENS)Antonio Torrelo, Isabel Colmenero, Leonard Kristal, et al.
European Journal of Dermatology : EJD|June 25, 2008
Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata"María del C Boente, Roxana Obeid, Raúl A Asial, et al.
Pigment Cell & Melanoma Research|August 18, 2018
Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2AMarc-Alexander Rauschendorf, Andreas D Zimmer, Astrid Laut, et al.
Acta Dermato-Venereologica|June 8, 2010
Phacomatosis pigmentokeratotica with nephroblastoma and juvenile hypertensionSimon Jacobelli, Stéphanie Leclerc-Mercier, Rémi Salomon, et al.
Pediatric Dermatology|May 27, 2005
Nevus psiloliparus and aplasia cutis: a further possible example of didymosisAntonio Torrelo, María del C Boente, Olga Nieto, et al.
The Journal of Investigative Dermatology|October 31, 2002
Interleukin-10-deficient mice are less susceptible to the induction of alopecia areataPia Freyschmidt-Paul, Kevin J McElwee, Rudolf Happle, et al.
The Journal of Investigative Dermatology|March 23, 2012
Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutationAndreas W Arnold, Dimitra Kiritsi, Rudolf Happle, et al.
Pediatric Dermatology|November 8, 2021
Conradi-Hünermann-Happle syndrome with minimal signsManuel Agud-Dios, Nelmar Valentina Ortiz Cabrera, Lucero Noguera-Morel, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|August 5, 2003
Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-affected skin from C3H/HeJ micePia Freyschmidt-Paul, Kevin J McElwee, Vladimir Botchkarev, et al.
Archives of Dermatology|May 20, 2009
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entityM Antonia González-Enseñat, Asunción Vicente, Pilar Poo, et al.
Pageof 23