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Peter Itin

Showing results (61-70 of 76) with videos related to

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Swiss Medical Weekly|December 25, 2014
Swiss clinical practice guidelines on field cancerization of the skinGünther Hofbauer, Mark Anliker, Wolf-Henning Boehncke, et al.
Human Mutation|September 22, 2011
Kindler syndrome: extension of FERMT1 mutational spectrum and natural historyCristina Has, Daniele Castiglia, Marcela del Rio, et al.
Journal of the American Academy of Dermatology|August 8, 2022
Validation of the Index for Facial Angiofibromas: A new scoring tool to assess facial angiofibromas in the tuberous sclerosis complexPatricia Elsa Dill, Didier Bessis, Beatrice Guidi, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Rothmund-Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) geneAude-Annick Suter, Peter Itin, Karl Heinimann, et al.
American Journal of Human Genetics|September 9, 2006
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14Jennie Lugassy, Peter Itin, Akemi Ishida-Yamamoto, et al.
Dermatology (Basel, Switzerland)|June 21, 2016
Swiss S1 Guidelines on the Systemic Treatment of Psoriasis VulgarisAntonios G A Kolios, Nikhil Yawalkar, Mark Anliker, et al.
Orphanet Journal of Rare Diseases|July 26, 2019
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patientsSara Guerrero-Aspizua, Claudio J Conti, Maria Jose Escamez, et al.
The Journal of Investigative Dermatology|December 1, 2007
KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndromeJennie Lugassy, John A McGrath, Peter Itin, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 24, 2014
Phase II metabolism in human skin: skin explants show full coverage for glucuronidation, sulfation, N-acetylation, catechol methylation, and glutathione conjugationNenad Manevski, Piet Swart, Kamal Kumar Balavenkatraman, et al.
The Journal of Investigative Dermatology|September 6, 2013
The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndromeCristina Has, Dimitra Kiritsi, Jemima E Mellerio, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Swiss Medical Weekly|December 25, 2014
Swiss clinical practice guidelines on field cancerization of the skinGünther Hofbauer, Mark Anliker, Wolf-Henning Boehncke, et al.
Human Mutation|September 22, 2011
Kindler syndrome: extension of FERMT1 mutational spectrum and natural historyCristina Has, Daniele Castiglia, Marcela del Rio, et al.
Journal of the American Academy of Dermatology|August 8, 2022
Validation of the Index for Facial Angiofibromas: A new scoring tool to assess facial angiofibromas in the tuberous sclerosis complexPatricia Elsa Dill, Didier Bessis, Beatrice Guidi, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Rothmund-Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) geneAude-Annick Suter, Peter Itin, Karl Heinimann, et al.
American Journal of Human Genetics|September 9, 2006
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14Jennie Lugassy, Peter Itin, Akemi Ishida-Yamamoto, et al.
Dermatology (Basel, Switzerland)|June 21, 2016
Swiss S1 Guidelines on the Systemic Treatment of Psoriasis VulgarisAntonios G A Kolios, Nikhil Yawalkar, Mark Anliker, et al.
Orphanet Journal of Rare Diseases|July 26, 2019
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patientsSara Guerrero-Aspizua, Claudio J Conti, Maria Jose Escamez, et al.
The Journal of Investigative Dermatology|December 1, 2007
KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndromeJennie Lugassy, John A McGrath, Peter Itin, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 24, 2014
Phase II metabolism in human skin: skin explants show full coverage for glucuronidation, sulfation, N-acetylation, catechol methylation, and glutathione conjugationNenad Manevski, Piet Swart, Kamal Kumar Balavenkatraman, et al.
The Journal of Investigative Dermatology|September 6, 2013
The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndromeCristina Has, Dimitra Kiritsi, Jemima E Mellerio, et al.
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