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The Journal of Investigative Dermatology
|
August 23, 2002
Phenotype diversity in familial cylindromatosis: a frameshift mutation in the tumor suppressor gene CYLD underlies different tumors of skin appendages
Pamela Poblete Gutiérrez, Thomas Eggermann, Daniela Höller, et al.
International Journal of Dermatology
|
November 15, 2008
Penile pyoderma gangrenosum: successful treatment with colchicine
Lizelotte J M T Parren, Ruud G L Nellen, Arienne M W van Marion, et al.
Genes
|
March 28, 2024
Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying <i>ABCA12</i> Mutations
Alrun Hotz, Regina Fölster-Holst, Vinzenz Oji, et al.
International Journal of Dermatology
|
November 15, 2008
Basal cell carcinoma and trichoepithelioma: a possible matter of confusion
Aimée H M M Arits, Lizelotte J M T Parren, Arienne M W van Marion, et al.
European Journal of Pediatrics
|
August 22, 2007
Erythropoietic protoporphyria without skin symptoms-you do not always see what they feel
Anne L Y Lecluse, Veronica C M Kuck-Koot, Huib van Weelden, et al.
Journal of Dermatological Science
|
November 30, 2010
A recurrent mutation in variegate porphyria patients from Chile and Sweden: Evidence for a common genetic background?
Anne Moniek van Tuyll van Serooskerken, Manon Ernst, Reno S Bladergroen, et al.
American Journal of Medical Genetics. Part A
|
July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes
Benjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
June 17, 2022
Phänotypische Vielfalt bei Varianten im TP63-Gen
Ariane Schmetz, Xing Xiong, Nicole Cesarato, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
May 20, 2022
Phenotype diversity associated with TP63 mutations
Ariane Schmetz, Xing Xiong, Nicole Cesarato, et al.
Orphanet Journal of Rare Diseases
|
June 12, 2023
Detect Acute Porphyrias in Emergency Departments (DePorED) - a pilot study
Eva Diehl-Wiesenecker, Sabine Blaschke, Nils Wohmann, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 136) with videos related to
Sort By:
Page
of 14
The Journal of Investigative Dermatology
|
August 23, 2002
Phenotype diversity in familial cylindromatosis: a frameshift mutation in the tumor suppressor gene CYLD underlies different tumors of skin appendages
Pamela Poblete Gutiérrez, Thomas Eggermann, Daniela Höller, et al.
International Journal of Dermatology
|
November 15, 2008
Penile pyoderma gangrenosum: successful treatment with colchicine
Lizelotte J M T Parren, Ruud G L Nellen, Arienne M W van Marion, et al.
Genes
|
March 28, 2024
Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying <i>ABCA12</i> Mutations
Alrun Hotz, Regina Fölster-Holst, Vinzenz Oji, et al.
International Journal of Dermatology
|
November 15, 2008
Basal cell carcinoma and trichoepithelioma: a possible matter of confusion
Aimée H M M Arits, Lizelotte J M T Parren, Arienne M W van Marion, et al.
European Journal of Pediatrics
|
August 22, 2007
Erythropoietic protoporphyria without skin symptoms-you do not always see what they feel
Anne L Y Lecluse, Veronica C M Kuck-Koot, Huib van Weelden, et al.
Journal of Dermatological Science
|
November 30, 2010
A recurrent mutation in variegate porphyria patients from Chile and Sweden: Evidence for a common genetic background?
Anne Moniek van Tuyll van Serooskerken, Manon Ernst, Reno S Bladergroen, et al.
American Journal of Medical Genetics. Part A
|
July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes
Benjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
June 17, 2022
Phänotypische Vielfalt bei Varianten im TP63-Gen
Ariane Schmetz, Xing Xiong, Nicole Cesarato, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
May 20, 2022
Phenotype diversity associated with TP63 mutations
Ariane Schmetz, Xing Xiong, Nicole Cesarato, et al.
Orphanet Journal of Rare Diseases
|
June 12, 2023
Detect Acute Porphyrias in Emergency Departments (DePorED) - a pilot study
Eva Diehl-Wiesenecker, Sabine Blaschke, Nils Wohmann, et al.
Page
of 14