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Nicole Cesarato

Showing results (1-10 of 17) with videos related to

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Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|August 2, 2024
First East Asian case of uncombable hair syndromeYe Li, Xing Xiong, Nicole Cesarato, et al.
Clinical and Experimental Dermatology|May 16, 2022
A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragilitySokounthie Ou, Nicole Cesarato, Pierre Mauran, et al.
The British Journal of Dermatology|February 8, 2026
A recurrent variant in two patients with EMP2-nEDDYunran Peng, Nicole Cesarato, Tsenka Tomova-Simitchieva, et al.
The Journal of Dermatology|August 29, 2025
Bi-Allelic DSG1 Splice-Site Variant Identified in a Family With Non-Syndromic Striate Palmoplantar KeratodermaSohail Ahmed, Nicole Cesarato, Ye Li, et al.
American Journal of Medical Genetics. Part A|July 28, 2021
Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypesNicole Cesarato, Maria Wehner, Mariam Ghughunishvili, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|June 17, 2022
Phänotypische Vielfalt bei Varianten im TP63-GenAriane 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 mutationsAriane Schmetz, Xing Xiong, Nicole Cesarato, et al.
The British Journal of Dermatology|July 19, 2024
A nonsense variant in KRT31 is associated with autosomal dominant monilethrixXing Xiong, Nicole Cesarato, Yasmina Gossmann, et al.
Frontiers in Immunology|May 4, 2026
Genome-wide association study of atopic and autoimmune comorbidities in alopecia areataMarisol Herrera-Rivero, Yasmina Gossmann, Swapnil Awasthi, et al.
Human Genome Variation|April 13, 2026
Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspotSheetal Kumar, Sohail Ahmed, Pietro Incardona, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|August 2, 2024
First East Asian case of uncombable hair syndromeYe Li, Xing Xiong, Nicole Cesarato, et al.
Clinical and Experimental Dermatology|May 16, 2022
A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragilitySokounthie Ou, Nicole Cesarato, Pierre Mauran, et al.
The British Journal of Dermatology|February 8, 2026
A recurrent variant in two patients with EMP2-nEDDYunran Peng, Nicole Cesarato, Tsenka Tomova-Simitchieva, et al.
The Journal of Dermatology|August 29, 2025
Bi-Allelic DSG1 Splice-Site Variant Identified in a Family With Non-Syndromic Striate Palmoplantar KeratodermaSohail Ahmed, Nicole Cesarato, Ye Li, et al.
American Journal of Medical Genetics. Part A|July 28, 2021
Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypesNicole Cesarato, Maria Wehner, Mariam Ghughunishvili, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|June 17, 2022
Phänotypische Vielfalt bei Varianten im TP63-GenAriane 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 mutationsAriane Schmetz, Xing Xiong, Nicole Cesarato, et al.
The British Journal of Dermatology|July 19, 2024
A nonsense variant in KRT31 is associated with autosomal dominant monilethrixXing Xiong, Nicole Cesarato, Yasmina Gossmann, et al.
Frontiers in Immunology|May 4, 2026
Genome-wide association study of atopic and autoimmune comorbidities in alopecia areataMarisol Herrera-Rivero, Yasmina Gossmann, Swapnil Awasthi, et al.
Human Genome Variation|April 13, 2026
Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspotSheetal Kumar, Sohail Ahmed, Pietro Incardona, et al.
Pageof 2