Francisco Cammarata-Scalisi

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Venues

Journal of pediatric genetics

Children (Basel, Switzerland)

Dermatologic therapy

Acta paediatrica (Oslo, Norway : 1992)

This page only lists publications with an associated author ORCID identifier.

Publications

Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby, Gunda Ruzaike, Antonio Cárdenas Tadich, Maykol Araya Castillo, Carmen Zara-Chirinos, Ana Bracho, Andrea Avendaño, Houweyda Jilani, Michele Callea
Erratum: Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1 . Journal of pediatric genetics 12 (4) (2024)
Francisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, Michele Callea
Challenges in Communicating a Genetic Diagnosis. Children (Basel, Switzerland) 10 (4) (2023)
Francisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, Michele Callea
Challenges in Communicating a Genetic Diagnosis. Children (Basel, Switzerland) 10 (4) (2023)
Michele Callea, Stefano Bignotti, Francesco Semeraro, Francisco Cammarata-Scalisi, Jinia El-Feghaly, Antonino Morabito, Vito Romano, Colin Eric Willoughby
Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia. Children (Basel, Switzerland) 9 (9) (2022)
Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby, Gunda Ruzaike, Antonio Cárdenas Tadich, Maykol Araya Castillo, Carmen Zara-Chirinos, Ana Bracho, Andrea Avendaño, Houweyda Jilani, Michele Callea
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1 . Journal of pediatric genetics 12 (4) (2021)
Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby, Gunda Ruzaike, Antonio Cárdenas Tadich, Maykol Araya Castillo, Carmen Zara-Chirinos, Ana Bracho, Andrea Avendaño, Houweyda Jilani, Michele Callea
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1 . Journal of pediatric genetics 12 (4) (2021)
Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby, Gunda Ruzaike, Antonio Cárdenas Tadich, Maykol Araya Castillo, Carmen Zara-Chirinos, Ana Bracho, Andrea Avendaño, Houweyda Jilani, Michele Callea
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1 . Journal of pediatric genetics 12 (4) (2021)
Francisco Cammarata-Scalisi, Colin Eric Willoughby, Antonio Cárdenas Tadich, Nancy Labrador, Adriana Herrera, Michele Callea
Clinical, etiopathogenic, and therapeutic aspects of KID syndrome. Dermatologic therapy 33 (4) (2020)
Francisco Cammarata-Scalisi, Andrea Diociaiuti, Blanca de Guerrero, Colin Eric Willoughby, Michele Callea
Membranous aplasia cutis congenita in trisomy 18. Italian journal of pediatrics 46 (1) (2020)
Michele Callea, Francisco Cammarata-Scalisi, Angela Galeotti, Alberto Villani, Diletta Valentini
COVID-19 and Down syndrome. Acta paediatrica (Oslo, Norway : 1992) 109 (9) (2020)
Michele Callea, Colin Eric Willoughby, Diana Perry, Ulrike Holzer, Giulia Fedele, Antonio Cárdenas Tadich, Francisco Cammarata-Scalisi
COVID-19 and ectodermal dysplasias. Recommendations are necessary. Dermatologic therapy 33 (5) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Francisco Cammarata-Scalisi