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F Cammarata-Scalisi

Showing results (1-10 of 8) with videos related to

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Actas Dermo-Sifiliograficas|January 21, 2019
Incontinentia PigmentiF Cammarata-Scalisi, F Fusco, M V Ursini
Anales De Pediatria (Barcelona, Spain : 2003)|May 21, 2013
[Mosaic trisomy 13]F Cammarata-Scalisi, D Araque, M A Lacruz-Rengel, et al.
Acta Ortopedica Mexicana|September 6, 2018
[Clinical and molecular study in a family with multiple osteochondromatosis]F Cammarata-Scalisi, F Stock, A Avendaño, et al.
Acta Ortopedica Mexicana|July 6, 2022
[Mutation c.3037G>A in the FBN1 gene associated with neonatal Marfan syndrome variant]F Cammarata-Scalisi, R Capolino, M Magliozzi, et al.
Acta Ortopedica Mexicana|April 10, 2014
[Hereditary multiple exostosis. Case report and differential diagnosis of enchondromatosis]F Cammarata-Scalisi, R Sánchez-Flores, F Stock-Leyton, et al.
European Journal of Paediatric Dentistry|January 4, 2017
A case of Beckwith-Wiedemann syndrome with peculiar dental findingsM Callea, I Yavuz, G Clarich, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2017
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complexF Cammarata-Scalisi, C Vidales Moreno, F Stock, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2016
Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A geneF Cammarata-Scalisi, K Natsuga, E Toyonaga, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Actas Dermo-Sifiliograficas|January 21, 2019
Incontinentia PigmentiF Cammarata-Scalisi, F Fusco, M V Ursini
Anales De Pediatria (Barcelona, Spain : 2003)|May 21, 2013
[Mosaic trisomy 13]F Cammarata-Scalisi, D Araque, M A Lacruz-Rengel, et al.
Acta Ortopedica Mexicana|September 6, 2018
[Clinical and molecular study in a family with multiple osteochondromatosis]F Cammarata-Scalisi, F Stock, A Avendaño, et al.
Acta Ortopedica Mexicana|July 6, 2022
[Mutation c.3037G>A in the FBN1 gene associated with neonatal Marfan syndrome variant]F Cammarata-Scalisi, R Capolino, M Magliozzi, et al.
Acta Ortopedica Mexicana|April 10, 2014
[Hereditary multiple exostosis. Case report and differential diagnosis of enchondromatosis]F Cammarata-Scalisi, R Sánchez-Flores, F Stock-Leyton, et al.
European Journal of Paediatric Dentistry|January 4, 2017
A case of Beckwith-Wiedemann syndrome with peculiar dental findingsM Callea, I Yavuz, G Clarich, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2017
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complexF Cammarata-Scalisi, C Vidales Moreno, F Stock, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2016
Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A geneF Cammarata-Scalisi, K Natsuga, E Toyonaga, et al.
Pageof 1