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X
Cammarata‐Scalisi, F.
9  Ergebnisse:
Personensuche X
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1

Two novel mutations in the TSC2 gene causing severe phenoty..:

Cammarata‐Scalisi, F. ; Vidales Moreno, C. ; Stock, F....
Journal of the European Academy of Dermatology and Venereology.  32 (2018)  6 - p. , 2018
Link: https://doi.org/10.1111/..
 
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2

Incontinentia Pigmenti:

Cammarata-Scalisi, F. ; Fusco, F. ; Ursini, M.V.
Actas Dermo-Sifiliográficas (English Edition).  110 (2019)  4 - p. 273-278 , 2019
Link: https://doi.org/10.1016/..
 
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3

Incontinencia pigmenti:

Cammarata-Scalisi, F. ; Fusco, F. ; Ursini, M.V.
Actas Dermo-Sifiliográficas.  110 (2019)  4 - p. 273-278 , 2019
Link: https://doi.org/10.1016/..
 
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4

Early severe pachyonychia congenita subtype PC-K6a with a n..:

Cammarata-Scalisi, F. ; Natsuga, K. ; Toyonaga, E....
Journal of the European Academy of Dermatology and Venereology.  31 (2016)  2 - p. e94-e96 , 2016
Link: https://doi.org/10.1111/..
 
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5

Mutación c.3037G>A en el gen FBN1 asociado a síndrome de Ma..:

Cammarata-Scalisi, F ; Capolino, R ; Magliozzi, M...
10.35366/105712.  , 2021
Link: http://www.scielo.org.mx..
 
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6

Oral manifestations and complications in childhood acute my..:

Cammarata-Scalisi F ; Girardi K ; Strocchio L...
info:eu-repo/semantics/altIdentifier/wos/WOS:000554931800001.  , 2020
Link: http://hdl.handle.net/21..
 
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7

Incontinentia Pigmenti:

F. Cammarata-Scalisi ; F. Fusco ; M.V. Ursini
url:https://www.openaccessrepository.it/communities/itmirror.  , 2019
Link: https://www.openaccessre..
 
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8

Estudio clínico y molecular en una familia con osteocondrom..:

Cammarata-Scalisi, F ; Stock, F ; Avendaño, A...
Acta ortopédica mexicana v.32 n.2 2018.  , 2018
Link: http://www.scielo.org.mx..
 
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9

Further Delineation of the Clinical Spectrum of KAT6B Disor..:

Zhang, Li Xin ; Lemire, Gabrielle ; Gonzaga-Jauregui, Claudia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737399/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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