Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

85 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family.
Callea M, Nieminen P, Willoughby CE, Clarich G, Yavuz I, Vinciguerra A, Di Stazio M, Giglio S, Sani I, Maglione M, Pensiero S, Tadini G, Bellacchio E. Callea M, et al. J Eur Acad Dermatol Venereol. 2016 Feb;30(2):341-3. doi: 10.1111/jdv.12747. Epub 2014 Sep 30. J Eur Acad Dermatol Venereol. 2016. PMID: 25266272 No abstract available.
Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasia.
Callea M, Bellacchio E, Fattori F, Bertini E, Callea F, Cammarata-Scalisi F. Callea M, et al. Among authors: callea f. Leuk Lymphoma. 2016 Sep;57(9):2189-91. doi: 10.3109/10428194.2015.1115030. Epub 2015 Dec 24. Leuk Lymphoma. 2016. PMID: 26700323 No abstract available.
Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene.
Cammarata-Scalisi F, Natsuga K, Toyonaga E, Nishie W, Shimizu H, Avendaño A, Araque D, Da Silva G, Bellacchio E, Callea M. Cammarata-Scalisi F, et al. Among authors: callea m. J Eur Acad Dermatol Venereol. 2017 Feb;31(2):e94-e96. doi: 10.1111/jdv.13800. Epub 2016 Jul 21. J Eur Acad Dermatol Venereol. 2017. PMID: 27445120 No abstract available.
[Mosaic trisomy 18. Series of cases].
Cammarata-Scalisi F, Lacruz-Rengel MA, Araque D, Da Silva G, Avendaño A, Callea M, Stock F, Guerrero Y, Aguilar E, Lacruz MJ, Sulbaran J. Cammarata-Scalisi F, et al. Among authors: callea m. Arch Argent Pediatr. 2017 Jun 1;115(3):e183-e186. doi: 10.5546/aap.2017.e183. Arch Argent Pediatr. 2017. PMID: 28504507 Free article. Spanish.
85 results