C. Pedicelli

发表

Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene

A. Christiano, A. Martinez-Mir, M. Paradisi, 2003, Clinical and experimental dermatology.

A novel recessive connexin 31 (GJB3) mutation in a case of erythrokeratodermia variabilis.

G. Melino, E. Candi, A. Terrinoni, 2004, The Journal of investigative dermatology.

Antibodies against human herpesvirus 8 in subjects with non‐venereal dermatological conditions

G. Fadda, P. Pasquini, M. Cattaruzza, 2000 .

Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome.

G. Zambruno, C. Pedicelli, L. Guerra, 2015, Acta dermato-venereologica.

Multicenter prospective study of the humoral autoimmune response in bullous pemphigoid.

F. Sera, L. Borradori, G. Zambruno, 2008, Clinical immunology.

Identification of categories at risk for high quality of life impairment in patients with vitiligo

F. Sampogna, C. Pedicelli, D. Abeni, 2008, The British journal of dermatology.

[Erythema nodosum induced by kerion celsi in a child with hypomelanosis of Ito].

M. Paradisi, C. Angelo, C. Pedicelli, 2003, Minerva pediatrica.

A Postzygotic ATP2A2 Novel Mutation Identified by Next-generation Sequencing in Mosaic Darier Disease.

C. Pedicelli, L. Guerra, D. Castiglia, 2018, Acta dermato-venereologica.

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress

Howard J Worman, H. Worman, M. Paradisi, 2005, BMC Cell Biology.

Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.

J. McGrath, C. Has, G. Zambruno, 2006, The Journal of investigative dermatology.

Trigeminal neurotrophic ulceration in Wallenberg's syndrome

M. Paradisi, C. Angelo, C. Pedicelli, 2009, International journal of dermatology.

Dermatitis Artefacta in a Child

M. Paradisi, C. Pedicelli, G. Palermi, 2007, Pediatric dermatology.

Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations.

C. Pedicelli, L. Guerra, D. Castiglia, 2017, Acta dermato-venereologica.

Dermatitis due to self-aggressive behaviors in pediatric age

M. Paradisi, C. Pedicelli, A. Paradisi, 2013 .

Novel and recurrent ALDH3A2 mutations in Italian patients with Sjögren-Larsson syndrome

E. Bertini, G. Melino, A. Terrinoni, 2007, Journal of Human Genetics.

Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization

N. Zoppi, M. Colombi, G. Zambruno, 2006, Clinical genetics.

Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesions.

A. Christiano, A. Martinez-Mir, H. Lam, 2005, European journal of dermatology : EJD.

[Neonatal adrenal hemorrhage associated with a scrotal hematoma. A case report].

V. Miele, C. Pedicelli, Alessandro Calisti, 2000, La Radiologia medica.