Suchergebnisse - "Codispoti, Andrea"

PubPharm (12)

1

Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss

enthalten in: Biochemical and biophysical research communications | 2010

von Terrinoni, A. | Codispoti, A. | Serra, V. | +8

2

Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss

enthalten in: Biochemical and biophysical research communications | 2010

von Terrinoni, A. | Codispoti, A. | Serra, V. | +8

3

Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation

enthalten in: Biochemical and biophysical research communications | 2010

von Terrinoni, A. | Codispoti, A. | Serra, V. | +7

4

Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation

enthalten in: Biochemical and biophysical research communications | 2010

von Terrinoni, A. | Codispoti, A. | Serra, V. | +7

5

Knuckle pads, in an epidermal palmoplantar keratoderma patient with Keratin 9 R163W transgrediens expression

enthalten in: European journal of dermatology : EJD | 2009

von Codispoti, A. | Colombo, E. | Zocchi, L. | +10

6

Transglutaminases expression in human supraspinatus tendon ruptures and in mouse tendons

enthalten in: Biochemical and biophysical research communications | 2009

von Oliva, F. | Zocchi, L. | Codispoti, A. | +5

7

Genes and skin - Knuckle pads, in an epidermal palmoplantar keratoderma patient with Keratin 9 R163W transgrediens expression

enthalten in: European journal of dermatology | 2009

von Codispoti, A. | Colombo, E. | Zocchi, L. | +10

8

Scotin : A new p63 target gene expressed during epidermal differentiation

enthalten in: Biochemical and biophysical research communications | 2008

von Zocchi, L. | Bourdon, J. | Codispoti, A. | +4

9

Cerebral cavernomas in a family with multiple cutaneous and uterine leiomyomas associated with a new mutation in the fumarate hydratase gene

enthalten in: The Journal of investigative dermatology | 2007

von Campione, E. | Terrinoni, A. | Orlandi, A. | +7

10

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

enthalten in: Journal of human genetics | 2007

von Didona, B. | Codispoti, A. | Bertini, E. | +8