Suchergebnisse - (Person:"Colombo, Enrico")

PubPharm (133)

21

Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders : First Report of Multilocus Syndrome in Piebaldism

enthalten in: Medicina (Kaunas, Lithuania) | 2019

von Gironi, L. | Colombo, E. | Brusco, A. | +8

22

A Modified Translaryngeal Tracheostomy Technique in the Neurointensive Care Unit. Rationale and Single-center Experience on 199 Acute Brain-damaged Patients

enthalten in: Journal of neurosurgical anesthesiology | 2019

von Spina, S. | Scaravilli, V. | Cavenaghi, G. | +6

23

Reactive arthritis secondary to Hafnia alvei enterocolitis

enthalten in: BMJ case reports | 2019

von Erre, G. | Colombo, E. | Bibbò, S. | +1

24

Congenital Hypopigmentary Disorders with Multiorgan Impairment : A Case Report and an Overview on Gray Hair Syndromes

enthalten in: Medicina (Kaunas, Lithuania) | 2019

von Gironi, L. | Zottarelli, F. | Savoldi, G. | +8

25

Melanoma-prone families : new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers

enthalten in: Archives of dermatological research | 2018

von Gironi, L. | Colombo, E. | Pasini, B. | +10

26

Local recurrence of a primary carcinoid of the skin : a first case report

enthalten in: Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia | 2018

von Celasco, M. | Veronese, F. | Meli, F. | +4

27

Eradication of basal cell carcinoma of the head and neck using the surgical excision with a new stained margin technique : a preliminary study

enthalten in: Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia | 2018

von Celasco, M. | Zavattaro, E. | Veronese, F. | +5

28

Gorlin-Goltz syndrome : a case series from north Italy

enthalten in: European journal of dermatology : EJD | 2018

von Veronese, F. | Miglino, B. | Boggio, P. | +4

29

Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers

enthalten in: Archives of dermatological research | 2018

von Gironi, L. | Colombo, E. | Pasini, B. | +10

30

Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers

enthalten in: Archives of dermatological research | 2018

von Gironi, L. | Colombo, E. | Pasini, B. | +10