Testo

NOTA! Questo sito utilizza i cookie e tecnologie simili.

Se non si modificano le impostazioni del browser, l'utente accetta. Per saperne di piu'

Approvo


Studi pubblicati nel 2012

  1. Putignani L, Raffa S, Pescosolido R, Rizza T, Del Chierico F, Leone L, Aimati L, Signore F, Carrozzo R, Callea F, Torrisi MR, Grammatico P. Preliminary evidences on mitochondrial injury and impaired oxidative metabolism in breast cancer. Mitochondrion. 2012 Feb 18.
  2. Castori M, Morrone A, Kanitakis J, Grammatico P. Genetic skin diseases predisposing to basal cell carcinoma. Eur J Dermatol. 2012 Mar 2.
  3. Castori M, Ritelli M, Zoppi N, Molisso L, Chiarelli N, Zaccagna F, Grammatico P, Colombi M. Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene. Am J Med Genet A. 158(A), 1164-9, 2012
  4. Saredi S, Ardissone A, Ruggieri A, Mottarelli E, Farina L, Rinaldi R, Silvestri E, Gandioli C, D'Arrigo S, Salerno F, Morandi L, Grammatico P, Pantaleoni C, Moroni I, Mora M. Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease. J Neurol Sci. 2012 May 1.
  5. Castori M. Morlino S, Dordoni C, Celletti C, Camerota F, Ritelli M, Morrone A, Venturini M, Grammatico P, Colombi M. Gynecologic and obstetric implicationes of the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome hypermobility type) in 82 Italian patients. Am J Med Genet A. Jul 27 2012
  6. Castori M, Morlino S, Celletti C, Celli M, Morrone A, Colombi M, Camerota F, Grammatico P. Managment of pain and fatigue in the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome hypermobility type): Principles and proposal for a multidisciplinary approach. Am J Med Genet A. 158A(8):2055-2070, 2012
  7. Gharbiya M, Moramarco A, Castori M, Parisi F, Celletti C, Marenco M, Mariani I, Grammatico P, Camerota F. Ocular features in joint hypermobility syndrome/ Ehlers-Danlos syndrome hypermobility type: a clinical and in vivo confocal mycroscopy study. Am J Ophtalmology May 23, 2012.
  8. Majore S, Ricerca BM, Radio FC, Binni F, Cosentino I, Gallusi G, De Bernardo C, Morrone A, Grammatico P. Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: Is there a link between African iron overload and TFR2 dysfunction? Blood Cells Mol Dis Sep 11 2012.

SCIENTIFIC COMMUNICATION: how to write a paper and prepare oral presentations and posters for a scie

Genova, 23-24 marzo 2018

Corso teorico-pratico, 16,2 crediti ECM

Direttore: Nancy Binkin

Rivolto a: medici (tutte le specializzazioni), farmacisti, biologi.

Approfondimento