Export 35 results:
[ Autore(Desc)] Titolo Tipo Anno
Filtri: First Letter Of Last Name è N  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
N
Naviglio S, Soncini E, Vairo D, Lanfranchi A, Badolato R, Porta F. Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency. J Clin Immunol 2017;37(7):701-706.
Nazzi F, Martinelli E, Del Fabbro S, Bernardinelli I, Milani N, Iob A, Pischiutti P, Campello C, D'Agaro P. Ticks and Lyme borreliosis in an alpine area in northeast Italy. Med Vet Entomol 2010;24(3):220-6.
Necchi V, Sommi P, Vitali A, Vanoli A, Savoia A, Ricci V, Solcia E. Polyubiquitinated proteins, proteasome, and glycogen characterize the particle-rich cytoplasmic structure (PaCS) of neoplastic and fetal cells. Histochem Cell Biol 2014;141(5):483-97.
Neri E, Barbi E, Rabach I, Zanchi C, Norbedo S, Ronfani L, Guastalla V, Ventura A, Guastalla P. Diagnostic accuracy of ultrasonography for hand bony fractures in paediatric patients. Arch Dis Child 2014;99(12):1087-90.
Neto JRibamar Co, da Silva MDaniel, Pandolfi V, Crovella S, Benko-Iseppon AMaria, Kido ÉAkio. Epigenetic Signals on Plant Adaptation: A Biotic Stress Perspective. Curr Protein Pept Sci 2016;
Nicchia E, Benedicenti F, De Rocco D, Greco C, Bottega R, Inzana F, Faleschini M, Bonin S, Cappelli E, Mogni M, Stanzial F, Svahn J, Dufour C, Savoia A. Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Birth Defects Res A Clin Mol Teratol 2015;103(12):1003-1010.
Nicchia E, Giordano P, Greco C, De Rocco D, Savoia A. Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing. Int J Lab Hematol 2016;38(4):412-8.
Nocerino A, Valencic E, Loganes C, Pelos G, Tommasini A. Low-dose sirolimus in two cousins with autoimmune lymphoproliferative syndrome-associated infection. Pediatr Int 2018;60(3):315-317.
Noetzli L, Lo RW, Lee-Sherick AB, Callaghan M, Noris P, Savoia A, Rajpurkar M, Jones K, Gowan K, Balduini CL, Pecci A, Gnan C, De Rocco D, Doubek M, Li L, Lu L, Leung R, Landolt-Marticorena C, Hunger S, Heller P, Gutierrez-Hartmann A, Xiayuan L, Pluthero FG, Rowley JW, Weyrich AS, Kahr WHA, Porter CC, Di Paola J. Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia. Nat Genet 2015;47(5):535-8.
Norbedo S, Naviglio S, Murru FMaria, Cavallin R, Giurici N, Rabusin M, Barbi E. A boy with sudden headache. Pediatr Emerg Care 2014;30(3):182-4.
Norbedo S, Bassanese G, Barbieri F, Barbi E. Acute Abdominal Pain: Recognition and Management of Constipation in the Emergency Department. Pediatr Emerg Care 2017;33(10):e75-e78.
Norbedo S, Perini R, Amaddeo A. A coughing spine. Emerg Med J 2012;29(1):14.

Amministrazione Trasparente