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Journal Article
Hauschner H, Mor-Cohen R, Messineo S, Mansour W, Seligsohn U, Savoia A, Rosenberg N. Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome. Blood Coagul Fibrinolysis 2015;26(3):302-8.
Hauschner H, Mor-Cohen R, Messineo S, Mansour W, Seligsohn U, Savoia A, Rosenberg N. Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome. Blood Coagul Fibrinolysis 2015;26(3):302-8.
Ura B, Scrimin F, Arrigoni G, Athanasakis E, Aloisio M, Monasta L, Ricci G. Abnormal expression of leiomyoma cytoskeletal proteins involved in cell migration. Oncol Rep 2016;35(5):3094-100.
Orzan E, Muzzi E, Marchi R, Falzone C, Battelino S, Ciciriello E. Achieving early functional auditory access in paediatric cochlear implantation. Acta Otorhinolaryngol Ital 2016;36(1):45-50.
Orzan E, Muzzi E, Marchi R, Falzone C, Battelino S, Ciciriello E. Achieving early functional auditory access in paediatric cochlear implantation. Acta Otorhinolaryngol Ital 2016;36(1):45-50.
Bastanza G, Gallus R, De Carlini M, Picciotti PM, Muzzi E, Ciciriello E, Orzan E, Conti G. Achieving effective hearing aid fitting within one month after identification of childhood permanent hearing impairment. Acta Otorhinolaryngol Ital 2016;36(1):38-44.
Marzuillo P, Benettoni A, Germani C, Ferrara G, D'Agata B, Barbi E. Acquired long QT syndrome: a focus for the general pediatrician. Pediatr Emerg Care 2014;30(4):257-61.
Faleschini M, Melazzini F, Marconi C, Giangregorio T, Pippucci T, Cigalini E, Pecci A, Bottega R, Ramenghi U, Siitonen T, Seri M, Pastore A, Savoia A, Noris P. ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. Br J Haematol 2018;183(2):276-288.
Faleschini M, Melazzini F, Marconi C, Giangregorio T, Pippucci T, Cigalini E, Pecci A, Bottega R, Ramenghi U, Siitonen T, Seri M, Pastore A, Savoia A, Noris P. ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. Br J Haematol 2018;183(2):276-288.
Bottega R, Marconi C, Faleschini M, Baj G, Cagioni C, Pecci A, Pippucci T, Ramenghi U, Pardini S, Ngu L, Baronci C, Kunishima S, Balduini CL, Seri M, Savoia A, Noris P. ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. Blood 2015;125(5):869-72.
Minen F, De Cunto A, Martelossi S, Ventura A. Acute and recurrent pancreatitis in children: exploring etiological factors. Scand J Gastroenterol 2012;47(12):1501-4.
Minen F, De Cunto A, Martelossi S, Ventura A. Acute and recurrent pancreatitis in children: exploring etiological factors. Scand J Gastroenterol 2012;47(12):1501-4.

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