Export 1075 results:
Autore Titolo [ Tipo] Anno Filtri: First Letter Of Last Name è G [Clear All Filters]
Achieving effective hearing aid fitting within one month after identification of childhood permanent hearing impairment. Acta Otorhinolaryngol Ital 2016;36(1):38-44.
. Acquired long QT syndrome: a focus for the general pediatrician. Pediatr Emerg Care 2014;30(4):257-61.
. Activation of the p53 pathway induces α-smooth muscle actin expression in both myeloid leukemic cells and normal macrophages. J Cell Physiol 2012;227(5):1829-37.
. . ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. Br J Haematol 2018;183(2):276-288.
. Acute lobar nephritis in children: Not so easy to recognize and manage. World J Clin Pediatr 2016;5(1):136-42.
. Acute lobar nephritis in children: Not so easy to recognize and manage. World J Clin Pediatr 2016;5(1):136-42.
. Acute myelitis as presenting symptom of HIV-HTLV-1 co-infection. J Neurovirol 2016;
. Acute small bowel obstruction in a child with a strict raw vegan diet. Arch Dis Child 2018;
. ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study. Ann Rheum Dis 2017;76(10):1648-1656.
. ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study. Ann Rheum Dis 2017;76(10):1648-1656.
. ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study. Ann Rheum Dis 2017;76(10):1648-1656.
.