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152. Vascular Endothelial Growth Factors and Angiopoietins As New Players in Mastocytosis

153. Authors’ Response to Letter to the Editor

158. Authors’ Response to Letter to the Editor

166. A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema

167. The experience of living with a chronic disease in pediatrics from the mothers’ narratives: The Clinical Interview on Parental Sense of Grip on the Disease

169. Impaired control of the contact system in hereditary angioedema with normal C1‐inhibitor

171. Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency

172. Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study

173. Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: A multicenter, prospective study

174. Effects on the incidence of cardiovascular events of the addition of pioglitazone versus sulfonylureas in patients with type 2 diabetes inadequately controlled with metformin (TOSCA.IT): a randomised, multicentre trial

180. Phenotypic and Functional Heterogeneity of Low-Density and High-Density Human Lung Macrophages

182. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

187. Late Breaking Poster Discussion LB PDS

194. Comparative effectiveness of breathing exercises in patients with chronic obstructive pulmonary disease

195. Gender in Japan: The Unseen Aspect of Natural Disaster Risks.

196. Altered Metabolism of Phospholipases, Diacylglycerols, Endocannabinoids, and

197. Biotelemetria: desenvolvimento de um negócio para saúde de idosos

198. Secreted Phospholipases A

199. Additional file 1: of Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study

200. Additional file 1: of Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study

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