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201. Drug-induced Glomerulonephritis: The Spectre of Biotherapeutic and Antisense Oligonucleotide Immune Activation in the Kidney

202. Reduced shear stress and associated aortic deformation in the thoracic aorta of patients with chronic obstructive pulmonary disease

203. Proximal pulmonary vascular stiffness as a prognostic factor in children with pulmonary arterial hypertension

204. Children with kawasaki disease present elevated stiffness of great arteries: Phase-contrast MRI study

205. Impact of different coarctation therapies on aortic stiffness: phase-contrast MRI study

206. Simulations of congenital septal defect closure and reactivity testing in patient-specific models of the pediatric pulmonary vasculature: a 3D numerical study with fluid-structure interaction

207. Short‐Term Effects of Inhaled Nitric Oxide on Right Ventricular Flow Hemodynamics by 4‐Dimensional–Flow Magnetic Resonance Imaging in Children With Pulmonary Arterial Hypertension

208. An overview of the Trilinos Project

214. Oncogenic signaling pathways in the Cancer Genome Atlas

218. Pancreas Annulare

219. Pulmonary Valve Incompetence

220. Precocious Puberty

221. Protein S Deficiency

222. Proliferative Diabetic Retinopathy

223. Purine Nucleoside Phosphorylase Deficiency

224. Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type

225. Pseudohypoaldosteronism, Autosomal Recessive

226. Pendred Syndrome

227. Protoporphyria, Erythropoietic

228. Premature Complexes, Atrial and Ventricular

229. PHT

230. Porphyria, Variegate

231. Paroxysmal Cold Hemoglobinuria

232. Polychondritis Recidivans

233. Pierre Robin Syndrome

234. Preauricular Cyst

235. Phrenic Nerve Palsy

236. Pancreatitis, Hereditary

237. Palmitoylcarnitine Transferase

238. PFK Deficiency

239. 5p Monosomy

240. Partial Tetrasomy 15(pter-q13)

241. Primary Empty Sella

242. Persistent Neonatal Hyperinsulinism

243. Periodic Vestibulocerebellar Ataxia

244. Pachyonychia Congenita Type I

245. Pterin-4a-Carbinolamine Dehydratase Deficiency

246. Progressive Tapetochoroidal Dystrophy

247. Pulmonary Valve Stenosis with Atrial Septal Defect

248. Pleural Inflammation

249. 9p Monosomy

250. Primary Hyperoxaluria Types I and II

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