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Shigeaki Kobayashi and Akio Morita

;78(6):987-93. 15. Kawashima M, Rhoton AJ, Tanriover N, Ulm AJ, Yasuda A, Fujii K. Microsurgical anatomy of cerebral revascularization. Part I: anterior circulation. J Neurosurg. 2005;102(1):116-31. 16. Kawashima M, Rhoton AJ, Tanriover N, Ulm AJ, Yasuda A, Fujii K. Microsurgical anatomy of cerebral revascularization. Part II: posterior circulation. J Neurosurg. 2005;102(1):132-47. 17. Funaki T, Matsushima T, Peris-Celda M, Valentine RJ, Joo W, Rhoton AJ. Focal transnasal approach to the upper, middle, and lower clivus. Neurosurgery. 2013

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Oliver Graupner, Christian Enzensberger, Larissa Wieg, Aline Wolter, Can Yerebakan, Markus Khalil and Roland Axt-Fliedner

myocardial deformation by Doppler strain rate echocardiography in humans: Validation against three-dimensional tagged magnetic resonance imaging. Circulation 2002;106:50-6. 23. Willruth AM, Geipel AK, Fimmers R, Gembruch UG. Assessment of right ventricular global and regional longitudinal peak systolic strain, strain rate and velocity in healthy fetuses and impact of gestational age using a novel speckle/feature-tracking based algorithm. Ultrasound Obstet Gynecol. 2011 Feb;37(2):143-9.

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Paulo Zielinsky

. Tada T, et al.: Human ductus arteriosus. A histological study on the relation between ductal maturation and gestational age. Acta Pathol Jpn 1985, 35 (1) : 23-34 5. Slomp J, et al.: Formation of intimal cushions in the ductus arteriosus as a model for vascular intimal thickening. An immunohistochemical study of changes in extracellular matrix components. Atherosclerosis 1992, 93 (1-2): 25-39 6. de Reeder EG, et al.: Distribution of prostacyclin synthase, 6-ketoprostaglandin F1 alpha, and 15-hydroxy-prostaglandin dehydrogenase in the

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Henu Kumar Verma, Saikrishna Lakkakula and Bhaskar V.K.S. Lakkakula

, HbD, HbE, and HbO. Figure 1 Classification of inherited hemoglobin disorders. The distribution of hemoglobinopathies varies from place to place, and much of the global burden of hemoglobinopathies is mainly correlated with malaria endemicity [ 3 ]. Further, hemoglobin SS disease (SCA) is the most common cause of sickle cell disease (SCD) and is most prevalent in Africa, Asia, and Mediterranean regions [ 4 ]. Beta-thalassemia is prevalent in populations of African descent and in regions of the Mediterranean, the Middle East, Transcaucasus, Central