نتایج جستجو برای: pfeiffer
تعداد نتایج: 963 فیلتر نتایج به سال:
1Department of Mathematics, Islamic Azad University, Science and Research Branch, Tehran, Iran 2Department of Mathematics, Islamic Azad University, Rasht Branch, Rasht, Iran 3Department of Health Administration, Pfeiffer University, Charlotte, USA 4Department of Mathematics, Shahid Beheshti University, Tehran, Iran 5Department of Management Science, University of Science and Technology of China...
Craniosynostosis syndromes are characterized by premature closure of one or more cranial sutures, associated with other malformations, the most frequent of which are the Crouzon and Apert syndromes. Few studies in the literature have addressed the oral health of these individuals. The purpose of this study was to compare the periodontal status of individuals with Apert, Crouzon, Pfeiffer and Sa...
http://adb.sagepub.com/content/1/2/123 The online version of this article can be found at: DOI: 10.1177/105971239200100201 1992 1: 123 Adaptive Behavior A.W. Dinges, M. Glagow and W.W. Schwippert J.-P. Ewert, H. Buxbaum-Conradi, S. Fingerling, E. Schürg-Pfeiffer, T.W. Beneke, Discrimination: A Neurobiological Analysis Toward Neural Engineering Adapted and Adaptive Properties in Neural Networks ...
Sophia Mueller ([email protected]) Nina Weichert ([email protected]) Veit Stoecklein ([email protected]) Ariane Hammitzsch ([email protected]) Giulia Pasciuto ([email protected]) Christian Krug ([email protected]) Matthias Holzer ([email protected]) Mona Pfeiffer ([email protected]) ...
A description is given of Physa acuta Draparnaud, 1805, based on topotypic specimens from the Garonne river basin, and additional samples from the environs of the French cities of Montpellier and Perpignan. It proved indistinguishable, in shell and anatomy, from topotypic Physa cubensis Pfeiffer, 1839, thus leading the authors to admit the synonymy of the two nominal species under the older nam...
Pfeiffer syndrome (PS) is mainly characterized by craniosysnostosis, midface hypoplasia, great toes with partial syndactyly of the digits, broad and medially deviated thumbs. It is caused by allelic mutations in the fibroblast growth factor receptor 1 and 2 (FGFR1 and 2) genes. This study describes the clinical and genetic features of five Brazilian families affected by PS. All patients exhibit...
Line 40 of Callimachus’ Coma Berenices (fr. 110 Pfeiffer = Harder 213 Massimilla) has been transmitted with an initial lacuna. This article aims to defend a supplement proposed by Lenchantin and discarded all subsequent editors. Este articulo trata sobre una laguna al principio de la línea del frg. (= [2012] Massimilla [2010]) Calímaco, conocido como El rizo Berenice. autor tiene objetivo defen...
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