Wheeler’s Dental Anatomy, Physiology and Occlusion, 10e 10th Edition
Author: Stanley J. Nelson DDS MS ID: 0323263232
Hardcover: 392 pagesPublisher: Saunders; 10 edition (January 2, 2015)Language: EnglishISBN-10: 0323263232ISBN-13: 978-0323263238 Product Dimensions: 1 x 8.8 x 11.2 inches Shipping Weight: 3.2 pounds (View shipping rates and policies) Best Sellers Rank: #505,640 in Books (See Top 100 in Books) #4 in Books > Medical Books > Dentistry > Anatomy & Physiology #160 in Books > Textbooks > Medicine & Health Sciences > Dentistry > General #494 in Books > Textbooks > Medicine & Health Sciences > Medicine > Basic Sciences > Anatomy Download Wheeler’s Dental Anatomy, Physiology and Occlusion, 10e 10th Edition PDF
Dental Anatomy Coloring Book, 2e 2nd Edition
Author: Margaret J. Fehrenbach RDH MS ID: 1455745898
Paperback: 448 pagesPublisher: Saunders; 2 edition (February 12, 2013)Language: EnglishISBN-10: 1455745898ISBN-13: 978-1455745890 Product Dimensions: 10.7 x 8.4 x 0.8 inches Shipping Weight: 2 pounds (View shipping rates and policies) Best Sellers Rank: #263,234 in Books (See Top 100 in Books) #30 in Books > Textbooks > Medicine & Health Sciences > Dentistry > Dental Hygiene #38 in Books > Medical Books > Dentistry > Dental Hygiene #51 in Books > Textbooks > Medicine & Health Sciences > Dentistry > Dental Assisting
This book is ok, but not spectacular like those I used for a regular Anatomy and Physiology class. This book contains a lot of information but not a variety of "sketches" for a student to color in in different colors in order to learn the different parts of the head, mouth, etc. I am wondering if there are "better" coloring books out there for this subject.
A must for my dental hygiene class.
I did not end up using this text because my professor had similar worksheets that she handed out in class, but this is a good way to learn anatomy if you are a visual learner. Download Dental Anatomy Coloring Book, 2e 2nd Edition PDF
Fundamentals of Clinical Trials 5th ed. 2015 Edition
Author: Lawrence M. Friedman ID: 3319185381
From the Back Cover
This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. Most chapters have been revised considerably from the fourth edition. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing, and international trials.
This book is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The authors use numerous examples of published clinical trials to illustrate the fundamentals.
The text is organized sequentially from defining the question to trial closeout. One chapter is devoted to each of the critical areas to aid the clinical trial researcher. These areas include pre-specifying the scientific questions to be tested and appropriate outcome measures, determining the organizational structure, estimating an adequate sample size, specifying the randomization procedure, implementing the intervention and visit schedules for participant evaluation, establishing an interim data and safety monitoring plan, detailing the final analysis plan, and reporting the trial results according to the pre-specified objectives.
Although a basic introductory statistics course is helpful in maximizing the benefit of this book, a researcher or practitioner with limited statistical background would still find most if not all the chapters understandable and helpful. While the technical material has been kept to a minimum, the statistician may still find the principles and fundamentals presented in this text useful. This book has been successfully used for teaching courses in clinical trial methodology.
About the Author
Lawrence M. Friedman received his M.D. from the University of Pittsburgh. After training in internal medicine, he went to the National Heart, Lung and Blood Institute of the National Institutes of Health. During his many years there, Dr. Friedman was involved in numerous clinical trials and epidemiology studies, having major roles in their design, management and monitoring. While at the NIH and subsequently, he served as a consultant on clinical trials to various NIH institutes and to other governmental and nongovernmental organizations. Dr. Friedman has been a member of many data monitoring and other safety committees.
Curt D. Furberg is Professor Emeritus of the Division of Public Health Sciences of the Wake Forest University School of Medicine. He received his M.D. and Ph.D. at the University of Umea, Sweden, and is a former chief, Clinical Trials Branch and Associate Director, Clinical Applications and Prevention Program, National Heart, Lung, and Blood Institute. Dr. Furberg established the Department of Public Health Sciences and served as its chair from 1986 to 1999. He has played major scientific and administrative roles in numerous multicenter clinical trials and has served in a consultative or advisory capacity on others. Dr. Furbergs research activities include the areas of clinical trials methodology and cardiovascular epidemiology. He is actively involved in the debate about the need for better documentation of meaningful clinical efficacy and long-term safety for drugs intended for chronic use.
David L. DeMets, PhD is currently the Max Halperin Professor of Biostatistics and former Chair of the Department of Biostatistics and Medical Informatics at the University of Wisconsin Madison He has co-authored numerous papers on statistical methods and four texts on clinical trials, two specifically on data monitoring. He has served on many NIH and industry-sponsored data monitoring committees for clinical trials in diverse disciplines. He served on the Board of Directors of the American Statistical Association, as well as having been President of the Society for Clinical Trials and President of the Eastern North American Region (ENAR) of the Biometric Society. In addition he was Elected Fellow of the International Statistics Institute, the American Statistical Association, the Association for the Advancement of Science, the Society for Clinical Trials and the American Medical Informatics Association. In 2013, he was elected as a member of the Institute of Medicine.
Christopher B. Granger is Professor of Medicine at Duke University, where he is an active clinical cardiologist and a clinical trialist at the Duke Clinical Research Institute. He received his M.D. at University of Connecticut and his residency training at the University of Colorado. He has had Steering Committee, academic leadership, and operational responsibilities for many clinical trials in cardiology. He has been on numerous Data Monitoring Committees. He serves on the National Heart, Lung, and Blood Institute Board of External Experts. He works with the Clinical Trials Transformation Initiative, a partnership between the U.S. Food and Drug Administration and Duke aiming to increase the quality and efficiency of clinical trials. He is a founding member of the Sensible Guidelines for the Conduct of Clinical Trials group, a collaboration between McMaster, Oxford, and Duke Universities.
David M. Reboussin is a Professor in the Department of Biostatistical Science at the Wake Forest University School of Medicine, where he has worked since 1992. He has a masters degree in Statistics from the University of Chicago and received his doctorate in Statistics from the University of Wisconsin at Madison. He is currently Principle Investigator for the Systolic Blood Pressure Intervention Trial Coordinating Center and has been a co-investigator in the coordinating centers for several NIH and industry funded clinical trials including Action to Control Cardiovascular Risk in Diabetes (ACCORD), Action for Health in Diabetes (Look AHEAD), the Combined Oral and Nutritional Treatment of Late-Onset Diabetes Trial (CONTROL DM) and the Estrogen Replacement and Atherosclerosis (ERA) Trial. Dr. Reboussin has served on the Data and Safety Monitoring Boards for many National Institutes of Health trials within areas including cardiology, diabetes, nephrology, pulmonology, liver disease, psychiatry, pediatrics, weight loss and smoking cessation. His work in statistical methodology has included techniques and software for sequential monitoring of clinical trials.
Hardcover: 550 pagesPublisher: Springer; 5th ed. 2015 edition (August 30, 2015)Language: EnglishISBN-10: 3319185381ISBN-13: 978-3319185385 Product Dimensions: 10.6 x 1.4 x 6.6 inches Shipping Weight: 1.6 pounds (View shipping rates and policies) Best Sellers Rank: #368,121 in Books (See Top 100 in Books) #97 in Books > Textbooks > Medicine & Health Sciences > Research > Biostatistics #154 in Books > Medical Books > Basic Sciences > Biostatistics #195 in Books > Textbooks > Medicine & Health Sciences > Research > Epidemiology Download Fundamentals of Clinical Trials 5th ed. 2015 Edition PDF
Wardlaw’s Perspectives in Nutrition 10th Edition
Author: Visit ‘s Carol Byrd-Bredbenner Page ID: 0078021413
About the Author
Danita Saxon Kelley, Ph.D., R.D., earned her doctorate in nutritional sciences from the University of Kentucky. She serves as Associate Dean of the College of Health and Human Services and is a Professor in the Family and Consumer Sciences Department at Western Kentucky University. Previously, Dr. Kelley was Director of the Didactic Program in Dietetics at Western Kentucky University. She is a Past President of the Board of Directors for the Kentucky Academy of Nutrition and Dietetics. Her scholarly work has focused on healthy eating of adolescents, communication skills of dietetic students, histaminergic activity and regulation of food intake, and dietary restriction effects on the antioxidant defense system. She has received awards for teaching from the Kentucky Academy of Nutrition and Dietetics and the Dietetic Educators of Practitioners of the Academy of Nutrition and Dietetics. She enjoys singing, walking her dog, cheering for her family in water-ski competitions, and watching her children participate in athletic and musical endeavors.
Carol Byrd-Bredbenner, Ph.D., R.D., FAND, received her doctorate from Pennsylvania State University. Currently, she is Professor in the Nutritional Sciences Department at Rutgers, The State University of New Jersey. She teaches a wide range of undergraduate and graduate nutrition courses. Her research interests focus on investigating environmental factors that affect dietary choices and health outcomes. Dr. Byrd-Bredbenner has authored numerous nutrition texts, journal articles, and computer software packages. She has received teaching awards from the American Dietetic Association (now called the Academy of Nutrition and Dietetics), Society for Nutrition Education, and U.S. Department of Agriculture. She was the recipient of the American Dietetic Associations Anita Owen Award for Innovative Nutrition Education Programs. She also was a Fellow of the United Nations, World Health Organization at the WHO Collaborating Center for Nutrition Education, University of Athens, Greece. She enjoys exploring food and culinary customs, traveling, diving, and gardening.
Jacqueline R. Berning, P h.D., R. D., CSSD , earned her doctorate in nutrition from Colorado State University in Fort Collins, Colorado. She is currently Professor and Chair of the Health Science Department at the University of Colorado at Colorado Springs (UCCS), where she has won numerous teaching awards. Dr. Berning is published in the area of sports dietetics and was the sport dietitian for the Denver Broncos for over 25 years, Cleveland Indians for 18 years, and Colorado Rockies for 10 years. Currently she is the sport dietitian for UCCS athletics and US Lacrosse. She is active in the Academy of Nutrition and Dietetics, where she served as the chair of the Program Planning Committee for FNCE and is currently Chair of the Appeals Committee. In 2014, Dr. Berning was awarded the Mary Abbot Hess Award for Culinary Events for teaching the University of Colorado football team how to grocery shop and cook. Additionally, she served 6 years as an ADA spokesperson and is a former chair of the Sports, Cardiovascular, and Wellness Nutritionists dietetics practice group. She enjoys walking, hiking, and gardening.
Gaile L. Moe, Ph. D., R.D., earned a doctorate in nutritional sciences at the University of Washington. She is a registered dietitian who has worked in clinical nutrition, research, and management, as well as education. She is currently Professor and Director of the Didactic Program in Dietetics at Seattle Pacific University. She has published in peer-reviewed journals in the areas of nutrition and cancer and media reporting of nutrition research. Gaile enjoys swimming, cycling, walking, and hiking, along with learning about culinary traditions, food, and food policy.
Hardcover: 992 pagesPublisher: McGraw-Hill Education; 10 edition (January 7, 2015)Language: EnglishISBN-10: 0078021413ISBN-13: 978-0078021411 Product Dimensions: 9.1 x 1.5 x 10.9 inches Shipping Weight: 4.6 pounds (View shipping rates and policies) Best Sellers Rank: #332,673 in Books (See Top 100 in Books) #133 in Books > Textbooks > Medicine & Health Sciences > Medicine > Clinical > Nutrition #316 in Books > Textbooks > Medicine & Health Sciences > Medicine > Basic Sciences > Physiology #553 in Books > Medical Books > Basic Sciences > Physiology
It’s was a great deal because it came with an acces code as well for only $30-$40 and when my school was charging $80 alone for the code and $120 alone for the text Download Wardlaw’s Perspectives in Nutrition 10th Edition PDF
s research activities include the areas of clinical trials methodology and cardiovascular epidemiology. He is actively involved in the debate about the need for better documentation of meaningful clinical efficacy and long-term safety for drugs intended for chronic use.
Madison He has co-authored numerous papers on statistical methods and four texts on clinical trials, two specifically on data monitoring. He has served on many NIH and industry-sponsored data monitoring committees for clinical trials in diverse disciplines. He served on the Board of Directors of the American Statistical Association, as well as having been President of the Society for Clinical Trials and President of the Eastern North American Region (ENAR) of the Biometric Society. In addition he was Elected Fellow of the International Statistics Institute, the American Statistical Association, the Association for the Advancement of Science, the Society for Clinical Trials and the American Medical Informatics Association. In 2013, he was elected as a member of the Institute of Medicine.