Maxillofacial examination

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  • 1. Introduction During the diagnosis of oral and maxillofacial diseases, clinical and radiological data play a major role. In this region, only a good clinical diagnosis along with a radiological examination may lead to a successful diagnosis. A successful diagnosis and evaluation of clinical examination are generally up to a profound knowledge of the normal anatomy of the region.

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  • It is difficult to overstress the importance of a good history and thorough clinical examination for every patient. On this the diagnosis is made and the treatment plan based. A full, clearly written record of the original consultation is essential to assess progress following treatment. Particularly is this true if a colleague should be called to see the patient in the practitioner's tioner's absenceT. he medicolegali mportanceo f accurater ecords cannot be overemphasised.

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  • This book brings together core text from the traditional subject areas of oral surgery, oral medicine, oral pathology and radiology to help readers to organise their knowledge in a useful way to solve clinical problems. We believe that this core text of knowledge is essential reading for university final examination success and will also be of help to graduates undertaking vocational training, their trainers and those preparing for postgraduate professional examinations such as MFDS.

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  • is with great pleasure and honor that I embrace the opportunity to write this book. After more than 25 years of practice, clinical observation, and case documentation, you get excited about what works and what does not work. The case study format is an excellent way to share this knowledge. All the cases are presented in a systematic format illustrating examination, diagnosis, diagnostic wax - up, treatment plan, treatment sequence, provisionalization, and the fi nished case.

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  • It is a great pleasure to introduce volume 19 of the book series Monographs in Human Genetics entitled ‘Craniosynostoses: Molecular Genetics, Principles of Diagnosis and Treatment’. The initial idea for this book was born during a workshop on craniosynostoses held at the Academy of Human Genetics in Würzburg (Germany). Hartmut Collmann and Wolfram Kress brought together many seemingly diverse aspects of craniosynostoses, including clinical approaches, genetics, molecular mechanisms and, most importantly, treatments.

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