Idioma: Inglés
Publicado por Princeton University Press, 2005
ISBN 10: 0691074429 ISBN 13: 9780691074429
Librería: WorldofBooks, Goring-By-Sea, WS, Reino Unido
EUR 7,86
Cantidad disponible: 1 disponibles
Añadir al carritoPaperback. Condición: Very Good. The book has been read, but is in excellent condition. Pages are intact and not marred by notes or highlighting. The spine remains undamaged.
ISBN 10: 711716140X ISBN 13: 9787117161404
Librería: liu xing, Nanjing, JS, China
EUR 188,97
Cantidad disponible: 1 disponibles
Añadir al carritoHardcover. Condición: New. Ship out in 2 business day, And Fast shipping, Free Tracking number will be provided after the shipment.By HardCover. Pub Date: December 2012 Pages: 447 Language: Chinese Publisher: People's Medical Publishing House system diseases of oral and maxillofacial characterization are the best-selling book of the first three editions. collected more than 1300 cases demonstrate oral maxillary facial performance of the disease. is undoubtedly the books in the field of visual system diseases of oral and maxillofacial characterization. The new version of the re-finishing neck anatomy in accordance with the type of disease and anatomical regions (new) classification. while increasing clinical guidance medication and adverse reactions chapter system diseases of oral and maxillofacial characterization of disease diagnosis and treatment Practical guide books. This book is the oral mucosal diseases. oral pathology. oral and maxillofacial surgery. head and neck surgery. ENT. Department of Infectious Diseases. dermatologists and other specialists in the diagnosis of diseases of the important books. Contents: 1. Systemic disease complications of maxillofacial 1.1 cardiovascular disease angina hemangioma anticoagulants congenital heart disease drugs giant cell arteritis hereditary hemorrhagic telangiectasia hypertension nodular arteritis organ the transplant Wegener granulomatosis Williams syndrome reference literature 1.2 endocrine and metabolic diseases. Addison's disease congenital parathyroid dysfunction. congenital hypothyroidism Cushing syndrome. diabetes insipidus diabetes gigantism / acromegaly parathyroid hyperfunction thyroid function hyperthyroidism hypothyroidism multiple endocrine neoplasia pituitary dwarfism precocious puberty pregnancy preterm children metabolic diseases References 1.3 gastrointestinal and pancreatic disease. chronic pancreatitis. chylous diarrhea Crohn disease cystic fibrosis. familial adenomatous polyposis gastroesophageal reflux disease pernicious anemia. malabsorption tumor Peutz-Jegher The deficiency syndrome short bowel syndrome. ulcerative colitis Reference 1.4 blood system diseases myeloid aplastic anemia. Fanconi anemia. nutritional deficiencies bleeding tendency hemoglobinopathy newborn hemolytic blood hematopoietic stem cell transplantation The low plasminogen hyperlipidemia leukemia leukocyte defects of the Friends of the disease eosinophilia syndrome lymphoma. multiple myeloma plasma cells histiocytosis Plummer-Vinson syndrome in polycythemia vera the disorder 2 thrombocytopenia of VOII Willeand disease References 1.5 liver disease cirrhosis hepatitis the jaundice of primary biliary cirrhosis liver transplantation References 1.6 iatrogenesis hematopoietic stem cell transplantation graft-versus-host disease in organ transplant drug treatment chemical treatment of the surgical treatment of Osteonecrosis of the jaw radiotherapy osteoradionecrosis immunosuppressants other drugs of the tetracycline class of drugs dry socket oral maxillary sinus fistula nose and mouth fistula dental materials References 1.7 immunodeficiency disease catalase deficiency ataxia - telangiectasia syndrome chronic mucocutaneous candidiasis the autoimmune polyendocrine - candidiasis ectoderm malnutrition common variable immunodeficiency disease Di George syndrome hereditary angioedema human immunodeficiency virus disease and acquired immune deficiency syndrome. hyper-IgM syndrome leukocytes defects myeloperoxidase deficiency neutropenia palm plantar keratosis - periodontal destruction syndrome. selective IgA deficiency with severe combined immunodeficiency sex-linked agammaglobulinemia T cell immunodeficiency. Wiskott-Aldrich syndrome reference literature 1.8 infections aspergillosis. blastomycosis actinomycosis candidiasis cat scratch disease Coxsackie and ECHO virus cytomegalovirus (CMV) EB virus gonorrhea herpes simplex virus (HsV) varicella zoster histoplasmosis patients class immunodeficiency virus (HIV) human herpes virus 6 (.