Oral and maxillofacial diseases : an illustrated guide to the diagnosis and management of diseases of the oral mucosa, gingivae, teeth, salivary glands, jaw bones and joints

Oral and maxillofacial diseases : an illustrated guide to the diagnosis and management of diseases of the oral mucosa, gingivae, teeth, salivary glands, jaw bones and joints / Crispian Scully [and others].

One of the most comprehensive illustrated coverages available of the oral and maxillofacial manifestations of diseases has now been revised and further extended to include problems with newer classes of drugs and systemic diseases.

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Bibliographic Details
Other Authors: Scully, Crispian
Format: eBook
Language:English
Published: London : Informa Healthcare, ©2010.
Edition:4th ed.
Subjects:
Mouth > Diseases.
Mouth > Diseases > Diagnosis.
Mouth > Diseases > Treatment.
Face > Diseases.
Face > Diseases > Diagnosis.
Face > Diseases > Treatment.
Maxilla > Diseases.
Maxilla > Diseases > Diagnosis.
Maxilla > Diseases > Treatment.
MEDICAL > Gastroenterology.
Face > Diseases
Face > Diseases > Diagnosis
Maxilla > Diseases
Mouth > Diseases
Mouth > Diseases > Diagnosis
Online Access:Click for online access
Table of Contents:
  • Front Cover; CONTENTS; PREFACE TO THE FOURTH EDITION; 1 MAXILLOFACIAL COMPLICATIONS IN SYSTEMIC CONDITIONS; 1.1 CARDIOVASCULAR DISEASE; ANGINA PECTORIS; ANGIOMAS; ANTICOAGULANTS; CONGENITAL HEART DISEASE; DRUGS; GIANT CELL ARTERITIS; HEREDITARY HAEMORRHAGIC TELANGIECTASIA (HHT); HYPERTENSION; POLYARTERITIS NODOSA; TRANSPLANTATION; WEGENER GRANULOMATOSIS; WILLIAMS SYNDROME; FURTHER READING; 1.2 ENDOCRINOLOGICAL AND METABOLIC CONDITIONS; ADDISON DISEASE; Clinical features; Diagnosis; Management; CONGENITAL HYPOPARATHYROIDISM; CONGENITAL HYPOTHYROIDISM; CUSHING SYNDROME; DIABETES INSIPIDUS.
  • DIABETES MELLITUSGIGANTISM/ACROMEGALY; HYPERPARATHYROIDISM; Clinical features; Diagnosis; Management; HYPERTHYROIDISM; HYPOTHYROIDISM; MULTIPLE ENDOCRINE NEOPLASIA (ADENOMA) (MEN OR MEA) SYNDROMES; PITUITARY DWARFISM; PRECOCIOUS PUBERTY; PREGNANCY; Clinical features; Pregnancy gingivitis; Pregnancy epulis; Diagnosis; Management; PRETERM CHILDREN; METABOLIC DISORDERS; FURTHER READING; 1.3 GASTROINTESTINAL AND PANCREATIC DISORDERS; CHRONIC PANCREATITIS; COELIAC DISEASE; CROHN DISEASE; Clinical features; Diagnosis; Management; CYSTIC FIBROSIS; FAMILIAL ADENOMATOUS POLYPOSIS (FAP).
  • Clinical featuresDiagnosis; Management; GASTRO-OESOPHAGEAL REFLUX DISEASE (GORD); MALABSORPTION; NEOPLASMS; PERNICIOUS ANAEMIA; PEUTZ-JEGHER SYNDROME; Clinical features; Diagnosis; Management; SHORT BOWEL SYNDROME; ULCERATIVE COLITIS; FURTHER READING; 1.4 HAEMATOLOGICAL DISEASE; AGRANULOCYTOSIS; APLASTIC ANAEMIA; BLEEDING TENDENCIES; FANCONI ANAEMIA; HAEMATINIC DEFICIENCY; Clinical features; Diagnosis; Management; HAEMATOPOIETIC STEM CELL TRANSPLANTATION; HAEMOGLOBINOPATHIES; HAEMOLYTIC DISEASE OF NEWBORN; HAEMOPHILIA; HYPEREOSINOPHILIC SYNDROME (HES); HYPOPLASMINOGENAEMIA; LEUKAEMIAS.
  • LEUKOCYTE DEFECTSLYMPHOMAS; MULTIPLE MYELOMA; Clinical features; Diagnosis; Management; PLASMACYTOSIS; PLUMMER-VINSON SYNDROME; POLYCYTHAEMIA; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE; FURTHER READING; 1.5 HEPATOLOGICAL DISEASE; CIRRHOSIS; HEPATITIS; JAUNDICE; PRIMARY BILIARY CIRRHOSIS; TRANSPLANTATION; FURTHER READING; 1.6 IATROGENIC CONDITIONS; HAEMATOPOIETIC STEM CELL TRANSPLANTATION; GRAFT-VERSUS-HOST DISEASE; Diagnosis; Management; ORGAN TRANSPLANTATION; Complications; PHARMACOTHERAPY; CHEMOTHERAPY; IMMUNOSUPPRESSIVE AGENTS; TETRACYCLINES; OTHER DRUGS; OSTEONECROSIS OF THE JAWS (ONJ.
  • OSTEOCHEMONECROSIS)Clinical features; Diagnosis; Management; RADIOTHERAPY; OSTEORADIONECROSIS; Clinical features; Diagnosis; Management; SURGERY; DRY SOCKET (ALVEOLAR OSTEITIS); Clinical features; Diagnosis; Management; OROANTRAL FISTULA; Clinical features; Diagnosis; Management; ORONASAL FISTULA; DENTAL MATERIALS; FURTHER READING; 1.7 IMMUNODEFICIENCIES; ACATALASIA; ATAXIA TELANGIECTASIA; CHRONIC MUCOCUTANEOUS CANDIDOSIS; AUTOIMMUNE POLYENDOCRINOPATHY
  • CANDIDOSIS
  • ECTODERMAL DYSTROPHY; COMMON VARIABLE IMMUNODEFICIENCY; DI GEORGE SYNDROME; HEREDITARY ANGIOEDEMA; Clinical features.

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