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    Clinical genomics : practical applications in adult patient care / editors, Michael F. Murray, Mark W. Babyatsky, Monica A. Giovanni ; associate editors, Fowzan S. Alkuraya, Douglas R. Stewart.

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    • Title:Clinical genomics : practical applications in adult patient care / editors, Michael F. Murray, Mark W. Babyatsky, Monica A. Giovanni ; associate editors, Fowzan S. Alkuraya, Douglas R. Stewart.
    •    
    • Other Contributors/Collections:Murray, Michael F.
      Babyatsky, Mark W.
      Giovanni, Monica A.
      Alkuraya, Fowzan S.
      Stewart, Douglas R.
    • Published/Created:New York : Mcgraw-Hill Education, ©2014.

    • Holdings

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    • Library of Congress Subjects:Genomics.
      Clinical medicine.
    • Medical Subjects: Genetics, Medical.
    • Description:xxx, 928 pages : illustrations ; 28 cm
    • Summary:The first book on the clinical application of genetics in primary care medicine, Clinical Genomics focuses on the everyday application of genetic assessment and its diagnostic, therapeutic, and preventive implications in clinical practice. Unlike traditional textbooks on medical genetics and dysmorphology, this is a clinical reference that covers many of the common diseases seen in everyday medical practice. Features: endorsed by the American College of Physicians; addresses the genetic basis of common chronic diseases, not just the classic diseases of dysmorphology.
    • Notes:Includes bibliographical references and index.
    • ISBN:0071622446
      9780071622448
    • Contents:Machine generated contents note: 1. Clinical Genomics
      -an Introduction
      2. Primary Care and Genomics
      Pharmacogenetics
      3. Pharmacogenomic Information in Drug Labeling
      4. Common Cytochrome P450 Polymorphisms and Pharmacogenetics
      5. Thiopurine Methyltransferase Pharmacogenetics
      6. Pharmacogenetics of Warfarin
      7. Clopidogrel Pharmacogenomics
      8. Tamoxifen Pharmacogenetics
      9. Statin-Induced Neuromyopathy
      10. Abacavir Pharmacogenomics
      Cardiovascular Disease
      11. Coronary Artery Disease
      12. Metabolic Syndrome
      13. Dyslipidemia
      14. Hypertriglyceridemia
      15. Familial Hypercholesterolemia
      16. Hypertension
      17. Stroke and Cerebrovascular Disease
      18. Thrombophilia
      19. Pulmonary Embolism and Deep Vein Thrombosis
      20. Arrhythmogenic Right Ventricular Cardiomyopathy
      21. Atrial Fibrillation
      22. Brugada Syndrome and Related Cardiac Diseases
      23. Long QT Syndrome
      24. Dilated Cardiomyopathy
      25. Hypertrophic Cardiomyopathy
      26. Bicuspid Aortic Valve Disease
      27. Thoracic Aortic Aneurysms and Acute Aortic Dissections
      28. Marfan Syndrome
      29. Loeys-Dietz Syndrome
      30. Abdominal Aortic Aneurysm
      Hematology
      31. Sickle Cell Anemia
      32. Hemophilia
      33. Aplastic Anemia, Bone Marrow Failure Syndromes
      34. Myeloproliferative Disorders
      35. Myelodysplastic Syndrome
      36. Acute Myeloid Leukemia
      37. Multiple Myeloma and Other Plasma Cell Disorders
      38. Alpha-Thalassemia
      39. Genetic Platelet Disorders
      Oncology
      40. Familial Cancer Syndromes
      41. Central Nervous System Tumors
      42. Esophageal Cancers
      43. Lung Cancer
      44. Cancers of the Small and Large Intestine
      45. Pancreatic Cancer
      46. Pancreatic Neuroendocrine Tumors
      47. Hereditary Pheochromocytoma and Paraganglioma
      48. Prostate Cancer
      49. Testicular Germ Cell Tumors
      50. Renal Cell Carcinoma
      51. PTEN Syndromes
      52. Hereditary Breast and Ovarian Cancer
      Endocrinology
      53. Obesity
      54. Diabetes Mellitus Type 1
      55. Diabetes Mellitus Type 2
      56. Maturity-Onset Diabetes of the Young
      57. Hypoglycemia
      58. Multiple Endocrine Neoplasia Type 1
      59. Multiple Endocrine Neoplasia Type 2
      60. Autoimmune Thyroid Diseases
      61. Adrenal Insufficiency
      62. Pituitary Tumors and Syndromes
      63. Disorders of Sexual Differentiation
      64. Congenital Adrenal Hyperplasia
      65. Osteopenia and Osteoporosis
      66. Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism Type 1
      67. Hypogonadotropic Hypogonadism
      Gastroenterology
      68. Celiac Disease
      69. Acute and Chronic Pancreatitis
      70. Inflammatory Bowel Disease
      71. Genetics of Constipation and Hirschsprung Disease
      72. Hereditary Hemochromatoses
      73. Wilson Disease
      74. Gilbert Syndrome
      75. Nonalcoholic Fatty Liver Disease
      76. Gallstone Disease
      Immunology
      77. Familial Autoinflammatory Diseases
      78. Common Variable Immune Deficiency
      79. Hereditary Angioedema
      80. Deficiency of Components of the Complement System
      81. Hemolytic Uremic Syndrome
      Infectious Disease
      82. Tuberculosis
      83. Malaria
      84. Genetics of HIV
      85. Hepatitis B and Hepatitis C Infection
      86. Bronchitis and Pneumonia
      Metabolic Disease
      87. Gaucher Disease
      88. Fabry Disease
      89. Porphyrias
      90. Hyperhomocysteinemia
      91. Hyperammonemia
      92. Hereditary Systemic Amyloidosis
      93. Glycogen Storage Disorders
      94. Cholesteryl Ester Storage Disease
      95. Organic Acidemias
      96. Primary Carnitine Deficiency
      97. Phenylketonuria
      Obstetrics
      98. Prenatal Testing, Noninvasive Screening, Invasive Testing, and Carrier Screening
      99. Recurrent Pregnancy Loss
      100. Folate and Neural Tube Defects
      101. Liver Disease in Pregnancy
      102. Pre-eclampsia
      Gynecology
      103. Genetic Basis of Female Infertility
      104. Polycystic Ovary Syndrome
      105. Uterine Leiomyomata
      Dermatology
      106. Psoriasis and Psoriatic Arthritis
      107. Hereditary Melanoma and Other High-Risk Skin Cancer Susceptibility Syndromes
      108. Neurofibromatosis Type 1
      109. Tuberous Sclerosis Complex
      110. Epidermolysis Bullosa
      111. Atopic Dermatitis
      112. Graft-Versus-Host Disease
      113. Nevoid Basal Cell Carcinoma Syndrome
      Pulmonology
      114. Cystic Fibrosis
      115. Alpha-1 Antitrypsin Deficiency
      116. Asthma
      117. Sarcoidosis
      118. Idiopathic Pulmonary Fibrosis
      119. Obstructive Sleep Apnea Syndrome
      120. Pulmonary Arterial Hypertension
      Neurology
      121. Epilepsy
      122. Autism Spectrum Disorders
      123. Frontotemporal Lobar Degeneration
      124. Alzheimer Disease
      125. Huntington Disease
      126. Parkinson Disease
      127. Multiple Sclerosis
      128. Ataxia-Telangiectasia
      129. von Hippel-Lindau Syndrome
      130. Amyotrophic Lateral Sclerosis
      131. Myotonic Dystrophy Type 1
      132. Charcot-Marie-Tooth Disease
      133. Genetic Prion Disease
      134. Hereditary Spastic Paraplegias
      135. Dystrophinopathics
      Psychiatry
      136. Depression
      137. Bipolar Mood Disorder
      138. Schizophrenia
      139. Genetics of Drug Addiction
      140. Nicotine Dependence
      Rheumatology
      141. Spondyloarthropathies
      142. Systemic Lupus Erythematosus
      143. Articular Chondrocalcinosis
      Nephrology
      144. Cystic Diseases of the Kidney, Polycystic Kidney Disease
      145. Nephrolithiasis
      146. Alport Syndrome
      Ophthalmology
      147. Age-related Cataract
      148. Primary Open Angle Glaucoma
      149. Age-Related Macular Degeneration
      150. Retinitis Pigmentosa
      Otolaryngology
      151. Nonsyndromic Sensorineural Hearing Loss
      152. Syndromic Hearing Loss
      153. Waardenburg Syndrome
      154. Vestibular Schwannoma and Neurofibromatosis 2
      Multisystem Disease
      155. Achondroplasia
      156. Malignant Hyperthermia
      157. Noonan Syndrome and Related Disorders
      158. Hereditary Hemorrhagic Telangiectasia
      159. Fragile X Syndrome and Related Conditions
      160. Werner Syndrome
      161. Prader-Willi and Angelman Syndromes: Examples of Genomic Imprinting
      162. Down Syndrome
      163. Turner Syndrome
      164. Klinefelter Syndrome and Related Sex Chromosome Aneuploidies
      165. 22q11.2 Deletion Syndrome
      166. Mitochondrial Disorders in Adult Patients
      167. Chromosomal Disorders in Adults
      168. Hereditary Disorders of Connective Tissue
      169. Ehlers-Danlos Syndrome, Hypermobility and Classical type
      Appendix
      170. Clinical Implications of Copy Number Variation in the Human Genome
      171. Genetic Privacy
      Race, Ancestry, and Genomics
      Population Genetics
      174. Transplantation Genetics and Genomics: Alloreactivity After Hematopoietic Stem Cell Transplantation
      175. Personalized Medicine in Clinical Practice
      176. Genomics and Evidence-Based Medicine
      177. MicroRNA in Cancer
      178. Genetic Syndromes of Childhood in Adults
      179. Clinical Interpretation of Genomic Data
      180. Genetic Risk Profiling in the Genomics Era
      181. Epigenetics and Clinical Medicine
      182. Clinical Potential of Stem Cells in Reproductive Medicine
      183. Effectively Integrating Genomic Clinical Decision Support into the EHR
      184. Genetic Assessment at the End of Life.
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