Blackwell's Underground Clinical Vignettes : Biochemistry,9780632045457

Blackwell's Underground Clinical Vignettes : Biochemistry

by ; ; ; ;
Edition: 3rd
ISBN13: 9780632045457
ISBN10: 0632045450
Format: Paperback
Pub. Date: 2002-01-01
Publisher(s): Lippincott Williams & Wilkins
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Summary

USMLE Step 1 ReviewBlackwell's Underground Clinical Vignettes (subject, ed.) is your primary source for clinically relevant, case-based material essential for Step 1 review. Each Clinical Vignette simulates USMLE format, and includes classic buzzwords in Hx, PE, lab, imaging and pathology. This revised edition contains:· Carefully selected cases templated to fit the way you are tested and taught to think · Valuable links to Step 1 and 2 Atlases for emphasis on photographic case studies· 50+ new cases compatible with the updated content of USMLE Step 1 Study with the student-to-student publisher you can trust!Blackwell's Underground Clinical Vignettes Step 1 Series:Anatomy, 3e 0-632-04541-8 Behavioral Sciences, 3e 0-632-04543-4 Biochemistry, 3e 0-632-04545-0Microbiology V.I, 3e 0-632-04547-7Microbiology V.II, 3e 0-632-04549-3Pathophysiology V.I, 3e 0-632-04551-5Pathophysiology V.II, 3e 0-632-04553-1Pathophysiology V.III, 3e 0-632-04555-8 Pharmacology, 3e 0-632-04557-4Basic Science Color Atlas 0-632-04635-X Perfect for medical students -- physician assistants, nurse practitioners and related health professionals will also find Undergrond Clinical Vignettes valuable.Available at Medical Bookstores everywhere!Or contact:1-800-449-2758email: csbooks@blacksci.com

Table of Contents

Acknowledgments x
Preface to the 3rd Edition xiii
How to Use This Book xvi
Abbreviations xvii
Endocrinology
17-Alpha-Hydroxylase Deficiency
5-Alpha-Reductase Deficiency
Acromegaly
Addison's Disease
Bartter's Syndrome
Congenital Adrenal Hyperplasia
Diabetes Insipidus
Diabetic Ketoacidosis
Glucagonoma
Hirsutism---Idiopathic
Hyperaldosteronism---Primary
Hypercalcemia
Hyperparathyroidism---Primary
Hyperthyroidism (Graves' Disease)
Hypocalcemia from Pancreatitis
Hypokalemia
Hypomagnesemia
Hyponatremia
Insulinoma
Kallmann's Syndrome
Kwashiorkor
Lactic Acidosis
Metabolic Alkalosis
Nonketotic Hyperosmolar Coma
Osteomalacia
Pheochromocytoma
Precocious Puberty
Pseudohypoparathyroidism
Rickets
SIADH
Thyroid Storm
Vitamin A Deficiency
Vitamin B1 Deficiency (Beriberi)
Vitamin B3 Deficiency (Pellagra)
Vitamin C Deficiency (Scurvy)
Vitamin K Deficiency
Gastroenterology
Carcinoid Syndrome
Crigler-Najjar Syndrome
Dubin-Johnson Syndrome
Gilbert's Disease
Wilson's Disease
Genetics
Acute Intermittent Porphyria
Albinism
Alkaptonuria
Cystic Fibrosis
Cystinuria
Ehlers-Danlos Syndrome
Fabry's Disease
Familial Hypercholesterolemia
Familial Hypertriglyceridemia
Fanconi's Anemia
Fragile X Syndrome
Galactosemia
Gaucher's Disease
Hereditary Fructose Intolerance
Homocystinuria
Hunter's Disease
Hurler's Disease
Kartagener's Syndrome
Klinefelter's Syndrome
Krabbe's Disease
Lesch-Nyhan Syndrome
Maple Syrup Urine Disease
Metachromatic Leukodystrophy
Niemann-Pick Disease
Orotic Aciduria
Phenylketonuria (PKU)
Phosphoenolpyruvate Carboxykinase Deficiency
Pompe's Disease
Porphyria Cutanea Tarda
Pyruvate Kinase Deficiency
Tay-Sachs Disease
von Gierke's Disease
Xeroderma Pigmentosum
Hematology/Oncology
Anemia---Folate Deficiency
Anemia---Iron Deficiency
Anemia---Vitamin B12 Deficiency
Glucose-6-Phosphate Dehydrogenase Deficiency
Hemophilia, Type A
Hereditary Spherocytosis
Methemoglobinemia
Paroxysmal Nocturnal Hemoglobinuria
Nephrology/Urology
Renal Tubular Acidosis
Rhabdomyolysis
Neurology
Duchenne's Muscular Dystrophy
Wernicke-Korsakoff Syndrome
Gynecology
Primary Amenorrhea---Testicular Feminization
Secondary Amenorrhea
Orthopedics
Osteogenesis Imperfecta
Psychopharmacology
Antabuse Effect
Pulmonary
Hyaline Membrane Disease
Alpha-1-Antitrypsin Deficiency
Hyperventilation
Carbon Monoxide Poisoning
Rheumatology
Gout

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