CHAPTER 92 VIRAL MENINGITIS AND ENCEPHALITIS Alan C. Jackson Acute viral infections of the central nervous system (CNS) are normally classified into two clinical syndromes, meningitis and encephalitis, which reflects…
CHAPTER 113 NEUROLOGY OF CARDIOLOGY Martin A. Samuels The neurology of cardiology may be divided into three categories: (1) the cardiac complications of neurological disease; (2) the neurological complications of…
CHAPTER 112 NEUROLOGY OF PREGNANCY AND THE PUERPERIUM Steven Feske, Autumn Klein The hormonal changes of pregnancy mediate a multitude of physiological effects that promote successful gestation and birth and…
CHAPTER 59 TRIGEMINAL AUTONOMIC CEPHALALGIAS: CLUSTER HEADACHE AND RELATED CONDITIONS Peter J. Goadsby*, The trigeminal autonomic cephalalgias (TACs) are a grouping of headache syndromes recognized in the second edition of…
CHAPTER 20 CONVERSION AND DISSOCIATION SYNDROMES Christopher Bass Social historians have confidently asserted that conversion hysteria has disappeared from clinical practice, to be replaced by syndromes characterized by fatigue and…
CHAPTER 46 CEREBRAL VENOUS THROMBOSIS Gian Luigi Lenzi, Alessio Mercurio, Marta Altieri Cerebral vein and sinus thrombosis (CVST) is a rare event in comparison with arterial stroke, accounting for less…
CHAPTER 74 EPIDEMIOLOGY AND GENETICS OF MULTIPLE SCLEROSIS Jan D. Lünemann, Roland Martin Multiple sclerosis is a chronic inflammatory disease of the central nervous system (CNS) that usually begins in…
CHAPTER 119 NEUROLOGY OF RHEUMATOLOGY, IMMUNOLOGY, AND TRANSPLANTATION Richard Rosenbaum Evaluation of patients with rheumatic, inflammatory, or post-transplantation neurological syndromes is challenging because these patients can have a wide variety…
CHAPTER 86 THE CONGENITAL MYOPATHIES Heinz Jungbluth, Caroline A. Sewry, Francesco Muntoni The congenital myopathies are a clinically and genetically heterogeneous group of congenital muscle disorders with characteristic structural abnormalities…
CHAPTER 108 WILSON DISEASE John H. Menkes Wilson Disease is an autosomal recessive disorder of copper metabolism caused by mutations in the ATP7B gene. The gene product, a P-type adenosine…
