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1

The child with febrile seizures. Wright, 1988.

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2

Parker, James N., and Philip M. Parker. The official parent's sourcebook on febrile seizures. Edited by Icon Group International Inc. Icon Health Publications, 2002.

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3

Febrile Seizures. Academic Press, 2001.

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4

(Editor), Tallie Z. Baram, and Shlomo Shinnar (Editor), eds. Febrile Seizures. Academic Press, 2001.

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5

Febrile Seizures. Elsevier, 2002. http://dx.doi.org/10.1016/b978-0-12-078141-6.x5000-8.

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6

Wallace, Sheila J. The Child With Febrile Seizures. Butterworth-Heinemann, 1988.

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7

Kaplan, Tamara, and Tracey Milligan. Seizures and Epilepsy (DRAFT). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190650261.003.0008.

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The video in this chapter explores seizures and epilepsy, including definitions or focal or generalized seizures and epilepsy, as well as the differences between the two. It discusses risk factors for epilepsy (family history, history of febrile seizures, brain injury) and its diagnosis (by history and EEG), as well as comorbidities of epilepsy (mood and cognitive disorders, accidents, and sudden unexpected death).
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8

Technical report: Treatment of the child with simple febrile seizures. BMJ Publishing, 1999.

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9

Hart, Yvonne. Epilepsy. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0226.

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Epilepsy is defined as the tendency to recurrent unprovoked seizures, while a seizure can be defined as a transient excessive discharge of nerve cells within the brain, causing an event which is discernible to the person experiencing the seizure or to an observer. The term ‘epilepsy’ excludes provoked seizures, such as febrile seizures.
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10

Shorter, Edward, and Max Fink. Delirious Mania and Febrile Catatonia. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190881191.003.0008.

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The acute onset of excited, aggressive, and destructive states, often febrile, described as Bell’s mania and Stauder’s delirium are hallmarks in the literature. Death is frequent. Subjects are disoriented, and delirious with catatonia signs of mutism, posturing, and repetitive speech. Treatments were ineffective until multiple daily induced seizures (ECT) were shown to be life-saving. A syndrome of nostalgia was also described in French and German armies among subjects pining to death. Delirious mania and its fatal variants were a rock-solid part of traditional psychiatric diagnosis. By the 19
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11

Publications, ICON Health. Febrile Seizures - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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12

Publications, ICON Health. The Official Parent's Sourcebook on Febrile Seizures: A Revised and Updated Directory for the Internet Age. ICON Health Publications, 2002.

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13

Sadleir, Lynette G., Jozef Gecz, and Ingrid E. Scheffer. Epilepsies That Occur Predominantly in Girls. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0041.

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Availability of DNA sequencing has led to an increase in the number of children being identified with mutations in specific genes in specific epilepsy phenotypes. The presence of mutations that cause epilepsy only in females is one of the discoveries revealed in the sequencing era. Mutations in PCDH19 and CDKL5 are distinctive and identifiable forms of female-only epilepsy, and clinicians should consider PCDH19 in normal girls presenting with clusters of afebrile or febrile seizures in the first 3 years of life, and CDKL5 in girls or boys presenting with severe developmental delay within the f
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14

Hesdorffer, Dale C. Epidemiology of Epilepsy. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0042.

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Epilepsy affects 1 out of every 26 people during their lifetime. Worldwide, the incidence of epilepsy ranges from 28.0/100,000 to 235.5/100,000, with the large variation attributable to differences in methodology across studies. The prevalence of active epilepsy provides important information about the burden of epilepsy in the population and spurs public health planner to assess the needs of the epilepsy population. The active prevalence of epilepsy ranges from 2.4/1,000 to 22.8/1,000 worldwide and more than 65 million people have active epilepsy. Risk factors for childhood-onset and adult-on
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15

Shorter, Edward, and Max Fink. The Neuroleptic Malignant Syndrome. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190881191.003.0009.

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Reports of fatal febrile, hypertensive, tachycardic neurotoxic cases followed quickly on the introduction of potent new neuroleptic drugs in the 1970s. Patients became mute, rigid, posturing, and staring, showing the signs of catatonia. Labeled the neuroleptic malignant syndrome (NMS), attention was first given to neuroleptic blockade of dopamine receptors as the cause, but treatments with dopamine agonists (bromocriptine) and muscle relaxants (dantrolene) offered little benefit. When catatonia was recognized, treatments with benzodiazepines (lorazepam, diazepam) and induced seizures (electros
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