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Books on the topic 'Epilepsis'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

The brainstorms companion: Epilepsy in our view. New York: Raven Press, 1994.

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2

Epilepsien: Fragen u. Antworten. München: Zuckschwerdt, 1987.

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3

Parkinson, Gill. Epilepsy. New York, NY: Continuum, 2006.

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4

Seizures and epilepsy. Philadelphia: F.A. Davis Co., 1989.

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5

Epilepsia: Enfermedad sagrada del cerebro. México, D.F: Fondo de Cultura Económica, 1999.

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6

Guberman, Alan. Essentials of clinical epilepsy. 2nd ed. Boston: Butterworth-Heinemann, 1999.

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7

Illinois. Dept. of Human Rights. An Employers guide to epilepsy. Chicago, Ill: Illinois Dept. of Human Rights, 1989.

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8

Shorvon, S. D. (Simon D.) and British Medical Association, eds. Understanding epilepsy. Poole: Family Doctor, 2009.

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9

The educator's guide to students with epilepsy. Springfield, Ill: Charles C. Thomas, 1995.

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10

Zarrina, Kurtz, ed. Special services for people with epilepsy in the 1970s. London: H.M.S.O., 1987.

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11

Status epilepticus: Its clinical features and treatment in children and adults. Cambridge: Cambridge University Press, 1994.

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12

Dannhardt, Gerd, Susann Seddigh, and Thomas Vogt. Epilepsie. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-56244-0.

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13

Bauer, Jürgen. Epilepsie. Heidelberg: Steinkopff, 2002. http://dx.doi.org/10.1007/978-3-642-57519-8.

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14

Elger, Christian E., and Anke Brockhaus. Epilepsie. Wiesbaden: Deutscher Universitätsverlag, 1997. http://dx.doi.org/10.1007/978-3-663-01651-9.

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15

Gunning, Boudewijn, and Frans Leijten. Epilepsie. Houten: Bohn Stafleu van Loghum, 2018. http://dx.doi.org/10.1007/978-90-368-2058-5.

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16

Levene, Anna. My friend has epilepsy. London: Chrysalis Children's Book, 2003.

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17

Rogan, Peter J. Epilepsy: A teacher's handbook. 2nd ed. (Liverpool): Roby Education for Mersey Region Epilepsy Association, 1986.

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18

Rogan, Peter J. Epilepsy: The detective's story. Lancaster: Quay, 1987.

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19

Singh, Anuradha. 100 questions and answers about your child's epilepsy. One hundred questions and answers about your child's epilepsy: Jones and Bartlett, 2009.

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20

The epilepsies: Diagnosis and management. Baltimore: Urban & Schwarzenberg, 1990.

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21

Williams, Michael V. Searching in the dark. Imperial Beach, CA: Aventine Press, 1993.

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22

Seized: Searching for health in the United States. Tamarac, FL: Llumina Press, 2013.

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23

Blume, Warren T., G. Bryan Young, Peter L. Carlen, Samuel Wiebe, and Ante Padjen. Intractable epilepsies. Philadelphia: Lippincott Williams & Wilkins, 2005.

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24

Epilepsy in children. 2nd ed. New York: Raven Press, 1994.

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25

Epilepsies of childhood. 2nd ed. London: Butterworths, 1985.

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26

Epilepsy in children. New York: Raven Press, 1986.

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27

Epilepsies of childhood. 3rd ed. Oxford: Butterworth-Heinemann, 1994.

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28

Keaney, Brian. That's what friends are for. Leeds: Epilepsy Action, 2003.

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29

Reese, Robert. Healing fits: The cure of an epileptic. Los Angeles: Big Sky Press, 1988.

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30

Fejerman, Natalio. Convivir Con Epilepsia/ Coexisting With Epilepsy. Editorial Medica Panamericana, 2007.

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31

Nita, Dragos A., Miguel A. Cortez, Jose Luis Perez Velazquez, and O. Carter Snead. Biological Bases of Symptomatic Generalized Epilepsies in Children. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0040.

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Symptomatic generalized epilepsies represent a group of challenging epilepsy syndromes, most often seen in children, which share the hallmark of a triad encompassing multiple seizure types, electroencephalographical (EEG) evidence of diffuse brain involvement, and dysfunction in the intellectual domain (global developmental delay or mental retardation). SGEs include the early myoclonic encephalopathy, early infantile epileptic encephalopathy (Ohtahara syndrome), West syndrome, epilepsy with myoclonic-astatic seizures, epilepsy with myoclonic absence, Lennox-Gastaut syndrome, and the progressive myoclonic epilepsies. SGEs may arise from various genetic, developmental, or acquired brain pathologies and also can be associated with other cerebral or systemic defects and thus being part of a broader epilepsy syndrome phenotype. SGEs are associated with significant mortality and morbidity and most patients with SGE grow up to have intractable epilepsy, mental retardation, and depend on parents and institutions for the activities of the daily living. The mechanisms of SGE are numerous and heterogeneous and the EEG findings usually reflect the age-related changes as the brain matures.

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32

1932-, Meinardi Harry, Bruyn G. W, and Vinken P. J, eds. The epilepsies. Amsterdam: Elsevier, 1999.

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33

Smith, P. E. M., and S. J. Wallace. Clinicians' Guide to Epilepsy. A Hodder Arnold Publication, 2001.

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34

The Epilepsies, Part I. Elsevier, 1999.

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35

Malafosse, A. Idiopathic Generalized Epilepsies (Current Problems in Epilepsy). John Libbey Eurotext Limited, 1994.

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36

Beal, Jules C., Monika Eisermann, Sunita Misra, Phillip L. Pearl, Perrine Plouin, Eli M. Mizrahi, and Solomon L. Moshe. Seizures and Epilepsy in Preterm and Term Neonates, Infants, Children, and Adolescents. Edited by Donald L. Schomer and Fernando H. Lopes da Silva. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228484.003.0018.

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Children are often affected by seizure types and epilepsy syndromes that are specific to their age group and distinct from those seen in adults. At the same time, certain epilepsy syndromes affecting the adult population, such as Lennox–Gastaut syndrome and juvenile myoclonic epilepsy, often begin during childhood, as do seizures related to genetic abnormalities. The use of electroencephalography (EEG) and prolonged EEG monitoring has allowed for further insight and greater specificity in identifying and understanding seizures and epilepsy syndromes in children. This chapter reviews the role of EEG in pediatric seizures and the pediatric epilepsies, including electrographic findings in the ictal state and in the interictal period, as well as the correlation with clinical seizure semiology as it contributes to the diagnosis of epileptic phenomena. The chapter discusses EEG patterns, seizure types, and epilepsy syndromes specific to neonates, infants, children, and adolescents.

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37

Bergin, Ann M. Ketogenic Diet in Established Epilepsy Indications. Edited by Eric H. Kossoff. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190497996.003.0006.

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The ketogenic diet is a metabolic therapy that provides an alternative strategy for seizure control in medication-resistant epilepsy. Many decades of continued use of diet therapy, amassing consistent observational evidence, was recently supported by a randomized, controlled study indicating benefit of diet treatment in children with refractory epilepsy as compared with a control group who continued with standard of care and delayed diet treatment for three months. Well-established uses include children with refractory, nonsurgical epilepsies and epileptic encephalopathies including infantile spasms and West syndrome, Lennox Gastaut syndrome, and Dravet and Doose syndromes. Current knowledge on the efficacy and role of diet therapy in these conditions are discussed.

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38

Kessler, Sudha Kilaru. The Ketogenic Diet and Related Therapies in “Novel” Situations. Edited by Eric H. Kossoff. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190497996.003.0008.

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The ketogenic diet (KD) is often considered as a treatment option for medication-resistant focal epilepsies and symptomatic generalized epilepsies, but is perhaps less commonly considered for idiopathic generalized epilepsies. The evidence for the use of the KD in two common idiopathic generalized epilepsy syndromes, childhood absence epilepsy and juvenile myoclonic epilepsy, is presented here.

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39

Wieser, H. G., E. H. Speckmann, and J. Engel. The Epileptic Focus (Current Problems in Epilepsy). Demos Medical Publishing, 1987.

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40

Shorvon, Simon, Renzo Guerrini, Mark Cook, and Samden Lhatoo, eds. Oxford Textbook of Epilepsy and Epileptic Seizures. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199659043.001.0001.

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41

Oxford Textbook of Epilepsy and Epileptic Seizures. Oxford University Press, 2013.

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42

Nehlig, Astrid. Childhood Epilepsies and Brain Development (Current Problems in Epilepsy). John Libbey Eurotext Limited, 1999.

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43

Epilepsy: 100 Elementary Principles. 3rd ed. W.B. Saunders Company, 1995.

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44

Wolf, P. Epileptic Seizures And Syndromes (Current Problems in Epilepsy). John Libbey Eurotext Limited, 1994.

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45

C, Schachter Steven, and Rowan A. J, eds. The brainstorms healer: Epilepsy in our experience : stories of health care professionals as care providers and patients. Philadelphia, PA: Lippincott-Raven, 1998.

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46

Crespel, Arielle, Philippe Gelisse, Michelle Bureau, and Pierre Genton. Atlas of Electroencephalography Vol 2. The Epilepsies. EEG and Epileptic Syndromes. John Libbey Eurotext Ltd, 2006.

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47

Massimo, Avoli, ed. Generalized epilepsy: Neurobiological approaches. Boston: Birkhäuser, 1990.

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48

National Society for Epilepsy (Corporate Author), ed. Epilepsy (Ward Lock Family Health Guides). Ward Lock Ltd, 1995.

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49

Duncan, J. S., and C. P. Panayiotopoulos. Typical Absences and Related Epileptic Syndromes. Elsevier, 1995.

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50

Levene, Anna. Has Epilepsy (My Friend). Chrysalis Children's Books, 2005.

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