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Books on the topic 'Epileptic Syndromes'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Panayiotopoulos, C. P. Reflex seizures and related epileptic syndromes. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4042-9.

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2

Lüders, Hans. Atlas of epileptic seizures and syndromes. Saunders, 2001.

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3

J, Roger, ed. Epileptic syndromes in infancy, childhood and adolescence. 2nd ed. J. Libbey, 1992.

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4

J, Roger, ed. Epileptic syndromes in infancy, childhood and adolescence. Libbey Eurotext, 1985.

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5

Panayiotopoulos, C. P. Benign Childhood Focal Seizures and Related Epileptic Syndromes. Springer London, 2011. http://dx.doi.org/10.1007/978-1-84996-477-7.

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6

Panayiotopoulos, C. P. A Clinical Guide to Epileptic Syndromes and their Treatment. Springer London, 2010. http://dx.doi.org/10.1007/978-1-84628-644-5.

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7

Panayiotopoulos, C. P. A clinical guide to epileptic syndromes and their treatment: Based on the new ILAE diagnostic scheme. Bladon Medical Pub., 2002.

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8

Panayiotopoulos, C. P. Panayiotopoulos syndrome: A common and benign childhood epileptic syndrome. John Libbey, 2002.

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9

Panayiotopoulos, C. P. Reflex seizures and related epileptic syndromes. Springer, 2012.

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10

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

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11

Panayiotopoulos, C. P. Reflex seizures and related epileptic syndromes. Springer, 2012.

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12

Mukhin, K. Yu, A. A. Kholin, M. B. Mironov, A. S. Petrukhin, and H. Holthausen. Epileptic Encephalopathies: & Related Syndromes in Children. Libbey Eurotext Limited, John, 2014.

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13

Atlas of Epileptic Seizures and Syndromes. W.B. Saunders Company, 2001.

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14

Dravet, Charlotte, Antonio Delgado-Escueta, Carlo Alberto Tassinari, Michelle Bureau, and Pierre Genton. Epileptic Syndromes in Infancy, Childhood and Adolescence. Editions John Libbey Eurotext, 2022.

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15

Dravet, Charlotte, Michelle Bureau, and Pierre Genton. Epileptic Syndromes in Infancy, Childhood and Adolescence. Editions John Libbey Eurotext, 2013.

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16

Dravet, Charlotte, Antonio Delgado-Escueta, Renzo Guerrini, Michelle Bureau, and Pierre Genton. Epileptic Syndromes in Infancy, Childhood and Adolescence-. Editions John Libbey Eurotext, 2019.

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17

Epileptic Syndromes in Infancy, Childhood and Adolescence. 3rd ed. John Libbey Eurotext, 2002.

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18

Wolf, Peter, J. Roger, M. Bureau, Ch Dravet, F. E. Dreifuss, and A. Perret. Epileptic Syndromes in Infancy, Childhood and Adolescence. 2nd ed. Butterworth-Heinemann, 2005.

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19

Panayiotopoulos, C. P. Clinical Guide to Epileptic Syndromes and Their Treatment. Springer London, Limited, 2007.

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20

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

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21

Benign Childhood Focal Seizures And Related Epileptic Syndromes. Springer, 2010.

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22

Panayiotopoulos, C. P. Benign Childhood partial Seizures and Related Epileptic Syndromes. John Libbey Eurotext Limited, 1999.

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23

Crespel, Arielle, Philippe Gelisse, Michelle Bureau, and Pierre Genton. Atlas of Electroencephalography: The Epilepsies, EEG and Epileptic Syndromes. Editions John Libbey Eurotext, 2019.

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24

A Clinical Guide to Epileptic Syndromes and their Treatment. Springer, 2010.

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25

Dravet, Charlotte, P. Genton, C. A. Tassinari, M. Bureau, and Joseph Roger. Epileptic Syndromes in Infancy, Childhood and Adolescence, 4th Edition. Editions John Libbey Eurotext, 2005.

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26

A Clinical Guide to Epileptic Syndromes and their Treatment. Bladon Medical Publishing, 2002.

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27

A Clinical Guide to Epileptic Syndromes and their Treatment. 2nd ed. Springer, 2007.

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28

Peter, Wolf, ed. Epileptic seizures and syndromes: With some of their theoretical implications. 1994.

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29

Dreifuss, Fritz E., J. Roger, D. Dravet, and M. Bureau. Epileptic Syndromes in Infancy, Childhood and Adolescence: Current Problems in Epilepsy. Demos Medical Publishing, 1985.

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30

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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31

Beal, Jules C., Monika Eisermann, Sunita Misra, et al. 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 o

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32

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

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33

Nobili, Lino, Paola Proserpio, Steve Gibbs, and Giuseppe Plazzi. Sleep and epilepsy. Edited by Sudhansu Chokroverty, Luigi Ferini-Strambi, and Christopher Kennard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199682003.003.0028.

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This chapter on sleep and epilepsy examines the activating and deactivating properties of NREM and REM sleep states on interictal epileptic activity and seizures. It reviews specific epileptic syndromes in which seizures manifest a tendency to present exclusively or predominantly during sleep or upon wakening. Particular attention is paid to the description of the different forms of nocturnal frontal lobe epilepsy: autosomal dominant and lesional. There is also a discussion of the negative bidirectional relationship between epilepsy and sleep disorders (sleep apneas and parasomnias) and the ef

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34

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 progressiv

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35

Forsyth, Rob, and Richard Newton. Specific conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198784449.003.0004.

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This chapter adopts a systematic approach to common diagnoses in paediatric neurology, aetiologies, management to include investigation and treatment, and outcome. For each condition current knowledge on cause and underlying biology is summarized. A rational approach to investigation and treatment is summarized for each topic. These include: acquired brain injury; autoimmune and autoinflammatory disease of the CNS; cerebral palsy and neurodisability which covers feeding, communication, special senses, and respiratory disease; demyelinating disease; epilepsy including its impact on daily life;

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36

Guzetta, Franco, Bernardo Dalla Bernadina, and Renzo Guerrini. Progress in Epileptic Spasms and West Syndrome. Libbey Eurotext Limited, John, 2007.

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37

Hodges, John R. Illustrative Cases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198749189.003.0008.

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This chapter comprises 16 case histories that illustrate methods of assessment described in the rest of this book and the use of the Addenbrooke’s Cognitive Examination (ACE)-III. Each case begins with a brief history from the patient and observations by the family followed by findings on cognitive examination focusing on the profile shown on the ACE-III, the results of imaging investigations, and a discussion of the diagnosis and its differential, with a final summary of the principal conclusions, indicating whether the services of a neuropsychologist are required or not. The cases present im

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38

Firth, Stacey. Understanding Canine Epileptoid Cramping Syndrome. CreateSpace Independent Publishing Platform, 2018.

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39

Meisner, Meike. Spektralanalytische Auswertung von Elektroenzephalogrammen bei Kindern mit BNS-Epilepsie und Lennox-Syndrom. 1988.

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40

Kaplan, Tamara, and Tracey Milligan. Neurologic Emergencies (DRAFT). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190650261.003.0023.

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The video in this chapter discusses neurologic emergencies, including the symptoms of increased intracranial pressure leading to herniation, subarachnoid haemorrhage (can be due to aneurysm, vascular malformation, or reversible cerebral vasoconstriction syndrome, and definition and management of status epilepticus.

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41

Caraceni, Augusto, Cinzia Martini, and Fabio Simonetti. Neurological problems in advanced cancer. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0141.

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Neurological complications are frequent in populations with advanced cancer. An adequate neurological assessment is always important in addressing pain, cognitive symptoms, and peripheral and central nervous system complications. This chapter discusses a variety of neurological problems found in advanced cancer together with their clinical aspects and management, including some suggested regimens for pharmacological therapy. Complications that are discussed include intracranial hypertension, seizures in patients with advanced illness (including a suggested algorithm for the management of statu

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42

Jolly, Elaine, Andrew Fry, and Afzal Chaudhry, eds. Acute medical emergencies and practical procedures. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199230457.003.0001.

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Chapter 1 covers the basic science and clinical topics relating to acute medical emergencies and practical procedures which trainees are required to learn as part of their basic training and demonstrate in the MRCP. It covers cardiorespiratory arrest, shock, acute coronary syndromes, tachycardia, bradycardia, hypertensive emergencies, pulmonary oedema, acute asthma, massive pulmonary embolism, acute upper gastrointestinal haemorrhage, acute kidney injury, coma, traumatic brain injury, status epilepticus, adrenal crisis, thyroid emergencies, acute poisoning, and burns.

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43

Friedman, Deborah I., Shamin Masrour, and Susan Hutchinson. Headache. Edited by Emma Ciafaloni, Cheryl Bushnell, and Loralei L. Thornburg. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190667351.003.0012.

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In most cases, women with headache disorders have normal pregnancy and delivery outcomes and should not be discouraged from becoming pregnant. Pre-pregnancy planning includes weaning of contraindicated medications. Most women with migraine without aura improve during pregnancy. Although there are limitations, various acute and preventive treatments may be employed, including non-pharmacologic options. Anti-epileptic medications should be avoided. For pseudotumor cerebri, the mainstay of treatment includes diuretics and therapeutic lumbar punctures, avoiding topiramate. Surgical treatment may b

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44

Waldmann, Carl, Neil Soni, and Andrew Rhodes. Neurological disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199229581.003.0022.

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Agitation and confusion 360Status epilepticus 362Meningitis 364Intracerebral haemorrhage 366Subarachnoid haemorrhage 368Ischaemic stroke 370Guillain–Barre syndrome 372Myasthenia gravis 374ICU neuromuscular disorders 376Tetanus 378Botulism 380Neurorehabilitation 382Hyperthermias 384Agitation and confusion are common features in critical illness. Agitation is a symptom or sign of numerous acute and chronic disease states that include pain, anxiety and delirium. Agitation is present in around half of ICU patients, with 15% experiencing severe agitation. Confusion may also be chronic or acute and

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45

Adam, Sheila, Sue Osborne, and John Welch. Neurological problems. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199696260.003.0008.

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This chapter provides an overview of the care and management of neurological disorders commonly seen in critical care, starting with an outline of the anatomy and physiology of the nervous system. The concepts of awareness, consciousness, and arousal, and the use of the Glasgow Coma Scale (GCS) to assess conscious level are discussed. The management and monitoring of raised intracranial pressure, cerebral perfusion pressure, and the impact on cerebral blood flow are detailed. The management of sodium and water balance, including diabetes insipidus, is outlined. There are overviews of the manag

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46

Smith, Martin, Giuseppe Citerio, W. Andrew Kofke, and Geert Meyfroidt. Oxford Textbook of Neurocritical Care. 2nd ed. Oxford University PressOxford, 2025. https://doi.org/10.1093/med/9780198864714.001.0001.

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Abstract Neurocritical care is a multidisciplinary specialty that provides comprehensive management for life-threatening disorders of the central nervous system and their complications. The second edition of the Oxford Textbook of Neurocritical Care brings together international experts from many disciplines to provide an overview of all aspects of neurocritical care. In 33 updated or new chapters, this textbook covers the pathophysiology of acute neurological conditions, including acute brain injury, advancements in neuromonitoring and neuroimaging techniques, evidenced-based treatment strate

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