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  1. Article ; Online: Towards equality in global epilepsy care and other neurological disorders.

    Cross, J Helen

    Developmental medicine and child neurology

    2023  Volume 66, Issue 2, Page(s) 140–141

    MeSH term(s) Humans ; Epilepsy/therapy ; Health Equity
    Language English
    Publishing date 2023-11-20
    Publishing country England
    Document type Letter
    ZDB-ID 80369-8
    ISSN 1469-8749 ; 0012-1622
    ISSN (online) 1469-8749
    ISSN 0012-1622
    DOI 10.1111/dmcn.15813
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  2. Book: Long term outcomes of epilepsy surgery in adults and children

    Malmgren, Kristina / Baxendale, Sallie / Cross, J. Helen

    2015  

    Title variant Long-term outcomes of epilepsy surgery in adults and children
    Author's details Kristina Malmgren ; Sallie Baxendale ; J. Helen Cross ed
    Keywords epilepsy surgery ; long-term outcome ; seizure outcome ; social outcome ; study methodology
    Language English
    Size IX, 283 S. : Ill., graph. Darst., 235 mm x 155 mm
    Publisher Springer
    Publishing place Cham u.a.
    Publishing country Switzerland
    Document type Book
    HBZ-ID HT018674894
    ISBN 978-3-319-17782-3 ; 3-319-17782-6 ; 9783319177830 ; 3319177834
    Database Catalogue ZB MED Medicine, Health

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    2015 A 2271 available for loan (reading room) Lesesaal EG

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  3. Article ; Online: Diagnosis of Lennox-Gastaut syndrome and strategies for early recognition.

    Pujar, Suresh / Cross, J Helen

    Expert review of neurotherapeutics

    2024  Volume 24, Issue 4, Page(s) 383–389

    Abstract: Introduction: Lennox Gastaut syndrome (LGS) as an electroclinical diagnosis has been utilized as a clinical entity for more than 70 years. However, with the recognition of other distinct electroclinical epilepsy syndromes, no consistent single etiology, ...

    Abstract Introduction: Lennox Gastaut syndrome (LGS) as an electroclinical diagnosis has been utilized as a clinical entity for more than 70 years. However, with the recognition of other distinct electroclinical epilepsy syndromes, no consistent single etiology, and the variability of criteria used in clinical trials, the clinical utility of such a diagnosis has been questioned. Recently, the International League Against Epilepsy for the first time defined diagnostic criteria for epilepsy syndromes, thereby allowing consistent language and inclusion criteria to be utilized.
    Areas covered: Recent diagnostic criteria for syndrome diagnosis are explored as defined by the International League Against Epilepsy, with further literature reviewed to highlight relevant features, and differential diagnosis explored.
    Expert opinion: Developmental and Epileptic Encephalopathy (DEE) is an overall term that may be descriptive of many different epilepsies, most of early onset, whether electroclinically or etiologically defined, of which LGS is one. Although we have moved forward in defining an increasing number of etiologically specific syndromes, this to date remains a minority of the DEEs. Although there is progress with precision medicine targeted at specific causes, the term LGS still remains useful as a diagnosis in defining treatment options, as well as overall prognosis.
    MeSH term(s) Humans ; Lennox Gastaut Syndrome/diagnosis ; Electroencephalography ; Epilepsy/diagnosis ; Epileptic Syndromes/diagnosis ; Diagnosis, Differential ; Status Epilepticus/diagnosis ; Epilepsy, Generalized
    Language English
    Publishing date 2024-02-28
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2112534-X
    ISSN 1744-8360 ; 1473-7175
    ISSN (online) 1744-8360
    ISSN 1473-7175
    DOI 10.1080/14737175.2024.2323568
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  4. Book: Pediatric epilepsy

    Duchowny, Michael S. / Cross, J. Helen / Arzimanoglou, Alexis

    2012  

    Abstract: Practical, easy-to-follow guidance on every aspect of the diagnosis and treatment of epilepsy in children 350 full-color illustrations Pediatric Epilepsy comprehensively addresses the needs of all physicians treating children with epilepsy -- from the ... ...

    Author's details ed. Michael Duchowny ; J. Helen Cross ; Alexis Arzimanoglou
    Abstract "Practical, easy-to-follow guidance on every aspect of the diagnosis and treatment of epilepsy in children 350 full-color illustrations Pediatric Epilepsy comprehensively addresses the needs of all physicians treating children with epilepsy -- from the specialized pediatric epileptologist to the general pediatric practitioner. Written by a team of international experts, this full-color text offers a consistent, age-based approach to the diagnosis and treatment of every type of seizure and epilepsy syndrome that may occur in childhood. The book's primary focus is on specific treatment modalities, both surgical and medical.Features Algorithms and drug-dosage tables throughout emphasize patient care Includes first, second, and combination drug treatments with recommended starting ranges and other essential information Specific types of seizures and syndromes are organized by the age group in which they most often present Logically organized by age group, then by the seizures and syndromes that tend to first occur at those ages Co-morbidities section addresses illnesses caused by epilepsy treatment and illnesses that often present with epilepsy treatment International authorship by a team of five award-winning pediatric epileptologists 350 full-color illustrations"--Provided by publisher
    Keywords Epilepsy ; Infant ; Child ; Adolescent
    Language English
    Size XVII, 507 S. : Ill., graph. Darst.
    Publisher McGraw-Hill Med
    Publishing place New York u.a.
    Publishing country United States
    Document type Book
    Note Includes bibliographical references and index
    HBZ-ID HT017400490
    ISBN 978-0-07-149621-6 ; 0-07-149621-1
    Database Catalogue ZB MED Medicine, Health

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    Shelf markLoan statusLocation
    2012 A 3879 order for loan Magazin

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  5. Article ; Online: Genetics in the epilepsies - A broadening concept.

    Cross, J Helen

    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

    2020  Volume 24, Page(s) 8

    MeSH term(s) Epilepsy ; Humans
    Language English
    Publishing date 2020-01-10
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 1397146-3
    ISSN 1532-2130 ; 1090-3798
    ISSN (online) 1532-2130
    ISSN 1090-3798
    DOI 10.1016/j.ejpn.2020.01.009
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  6. Article ; Online: Raising the bar: Fenfluramine sets new treatment standards for Dravet syndrome.

    Sullivan, Joseph / Helen Cross, J

    Epilepsy & behavior : E&B

    2021  Volume 121, Issue Pt A, Page(s) 108061

    MeSH term(s) Anticonvulsants/therapeutic use ; Epilepsies, Myoclonic/drug therapy ; Fenfluramine/therapeutic use ; Humans ; Spasms, Infantile/drug therapy
    Chemical Substances Anticonvulsants ; Fenfluramine (2DS058H2CF)
    Language English
    Publishing date 2021-05-28
    Publishing country United States
    Document type Editorial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2010587-3
    ISSN 1525-5069 ; 1525-5050
    ISSN (online) 1525-5069
    ISSN 1525-5050
    DOI 10.1016/j.yebeh.2021.108061
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  7. Article ; Online: Implications of the KIWE trial for low-income and lower-middle-income countries - Authors' reply.

    Cross, J Helen / Schoeler, Natasha E / Marston, Louise / Freemantle, Nick

    The Lancet. Neurology

    2024  Volume 23, Issue 4, Page(s) 332–333

    MeSH term(s) Humans ; Developing Countries ; Poverty ; Income
    Language English
    Publishing date 2024-02-27
    Publishing country England
    Document type Letter
    ZDB-ID 2081241-3
    ISSN 1474-4465 ; 1474-4422
    ISSN (online) 1474-4465
    ISSN 1474-4422
    DOI 10.1016/S1474-4422(24)00080-2
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  8. Article ; Online: Epilepsy in 2020-a new dawn.

    Cross, J Helen

    The Lancet. Neurology

    2020  Volume 20, Issue 1, Page(s) 8–10

    MeSH term(s) Animals ; Clinical Trials as Topic ; Databases as Topic ; Epilepsies, Myoclonic/therapy ; Epilepsy/drug therapy ; Epilepsy/genetics ; Epilepsy/pathology ; Epilepsy/therapy ; Fenfluramine/pharmacology ; Genetic Therapy ; Humans ; NAV1.1 Voltage-Gated Sodium Channel ; Neuroimaging ; Serotonin Uptake Inhibitors/pharmacology
    Chemical Substances NAV1.1 Voltage-Gated Sodium Channel ; SCN1A protein, human ; Serotonin Uptake Inhibitors ; Fenfluramine (2DS058H2CF)
    Language English
    Publishing date 2020-12-10
    Publishing country England
    Document type Journal Article
    ZDB-ID 2081241-3
    ISSN 1474-4465 ; 1474-4422
    ISSN (online) 1474-4465
    ISSN 1474-4422
    DOI 10.1016/S1474-4422(20)30438-5
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  9. Article ; Online: Newer versus older antiseizure medications: further forward?

    Cross, J Helen / Tomson, Torbjorn

    Lancet (London, England)

    2021  Volume 397, Issue 10282, Page(s) 1327–1329

    MeSH term(s) Anticonvulsants/therapeutic use ; Humans ; Seizures/drug therapy
    Chemical Substances Anticonvulsants
    Language English
    Publishing date 2021-04-07
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(21)00435-9
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  10. Article ; Online: Ketogenic dietary therapy utilization in Kenya: A qualitative exploration of dietitian's perceptions.

    Samia, Pauline / Naanyu, Violet / Helen Cross, J / Idro, Richard / Boon, Paul / Wilmshurst, Jo / Luchters, Stanley

    Epilepsy & behavior reports

    2024  Volume 26, Page(s) 100661

    Abstract: This study utilized a qualitative design to explore dietitians' perceptions regarding Ketogenic Diet Therapy (KDT) for patients with drug-resistant epilepsy in Kenya. Dietitians from Kenya were selected and consented. Audio-recorded interviews were ... ...

    Abstract This study utilized a qualitative design to explore dietitians' perceptions regarding Ketogenic Diet Therapy (KDT) for patients with drug-resistant epilepsy in Kenya. Dietitians from Kenya were selected and consented. Audio-recorded interviews were conducted, followed by thematic analysis of verbatim transcripts to identify recurring patterns. The study enrolled 18 dietitians, fourteen of whom correctly described their understanding of KDT for managing drug-resistant epilepsy. There was a lack of confidence in their capacity to initiate the KDT with all expressing the need for further training and facilitation. Only one dietitian reported having initiated and maintained KDT. There was an overall positive view regarding KDT and willingness to implement KDT for patients with drug-resistant epilepsy. Dietitians expressed concerns regarding the availability of national policies, inadequate staffing to support families who require KDT, and the cost of implementing this intervention. Dietitians expressed interest in virtual training to enhance their understanding of KDT. Dietitians in Kenya are mostly aware of KDT utilization for the management of drug-resistant epilepsy. However, they cited poor capability and various barriers to implementation. There is a need for policies to facilitate KDT as a treatment option for the benefit of patients with drug-resistant epilepsy.
    Language English
    Publishing date 2024-03-20
    Publishing country United States
    Document type Journal Article
    ISSN 2589-9864
    ISSN (online) 2589-9864
    DOI 10.1016/j.ebr.2024.100661
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