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  1. Book: Chiari I malformation

    Limbrick, David D.

    (Neurosurgery clinics of North America ; volume 34, number 1 (January 2023))

    2023  

    Author's details editors David D. Limbrick, Jr, Jeffrey R. Leonard
    Series title Neurosurgery clinics of North America ; volume 34, number 1 (January 2023)
    Collection
    Language English
    Size xv, 192 Seiten, Illustrationen
    Publisher Elsevier
    Publishing place Philadelphia, Pennsylvania
    Publishing country United States
    Document type Book
    HBZ-ID HT021716226
    ISBN 978-0-323-93855-6 ; 0-323-93855-8
    Database Catalogue ZB MED Medicine, Health

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  2. Book ; Online ; E-Book: Cerebrospinal fluid disorders

    Limbrick Jr, David D. / Leonard, Jeffrey Russell

    lifelong implications

    2019  

    Author's details David D. Limbrick Jr., Jeffrey R. Leonard editors
    Keywords Neurosurgery ; Emergency medicine ; Neurology
    Subject code 617.48
    Language English
    Size 1 Online-Ressource (xi, 387 Seiten)
    Publisher Springer
    Publishing place Cham
    Publishing country Switzerland
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT019932434
    ISBN 978-3-319-97928-1 ; 9783319979274 ; 3-319-97928-0 ; 3319979272
    DOI 10.1007/978-3-319-97928-1
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  3. Article ; Online: Advances in the Field of Chiari I Malformation and Integrating Them into Clinical Practice.

    Limbrick, David D / Leonard, Jeffrey R

    Neurosurgery clinics of North America

    2022  Volume 34, Issue 1, Page(s) xv

    Language English
    Publishing date 2022-11-24
    Publishing country United States
    Document type Editorial
    ZDB-ID 1196855-2
    ISSN 1558-1349 ; 1042-3680
    ISSN (online) 1558-1349
    ISSN 1042-3680
    DOI 10.1016/j.nec.2022.10.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Posterior Fossa Decompression with or Without Duraplasty for Chiari I Malformation.

    Yahanda, Alexander T / Limbrick, David D

    Neurosurgery clinics of North America

    2022  Volume 34, Issue 1, Page(s) 105–111

    Abstract: Posterior fossa decompression (PFD) with/without duraplasty is the standard surgical treatment for symptomatic CM-1. Posterior fossa decompression without duraplasty (PFD) may be associated with shorter operative times and hospital stays, fewer ... ...

    Abstract Posterior fossa decompression (PFD) with/without duraplasty is the standard surgical treatment for symptomatic CM-1. Posterior fossa decompression without duraplasty (PFD) may be associated with shorter operative times and hospital stays, fewer complications, and may yield improvements in symptoms and syrinx sizes. Posterior fossa decompression with duraplasty (PFDD) may be associated with superior long-term symptomatic improvements, larger syrinx reductions, and a lower need for revision decompression. Various dural graft materials may be used for PFDD, though the ideal type of graft has not been definitively established. Other adjunct surgical procedures may be added to PFD/PFDD given certain symptomatic or anatomical considerations.
    MeSH term(s) Humans ; Dura Mater/surgery ; Decompression, Surgical/methods ; Arnold-Chiari Malformation/surgery ; Syringomyelia/surgery
    Language English
    Publishing date 2022-11-03
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1196855-2
    ISSN 1558-1349 ; 1042-3680
    ISSN (online) 1558-1349
    ISSN 1042-3680
    DOI 10.1016/j.nec.2022.08.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Introduction. Stability and motion: addressing the pathology of Chiari malformation and craniocervical junction.

    Limbrick, David D / Brockmeyer, Douglas L / Goel, Atul / Strahle, Jennifer M

    Neurosurgical focus

    2023  Volume 54, Issue 3, Page(s) E1

    MeSH term(s) Humans ; Arnold-Chiari Malformation ; Motion
    Language English
    Publishing date 2023-03-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2026589-X
    ISSN 1092-0684 ; 1092-0684
    ISSN (online) 1092-0684
    ISSN 1092-0684
    DOI 10.3171/2022.12.FOCUS22636
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Neurosurgical management of non-spastic movement disorders.

    McEvoy, Sean D / Limbrick, David D / Raskin, Jeffrey Steven

    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

    2023  Volume 39, Issue 10, Page(s) 2887–2898

    Abstract: Background: Non-spastic movement disorders in children are common, although true epidemiologic data is difficult to ascertain. Children are more likely than adults to have hyperkinetic movement disorders defined as tics, dystonia, chorea/athetosis, or ... ...

    Abstract Background: Non-spastic movement disorders in children are common, although true epidemiologic data is difficult to ascertain. Children are more likely than adults to have hyperkinetic movement disorders defined as tics, dystonia, chorea/athetosis, or tremor. These conditions manifest from acquired or heredodegenerative etiologies and often severely limit function despite medical and surgical management paradigms. Neurosurgical management for these conditions is highlighted.
    Methods: We performed a focused review of the literature by searching PubMed on 16 May 2023 using key terms related to our review. No temporal filter was applied, but only English articles were considered. We searched for the terms (("Pallidotomy"[Mesh]) OR "Rhizotomy"[Mesh]) OR "Deep Brain Stimulation"[Mesh], dystonia, children, adolescent, pediatric, globus pallidus, in combination. All articles were reviewed for inclusion in the final reference list.
    Results: Our search terms returned 37 articles from 2004 to 2023. Articles covering deep brain stimulation were the most common (n = 34) followed by pallidotomy (n = 3); there were no articles on rhizotomy.
    Discussion: Non-spastic movement disorders are common in children and difficult to treat. Most of these patients are referred to neurosurgery for the management of dystonia, with modern neurosurgical management including pallidotomy, rhizotomy, and deep brain stimulation. Historically, pallidotomy has been effective and may still be preferred in subpopulations presenting either in status dystonicus or with high risk for hardware complications. Superiority of DBS over pallidotomy for secondary dystonia has not been determined. Rhizotomy is an underutilized surgical tool and more study characterizing efficacy and risk profile is indicated.
    MeSH term(s) Adult ; Adolescent ; Humans ; Child ; Dystonia/surgery ; Movement Disorders/surgery ; Tremor/surgery ; Dystonic Disorders/surgery ; Neurosurgical Procedures ; Globus Pallidus/surgery ; Deep Brain Stimulation ; Treatment Outcome
    Language English
    Publishing date 2023-07-31
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 605988-0
    ISSN 1433-0350 ; 0302-2803 ; 0256-7040
    ISSN (online) 1433-0350
    ISSN 0302-2803 ; 0256-7040
    DOI 10.1007/s00381-023-06100-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Co-occurrence of subcutaneous myxopapillary ependymoma, dermal sinus tract, and filum terminale lipoma: a review of the pathobiology of caudal spinal cord development and spinal cord tethering. Illustrative case.

    Johnson, Gabrielle W / Xu, Yuxiao / Mian, Ali Y / Limbrick, David D

    Journal of neurosurgery. Case lessons

    2023  Volume 5, Issue 4

    Abstract: Background: Myxopapillary ependymoma (MPE) is typically benign and found in the conus medullaris and/or filum terminale, although rare cases of subcutaneous and extra-axial MPE have been reported. The co-occurrence of MPE, tethered cord syndrome (TCS) ... ...

    Abstract Background: Myxopapillary ependymoma (MPE) is typically benign and found in the conus medullaris and/or filum terminale, although rare cases of subcutaneous and extra-axial MPE have been reported. The co-occurrence of MPE, tethered cord syndrome (TCS) with lipoma of the filum terminale, and a dermal sinus tract is extremely rare, with only 6 reported cases in the literature. Here, the authors present the first case, to their knowledge, of an extra-axial, subcutaneous MPE co-presenting with TCS, lipoma of the filum terminale, and a dermal sinus tract and discuss the underlying pathobiology.
    Observations: A 14-month-old male who presented for evaluation of a dermal sinus tract underwent magnetic resonance imaging, which revealed a tethered cord with associated lipoma. At 14 months, the patient underwent spinal cord detethering with resection of his sacral dimple and sinus tract. Histopathological evaluation revealed an incidentally found MPE within the dermal sinus tract.
    Lessons: The authors review the underlying biology of MPEs, tethered cord syndrome, and dermal sinus tracts, and explore possible points of convergence within the developmental pathways that may result in this unique concomitant presentation. Additionally, they suggest that extra-axial MPE may be underappreciated and underdiagnosed; this case suggests that extra-axial MPE may be only effectively diagnosed with histological studies.
    Language English
    Publishing date 2023-01-23
    Publishing country United States
    Document type Journal Article
    ISSN 2694-1902
    ISSN (online) 2694-1902
    DOI 10.3171/CASE22451
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: New insights into the management of post-hemorrhagic hydrocephalus.

    Limbrick, David D / de Vries, Linda S

    Seminars in perinatology

    2022  Volume 46, Issue 5, Page(s) 151597

    Abstract: During the last decade, an increasing number of studies have been conducted to improve the outcome of post-hemorrhagic hydrocephalus (PHH), a complication of severe intraventricular hemorrhage (IVH) in preterm infants. Two randomized controlled trials ... ...

    Abstract During the last decade, an increasing number of studies have been conducted to improve the outcome of post-hemorrhagic hydrocephalus (PHH), a complication of severe intraventricular hemorrhage (IVH) in preterm infants. Two randomized controlled trials have shown that treatment should be initiated prior to the onset of clinical symptoms. Ventricular access devices and subgaleal shunts are used as temporary neurosurgical interventions whereas ventriculoperitoneal shunts are performed for infants with progressive hydrocephalus. Recently, techniques such as neuro-endoscopic lavage have also been introduced to eliminate toxic blood products and debris from the cerebral ventricles and have shown promise in early clinical studies. The objective of this review is to provide an update on management of PHVD and PHH in the preterm infant.
    MeSH term(s) Cerebral Hemorrhage/surgery ; Cerebral Hemorrhage/therapy ; Cerebral Ventricles ; Humans ; Hydrocephalus/complications ; Hydrocephalus/therapy ; Infant ; Infant, Newborn ; Infant, Premature ; Infant, Premature, Diseases ; Retrospective Studies
    Language English
    Publishing date 2022-03-12
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 752403-1
    ISSN 1558-075X ; 0146-0005
    ISSN (online) 1558-075X
    ISSN 0146-0005
    DOI 10.1016/j.semperi.2022.151597
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Letter to the Editor. The Chiari Severity Index and the role of external validation.

    Greenberg, Jacob K / Limbrick, David D

    Journal of neurosurgery. Pediatrics

    2020  Volume 27, Issue 2, Page(s) 241–242

    MeSH term(s) Arnold-Chiari Malformation/diagnostic imaging ; Arnold-Chiari Malformation/surgery ; Decompression, Surgical ; Humans
    Language English
    Publishing date 2020-12-11
    Publishing country United States
    Document type Journal Article ; Letter ; Comment
    ZDB-ID 2403985-8
    ISSN 1933-0715 ; 1933-0707
    ISSN (online) 1933-0715
    ISSN 1933-0707
    DOI 10.3171/2020.9.PEDS20796
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Pediatric Neurocritical Care: Off to a Good Start.

    Pineda, Jose A / Limbrick, David D

    Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies

    2019  Volume 20, Issue 1, Page(s) 97–98

    MeSH term(s) Child ; Critical Care ; Humans ; Intensive Care Units, Pediatric ; United States
    Language English
    Publishing date 2019-01-07
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 2052349-X
    ISSN 1947-3893 ; 1529-7535
    ISSN (online) 1947-3893
    ISSN 1529-7535
    DOI 10.1097/PCC.0000000000001771
    Database MEDical Literature Analysis and Retrieval System OnLINE

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