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  1. Article ; Online: Keeping expanded access programs in context.

    Caress, James B

    Muscle & nerve

    2023  Volume 67, Issue 5, Page(s) 337–338

    MeSH term(s) Humans ; United States ; United States Food and Drug Administration ; Amyotrophic Lateral Sclerosis
    Language English
    Publishing date 2023-03-09
    Publishing country United States
    Document type Editorial ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.27802
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Neuromuscular Ultrasound in Cervical Nerve Root Avulsion.

    Miller, Nicholas J / Meiling, James B / Caress, James B / Cartwright, Michael S

    Annals of neurology

    2024  

    Language English
    Publishing date 2024-03-19
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80362-5
    ISSN 1531-8249 ; 0364-5134
    ISSN (online) 1531-8249
    ISSN 0364-5134
    DOI 10.1002/ana.26924
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Another step forward for neuromuscular ultrasound.

    Caress, James B / Wiesler, Ethan R

    Muscle & nerve

    2023  Volume 69, Issue 3, Page(s) 255–256

    MeSH term(s) Humans ; Ultrasonography ; Neuromuscular Diseases/diagnostic imaging
    Language English
    Publishing date 2023-12-20
    Publishing country United States
    Document type Editorial
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.28025
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Bilateral hypertrophic olivary degeneration in a syndrome of sensory ataxic neuropathy with dysarthria and ophthalmoplegia.

    Aldendail, Carolyn F / Caress, James B

    Muscle & nerve

    2022  Volume 66, Issue 4, Page(s) E15–E18

    MeSH term(s) Dysarthria/etiology ; Humans ; Hypertrophy ; Ophthalmoplegia/complications ; Peripheral Nervous System Diseases
    Language English
    Publishing date 2022-08-15
    Publishing country United States
    Document type Letter
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.27689
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Identification and Management of Acute Neuromuscular Respiratory Failure in the ICU.

    Krall, Jennifer T W / Chakravartty, Akash / Caress, James B / Files, D Clark

    Chest

    2023  Volume 164, Issue 6, Page(s) 1454–1461

    Abstract: Respiratory failure is a common and potentially life-threatening complication of neuromuscular diseases. Prompt recognition and accurate diagnosis of new or worsening chronic neuromuscular disease have important clinical management and prognostic ... ...

    Abstract Respiratory failure is a common and potentially life-threatening complication of neuromuscular diseases. Prompt recognition and accurate diagnosis of new or worsening chronic neuromuscular disease have important clinical management and prognostic implications. In this article, we present an approach to the acute presentation of undifferentiated neuromuscular respiratory failure in the ICU and guidance for determination and respiratory management of the underlying disorder.
    MeSH term(s) Humans ; Neuromuscular Diseases/complications ; Neuromuscular Diseases/diagnosis ; Neuromuscular Diseases/therapy ; Respiratory Insufficiency/diagnosis ; Respiratory Insufficiency/etiology ; Respiratory Insufficiency/therapy ; Prognosis ; Intensive Care Units
    Language English
    Publishing date 2023-12-08
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 1032552-9
    ISSN 1931-3543 ; 0012-3692
    ISSN (online) 1931-3543
    ISSN 0012-3692
    DOI 10.1016/j.chest.2023.09.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Optimal muscle selection in amyotrophic lateral sclerosis and the end of the 4-limb EMG.

    Caress, James B

    Muscle & nerve

    2017  Volume 56, Issue 1, Page(s) 4–6

    MeSH term(s) Amyotrophic Lateral Sclerosis ; Electromyography ; Extremities ; Humans ; Muscles
    Language English
    Publishing date 2017-06-02
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.25662
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Clinical Utility and Diagnostic Yield of Genetic Testing for Inherited Neuromuscular Disorders in a Single, Large Neuromuscular Center.

    Ebert, Suzahn E / Meiling, James B / Caress, James B / Gandhi Mehta, Rachana K / Baute Penry, Vanessa / Puwanant, Araya / Cartwright, Michael S

    Neurology. Clinical practice

    2024  Volume 14, Issue 2, Page(s) e200268

    Abstract: Background and objectives: Most published studies on the clinical utility of genetic testing for neuromuscular diseases (NMDs) focus on disease-specific cohorts and/or involve multiple centers. The aim of this study was to examine the clinical utility ... ...

    Abstract Background and objectives: Most published studies on the clinical utility of genetic testing for neuromuscular diseases (NMDs) focus on disease-specific cohorts and/or involve multiple centers. The aim of this study was to examine the clinical utility and diagnostic yield of genetic testing at a single, large neuromuscular center. Unlike previous studies, this study is unique in that it includes a broad array of patients at a single, large neuromuscular center, providing real-world data that may assist both neuromuscular specialists as well as general neurologists in decision-making regarding the need for genetic testing in patients with suspected NMDs.
    Methods: Genetic testing results were reviewed for all patients who underwent testing through a single genetic testing company for NMDs in this single laboratory at a large neuromuscular center from 2015 to 2020. Retrospective chart reviews were performed to determine whether genetic testing results conferred a specific NMD diagnosis, including cases where a variant of uncertain significance (VUS) was identified.
    Results: Genetic testing was pursued for 192 patients. A positive result, defined as a pathogenic mutation, a VUS, or both, was found in 77.1%. A definitive diagnosis was conferred in 35.9%. The most common testing indication was suspected neuropathy (53.3%), and the indication with the highest diagnostic yield was suspected myopathy (48.7%).
    Discussion: This study provides further evidence of the clinical utility of genetic testing for NMDs in a real-world setting with over one-third of patients tested receiving a definitive diagnosis. Over time, genetic testing will continue to become increasingly accessible, cost-effective, and sensitive, which will lead to even more utilization.
    Language English
    Publishing date 2024-02-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2645818-4
    ISSN 2163-0933 ; 2163-0402
    ISSN (online) 2163-0933
    ISSN 2163-0402
    DOI 10.1212/CPJ.0000000000200268
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Thrombotic risks from pulling the "trigger" on intravenous immunoglobulin and plasma exchange.

    Caress, James B / Yang, Chengwu

    Muscle & nerve

    2020  Volume 62, Issue 3, Page(s) 295–296

    MeSH term(s) Cross-Over Studies ; Humans ; Immunoglobulins, Intravenous ; Inpatients ; Plasma Exchange ; Plasmapheresis
    Chemical Substances Immunoglobulins, Intravenous
    Language English
    Publishing date 2020-07-04
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.26986
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Arg953* mutation in Periaxin causes CMT4F without nerve hypertrophy on ultrasound imaging: A case report and review of the literature.

    Castoro, Ryan / Caress, James B / Li, Jun / Cartwright, Michael S

    Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

    2022  Volume 147, Page(s) 14–16

    MeSH term(s) Humans ; Hereditary Sensory and Motor Neuropathy ; Mutation ; Membrane Proteins/genetics ; Hypertrophy
    Chemical Substances periaxin ; Membrane Proteins
    Language English
    Publishing date 2022-12-26
    Publishing country Netherlands
    Document type Review ; Case Reports ; Letter
    ZDB-ID 1463630-x
    ISSN 1872-8952 ; 0921-884X ; 1388-2457
    ISSN (online) 1872-8952
    ISSN 0921-884X ; 1388-2457
    DOI 10.1016/j.clinph.2022.12.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Neuromuscular ultrasound as a biomarker in amyotrophic lateral sclerosis.

    Caress, James B / Cartwright, Michael S

    Muscle & nerve

    2018  Volume 58, Issue 6, Page(s) 747–748

    MeSH term(s) Amyotrophic Lateral Sclerosis ; Biomarkers ; Cross-Sectional Studies ; Humans ; Nerve Tissue ; Ultrasonography
    Chemical Substances Biomarkers
    Language English
    Publishing date 2018-10-06
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.26343
    Database MEDical Literature Analysis and Retrieval System OnLINE

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