Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis

Published:2010-01 Issue:1-2 Volume:11 Page:194-202
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Baumann Fusun,Henderson Robert D.,Morrison Stephen C.,Brown Michael,Hutchinson N.,Douglas James A.,Robinson Peter J.,McCombe Pamela A.

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482960902991773

Reference26 articles.

1. Causes of death in a post‐mortem series of ALS patients

2. Clinical phenotypes and natural progression for motor neuron disease: Analysis from an Australian database

3. Practice parameter: The care of the patient with amyotrophic lateral sclerosis (An evidence-based review)

4. Pulmonary Function at Diagnosis of Amyotrophic Lateral Sclerosis

5. Prognostic indicators of survival in ALS

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1. Neutrophil-to-lymphocyte ratio at diagnosis as a biomarker for survival of amyotrophic lateral sclerosis;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2024-05-14

2. Sleep Disorders in Neuromuscular Diseases: A Narrative Review;Clinical and Translational Neuroscience;2023-08-18

3. Respiratory Management of Patients With Neuromuscular Weakness;CHEST;2023-08

4. The role of lung volume recruitment therapy in neuromuscular disease: a narrative review;Frontiers in Rehabilitation Sciences;2023-07-26

5. Maximum Phonation Time as a Surrogate Marker for Airway Clearance Physiologic Capacity and Pulmonary Function in Individuals With Amyotrophic Lateral Sclerosis;Journal of Speech, Language, and Hearing Research;2023-04-12

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