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Author

Vinay Goyal

Other affiliations: Medanta
Bio: Vinay Goyal is an academic researcher from All India Institute of Medical Sciences. The author has contributed to research in topics: Parkinson's disease & Medicine. The author has an hindex of 19, co-authored 175 publications receiving 1294 citations. Previous affiliations of Vinay Goyal include Medanta.


Papers
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Journal ArticleDOI
TL;DR: RBD may precede or follow PD onset, and has association with higher occurrence of hallucinations and other nocturnal problems; although most of these episodes were brief, had static course and were not associated with violent behavior.

65 citations

Journal ArticleDOI
TL;DR: Findings suggest significantly better stroke outcomes and statistically nonsignificant favorable outcomes in terms of recurrence of vascular events for patients with stroke and OSA who use CPAP treatment.
Abstract: Study Objectives:Obstructive sleep apnea (OSA) is an independent risk factor for stroke. The objective of this study was to assess the effect of continuous positive airway pressure (CPAP) treatment...

58 citations

Journal ArticleDOI
TL;DR: The clinical practice guidelines provide recommendations for a comprehensive management of WD which will be of value to all specialties and differences in pharmacological approach to neurological and hepatic disease and global monitoring scales have been included.
Abstract: Clinical practice guidelines for Wilson's disease (WD) have been published by the American Association for the Study of Liver Diseases and European Association for the Study of the Liver in 2008 and 2012, respectively Their focus was on the hepatic aspects of the disease Recently, a position paper on pediatric WD was published by the European Society of Pediatric Gastroenterology Hepatology and Nutrition A need was felt to harmonize guidelines for the hepatic, pediatric, and neurological aspects of the disease and contextualize them to the resource-constrained settings Therefore, experts from national societies from India representing 3 disciplines, hepatology (Indian National Association for Study of the Liver), pediatric hepatology (Indian Society of Pediatric Gastroenterology, Hepatology and Nutrition), and neurology (Movement Disorders Society of India) got together to evolve fresh guidelines A literature search on retrospective and prospective studies of WD using MEDLINE (PubMed) was performed Members voted on each recommendation, using the nominal voting technique The Grades of Recommendation, Assessment, Development and Evaluation system was used to determine the quality of evidence Questions related to diagnostic tests, scoring system, and its modification to a version suitable for resource-constrained settings were posed While ceruloplasmin and 24-h urine copper continue to be important, there is little role of serum copper and penicillamine challenge test in the diagnostic algorithm A new scoring system – Modified Leipzig score has been suggested with extra points being added for family history and serum ceruloplasmin lower than 5 mg/dl Liver dry copper estimation and penicillamine challenge test have been removed from the scoring system Differences in pharmacological approach to neurological and hepatic disease and global monitoring scales have been included Rising bilirubin and worsening encephalopathy are suggested as indicators predicting need for liver transplant but need to be validated The clinical practice guidelines provide recommendations for a comprehensive management of WD which will be of value to all specialties

56 citations

Journal ArticleDOI
TL;DR: In this paper, the authors presented a comprehensive analysis of the disease burden and trends of neurological disorders at the state level in India, and assessed the Pearson correlation coefficient between Socio-demographic Index (SDI) of the states and the prevalence or incidence and disability-adjusted life-years (DALY) rates of each neurological disorder.

49 citations

Journal ArticleDOI
TL;DR: Sleep related complaints are commonly reported in patients with PD and may form an important determinant of their quality of life and interactions among genetic and environmental factors may play an important role in the development of and also explain the difference in sleep disturbances in these groups.

47 citations


Cited by
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Journal ArticleDOI
TL;DR: The Eighth Edition of the JCA Special Issue seeks to continue to serve as a key resource that guides the utilization of TA in the treatment of human disease.
Abstract: The American Society for Apheresis (ASFA) Journal of Clinical Apheresis (JCA) Special Issue Writing Committee is charged with reviewing, updating, and categorizing indications for the evidence-based use of therapeutic apheresis in human disease. Since the 2007 JCA Special Issue (Fourth Edition), the Committee has incorporated systematic review and evidence-based approaches in the grading and categorization of apheresis indications. This Seventh Edition of the JCA Special Issue continues to maintain this methodology and rigor to make recommendations on the use of apheresis in a wide variety of diseases/conditions. The JCA Seventh Edition, like its predecessor, has consistently applied the category and grading system definitions in the fact sheets. The general layout and concept of a fact sheet that was used since the fourth edition has largely been maintained in this edition. Each fact sheet succinctly summarizes the evidence for the use of therapeutic apheresis in a specific disease entity. The Seventh Edition discusses 87 fact sheets (14 new fact sheets since the Sixth Edition) for therapeutic apheresis diseases and medical conditions, with 179 indications, which are separately graded and categorized within the listed fact sheets. Several diseases that are Category IV which have been described in detail in previous editions and do not have significant new evidence since the last publication are summarized in a separate table. The Seventh Edition of the JCA Special Issue serves as a key resource that guides the utilization of therapeutic apheresis in the treatment of human disease. J. Clin. Apheresis 31:149-162, 2016. © 2016 Wiley Periodicals, Inc.

1,691 citations

Journal ArticleDOI
TL;DR: The discovery of the Wilson's disease gene has opened up a new molecular diagnostic approach, and could form the basis of future gene therapy.

1,207 citations

Journal ArticleDOI
TL;DR: Intended for use by physicians, these recommendations suggest preferred approaches to the diagnostic, therapeutic, and preventive aspects of care are intended to be flexible, in contrast to standards of care, which are inflexible policies to be followed in every case.

1,068 citations

Book ChapterDOI
01 Jan 2010

691 citations