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Hyperreflexia
Treatment of Autonomic Dysreflexia for Adults & Adolescents with Spinal
Scienti®C Review Spastic Movement Disorder
Neuromuscular Disorders Neurology in Practice: Series Editors: Robert A
Non-Progressive Congenital Ataxia with Cerebellar Hypoplasia in Three Families
Autonomic Hyperreflexia Associated with Recurrent Cardiac Arrest
Late-Onset Oro-Facial Dyskinesia in Spinocerebellar Ataxia Type 2: a Case Report Floriana Giardina1†, Giuseppe Lanza2,3*† , Francesco Calì3 and Raffaele Ferri3
History-Of-Movement-Disorders.Pdf
Tremor, Abnormal Movement and Imbalance Differential
Hemiballismus: /Etiology and Surgical Treatment by Russell Meyers, Donald B
PREVENTING SECONDARY MEDICAL COMPLICATIONS: a Guide for Personal Assistants to People with Spinal Cord Injury
Autonomic Hyperreflexia After Spinal Cord Injury
Recognition and Management of Intraoperative Autonomic Dysreflexia Thomas Lyford1, Katherine Borowczyk1, Simon Danieletto1 and Ruan Vlok1,2*
Movement Disorders and Neurodegenerative Diseases
Managing Tetraplegia and Its Associated Risks in Pregnancy and Labour- a Case Report Fatima Rashed1*, Summia Zaher2, and Marion Beard2
Pregnancy and Autonomic Hyperreflexia in Patients with Spinal
Myelopathy in Cervical Spondylosis with Vertebral Subluxation and Hyperlordosis
An Approach to Late Onset Cerebellar Ataxia
Acute Or Recurrent Ataxia
Top View
Puremotor Hemiplegia Secondaryto Brain-Stemtumour
Muscle Tone Physiology and Abnormalities
Blood Pressure Variability in Tetraplegic Patients with Autonomic Hyperreflexia
Spinocerebellar Ataxia Type 14: Study of a Family with an Exon 5 Mutation in the PRKCG Gene
Spastic Movement Disorder: Impaired Reflex Function and Altered Muscle
Headache Attributed to Autonomic Dysreflexia: Clinical Presentation, Pathophysiology, and Treatment
Neuro-Immunology AKA Neurologic Manifestations of Autoimmune
The Genetic Nomenclature of Recessive Cerebellar Ataxias
The Main Neurological Dysfunctions in Hyperargininemia-Literature
Title: Ocular Manifestations of Spinocerebellar Ataxia 3 Abstract: Spinocerebellar Ataxia(SCA) Is a Group of Progressive, Neuro
Hemiparetic Multiple Sclerosis
Hereditary Ataxias: Overview
The Neurologic Diagnosis
Review Historical Overview of Hereditary Ataxias with An
Pseudoathetosis: Three Cases of Delayed-Onset Movement Disorder
Paroxysmal Movement Disorders Paroxysmal Dyskinesias
Initial and Subsequent Medication Therapy of Parkinson's Disease
Movement Disorders, 25(13), Pp