Early diagnosis of peripheral nervous system involvement in Fabry disease and treatment of neuropathic pain: the report of an expert panel

Vibrameter testing facilitates the diagnosis of uremic and alcoholic polyneuropathy

(2010) M.J. Hilz et al.   ACTA NEUROLOGICA SCANDINAVICA

Vibratory perception threshold compared with nerve conduction velocity in the evaluation of uremic neuropathy

(2010) Richard Tegnér et al.   ACTA NEUROLOGICA SCANDINAVICA

Autonomic neuropathy in Fabry disease: a prospective study using the Autonomic Symptom Profile and cardiovascular autonomic function tests

(2010) Marieke Biegstraaten et al.   BMC Neurology

Assessment of Renal Pathology and Dysfunction in Children with Fabry Disease

(2010) U. Ramaswami et al.   Clinical Journal of the American Society of Nephrology

Prognostic Indicators of Renal Disease Progression in Adults with Fabry Disease: Natural History Data from the Fabry Registry

(2010) C. Wanner et al.   Clinical Journal of the American Society of Nephrology

Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study

(2010) C. Tanislav et al.   EUROPEAN JOURNAL OF NEUROLOGY

EFNS guidelines on neuropathic pain assessment: revised 2009

(2010) G. Cruccu et al.   EUROPEAN JOURNAL OF NEUROLOGY

Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: Findings from the Fabry Registry

(2010) Torquil Watt et al.   GENETICS IN MEDICINE

Enzyme replacement therapy improves cardiovascular responses to orthostatic challenge in Fabry patients

(2010) Max J Hilz et al.   JOURNAL OF HYPERTENSION

Misdiagnosis in Fabry Disease

(2010) Cintia L. Marchesoni et al.   JOURNAL OF PEDIATRICS

Neuropathic pain: diagnosis, pathophysiological mechanisms, and treatment

(2010) Ralf Baron et al.   LANCET NEUROLOGY

Recommendations for the Pharmacological Management of Neuropathic Pain: An Overview and Literature Update

(2010) Robert H. Dworkin et al.   MAYO CLINIC PROCEEDINGS

Utilidad del tratamiento de sustitución enzimática en la enfermedad de Fabry

(2010) Juan Manuel Politei et al.   MEDICINA CLINICA

Small fiber neuropathy in female patients with fabry disease

(2010) Rocco Liguori et al.   MUSCLE & NERVE

Long-Term Effects of Enzyme Replacement Therapy on Fabry Cardiomyopathy

(2009) Frank Weidemann et al.   CIRCULATION

Psychological aspects of patients with Fabry disease

(2009) T. Wilson Crosbie et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Can we use statins to prevent stroke in Fabry disease?

(2009) J. M. Politei   JOURNAL OF INHERITED METABOLIC DISEASE

Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy

(2009) R. Schiffmann et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Functional and structural nerve fiber findings in heterozygote patients with Fabry disease

(2009) Anette Torvin Møller et al.   PAIN

Development and initial validation of an expanded and revised version of the Short-form McGill Pain Questionnaire (SF-MPQ-2)

(2009) Robert H. Dworkin et al.   PAIN

The Pediatric Quality of Life Inventory: Measuring Pediatric Health-Related Quality of Life from the Perspective of Children and Their Parents

(2009) James W. Varni et al.   PEDIATRIC CLINICS OF NORTH AMERICA

Fabry disease

(2009) Raphael Schiffmann   PHARMACOLOGY & THERAPEUTICS

Stroke in Fabry Disease Frequently Occurs Before Diagnosis and in the Absence of Other Clinical Events

(2009) Katherine Sims et al.   STROKE

Neuropathic symptoms and findings in women with Fabry disease

(2008) Satu M. Laaksonen et al.   CLINICAL NEUROPHYSIOLOGY

Misleading terms in Anderson-Fabry disease

(2008) F. Weidemann et al.   EUROPEAN JOURNAL OF CLINICAL INVESTIGATION

Diagnosis of Fabry Disease via Analysis of Family History

(2008) Dawn A. Laney et al.   Journal of Genetic Counseling

Fabry's disease

(2008) Yuri A Zarate et al.   LANCET

Detection of a Characteristic Painful Neuropathy in Fabry Disease: A Pilot Study

(2008) Rainer Maag et al.   PAIN MEDICINE

Characterization of Fabry Disease in 352 Pediatric Patients in the Fabry Registry

(2008) Robert J Hopkin et al.   PEDIATRIC RESEARCH

Elevated globotriaosylsphingosine is a hallmark of Fabry disease

(2008) J. M. Aerts et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Ocular Features of Fabry Disease: Diagnosis of a Treatable Life-threatening Disorder

(2008) Nasi Samiy   SURVEY OF OPHTHALMOLOGY

Safety and Efficacy of Enzyme Replacement Therapy with Agalsidase Beta: An International, Open-label Study in Pediatric Patients with Fabry Disease

(2007) J. Edmond Wraith et al.   JOURNAL OF PEDIATRICS

Females with Fabry disease frequently have major organ involvement: Lessons from the Fabry Registry

(2007) William R. Wilcox et al.   MOLECULAR GENETICS AND METABOLISM