(Q36892306)

English

Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group

scientific article published on August 2007

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group (English)

1 reference

Europe PubMed Central

16 August 2017

amyotrophic lateral sclerosis

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4

1 reference

Europe PubMed Central

16 August 2017

Vincenzo Silani

object named as

Vincenzo Silani

8

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Gian Domenico Borasio

object named as

Gian Domenico Borasio

2

0 references

Reinhard Dengler

3

object named as

Reinhard Dengler

1 reference

Europe PubMed Central

16 August 2017

Pierre-François Pradat

7

object named as

Pierre-Francois Pradat

1 reference

Europe PubMed Central

16 August 2017

9

object named as

Barbara Tomik

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Europe PubMed Central

16 August 2017

author name string

Peter Munch Andersen

1

1 reference

Europe PubMed Central

16 August 2017

Katja Kollewe

5

1 reference

Europe PubMed Central

16 August 2017

Peter Nigel Leigh

6

1 reference

Europe PubMed Central

16 August 2017

EALSC Working Group

10

1 reference

Europe PubMed Central

16 August 2017

publication date

1 August 2007

1 reference

Europe PubMed Central

16 August 2017

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

1 reference

Europe PubMed Central

16 August 2017

8

1 reference

Europe PubMed Central

16 August 2017

4

1 reference

Europe PubMed Central

16 August 2017

195-213

1 reference

Europe PubMed Central

16 August 2017

Frontal lobe dysfunction in amyotrophic lateral sclerosis. A PET study.

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21 January 2018

Epidemiology of motor neuron disease in northern Sweden.

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Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction.

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21 January 2018

Epidemiology of Motor-Neuron Diseases

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21 January 2018

Amyotrophic lateral sclerosis: current issues in classification, pathogenesis and molecular pathology.

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21 January 2018

EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives

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Getting the diagnosis right: beyond El Escorial.

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ISIS Survey: an international study on the diagnostic process and its implications in amyotrophic lateral sclerosis

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Detection of preclinical motor neurone loss in SOD1 mutation carriers using motor unit number estimation

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Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

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El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

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Toward earlier diagnosis of amyotrophic lateral sclerosis: revised criteria. rhCNTF ALS Study Group

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Good practice in the management of adults with malignant cerebral glioma: clinical guidelines. Working Group, Royal College of Physicians.

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21 January 2018

Practice parameter: the care of the patient with amyotrophic lateral sclerosis (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology: ALS Practice Parameters Task Force

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Amyotrophic lateral sclerosis care in Italy: a nationwide study in neurological centers.

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Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996-2000.

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21 January 2018

Prognosis of amyotrophic lateral sclerosis and the effect of referral selection.

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21 January 2018

Prognostic modelling of therapeutic interventions in amyotrophic lateral sclerosis

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An outcome study of riluzole in amyotrophic lateral sclerosis--a population-based study in Ireland, 1996-2000.

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Stem-cell therapy for amyotrophic lateral sclerosis.

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21 January 2018

A survey of clinicians' practice in the symptomatic treatment of ALS.

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21 January 2018

Sublingual atropine for sialorrhea secondary to parkinsonism: a pilot study.

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Treatment of sialorrhea with glycopyrrolate: A double-blind, dose-ranging study

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Reduction of salivary flow with transdermal scopolamine: a four-year experience

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Botulinum toxin treatment of sialorrhea: comparing different therapeutic preparations

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21 January 2018

Injections of botulinum toxin A into the salivary glands improve sialorrhoea in amyotrophic lateral sclerosis

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21 January 2018

Treatment of sialorrhoea with ultrasound guided botulinum toxin type A injection in patients with neurological disorders

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21 January 2018

Ultrasound-guided versus 'blind' intraparotid injections of botulinum toxin-A for the treatment of sialorrhoea in patients with Parkinson's disease.

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21 January 2018

Botulinum toxin for the treatment of sialorrhoea in ALS: serious side effects of a transductal approach

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21 January 2018

The control of oral secretions in bulbar ALS/MND.

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21 January 2018

Efficacy of mechanical insufflation-exsufflation in medically stable patients with amyotrophic lateral sclerosis.

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21 January 2018

Pathologic laughter and crying in ALS: a search for their origin

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Treatment of pseudobulbar affect in ALS with dextromethorphan/quinidine: a randomized trial

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Treatment of pathologic laughing and weeping with amitriptyline

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Citalopram for post-stroke pathological crying

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The use of hydrotherapy for the management of spasticity.

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Use of intrathecal baclofen for treatment of spasticity in amyotrophic lateral sclerosis

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Diagnostic investigation and multidisciplinary management in motor neuron disease

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Recurrent trismus and stridor in an ALS patient: successful treatment with botulinum toxin.

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Examining the evidence about treatment in ALS/MND.

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Amyotrophic lateral sclerosis in Middle-Finland: an epidemiological study.

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Comparison of sporadic and familial disease amongst 580 cases of motor neuron disease

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Epidemiologic study of amyotrophic lateral sclerosis in Sardinia, Italy.

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Incidence and prevalence of motor neuron disease in two Danish counties.

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Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

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Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients

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Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.

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Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

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10.1080/17482960701262376

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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