(Q37873725)

24 August 2017

1 reference

title

Clinical and pathophysiological concepts of neuralgic amyotrophy (English)

1 reference

24 August 2017

1 reference

Nens van Alfen

1

1 reference

24 August 2017

language of work or name

English

0 references

publication date

10 May 2011

1 reference

24 August 2017

published in

Nature Reviews Neurology

1 reference

24 August 2017

volume

7

1 reference

24 August 2017

issue

6

1 reference

24 August 2017

page(s)

315-322

1 reference

The clinical spectrum of neuralgic amyotrophy in 246 cases

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The neuralgic amyotrophy consultation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Brachial plexus neuropathy in the population of Rochester, Minnesota, 1970-1981

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The incidence and lifetime prevalence of neurological disorders in a prospective community-based study in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Neuralgic amyotrophy: variable expression in 40 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Natural history of brachial plexus neuropathy. Report on 99 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Long-term pain, fatigue, and impairment in neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Chronic pain in persons with neuromuscular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Dyspnea as the predominant manifestation of bilateral phrenic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Phrenic neuropathy due to neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Laparoscopic diaphragmatic plication: long-term results of a novel surgical technique for postoperative phrenic nerve palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Diabetic and nondiabetic lumbosacral radiculoplexus neuropathies: new insights into pathophysiology and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Scapular winging: anatomical review, diagnosis, and treatments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

AAEM case report #25: anterior interosseous nerve syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Unusual compression neuropathies of the forearm, part I: radial nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Disputed radial tunnel syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Mutation analysis of a putative sialyltransferase gene, theSFRS2splicing factor gene and thec-mybET-locus in two families with hereditary neuralgic amyotrophy (HNA)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Genomic organization, complex splicing pattern and expression of a human septin gene on chromosome 17q25.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Conquering the complex world of human septins: implications for health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The pathobiology of the septin gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Large-scale characterization of HeLa cell nuclear phosphoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Global proteomic profiling of phosphopeptides using electron transfer dissociation tandem mass spectrometry.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Multimodality expression profiling shows SEPT9 to be overexpressed in a wide range of human tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Properties of SEPT9 isoforms and the requirement for GTP binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Translational control of SEPT9 isoforms is perturbed in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Inflammation and neuropathic attacks in hereditary brachial plexus neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Histology of hereditary neuralgic amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Extended neuralgic amyotrophy syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The variations of neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

So-called neuralgic amyotrophy: clinical features and long term follow-up

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The natural history of hereditary neuralgic amyotrophy in the Dutch population: two distinct types?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Treatment for idiopathic and hereditary neuralgic amyotrophy (brachial neuritis)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Distal neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Isolated sensory manifestations in neuralgic amyotrophy: report of eight cases

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Neuralgic amyotrophy with phrenic nerve involvement

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Long-term recovery of diaphragm strength in neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

The natural history of long thoracic and spinal accessory neuropathies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Sensory nerve conduction studies in neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Painful brachial plexopathies in SEPT9 mutations: adverse outcome related to comorbid states

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Hereditary neuralgic amyotrophy: mutation analysis of candidate genes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Cytoskeletal modification of Rho guanine nucleotide exchange factor activity: identification of a Rho guanine nucleotide exchange factor as a binding partner for Sept9b, a mammalian septin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Phenotypic spectrum of hereditary neuralgic amyotrophy caused by the SEPT9 R88W mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Neuralgic amyotrophy associated with Bartonella henselae infection

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Immune brachial plexus neuropathy: suggestive evidence for an inflammatory-immune pathogenesis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Anti-peripheral nerve myelin antibodies and terminal activation products of complement in serum of patients with acute brachial plexus neuropathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Blood lymphocytes are sensitized to branchial plexus nerves in patients with neuralgic amyotrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2011.62

Lumbosacral plexus neuropathy: a case report and review of the literature

31 March 2020

1 reference

12 December 2020

Kiloh-Nevin syndrome: a compression neuropathy or brachial plexus neuritis?

1 reference

12 December 2020

Epidemiologic study of a brachial plexus neuritis outbreak in northeast Czechoslovakia

1 reference

12 December 2020

The anterior interosseous nerve syndrome (the Kiloh-Nevin syndrome). Report and follow-up study of three cases.

1 reference

12 December 2020

Brachial plexus neuropathy. A long-term outcome study

1 reference

12 December 2020

[An unusual cause of acute dyspnoea: neuralgic amyotrophy]

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEUROL.2011.62

1 reference

Dimensions Publication ID

24 August 2017

1022451870

0 references

1 reference