Literature DB >> 10996784

Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT Consortium.

G Kuhlenbäumer1, F Stögbauer, V Timmerman, P De Jonghe.   

Abstract

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Year:  2000        PMID： 10996784     DOI： 10.1016/s0960-8966(00)00109-7

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN： 0960-8966            Impact factor:   4.296


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  8 in total

Review 1.  Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.

Authors:  Phillip F Chance
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

2.  SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.

Authors:  M C Hannibal; E K Ruzzo; L R Miller; B Betz; J G Buchan; D M Knutzen; K Barnett; M L Landsverk; A Brice; E LeGuern; H M Bedford; B B Worrall; S Lovitt; S H Appel; E Andermann; T D Bird; P F Chance
Journal:  Neurology       Date:  2009-05-19       Impact factor: 9.910

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

Authors:  Megan L Landsverk; Elizabeth K Ruzzo; Heather C Mefford; Karen Buysse; Jillian G Buchan; Evan E Eichler; Elizabeth M Petty; Esther A Peterson; Dana M Knutzen; Karen Barnett; Martin R Farlow; Judy Caress; Gareth J Parry; Dianna Quan; Kathy L Gardner; Ming Hong; Zachary Simmons; Thomas D Bird; Phillip F Chance; Mark C Hannibal
Journal:  Hum Mol Genet       Date:  2009-01-12       Impact factor: 6.150

Review 4.  Treatment for idiopathic and hereditary neuralgic amyotrophy (brachial neuritis).

Authors:  Nens van Alfen; Baziel G M van Engelen; Richard A C Hughes
Journal:  Cochrane Database Syst Rev       Date:  2009-07-08

5.  Incidence of neuralgic amyotrophy (Parsonage Turner syndrome) in a primary care setting--a prospective cohort study.

Authors:  Nens van Alfen; Jeroen J J van Eijk; Tessa Ennik; Sean O Flynn; Inge E G Nobacht; Jan T Groothuis; Sigrid Pillen; Floris A van de Laar
Journal:  PLoS One       Date:  2015-05-27       Impact factor: 3.240

6.  Hereditary Neuropathy with Liability to Pressure Palsy Presenting as an Acute Brachial Plexopathy: A Lover's Palsy.

Authors:  Sarah Wedderburn; Puraskar Pateria; Peter K Panegyres
Journal:  Case Rep Neurol       Date:  2014-12-12

7.  Chronic Brachial Plexus Neuritis That Developed into Typical Neuralgic Amyotrophy and Positively Responded to Immunotherapy.

Authors:  Ryo Morishima; Utako Nagaoka; Masahiro Nagao; Eiji Isozaki
Journal:  Intern Med       Date:  2017-12-21       Impact factor: 1.271

8.  Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study.

Authors:  Katharina Neubauer; Doris Boeckelmann; Udo Koehler; Julia Kracht; Janbernd Kirschner; Manuela Pendziwiat; Barbara Zieger
Journal:  Cytoskeleton (Hoboken)       Date:  2018-10-10
  8 in total

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