Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection

Neuromuscular Disorders

Volumn 10, Issue 7, 2000, Pages 515-517

  Kuhlenbäumer, Gregor ^a   Stögbauer, Florian ^a   Timmerman, Vincent ^b   De Jonghe, Peter ^b,c  

^a UNIVERSITY OF MÜNSTER   (Germany)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c ANTWERP UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRACHIAL PLEXUS; CHROMOSOME 17P; DIAGNOSTIC PROCEDURE; GENE MUTATION; HEREDITARY NEURALGIC AMYOTROPHY; HUMAN; MUSCLE ATROPHY; NEURITIS; PRACTICE GUIDELINE; PRIORITY JOURNAL;

EID: 0034308262     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(00)00109-7     Document Type: Article

References (8)

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2. Chance PF, Lensch MW, Lipe H, Brown RS, Brown RJ, Bird TD. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders. Neurology 1994;44(12):2253-2257.
3. Gouider R, LeGuern E, Emile J, et al. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities. Neurology 1994;44(12):2250-2252.
4. Pellegrino JE, Rebbeck TR, Brown MJ, Bird TD, Chance PF. Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q. Neurology 1996;46(4):1128-1132.
5. Wehnert M, Timmerman V, Spoelders P, Meuleman J, Nelis E, Van Broeckhoven C. Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q. Neurology 1997;48(6):1719-1721.
6. Stogbauer F, Young P, Timmerman V, et al. Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25. Hum Genet 1997;99(5):685-687.
7. Meuleman J, Kuhlenbäumer G, Schirmacher A, et al. Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25. Eur J Hum Genet; 1999;7(8):920-928.
8. Kuhlenbäumer G, Schirmacher A, Meuleman J, et al. A sequence ready BAC/PAC contig and partial transcript map of approximately 1,5 Mb in human chromsome 17q25 comprising multiple disease genes. Genomics 1999;62:242-250.