Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 83, Issue 7, 2012, Pages 763-764

  Saiga, Toru ^a   Tateishi, Takahisa ^a   Torii, Takako ^a   Kawamura, Nobutoshi ^a   Nagara, Yuko ^a   Shigeto, Hiroshi ^a   Hashiguchi, Akihiro ^b   Takashima, Hiroshi ^b   Honda, Hiroyuki ^a   Ohyagi, Yasumasa ^a   Kira, Jun Ichi ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b KAGOSHIMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN; METHYLPREDNISOLONE; PREDNISOLONE;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; CASE REPORT; CLINICAL FEATURE; COMORBIDITY; DNA DETERMINATION; DRUG DOSE REDUCTION; DRUG RESPONSE; EVOKED SOMATOSENSORY RESPONSE; GENE MUTATION; GRIP STRENGTH; HETEROZYGOTE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JAPANESE; LETTER; MALE; MISSENSE MUTATION; NERVE BIOPSY; NERVE CONDUCTION; POLYRADICULONEUROPATHY; PRIORITY JOURNAL; SETX GENE; SURAL NERVE; WALKING DIFFICULTY;

EID: 84861861627     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp-2012-302281     Document Type: Letter

References (5)

1. Chance PF, Rabin BA, Ryan SG, et al. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34. Am J Hum Genet 1998;62:633-40. (Pubitemid 28164621)
2. De Jonghe P, Auer-Grumbach M, Irobi J, et al. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? Brain 2002;125:1320-5. (Pubitemid 34587141)
3. Chen YZ, Bennett CL, Huynh HM, et al. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet 2004;74:1128-35. (Pubitemid 38669312)
4. Chentanez V, Cha-oumphol P, Kaewsema A, et al. Accuracy of the three-window sampling method in morphometric analysis of human sural nerve. J Neurosci Methods 2006;157:154-7. (Pubitemid 44308361)
5. Hirano M, Quinzii CM, Mitsumoto H, et al. Senataxin mutations and amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2011;12:223-7.