Thickened skull, scoliosis and other skeletal findings in Unverricht–Lundborg disease link cystatin B function to bone metabolism-Reference-Cited by-同舟云学术

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Thickened skull, scoliosis and other skeletal findings in Unverricht–Lundborg disease link cystatin B function to bone metabolism

Published:2012-12 Issue:6 Volume:51 Page:1016-1024
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Suoranta Sanna,Manninen Hannu,Koskenkorva Päivi,Könönen Mervi,Laitinen Rita,Lehesjoki Anna-Elina,Kälviäinen Reetta,Vanninen Ritva

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference85 articles.

1. Diagnosis of infantile spasms, Lennox–Gastaut syndrome, and progressive myoclonic epilepsy;Shields;Epilepsia,2004

2. Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patients;Norio;Clin Genet,1979

3. Clinical picture of EPM1-Unverricht–Lundborg disease;Kalviainen;Epilepsia,2008

4. The natural history of Unverricht–Lundborg disease: a report of eight genetically proven cases;Chew;Mov Disord,2008

5. T2-weighted high-intensity signals in the basal ganglia as an interesting image finding in Unverricht–Lundborg disease;Korja;Epilepsy Res,2007

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