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Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation.
Timmermann L, Pauls KA, Wieland K, Jech R, Kurlemann G, Sharma N, Gill SS, Haenggeli CA, Hayflick SJ, Hogarth P, Leenders KL, Limousin P, Malanga CJ, Moro E, Ostrem JL, Revilla FJ, Santens P, Schnitzler A, Tisch S, Valldeoriola F, Vesper J, Volkmann J, Woitalla D, Peker S. Timmermann L, et al. Among authors: haenggeli ca. Brain. 2010 Mar;133(Pt 3):701-12. doi: 10.1093/brain/awq022. Epub 2010 Mar 5. Brain. 2010. PMID: 20207700 Free PMC article.
CT in Wilson disease.
Haenggeli CA, Hauser H, Paunier L. Haenggeli CA, et al. Neurology. 1981 Aug;31(8):1056-7. doi: 10.1212/wnl.31.8.1056. Neurology. 1981. PMID: 7196520 No abstract available.
Plant-induced seizures: reappearance of an old problem.
Burkhard PR, Burkhardt K, Haenggeli CA, Landis T. Burkhard PR, et al. Among authors: haenggeli ca. J Neurol. 1999 Aug;246(8):667-70. doi: 10.1007/s004150050429. J Neurol. 1999. PMID: 10460442
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases.
Ferreiro A, Estournet B, Chateau D, Romero NB, Laroche C, Odent S, Toutain A, Cabello A, Fontan D, dos Santos HG, Haenggeli CA, Bertini E, Urtizberea JA, Guicheney P, Fardeau M. Ferreiro A, et al. Among authors: haenggeli ca. Ann Neurol. 2000 Nov;48(5):745-57. Ann Neurol. 2000. PMID: 11079538
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene.
Ferreiro A, Monnier N, Romero NB, Leroy JP, Bönnemann C, Haenggeli CA, Straub V, Voss WD, Nivoche Y, Jungbluth H, Lemainque A, Voit T, Lunardi J, Fardeau M, Guicheney P. Ferreiro A, et al. Among authors: haenggeli ca. Ann Neurol. 2002 Jun;51(6):750-9. doi: 10.1002/ana.10231. Ann Neurol. 2002. PMID: 12112081
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.
Guicheney P, Vignier N, Zhang X, He Y, Cruaud C, Frey V, Helbling-Leclerc A, Richard P, Estournet B, Merlini L, Topaloglu H, Mora M, Harpey JP, Haenggeli CA, Barois A, Hainque B, Schwartz K, Tomé FM, Fardeau M, Tryggvason K. Guicheney P, et al. Among authors: haenggeli ca. J Med Genet. 1998 Mar;35(3):211-7. doi: 10.1136/jmg.35.3.211. J Med Genet. 1998. PMID: 9541105 Free PMC article.
Two sisters with Rett syndrome.
Haenggeli CA, Moura-Serra J, DeLozier-Blanchet CD. Haenggeli CA, et al. J Autism Dev Disord. 1990 Mar;20(1):129-38. doi: 10.1007/BF02206862. J Autism Dev Disord. 1990. PMID: 2108956
63 results