AAAAAA

   
Results: 1-9 |
Results: 9
Neurodegenerative Huntington-like disorder
Authors: Bohlega, S Al-Tahan, A Kambouris, M Divakaran, M
Citation: S. Bohlega et al., Neurodegenerative Huntington-like disorder, MOVEMENT D, 16(3), 2001, pp. 533-534
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
Authors: Aoki, M Liu, J Richard, I Bashir, R Britton, S Keers, SM Oeltjen, J Brown, HEV Marchand, S Bourg, N Beley, C McKenna-Yasek, D Arahata, K Bohlega, S Cupler, E Illa, I Majneh, I Barohn, RJ Urtizberea, JA Fardeau, M Amato, A Angelini, C Bushby, K Beckmann, JS Brown, RH
Citation: M. Aoki et al., Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy, NEUROLOGY, 57(2), 2001, pp. 271-278
Transcranial magnetic stimulation in Behcet's disease: a cross-sectional and longitudinal study with 44 patients comparing clinical, neuroradiological, somatosensory and brain-stem auditory evoked potential findings
Authors: Stigsby, B Bohlega, S McLean, DR Al-Kawi, MZ
Citation: B. Stigsby et al., Transcranial magnetic stimulation in Behcet's disease: a cross-sectional and longitudinal study with 44 patients comparing clinical, neuroradiological, somatosensory and brain-stem auditory evoked potential findings, CLIN NEU, 111(7), 2000, pp. 1320-1329
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
Authors: Hentati, A Deng, HX Zhai, H Chen, W Yang, Y Hung, WY Azim, AC Bohlega, S Tandan, R Warner, C Laing, NG Cambi, F Mitsumoto, H Roos, RP Boustany, RM Ben Hamida, M Hentati, F Siddique, T
Citation: A. Hentati et al., Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, NEUROLOGY, 55(9), 2000, pp. 1388-1390
Gaucher disease with oculomotor apraxia and cardiovascular calcification -Reply
Authors: Bohlega, S
Citation: S. Bohlega, Gaucher disease with oculomotor apraxia and cardiovascular calcification -Reply, NEUROLOGY, 55(5), 2000, pp. 742-742
Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC)
Authors: Bohlega, S Kambouris, M Shahid, M Al Homsi, M Al Sous, W
Citation: S. Bohlega et al., Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC), NEUROLOGY, 54(1), 2000, pp. 261-263
Localization of the gene for a novel autosomal recessive neurodegenerativeHuntington-like disorder to 4p15.3
Authors: Kambouris, M Bohlega, S Al-Tahan, A Meyer, BF
Citation: M. Kambouris et al., Localization of the gene for a novel autosomal recessive neurodegenerativeHuntington-like disorder to 4p15.3, AM J HU GEN, 66(2), 2000, pp. 445-452
A novel autosomal recessive "Huntington's disease-like" neurodegenerative disorder in a Saudi family
Authors: Al-Tahan, AY Divakaran, MP Kambouris, M Bohlega, S Salih, M Ogunniyi, A Al-Ghanmi, H
Citation: Ay. Al-tahan et al., A novel autosomal recessive "Huntington's disease-like" neurodegenerative disorder in a Saudi family, SAUDI MED J, 20(1), 1999, pp. 85-89
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy
Authors: Minassian, BA Sainz, J Serratosa, JM Gee, M Sakamoto, LM Bohlega, S Geoffroy, G Barr, C Scherer, SW Tomiyasu, U Carpenter, S Wigg, K Sanghvi, AV Delgado-Escueta, AV
Citation: Ba. Minassian et al., Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy, ANN NEUROL, 45(2), 1999, pp. 262-265
Risultati: 1-9 |