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Results: 1-23 |
Results: 23
EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts
Authors: Gasser, T Dichgans, M Finsterer, J Hausmanowa-Petrusewicz, I Jurkat-Rott, K Klopstock, T Leguern, E Lehesjoki, AE Lehmann-Horn, F Lynch, T Morris, H Rossor, M Steinlein, OK Wood, N Zaremba, J Zeviani, M Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts, EUR J NEUR, 8(5), 2001, pp. 407-424
EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts
Authors: Gasser, T Dichgans, M Finsterer, J Hausmanowa-Petrusewicz, I Jurkat-Rott, K Klopstock, T LeGuern, E Lehesjoki, AE Lehmann-Horn, F Lynch, T Morris, H Rossor, M Steinlein, OK Wood, N Zaremba, J Zeviani, M Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts, EUR J NEUR, 8(4), 2001, pp. 299-314
Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families
Authors: Asmus, F Zimprich, A Naumann, M Berg, D Bertram, M Ceballos-Baumann, A Pruszak-Seel, R Kabus, C Dichgans, M Fuchs, S Muller-Myhsok, B Gasser, T
Citation: F. Asmus et al., Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families, ANN NEUROL, 49(1), 2001, pp. 121-124
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Decrease in regional cerebral blood volume in hyperintense subcortical lesions inversely correlates with disability and cognitive performance
Authors: Bruening, R Dichgans, M Berchtenbreiter, C Yousry, T Seelos, KC Wu, RH Mayer, M Brix, G Reiser, M
Citation: R. Bruening et al., Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Decrease in regional cerebral blood volume in hyperintense subcortical lesions inversely correlates with disability and cognitive performance, AM J NEUROR, 22(7), 2001, pp. 1268-1274
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Authors: Iannucci, G Dichgans, M Rovaris, M Bruning, R Gasser, T Giacomotti, L Yousry, TA Filippi, M
Citation: G. Iannucci et al., Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, STROKE, 32(3), 2001, pp. 643-648
Reduced cerebrovascular CO2 reactivity in CADASIL - A transcranial Dopplersonography study
Authors: Pfefferkorn, T von Stuckrad-Barre, S Herzog, J Gasser, T Hamann, GF Dichgans, M
Citation: T. Pfefferkorn et al., Reduced cerebrovascular CO2 reactivity in CADASIL - A transcranial Dopplersonography study, STROKE, 32(1), 2001, pp. 17-21
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison
Authors: Auer, DP Putz, B Gossl, C Elbel, GK Gasser, T Dichgans, M
Citation: Dp. Auer et al., Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison, RADIOLOGY, 218(2), 2001, pp. 443-451
NOTCH3 mutation involving three cysteine residues in a family with typicalCADASIL
Authors: Dichgans, M Herzog, J Gasser, T
Citation: M. Dichgans et al., NOTCH3 mutation involving three cysteine residues in a family with typicalCADASIL, NEUROLOGY, 57(9), 2001, pp. 1714-1717
Altered white and gray matter metabolism in CADASIL - A proton MR spectroscopy and H-1-MRSI study
Authors: Auer, DP Schirmer, T Heidenreich, JO Herzog, J Putz, B Dichgans, M
Citation: Dp. Auer et al., Altered white and gray matter metabolism in CADASIL - A proton MR spectroscopy and H-1-MRSI study, NEUROLOGY, 56(5), 2001, pp. 635-642
A magnetic resonance imaging study of the cervical cord of patients with CADASIL
Authors: Rocca, MA Filippi, M Herzog, J Sormani, MP Dichgans, M Yousry, TA
Citation: Ma. Rocca et al., A magnetic resonance imaging study of the cervical cord of patients with CADASIL, NEUROLOGY, 56(10), 2001, pp. 1392-1394
Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains
Authors: Dichgans, M Ludwig, H Muller-Hocker, J Messerschmidt, A Gasser, T
Citation: M. Dichgans et al., Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains, EUR J HUM G, 8(4), 2000, pp. 280-285
Motor cortex excitability in patients with migraine with aura and hemiplegic migraine
Authors: Werhahn, KJ Wiseman, K Herzog, J Forderreuther, S Dichgans, M Straube, A
Citation: Kj. Werhahn et al., Motor cortex excitability in patients with migraine with aura and hemiplegic migraine, CEPHALALGIA, 20(1), 2000, pp. 45-50
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients
Authors: Winkelmann, J Wetter, TC Collado-Seidel, V Gasser, T Dichgans, M Yassouridis, A Trenkwalder, C
Citation: J. Winkelmann et al., Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients, SLEEP, 23(5), 2000, pp. 597-602
Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine
Authors: Kaube, H Herzog, J Kaufer, T Dichgans, M Diener, HC
Citation: H. Kaube et al., Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine, NEUROLOGY, 55(1), 2000, pp. 139-141
Molecular diagnosis of hereditary neurological diseases. A position paper
Authors: Gasser, T Dichgans, M Jurkat-Rott, K Klockgether, T Klopstock, T Kretzschmar, H Lehmann-Horn, F Reichmann, H Rolfs, A Sander, T Stogbauer, F
Citation: T. Gasser et al., Molecular diagnosis of hereditary neurological diseases. A position paper, NERVENARZT, 71(10), 2000, pp. 774-796
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL
Authors: Mayer, M Straube, A Bruening, R Uttner, I Pongratz, D Gasser, T Dichgans, M Muller-Hocker, J
Citation: M. Mayer et al., Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL, J NEUROL, 246(7), 1999, pp. 526-532
Clinical findings and diagnostic approach in CADASIL
Authors: Dichgans, M Gasser, T
Citation: M. Dichgans et T. Gasser, Clinical findings and diagnostic approach in CADASIL, AKT NEUROL, 26(6), 1999, pp. 260-269
Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Authors: Yousry, TA Seelos, K Mayer, M Bruning, R Uttner, I Dichgans, M Mammi, S Straube, A Mai, N Filippi, M
Citation: Ta. Yousry et al., Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), AM J NEUROR, 20(1), 1999, pp. 91-100
Cerebrospinal fluid findings in CADASIL
Authors: Dichgans, M Wick, M Gasser, T
Citation: M. Dichgans et al., Cerebrospinal fluid findings in CADASIL, NEUROLOGY, 53(1), 1999, pp. 233-233
Quantitative MRI in CADASIL - Correlation with disability and cognitive performance
Authors: Dichgans, M Filippi, M Bruning, R Iannucci, G Berchtenbreiter, C Minicucci, L Uttner, I Crispin, A Ludwig, H Gasser, T Yousry, TA
Citation: M. Dichgans et al., Quantitative MRI in CADASIL - Correlation with disability and cognitive performance, NEUROLOGY, 52(7), 1999, pp. 1361-1367
Bacterial meningitis in adults - Demonstration of inner ear involvement using high-resolution MRI
Authors: Dichgans, M Jager, L Mayer, T Schorn, K Pfister, HW
Citation: M. Dichgans et al., Bacterial meningitis in adults - Demonstration of inner ear involvement using high-resolution MRI, NEUROLOGY, 52(5), 1999, pp. 1003-1009
Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families
Authors: Dichgans, M Schols, L Herzog, J Stevanin, G Weirich-Schwaiger, H Rouleau, G Burk, K Klockgether, T Zuhlke, C Laccone, F Riess, O Gasser, T
Citation: M. Dichgans et al., Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families, NEUROLOGY, 52(4), 1999, pp. 849-851
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis
Authors: Spranger, M Spranger, S Schwab, S Benninger, C Dichgans, M
Citation: M. Spranger et al., Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis, EUR NEUROL, 41(3), 1999, pp. 150-152
Risultati: 1-23 |