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M Finkenstaedt

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Articles 16
Citations 277
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Recent Articles
1.
Meissner B, Kortner K, Bartl M, Jastrow U, Mollenhauer B, Schroter A, et al.
Neurology . 2004 Aug; 63(3):450-6. PMID: 15314808
Objective: To assess if clinical features, prion protein codon 129, and molecular subtype correlate with MRI basal ganglia hyperintensity in sporadic Creutzfeldt-Jakob disease (CJD). Methods: The authors studied 219 patients...
2.
Schroter A, Zerr I, Henkel K, Tschampa H, Finkenstaedt M, Poser S
Arch Neurol . 2000 Dec; 57(12):1751-7. PMID: 11115241
Objective: To evaluate the diagnostic usefulness of magnetic resonance imaging (MRI) in the clinical diagnosis of Creutzfeldt-Jakob disease (CJD). Background: Creutzfeldt-Jakob disease is a rare neurodegenerative disease that belongs to...
3.
Ziemann U, Koc J, Reimers C, Finkenstaedt M, Paulus W
Mov Disord . 2000 Sep; 15(5):1000-5. PMID: 11009213
Hemiballism-hemichorea in older patients with hyperglycemia, associated with high signal intensity in the contralateral striatum on T1-weighted magnetic resonance scans, is now an accepted clinical entity. We present an additional...
4.
Kropp S, Finkenstaedt M, Zerr I, Schroter A, Poser S
Nervenarzt . 2000 Mar; 71(2):91-5. PMID: 10703009
Today the diagnosis of Creutzfeldt-Jakob disease (CJD) is proven only postmortem or by evidence of neuropathology. During the patient's lifetime EEG recordings or cerebrospinal fluid analysis may support the diagnosis....
5.
Christen H, Hanefeld F, Kruse E, Imhauser S, ERNST J, Finkenstaedt M
Dev Med Child Neurol . 2000 Mar; 42(2):122-32. PMID: 10698330
Foix-Chavany-Marie syndrome (FCMS) is a distinct clinical picture of suprabulbar (pseudobulbar) palsy due to bilateral anterior opercular lesions. Symptoms include anarthria/severe dysarthria and loss of voluntary muscular functions of the...
6.
Vogelsang J, Finkenstaedt M, Vogelsang M, Markakis E
Eur Spine J . 2000 Feb; 8(6):475-9. PMID: 10664306
The association between peridural scarring and recurrent pain after lumbar discectomy is much debated. A recently published study found that patients with extensive peridural fibrosis were 3.2 times more likely...
7.
Poser S, Mollenhauer B, Kraubeta A, Zerr I, Steinhoff B, Schroeter A, et al.
Brain . 1999 Dec; 122 ( Pt 12):2345-51. PMID: 10581227
This paper describes a prospective follow-up of 364 patients initially notified as suspected Creutzfeldt-Jakob disease to a Surveillance Unit in Göttingen, Germany. Six patients were diagnosed as having genetic prion...
8.
Kropp S, Schulz-Schaeffer W, Finkenstaedt M, Riedemann C, Windl O, Steinhoff B, et al.
Arch Neurol . 1999 Jan; 56(1):55-61. PMID: 9923761
Objective: To investigate whether typical neuropathological and radiological findings can be identified in patients with the clinical diagnosis of the Heidenhain variant of Creutzfeldt-Jakob disease (CJD). Design: Case study. The...
9.
Nolte W, Wiltfang J, Schindler C, Unterberg K, Finkenstaedt M, Niedmann P, et al.
J Hepatol . 1998 Oct; 29(3):443-9. PMID: 9764992
Background/aims: Deposition of paramagnetic substances in basal ganglia, resulting in increased signals in T1-weighted magnetic resonance images (bright basal ganglia), is frequently seen in liver cirrhosis. The present study describes...
10.
Reimers C, Finkenstaedt M
Curr Opin Rheumatol . 1998 Feb; 9(6):475-85. PMID: 9375276
Myositides are characterized by perivascular and intrafascicular inflammatory infiltrates and often by fiber de- and regeneration. In chronic disease, muscle size decreases, and replacement of muscle parenchyma by adipose and...