Schizophasie: Verschleierung einer Sprachstörung durch Sprache?
in: European archives of psychiatry and clinical neuroscience , ISSN 1433-8491, Vol. 219 (3. 1974), p. 277-284 Zugang:
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1974
Summary Schizophasics give the impression that they have command of colloquial language, but for inexplicable reasons this does not seem to be the case. We refer, for example, to a lengthy quotation from a patient that indicates by what linguistic means the impression of Schizophasia is produced.... mehr Zusammenfassung Ausgehend von dem vorwissenschaftlichen Eindruck, daß Schizophasiker durchaus imstande sind, die gewöhnliche Umgangssprache zu benutzen, sich aber aus einem unerklärlichen Grunde anders verhalten, wird an Hand einer Textstelle aufgezeigt, mit welchen sprachlichen Mitteln der... mehr
Desmin and Vimentin as markers of regeneration in muscle diseases
in: Acta neuropathologica , ISSN 1432-0533, Vol. 85 (1. 1992), p. 88-92 Zugang:
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1992
Summary Localization and distribution of desmin and vimentin have been studied in different neuromuscular disorders using monoclonal antibodies. We have demonstrated that vimentin, although virtually absent in normal human muscle fibers, is expressed in regenerating fibers in different... mehr
Dystrophin deficiency in a case of congenital myopathy
in: Journal of neurology , ISSN 1432-1459, Vol. 239 (2. 1992), p. 76-78 Zugang:
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1992
Summary We studied a 5-year-old boy who had the “floppy infant syndrome” and a dystrophic pattern on muscle biopsy. According to the clinical presentation and the histopathological findings the diagnosis of congenital muscular dystrophy with associated intellectual retardation was made.... mehr
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsy
in: Acta neuropathologica , ISSN 1432-0533, Vol. 90 (6. 1995), p. 660-664 Zugang:
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1995
Abstract We studied the muscle biopsy from an asymptomatic patient with high serum creatine kinase values. Subsarcolemmal and intermyofibrillar granular inclusions were seen at the light microscopy level. Ultrastructural observation showed clusters of cylindrical spirals (CS). CS are a... mehr
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsy
in: Acta neuropathologica , ISSN 1432-0533, Vol. 90 (6. 1995), p. 660-664 Zugang:
zum Volltext ähnliche Vorschläge
1995
Abstract We studied the muscle biopsy from an asymptomatic patient with high serum creatine kinase values. Subsarcolemmal and intermyofibrillar granular inclusions were seen at the light microscopy level. Ultrastructural observation showed clusters of cylindrical spirals (CS). CS are a... mehr
Copyright: Copyright 1995 Springer-Verlag Berlin Heidelberg mehr
Interpersonal attraction and descriptions of the traits of others: Ideal similarity, self similarity, and liking
in: Journal of Research in Personality, in: Journal of Research in Personality . - Amsterdam : Elsevier, ISSN 0092-6566, ZDB-ID 1469785-3 Vol. 24, No. 2 (1990), p. 216-240
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Congenital Myopathy with Type 2A Muscle Fiber Uniformity and Smallness
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 23, No. 01 (2. 1992), p. 10-13 Zugang:
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1992
We describe a 12-year-old girl with congenital myopathy. ATPase histochemical reactions and immunocytochemical analysis of muscle fiber-type composition with monoclonal antibodies against slow, fast (2 A and 2 B) and fetal myosin demonstrate that this congenital disease is characterized by type 2... mehr
A case of mitochondrial myopathy, lactic acidosis and complex I deficiency
in: Journal of neurology , ISSN 1432-1459, Vol. 237 (7. 1990), p. 399-404 Zugang:
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1990
Summary A 34-year-old man affected by exercise intolerance, mild proximal weakness and severe lactic acidosis is described. Muscle biopsy revealed mitochondrial abnormalities and an increase of cytochrome c oxidase histochemical reaction. Biochemical investigations on isolated muscle mitochondria... mehr
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level
in: Acta neuropathologica , ISSN 1432-0533, Vol. 87 (4. 1994), p. 371-376 Zugang:
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1994
Abstract In situ hybridization combined with immunohistochemical techniques has been applied to study patients affected by mitochondrial myopathies with large mitochondrial (mt)DNA deletions. All patients' muscle biopsies showed ragged red fibers (RRFs) and cytochrome oxidase (COX) deficiency.... mehr
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level
in: Acta neuropathologica , ISSN 1432-0533, Vol. 87 (4. 1994), p. 371-376 Zugang:
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1994
Abstract. In situ hybridization combined with immunohistochemical techniques has been applied to study patients affected by mitochondrial myopathies with large mitochondrial (mt)DNA deletions. All patients' muscle biopsies showed ragged red fibers (RRFs) and cytochrome oxidase (COX) deficiency.... mehr
Copyright: Copyright 1994 Springer-Verlag Berlin Heidelberg mehr
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C
in: Journal of neurology , ISSN 1432-1459, Vol. 242 (4. 1995), p. 203-209 Zugang:
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1995
Abstract A 16-year-old girl presented with early-onset cerebellar ataxia, myoclonus, elevated lactic acidosis and hypogonadotropic hypogonadism. Muscle biopsy specimens revealed fibres with a “ragged” appearance with increased mitochondria and lipid droplets. Biochemical investigation... mehr
Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (8. 1994), p. 511-516 Zugang:
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1994
Abstract A woman with definite multiple sclerosis (MS) and mitochondrial myopathy is described. There were widespread white matter lesions on magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) abnormalities and evoked response changes. Muscle biopsy showed ragged red fibres (RRFs) and... mehr
An atypical case of partial merosin deficiency congenital muscular dystrophy
in: Journal of neurology , ISSN 1432-1459, Vol. 244 (6. 1997), p. 391-395 Zugang:
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1997
Copyright: Copyright 1997 Springer-Verlag Berlin Heidelberg mehr
Sarcoglycan deficiency in a large Italian population of myopathic patients
in: Acta neuropathologica , ISSN 1432-0533, Vol. 96 (5. 1998), p. 509-514 Zugang:
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1998
Abstract Autosomal recessive limb-girdle muscular dystrophies are a heterogeneous group of genetic diseases with a wide spectrum of clinical severity and age of onset; mutations in the gene encoding the dystrophin-associated sarcoglycan proteins (α, β, γ and δ) have recently been shown to... mehr
Copyright: Copyright 1998 Springer-Verlag Berlin Heidelberg mehr
A novel mitochondrial tRNAIle point mutation in chronic progressive external ophthalmoplegia
in: Journal of neurology , ISSN 1432-1459, Vol. 245 (11. 1998), p. 755-758 Zugang:
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1998
Copyright: Copyright 1998 Springer-Verlag Berlin Heidelberg mehr
Fourth metting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (1. 1994), p. 1-164 Zugang:
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