Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Michael Krasnianski"'
Publikováno v:
Journal of Neurology. 253:1442-1446
In comparison with the lateral (Wallenberg), medial (Dejerine) and hemimedullary (Reinhold) medulla oblongata syndromes, the Babinski-Nageotte and Cestan-Chenais syndromes are much less familiar cerebrovascular disorders. While the Babinski-Nageotte
Publikováno v:
Acta Ophthalmologica Scandinavica. 84:415-418
Purpose: To explain the rare phenomenon of acute transient bilateral blindness without additional ophthalmological or neurological symptoms and signs. Methods: Six patients with isolated bilateral visual loss lasting 1–15 mins and occurring simulta
Publikováno v:
Obstetrics & Gynecology. 107:446-449
BACKGROUND:The postpartum angiopathy (Call-Fleming syndrome) is a rare, reversible cerebral vasoconstriction syndrome. Unlike in eclampsia, neither proteinuria nor hypertension have been observed in the Call-Fleming syndrome.CASE:A 17-year-old woman
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 72:460-468
Definitions of classical crossed brainstem syndromes in the modern neurological literature are often inaccurate and inconsistent. As a result, different clinical syndromes are designated with the same eponym, other crossed syndromes are nearly comple
Publikováno v:
Neuromuscular Disorders. 14:438-441
External ocular muscle palsies in patients with ophthalmic zoster are traditionally interpreted as diseases of III, IV or VI cranial nerves. Orbital myositis associated with zoster ophthalmicus has been diagnosed only rarely. We describe a patient wi
Autor:
Michael Krasnianski, Wolfgang Hirsch, Rolf Peter Spielmann, Mirko Krivokuca, Andreas Schluter, Stephan Neudecker
Publikováno v:
Clinical Neurology and Neurosurgery. 106:110-113
Vasculitits of the central nervous system (CNS) is a known complication of chronic inflammatory bowel diseases. We report the case of a female patient with Crohn's disease, developing vasculitis of the CNS with evidence of pathological vessel depicti
Publikováno v:
Der Nervenarzt. 74:1150-1154
In contrast to the majority of classic brainstem syndromes, the interpretation of Schmidt's syndrome (ipsilateral palsy of the IX, X, XI, and XII cranial nerves with contralateral hemiparesis) and Vernet's syndrome (ipsilateral palsy of the IX, X, an
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 71:650-653
In 1891 Georg Avellis described a so-called "laryngeal hemiplegia" that can be caused by peripheral lesions of the vagal and glossopharyngeal nerves and rarely by infarctions of the medulla oblongata, thus representing a classical brainstem syndrome.
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 71:397-405
Historical publications of the classical alternating medulla oblongata syndromes of Wallenberg, Babinski-Nageotte, Cestan-Chenais, Hughlings Jackson, Avellis, Schmidt, Dejerine, Spiller and Tapia were reviewed and critically analysed. We compare thes
Publikováno v:
Der Nervenarzt. 74:151-158
Although the gene for facioscapulohumeral muscular dystrophy (FSHD) has not been identified so far, 4q35 deletion represents a diagnostic marker of the disease. In the present study, 46 consecutive symptomatic patients with 4q35 FSHD deletions or typ