Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
  • 1
    Digitale Medien
    Digitale Medien
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Phytopathology 3 (1965), S. 69-84 
    ISSN: 0066-4286
    Quelle: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft , Biologie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    ISSN: 1434-6052
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract We present data on the multiplicity structure of inclusive charged hadron production in charged current neutrino and antineutrino freon interactions in the energy range 3–30 GeV resulting from an experiment with the bubble chamber SKAT. Average multiplicities, dispersions and correlation coefficients are investigated. Furthermore, KNO-scaling is studied and average net charges are calculated in different kinematical regions. Our data are compared with results from $$\begin{array}{*{20}c} {( - )} \\ v \\ \end{array} $$ -interactions on an isoscalar target of “free” nucleons to study the influence of nuclear effects.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Cellular and molecular life sciences 21 (1965), S. 46-47 
    ISSN: 1420-9071
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Résumé La production d'anticorps antiprotéiques a été étudiée comparativement chez des rats de 3 mois et de 22 mois, par la méthode d'hémagglutination passive. Les résultats montrent et précisent la différence de comportement immunologique entre animaux jeunes et animaux âgés.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Pediatric radiology 26 (1996), S. 280-281 
    ISSN: 1432-1998
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract From April 1992 to May 1994, 780 patients aged from 1 day to 8 years were examined. Sedation of these patients was conducted by giving chlorprothixene orally and, in some cases, chloral hydrate had to be added. The patients were monitored with a pulse oxymeter. Investigations could begin after 50–120 min. In 710 patients (91 %) the first attempt to perform the examination was successful; 70 patients required one or two further attempts. Only two of the 780 patients (0.5 %) showed evidence of respiratory depression. The total number of pediatric MRI examinations performed in 1 year is almost 1000. In the hands of an experienced pediatric radiologist these examinations can be performed entirely without anesthesia.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    facet.materialart.
    Unbekannt
    New York : Periodicals Archive Online (PAO)
    Journal of Memory and Language. 6:5 (1967:Oct.) 699 
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    ISSN: 1432-0533
    Schlagwort(e): Key words Pure autonomic failure ; Lewy bodies ; Autopsy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Pure autonomic failure (PAF; also known as idiopathic orthostatic hypotension or Bradbury-Eggleston syndrome) is an uncommon sporadic disorder, characterized by autonomic failure without other neurological deficits and histopathologically by cell loss in intermediolateral columns and sympathetic ganglia. Few postmortem studies of patients with PAF have been reported in the literature, and none have demonstrated Lewy bodies in distal axons, although this has been described as a feature in Parkinson’s disease with autonomic failure. We report a patient with PAF who had orthostatic hypotension and urinary symptoms for 15 years prior to death at the age of 63 years. Postmortem findings included typical and atypical Lewy bodies in the substantia nigra, locus ceruleus, substantia innominata, and sympathetic ganglia, as well as in autonomic axons in the epicardial fat, autonomic nerve fascicles in periadrenal adipose tissue, and autonomic nerves in the muscularis of the urinary bladder. Sites of autonomic nerve involvement correlated with clinical symptomatology, and thus were a valuable observation in the complete autopsy. Systemic autopsy results should be reviewed carefully in patients with PAF, as Lewy bodies in this disease may be seen in distal axons at a great length from their primary cell bodies.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Cellular and molecular life sciences 24 (1968), S. 119-121 
    ISSN: 1420-9071
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Zusammenfassung Katalase aus Erythrocyten vom Menschen (und Pferd) lässt sich säulenchromatographisch und elektrophoretisch in drei Fraktionen A, B und C auftrennen, wobei die Fraktionen A und B die Tendenz haben, in die Fraktion C überzugehen. Durch Chromatographie unter Ausschluss von Luftsauerstoff konnte gezeigt werden, dass die Katalase in den Erythrozyten in der Form A vorliegt. Setzt man das Hämolysat dagegen einige Zeit Luftsauerstoff aus, wird die Katalase bei der Chromatographie in Form C eluiert. SH-blockierende Reagentien verhindern die Umwandlung von A in C, während C mit Mercaptoäthanol zu A reduziert werden kann. Es wird angenommen, dass dem Übergang von Fraktion A in B und C eine Bildung von Disulfidbrücken zugrunde liegt und dass es sich bei den beobachteten alternativen Formen möglicherweise um Katalase-Konformere handelt.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    Springer
    European journal of pediatrics 140 (1983), S. 5-12 
    ISSN: 1432-1076
    Schlagwort(e): Proteus syndrome ; Macrodactyly ; Hemihypertrophy ; Pigmented nevi ; Skull anomalies ; Lipomas
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Four boys are described with partial gigantism of the hands and/or feet, pigmented nevi, hemihypertrophy, subcutaneous hamartomatous tumors and macrocephaly, and/or other skull anomalies. Three of these patients showed an accelerated growth in their first years of life. Two suffered from cystiform pulmonary abnormalities. The children showed normal mental development with the exception of one with traumatic brain damage. Parental consanguinity was not disclosed. As a result of a review of the literature, we can say that these cases do not conform to any well defined entity and would appear to represent a ‘new’ syndrome to be categorized under congenital hamartomatous disorders. The mode of inheritance of the undoubtedly genetically determined syndrome is yet not clearly understood. We propose the term Proteus syndrome for this ‘new’ syndrome.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    ISSN: 1432-1076
    Schlagwort(e): New skeletal dysplasia ; Multiple epiphyseal dysplasia ; Delayed maturation of hand feet pelvis sacrum
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Three brothers with a constitutional skeletal dysplasia characterized by an excessively retarded ossification, principally of the epiphyses, the pelvis, the hands and the feet, are reported. In the hands and feet the retarded ossification is combined with an abnormal modeling of the bones. All the children appeared normal at birth. At the time of examination a moderate degree of dwarfism could be predicted. There was no mental retardation. All laboratory investigations including chromosomal analyses and examination for acid mucopolysaccharides in the urine were normal. Parental consanguinity suggest an autosomal recessive inheritance. There is no resemblance of this disorder to any of the hitherto described groups of constitutional diseases of bones.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Skeletal radiology 7 (1981), S. 173-177 
    ISSN: 1432-2161
    Schlagwort(e): Cockayne's syndrome ; Bone deformities ; Children, growth and development ; Premature aging ; Thymic hormone
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Cockayne's syndrome is a rare familial disorder characterised clinically by premature aging, appearing progressively from the third year on. The radiological manifestations of eight affected children have been studied and summarised. It is concluded that a skeletal survey can provide a roentgenologic pattern suggesting the diagnosis, even when it is inconclusive from the clinical signs during the first years of life. The aetiology of this syndrome is unknown, but the authors postulate the possible role of a defect of thymic hormone which has been found in all their cases.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...