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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 17 (1968), S. 152-154 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über einen Patienten mit chronischer mycloischer Leukämie berichter, bei demsich nach Injektionen eines Eisen-Sorbit-Komplexes eine blastische Krise entwickelte. Zum Zeitpunkt des Eintritts dieser blastischen Krise befand sich der Patient im Stadium einer Remission nach Behandlung mit Myleran. Die möglichen ursächlichen Zusammenhänge zwischen der Entstehung der blastischen Krise und der parenteralen Verabfolgung des Eisen-Sorbit-Komplexes werden diskutiert.
    Notes: Summary A case of chronic myeloid leukemia who developed a blastic crisis following injections of iron sorbitol complex is presented. When the blastic crisis occurred the patient was in myleran induced remission. The caudal relationship between the development of blastic crisis and parenteral administration of iron sorbitol complex is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 19 (1969), S. 57-63 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Der Verfasser schildert einen Fall von Hodgkin, bei dem es nach Behandlung mit Vinblastinsulfat zu einer Megaloblasten-Anämie kam. Der ursächliche Zusammenhang wird diskutiert. Dieser Fall war aus folgenden Gründen interessant: 1. Bei diesem Patienten wurde der Hodgkin durch reine Erythrozyten-Aplasie angekündigt. 2. Für die Behandlung der Erythrozyten-Aplasie und für die Beeinflussung der Leukopenie, die während der Therapie mit Stickstoffsenf auftrat, wurde Phytohämagglutinin mit teilweisem Erfolg im ersten und vollständigem Erfolg in den letzteren Fällen angewendet.
    Notes: Summary A case of Hodgkin's disease who developed a megaloblastic anemia following treatment with Vinblastine sulfate is presented. The causal relationship is discussed. This case was also interesting for following reasons: 1. In this patient, Hodgkin's disease was heralded by pure red cell aplasia. 2. Phytohaemagglutinin was used for the treatment of pure red cell aplasia and for the correction of leukopenia which occured during nitrogen mustard therapy, with partial success in the former and complete success in the latter instances.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei 3 Patienten mit aplastischer Anämie, die durch eine chronische Benzol-Vergiftung verursacht war, wurde die osmotische Resistenz der Blutkörperchen untersucht. Die Messungen erfolgten vor und nach 24stündiger Inkubation bei 37°C. Obwohl die osmotische Resistenz vor der Inkubation normal war, war sie bei 2 Patienten nach 24 Stunden bei 37° C leicht bis mäßig erniedrigt.
    Notes: Summary In three patients with aplastic anaemia due to chronic benzene poisoning osmotic fragility before and after incubation at 37°C. for 24 hours was performed. Although the results of osmotic fragility before incubation were within normal limits, a mild or moderate increase in osmotic fragility after incubation at 37 C.° for 24 hours was observed in two of them.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 10 (1964), S. 329-332 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es werden zwei Beobachtungen von Thalassaemia minor mit leicht erhöhtem fetalem Hämoglobin beschrieben. Die Krankheitsbilder ähnelten in jeder Beziehung dem intermediären Typ vonCooley-Anämie oder der Thalassaemia minor mit starker Erhöhung, des fetalen Hämoglobins. Der einzige Unterschied war aber die weniger als 5%ige Erhöhung des HbF. Die möglichen genetischen Hintergründe der ungewöhnlichen Fälle werden diskutiert.
    Notes: Summary Two cases of thalassaemia minor with slightly elevated fetal haemoglobin are described. The patients resembled in every respect to intermediate type of Cooley's anaemia or thalassaemia minor with large amount of fetal haemoglobin. But there was only one difference between them, namely, the amount of fetal haemoglobin was less than 5%. The possible genetic explanation for this unusual observation is discussed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 15 (1967), S. 153-156 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über zwei Fälle der angeborenen Hüftluxation im Zusammenhang mit einer chronischen, ernährungsbedingten Eisenmangelanämie, die während der Fötalentwicklung begann, sowohl als auch über die Unterfunktion der Geschlechtsdrüsen, Zwergwuchs und Hepatosplenomegalie als Ausdruck der Leberzirrhose, berichtet. Über die Rolle der chronischen Eisenmangelanämie und anderer gleichzeitig existierender Ernährungsfaktoren, wie z. B. Mangel an Aminosäuren als mitwirkende Faktoren bei der Entwicklung einer angeborenen Hüftluxation wird berichtet.
    Notes: Summary Two cases of congenital dislocation of the hip associated with chronic iron deficiency anaemia of nutritional origin which had its onset in foetal life, hypogonadism, dwarfism and hepatosplenomegaly as a manifestation of liver cirrhosis are presented. The role of chronic iron deficiency anaemia and other coexistent nutritional factors such as deficiency of amino-acids as a contributary factor in the development of congenital dislocation of the hip is discussed.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary By using oligonucleotide hybridization, restriction endonuclease analysis and direct sequencing of amplified genomic DNA, we have been able to characterize 18 different mutations in the β-globin genes of 161 β thalassemia homozygotes and 107 β-thalassemia heterozygotes from Turkey (429 β-thalassemia chromosomes). Previous studies dealing with β-thalassemia in Mediterranean countries have shown that, in most Mediterranean populations, only a few mutations are prevalent. In contrast, β-thalassemia in Turkey does not seem to be associated with a few predominant mutations. The six most frequent alleles, IVS-I-110 (G→A), IVS-I-6(T→C), FSC-8 (-AA), IVS-I-1(G→A), -30(T→A) and FSC-5 (CT), account for only 69.3% of the disease genes; indeed, all 26 mutations assayed represent 85.8% of the disease genes, confirming the considerable molecular heterogeneity of β-thalassemia among Turks, and indicating the possible presence of rare, previously undefined, mutations in the population. Two mutations observed in this study, IVS-I-116 (T→G) and Cd44(-C), have not been reported in the Turkish population to date. Since preventive medical services, such as genetic counseling and prenatal diagnosis, are greatly improved by detailed knowledge of the molecular pathology of β thalassemia, we strongly believe that the presented data will facilitate the intended establishment of a prenatal diagnosis center, based on DNA analysis, in Turkey.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 179 (1957), S. 1248-1249 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] It was therefore a fortunate chance when, after an interval of two years, one Eti-Turk was examined at Mersin State Hospital and was found to possess two haemoglobins, one of them sickle-cell haemoglobin and the other haemoglobin E. This was the first time that 'sickle-cell haemoglobin E disease' ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Clinica Chimica Acta 12 (1965), S. 696-698 
    ISSN: 0009-8981
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1365-2095
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: A study was conducted to evaluate the effect of free gossypol from glanded-cottonseed meal (G-CSM) (natural free gossypol) or gossypol-acetic acid on growth performance, body composition, haematology, immune response and resistance of channel catfish (Ictalurus punctatus) to Edwardsiella ictaluri challenge. Soya bean meal-based diets supplemented with 0, 100, 200, 400, and 800 mg kg−1 free gossypol from G-CSM or gossypol-acetic acid were fed to juvenile channel catfish in triplicate aquaria to apparent satiation twice daily for 12 weeks. Neither sources nor levels of dietary gossypol significantly influenced the final weight gain, feed intake, feed efficiency and survival of channel catfish. Similarly, whole-body proximate composition, haematological parameters (red blood cell, white blood cell counts, haemoglobin and haematocrit), serum protein concentration, macrophage chemotaxis ratio, phagocytic activity and antibody production against E. ictaluri 21-day postinfection were not significantly affected at either dietary sources or levels of gossypol. Gossypol concentrations of liver were linearly related to dietary level of gossypol but the retention rate varied dependent on sources of the dietary gossypol. At dietary gossypol levels of 400 or 800 mg kg−1, total gossypol concentrations in liver of fish fed dietary gossypol from G-CSM were significantly higher than those of fish fed the corresponding levels of gossypol from gossypol-acetic acid. The (+)-isomer of gossypol was predominantly retained in liver regardless of dietary sources of gossypol. The ratio of (+) to (−) gossypol isomers in liver decreased with increasing dietary concentrations of gossypol. Serum lysozyme activity of fish fed dietary gossypol levels of 200 mg kg−1 or higher, either from G-CSM or gossypol-acetic acid, was significantly higher than that of the control. At a level of 800 mg kg−1 diet, gossypol from G-CSM stimulated significantly higher lysozyme activity than gossypol from gossypol-acetic acid. Fish fed diets containing 400 mg kg−1 gossypol or higher from G-CSM or 800 mg kg−1 gossypol from gossypol-acetic acid had significantly increased superoxide anion (O〈inlineGraphic alt="inline image" href="urn:x-wiley:13535773:ANU281:ANU_281_mu1" location="equation/ANU_281_mu1.gif"/〉) production. However, neither the sources nor the levels of dietary free gossypol influenced the resistance of juvenile channel catfish to E. ictaluri challenge.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 110 (1985), S. 244-246 
    ISSN: 1432-1335
    Keywords: High fat diet ; Vitamin A ; Vitamin E ; Reduced glutathione
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Mammary tumor development induced by methylnitrosourea in female Sprague-Dawley rats had no significant effect on hepatic glutathione levels. If the diets of methylnitrosourea-treated animals were supplemented with vitamin A and E an increased hepatic glutathione level was observed initially. A high fat diet (21% per weight) supplemented with the two vitamins led to a decreased hepatic glutathione level 2 months after tumor induction. Advanced tumor development under any of the diets tested had no effect on hepatic glutathione.
    Type of Medium: Electronic Resource
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