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  • 1
    ISSN: 1432-0428
    Keywords: Keywords Gastric emptying ; diabetic gastroparesis ; scintigraphy ; breath test ; cardiovascular autonomic function.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Since there is a need for a widely applicable non-invasive test to assess gastric emptying in diabetic patients, we evaluated the sensitivity, specificity, and reproducibility of the [13C]octanoic acid breath test as compared with scintigraphy. Moreover, we examined the relationship between the breath test indices and gastric symptoms, cardiovascular autonomic function, and metabolic parameters. Forty healthy control subjects and 34 diabetic patients were studied. Three indices of gastric emptying, assessed by the breath test, were computed: half-emptying time (t1/2breath), gastric emptying coefficient (GEC), and lag phase. Furthermore, the half-emptying time, measured by scintigraphy (t1/2scint), was calculated and gastric symptoms and cardiovascular autonomic neuropathy (CAN) were scored. The coefficients of variation of day-to-day reproducibility in 10 healthy subjects were 29.6 % for t1/2breath, 7.4 % for GEC, and 46.5 % for lag phase. An abnormal delay for t1/2scint (〉 100 min) or t1/2breath (〉 200 min) was noted in 12 patients. Based on the results for t1/2scint, the sensitivity of t1/2breath and GEC was 75 % and the specificity was 86 %. Both t1/2breath (r s = 0.523; p 〈 0.05) and GEC (r 2 = − 0.594; p 〈 0.05) were significantly associated with the gastric symptom score. A significant relationship to the CAN score was demonstrated for t1/2breath (r s = 0.448; p 〈 0.05), GEC (r s = − 0.467; p 〈 0.05), and t1/2scint (r s = 0.602; p 〈 0.05). There were no significant associations of the breath test indices with the blood glucose levels during the test, HbA1c, age, and duration of diabetes. In patients with abnormal t1/2scint (n = 12) not only was t1/2breath significantly prolonged and GEC reduced, but also the scores of CAN and gastric symptoms were significantly increased as compared with those who had a normal t1/2scint (n = 22). We conclude that the [13C]octanoic acid breath test represents a suitable measure of delayed gastric emptying in diabetic patients which is associated with the severity of gastric symptoms and CAN but not affected by the blood glucose level. [Diabetologia (1996) 39: 823–830]
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 68 (1976), S. 456-464 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0888-7543
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0888-7543
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1437-3262
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Abstract Widely accepted plate tectonic models suggest that an inactive subduction zone lies along the north-west continental margin of Sabah. In contrast, interpretation of reflection seismic data acquired by BGR shows an autochthonous continental terrane comprising an Oligocene to Early Miocene carbonate platform being progressively overthrust by an allochthonous rock complex. Progressive compression resulted in the development of four structural zones: Imbricated thrust sheets (Zone III); two thrust sheet systems one on top of the other (Zone IV); a complex zone with multiphase deformation (Zone V); and piercement ridges (Zone VI).
    Abstract: Résumé Les modèles géodynamiques que l'on admet habituellement comportent une zone de subduction inactive le long de la marge continentale nord-occidentale de Sabah. Toutefois, des mesures de sismique-réflexion exécutées par le BGR font apparaître qu'à cet endroit, une croûte continentale autochtone, comportant une plateforme carbonatée oligocène à éomiocène, est chevauchée progressivement par un complexe allochtone. La compression, qui s'est manifestée progressivement depuis le Miocène inférieur, a engendré quatre zones structurales: un ensemble d'écailles tectoniques (zone III); deux systèmes de lames tectoniques charriés l'un sur l'autre (zone IV); une zone complexe à déformation multiphasée (zone V); des structures d'extrusion tectonique (zone VI).
    Notes: Zusammenfassung Nach herkömmlichen plattentektonischen Vorstellungen soll eine inaktive Subduktionszone am nordwestlichen Kontinentalrand von Sabah liegen. Reflexionsseismische Meßdaten der BGR zeigen jedoch, daß hier autochthone kontinentale Kruste mit einer oligozänen-frühmiozänen Karbonatplattform progressiv von einem allochthonen Gesteinsverband überschoben wird. Fortschreitender Zusammenschub seit dem frühen Miozän führte zur Anlage von vier Deformationszonen: Tekonische Schuppen (Zone III); zwei übereinander geschobene Verschuppungssysteme (Zone IV); Gürtel mit mehrphasiger Deformation (Zone V) und Durchspießungsstrukturen (Zone VI).
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1435-1285
    Keywords: Schlüsselwörter Myokarditis – Antimyosin-Szintigraphie – Myokardbiopsie – Antimyosin-Autoantikörper ; Key words Myocarditis – antimyosin-scintigraphy – endomyocardial biopsy – antimyosin-autoantibodies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Antimyosin-scintigraphy is believed to have a high specificity but a low sensitivity for the diagnosis of myocarditis when histological analysis of endomyocardial biopsy is used as the reference method. However, the histological evaluation itself seems to have a low sensitivity for the diagnosis of myocarditis. Therefore, immunohistological techniques have been developed for the detection of lymphocytic infiltrates and increased expression of HLA antigens in the myocardium. The present study compares the results of antimyosin-scintigraphy with histological and immunohistological analysis of the endomyocardial biopsy. 65 patients with clinically suspected myocarditis underwent antimyosin-scintigraphy and histological and immunohistological analysis of the endomyocardial biopsy. Myocarditis could be diagnosed histologically in only 9/36 (25%) patients with a positive antimyosin scan but additional immunohistological analysis revealed lymphocytic infiltrates in 31 (86%) of these patients. In 29 patients with a normal antimyosin scan, histological analysis showed evidence of myocarditis in 3 (10%) patients; additional immunohistological evaluation disclosed lymphocytic infiltrates in 17 (59%) patients. With immunohistological analysis of the endomyocardial biopsy as the reference method, antimyosin-scintigraphy has a high sensitivity but a lower specificity for the diagnosis of myocarditis. Detection of autoantibodies against human cardiac myosin in patients with myocarditis is associated with a significantly lower incidence of positive antimyosin scans in these patients. Antimyosin-scintigraphy was repeated after six months in 14 patients with myocarditis. Histological and immunohistological evaluation of the endomyocardial biopsy now showed persistent myocarditis in 3/8 patients with a positive antimyosin scan and in 5/6 patients with a normal antimyosin scan.
    Notes: Zusammenfassung Für die Diagnostik der Myokarditis wird bisher der Antimyosin-Szintigraphie eine hohe Spezifität, jedoch eine geringe Sensitivität zugewiesen. Hierfür wurde bisher die Antimyosin-Szintigraphie mit der allein histologischen Aufarbeitung der Endomyokardbiopsie verglichen. Die histologische Analyse der Myokardbiopsie scheint jedoch selbst nur eine geringe Sensitivität für die Diagnose einer Myokarditis zu haben. Daher wurden in den letzten Jahren zusätzlich immunhistologische Methoden zum Nachweis lymphozytärer Infiltrate im Myokard etabliert. In der vorliegenden Studie werden die Ergebnisse der Antimyosin-Szintigraphie mit den Befunden der histologischen sowie zusätzlich der immunhistologischen Analyse der Myokardbiopsie verglichen. Bei 65 Patienten mit klinischem Verdacht auf eine Myokarditis wurden eine Antimyosin-Szintigraphie durchgeführt sowie die Myokardbiopsie mit histologischen und immunhistologischen Methoden analysiert. Bei 36 Patienten mit positivem Antimyosin-Szintigramm konnte durch die allein histologische Beurteilung der Myokardbiopsie nur bei 9 (25%) Patienten eine Myokarditis diagnostiziert werden, die immunhistologische Aufarbeitung wies jedoch lymphozytäre Infiltrate bei 31 (86%) dieser Patienten nach. Bei 29 Patienten mit unauffälligem Antimyosin-Szintigramm diagnostizierte die allein histologische Beurteilung der Myokardbiopsie eine Myokarditis bei 3 (10%) Patienten, die immunhistologische Analyse zeigte lymphozytäre Infiltrate bei 17 (59%) dieser Patienten. Bei immunhistologischer Aufarbeitung der Myokardbiopsie als Referenzmethode muß somit der Antimyosin-Szintigraphie eine hohe Sensitivität, jedoch eine geringere Spezifität für die Diagnostik der Myokarditis zugerechnet werden. Bei Patienten mit einer Myokarditis, bei denen im Serum Autoantikörper gegen kardiales Myosin nachgewiesen werden konnten, lag die Inzidenz positiver Antimyosin-Szintigramme deutlich niedriger als bei Patienten mit Myokarditis ohne Antimyosin-Autoantikörper. Bei 14 Patienten mit Myokarditis wurde nach 6 Monaten erneut eine Antimyosin-Szintigraphie durchgeführt. Jetzt konnte histologisch oder immunhistologisch eine Myokarditis bei 3/8 Patienten mit positivem Antimyosin-Szintigramm sowie bei 5/6 Patienten mit unauffälligem Antimyosin-Szintigramm nachgewiesen werden. Somit erscheint die Antimyosin-Szintigraphie zur Verlaufskontrolle einer Myokarditis weniger hilfreich.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1435-1285
    Keywords: Schlüsselwörter Apikale ; hypertrophe Kardiomyopathie ; βMHC-de novo-Mutation ; Plötzlicher Herztod ; Key words Apical hypertrophic ; cardiomyopathy ; β-myosin heavy chain de novo mutation ; codon 719 ; sudden death
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Hypertrophic cardiomyopathy (HCM) is a myocardial disease with variable phenotpye and genotype. To demonstrate that the mutation Arg719Trp in the cardiac β-myosin heavy chain (βMHC) gene is a high risk factor for sudden death and can be associated with an unusual apical non-obstructive HCM, we report the case of a 61/2 year old boy, who suffered cardiac arrest.    The proband had a de novo mutation of the βMHC gene (Arg719Trp) on the paternal βMHC allele and a second maternally transmitted mutation (Met349Thr), as was shown previously (Jeschke et al. 1998 (11)). Here we report the clinical phenotype of the proband and of his relatives in detail. The proband had a marked apical and midventricular hypertrophy of the left and right ventricle without obstruction. There was an abnormal relaxation of both ventricles. Holter monitoring detected no arrhythmia. Ventricular fibrillation was inducible only by aggressive programmed stimulation. The boy died 31/2years later after another cardiac arrest due to arrhythmia.    Five carriers of the Met349Thr mutation in the family were asymptomatic and had no echocardiographic changes in the heart, suggesting a neutral inherited polymorphism or a recessive mutation. It is concluded that there is an association of the mutation Arg719Trp in the β-myosin heavy chain with sudden cardiac death in a young child. Disease history in conjunction with the genetic analysis suggests that the implantation of a defibrillator converter would have been a beneficial and probably life saving measure.
    Notes: Zusammenfassung Die hypertrophe Kardiomyopathie (HCM) ist eine Erkrankung des Myokards mit variablem Geno- und Phänotyp. Um zu zeigen, dass die Mutation Arg719Trp ein Risikofaktor bedeutet und mit einer apikalen HCM (AHCM) einhergehen kann, berichten wir über einen Jungen, der im Alter von 61/2 Jahren als Erstmanifestation eine reanimationsbedürftige tachycarde Syncope erlitt und 31/2 Jahre später an einem zweiten Anfall verstarb.    Bei diesem Jungen war eine denovo Mutation im β-Myosingen (βMHC) (Arg719Trp) auf den paternalen sowie eine Met349Thr-Mutation auf dem maternalen Allel identifiziert worden (11). Die vorliegende Studie beschreibt den Phänotyp des Patienten, seine Familie und den weiteren klinischen Verlauf. Doppler-echocardiographisch zeigt sich eine nicht obstruktive apikale HCM mit abnormer Relaxation des linken und rechten Ventrikels. Elektrophysiologisch ließ sich nur unter aggressivem Stimulationsprotokoll und Suprarenin Kammerflimmern auslösen. In den 31/2 Jahren waren in den Langzeit-EKG‘s Arrythmien nicht nachweisbar, bis der Junge im zweiten Anfall verstarb.    Die fünf Träger der Mutation Met349Thr hatten keine Symptome der HCM.    Schlussfolgerung: Assoziation der Arg719Trp-Mutation im β-Myosin-Gen mit plötzlichem Herztod bei einem Kind.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 65 (1983), S. 195-197 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A cloned rabbit heart muscle myosin heavy-chain cDNA was hybridized in situ with human metaphase chromosomes. The probe was known to have sequence homology with human genomic heavy-chain DNA. Only one site in the human haploid karyotype was labeled with the cDNA, and this site was found on the short arm of chromosome 17. The localization of autoradiographic grains suggests a subregional assignment of the myosin heavy-chain locus to 17p 1,2-pter.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 65 (1983), S. 198-203 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A DNA segment from the human genome with information for myosin heavy chain (MHC) was isolated from a human genomic DNA library cloned in λ Charon 4A phages. The isolation was accomplished by a myosin cDNA probe obtained from rabbit heart muscle mRNA (Sinha et al. 1982). The selected human DNA clone, designated λ gMHCl, contains a genomic DNA fragment of about 14 kilobase pairs. The transcriptional polarity of this DNA was determined. The 5′-end of the gene is missing from the cloned fragment. This human gene exhibits sequence homology to MHC DNA of rabbit and chicken, but not to an MHC sequence of nematode. The isolated gene fragment is a member of the human MHC multigene family, which is presumed to consist of probably more than ten separate sarcomeric MHC genes per haploid genome.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of nuclear medicine 12 (1986), S. S34 
    ISSN: 1619-7089
    Keywords: T-butylisonitrile-technetium ; Pharmacokinetics ; Coronary heart disease ; Myocardial scintigraphy ; TBI
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract T-butylisonitrile-technetium-99 m (TBI), a technetium labeled myocardium imaging agent was investigated in ten male patients with coronary heart disease. Kinetics of TBI were evaluated by means of transfer function analysis of organ time-activity curves. First-pass uptake values at rest showed the following decreasing order: liver, spleen, normal myocardium, lung and ischemic myocardium. Mean turnover times were shortest in the lung and of increasing order longer in spleen, normal myocardium, ischemic myocardium and liver. Under stress first pass uptake increased in myocardium and decreased in liver and spleen, while turnover times became prolonged. Thus kinetics of TBI are characterized by definite turnover rates and not by trapping in various tissues, which has to be considered during evaluation of scintigraphic images.
    Type of Medium: Electronic Resource
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