Zobrazeno 1 - 10 of 63 pro vyhledávání: '"C Whybra"'
1
Charakteristika und klinische Manifestation katheterassoziierter Thrombosen bei Frühgeborenen
Autor: S. Tippmann, K. Schmitz, C. Whybra, G. Staatz, C. Kampmann, E. Mildenberger
Zusammenfassung Hintergrund In der Neonatologie sind peripher eingeführte zentrale Katheter ein häufiger Zugangsweg zur parenteralen Ernährung und Verabreichung von Medikamenten und Flüssigkeit. Die Vorteile stehen den Risiken wie Infektion, Thro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5806ab7f959e2fa0cabe5bbc47a9b61c
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5
[Female Preterm Monozygotic Twins Discordant for Fetal Megacystis due to Cloacal Dysgenesis After Conception by Intracytoplasmatic Sperm Injection - Case Report and Review of Literature]
Autor: M, Schneider, I, Schmeh, A, Fruth, C, Whybra-Trümpler, E, Mildenberger
Publikováno v: Zeitschrift fur Geburtshilfe und Neonatologie. 220(5)
Monozygotic twins were previously regarded as "identical". By now an increasing number of case reports of monozygotic but discordant twins have been reported, and therefore discordance between monozygotic twins is being investigated intensively. We r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32f430e1f0b5e18689812c6992f0a564
https://pubmed.ncbi.nlm.nih.gov/27764886
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7
Average square atomic displacement: A comparison of the Monte-Carlo and Green's function results
Autor: R. C. Shukla, J. C. Whybra, F. Boseglav
Publikováno v: physica status solidi (b). 195:73-83
Highly accurate results for the mean-square displacement (MSD) of an atom for a nearest-neighbor Lennard-Jones model of a f.c.c. solid are presented. These results are obtained from the Monte-Carlo (MC) method and the Green's function method. The dep
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ff536f5f1be3fd1b5494906d712f780
https://doi.org/10.1002/pssb.2221950109
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9
[Psychiatric and neuropsychological signs and symptoms in patients with fabry disease: literature review]
Autor: M J, Müller, K-M, Müller, A, Dascalescu, C, Whybra, K, Baron, A, Scheurich, K, Mann, M, Beck, L G, Schmidt, A, Fellgiebel
Publikováno v: Fortschritte der Neurologie-Psychiatrie. 73(11)
Fabry Disease (FD) is an X-linked lysosomal storage disorder (prevalence about 1 : 100 000) caused by a genetic defect associated with a lack of alpha-galactosidase A (alpha-GAL) enzyme activity. As a consequence, neutral glycosphingolipides can not
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2999bf8335c5e5fef1317da41afbc3c0
https://pubmed.ncbi.nlm.nih.gov/16283613
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10
The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy
Autor: C, Whybra, C, Kampmann, F, Krummenauer, M, Ries, E, Mengel, E, Miebach, F, Baehner, K, Kim, M, Bajbouj, A, Schwarting, A, Gal, M, Beck
Publikováno v: Clinical genetics. 65(4)
Anderson-Fabry disease (AFD) is an X-linked disorder caused by deficient activity of the lysosomal enzyme alpha-galactosidase A. The availability of enzyme replacement therapy (ERT) for this debilitating condition has led to the need for a convenient
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::57ab2168eb0b6fbf0cb1c77acb9f5d8d
https://pubmed.ncbi.nlm.nih.gov/15025723
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