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Chorea Huntington: A Rare Case with Childhood Onset

Autor: N. Wagner, M. Gencik, C. Hammans, J. T. Epplen, H. Strehl

Publikováno v: Neuropediatrics. 33:90-92

Chorea Huntington (CH) is a dominantly inherited, neurodegenerative disease usually with adult onset. The course of CH is characterized by movement disturbances, psychiatric symptoms and it may lead to dementia. Typically death occurs after 10 to 20

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c533e5a4ce0aa92d07416e61ff28e7eb
https://doi.org/10.1055/s-2002-32367

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Pyridoxal 5′-phosphate may be curative in early-onset epileptic encephalopathy

Autor: Johannes Zschocke, Beat Steinmann, Georg F. Hoffmann, Peter E. Clayton, Philippa B. Mills, N. Wagner, H. Strehl, Nicole I. Wolf, Axel R. Franz, Matthias R. Baumgartner, Thomas Bast, Bernhard Schmitt, Soyhan Bagci, M. Windfuhr

Publikováno v: Hoffmann, G F, Schmitt, B, Windfuhr, M, Wagner, N, Strehl, H, Bagci, S, Franz, A R, Mills, P B, Clayton, P T, Baumgartner, M R, Steinmann, B, Bast, T, Wolf, N I & Zschocke, J 2007, ' Pyridoxal 5′-phosphate may be curative in early-onset epileptic encephalopathy ', Journal of Inherited Metabolic Disease, vol. 30, no. 1, pp. 96-99 . https://doi.org/10.1007/s10545-006-0508-4
Journal of Inherited Metabolic Disease, 30(1), 96-99. Springer Netherlands

Neonatal epileptic encephalopathy can be caused by inborn errors of metabolism. These conditions are often unresponsive to treatment with conventional antiepileptic drugs. Six children with pyridox(am)ine-5′-phosphate oxidase (PNPO) deficiency pres

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d450b53b1689051294192ad341c4284b
https://research.vumc.nl/en/publications/31aa85ef-f987-489c-907a-11030caf2a70

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[Radiosensitivity of hyperpentaploid cell clones in vulvar neoplasms]

Autor: S, Dahlhäuser, H, Strehl, N, Zamboglou

Publikováno v: Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]. 171(2)

Intension of our examination is to investigate changes in ploidy during radiotherapy and to find out radiosensitive cloni of tumors.In November 1993 a 83-year old patient with a carcinoma of the vulva was introduced to the Strahlenklinik der Städtis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9967f70df54f8e5ae229b406467ad8bd
https://pubmed.ncbi.nlm.nih.gov/7863432

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Carboplatin and radiotherapy in the treatment of head and neck cancer: six years' experience

Autor: N, Zamboglou, T, Schnabel, C, Kolotas, W, Achterrath, H, Strehl, S, Dalhäuser, H G, Vogt, L, Lenaz, G, Schmitt

Publikováno v: Seminars in oncology. 21(5 Suppl 12)

Between 1987 and 1991, 103 patients with advanced head and neck carcinoma were treated with radiochemotherapy plus carboplatin. Tumors were located in the oral cavity in 33 patients, the oropharynx in eight, and the hypopharynx in seven. Four patient

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0769419bd09b38b54bfd1d0a1d8dbe81
https://pubmed.ncbi.nlm.nih.gov/7992066

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Phase I study of hyperfractionated accelerated radiation and simultaneous Carboplatin therapy for advanced head and neck carcinomas

Autor: T, Schnabel, N, Zamboglou, C, Kolotas, W, Jiménez, H, Strehl, G, Schmitt

Publikováno v: Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]. 168(6)

From 1990 to 1991 15 patients with advanced head and neck carcinomas underwent hyperfractionated accelerated radiotherapy (2 x 1.6 Gy/day, five days/week, total dose 64.0 to 67.2 Gy) and simultaneous intravenous application of Carboplatin (60 mg/m2,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c46fa1b053e12e0371b821ea37391275
https://pubmed.ncbi.nlm.nih.gov/1621209

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