Zobrazeno 1 - 10
of 35
pro vyhledávání: '"H. G. Scheel-Walter"'
Autor:
Hartmut Liebich, Bernd Kammerer, H.-G. Scheel-Walter, H. Gérard, M. Bacher, Xin Lu, S. Müller-Hagedorn, Kwhanmien Kim, Antje Frickenschmidt
Publikováno v:
Journal of Chromatography B. 814:275-283
Modified nucleosides have been characterized as tumor markers for a number of malignant diseases. In order to use these markers in children, the age-dependence of the nucleoside levels in healthy children has to be established and taken into account
Autor:
B. Smyczek-Gargya, U. Krainick, G. C. Meyberg-Solomayer, B. Bültmann, D. Wallwiener, H.-G. Scheel-Walter, Karl Sotlar, Nikos Fersis
Publikováno v:
Geburtshilfe und Frauenheilkunde. 62:897-900
Breast malignancy is a rare event in adolescent. The case history described an adolescent girl presenting with breast enlargement. Clinical and sonographic features remind on malignancy. She had a history of rhabdomyosarcoma of the parotis. Core need
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 213:64-66
Down's syndrome is the most frequent autosomale chromosomal anomaly in newborns. In up to 10% of the cases these children develop a transient myeloproliferative disorder (TMD). Clinical symptoms are blood count disorders and raised liver enzymes. 15%
Publikováno v:
Klinische Pädiatrie. 206:381-384
Two sickle cell patients with cerebral accidents, infarct and bleeding, are presented. Up to 15% of all sickle cell patients suffer cerebral events, 75% of which are infarcts, 25% intracranial hemorrhages. Infarcts occur predominantly in children wit
Publikováno v:
Zeitschrift fur Geburtshilfe und Neonatologie. 215(5)
Anaplastic astrocytomas presenting as gliomatosis cerebri in neonates are extremely rare. Tumours in newborns are mostly of neuroectodermal origin.We report about a female newborn at term [birth weight 3 600 g (P 90), head circumference 35 cm (P 95)
Publikováno v:
Zeitschrift fur Geburtshilfe und Neonatologie. 213(2)
Down's syndrome is the most frequent autosomale chromosomal anomaly in newborns. In up to 10% of the cases these children develop a transient myeloproliferative disorder (TMD). Clinical symptoms are blood count disorders and raised liver enzymes. 15%
Autor:
Jens Martin Rohrbach, H. Pressler, G. Schaumburg-Lever, Edwin Kaiserling, Klaus-Peter Steuhl, H. G. Scheel-Walter
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 229:172-177
A 15-year-old girl presented with a painless nodule in the nasal lower-lid portion of the left eye at the beginning of 1989. The tumor was excised in March 1989, and the histopathologic diagnosis was - erroneously - a chondromatous choristoma of the
Autor:
Günther Schellong, Jörg Ritter, R. Dickerhoff, C. Eschenbach, S. Burdach, Josef Vormoor, H. G. Scheel-Walter, U. Creutzig, J Kühl
Publikováno v:
Klinische Pädiatrie. 202:253-257
Transient neonatal myeloproliferative disorders (TMD's) indistinguishable from acute leukaemia by clinical and morphological criteria have been described in neonates with Down's syndrome. To analyse its clinical significance, 10 infants under 1 year
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 211
Autor:
Ernemann U, R Beschorner, H-G Scheel-Walter, Marcos Tatagiba, Andrei Koerbel, Richard Meyermann, M Mittelbronn, Dietmar Rudolf Thal
Publikováno v:
Pediatric neurosurgery. 42(4)
We here describe the case of a boy with an atypical teratoid-rhabdoid tumor (ATRT) of the 4th ventricle at 1 year of age and a local tumor recurrence at 19 months of age. Due to brainstem infiltration, only incomplete tumor resection was possible eac