Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Dietmar Roesner"'
Autor:
Beate Häberle, Guido Fitze, Inke R. König, Alexandre Serra, Hans K. Schackert, Dietmar Roesner, Roland Kappler, Meinolf Suttorp
Publikováno v:
Journal of Pediatric Hematology/Oncology. 30:728-732
Neuroblastomas (NBs) are frequent solid tumors in childhood for which no specific genetic marker linked to their development has been identified to date. PHOX2b, which regulates the autonomic neuron development, has been associated with the developme
Autor:
E. Paditz, Guido Fitze, Andreas Ziegler, Dietmar Roesner, Marianne E. Schläfke, Inke R. König, Hans K. Schackert, Alexandre Serra
Publikováno v:
American Journal of Medical Genetics Part A. :1486-1489
Publikováno v:
European Journal of Pediatric Surgery. 18:32-37
INTRODUCTION: We aimed to critically evaluate elective preterm delivery and immediate abdominal wall closure and other techniques for the management of gastroschisis, hypothesizing that the advantages of an elective preterm delivery outweigh possible
Publikováno v:
Journal of Cranio-Maxillofacial Surgery. 35:218-221
Summary Aim Biodegradable osteosynthesis materials are often used for fixation of bone fragments when repairing craniosynostoses. When compared with titanium plates they have the disadvantage of difficult handling and time-consuming thread cutting. A
Publikováno v:
Klinische Pädiatrie. 216:270-276
Introduction Heredity of MEN2 syndromes is caused by a heterozygous germline mutation in the RET proto-oncogene. This study describes families with rare noncysteine codon 790/791 mutations and discusses the genotype-phenotype correlation plus the the
Die Beiträge dieses Tagungsbands befassen sich aus der Sicht der Linguistischen Datenverarbeitung und ihrer benachbarten Disziplinen mit den Interaktionsmöglichkeiten zwischen Mensch und Computer. Zu diesen Disziplinen gehören z. B. Informatik, in
Autor:
Wolfgang Walther, Dietmar Roesner, Andreas Ziegler, Hella Appelt, Guido Fitze, Inke R. König, Hans K. Schackert, Matthias Schreiber, Ulrike Stein, Manfred Gossen, Heike Görgens
Publikováno v:
Human Molecular Genetics. 12:3207-3214
The activation of the RET signaling pathway during embryogenesis is a crucial prerequisite for a directional migration of enteric nervous system progenitor cells. Loss-of-function germline mutations of the RET proto-oncogene are reported in familial
Autor:
Jakob Cramer, Hans Konrad Schackert, Dietmar Roesner, Mandy Schierz, Matthias Schreiber, Eberhard Kuhlisch, Andreas Ziegler, Guido Fitze
Publikováno v:
The Lancet. 359:1200-1205
Summary Background Several genes, including the major susceptibility gene RET , have roles in development of Hirschsprung's disease. Results of genetic-linkage analysis of patients with familial disease with both long-segment and short-segment phenot
Publikováno v:
Journal of Pediatric Surgery. 35:1482-1488
Background/Purpose: Congenital diaphragmatic hernia (CDH) is associated with pulmonary hypoplasia that limits survival. The authors' knowledge on lung mechanics and lung volumes in these patients with hypoplastic lungs is still limited. Therefore, th
Publikováno v:
Medizinische Klinik. 94:93-96
PATIENTS AND METHOD At the Clinic for Paediatric Surgery of the University of Dresden, in a time period ranging from 5/1994 to 12/1996, all patients aged between 1 and 16 years with severe inflammatory surgical diseases or extended scalded skin, were