Roesner D[au] - Search Results

Year	Number of Results
1969	1
1980	1
1981	3
1984	2
1985	2
1986	1
1988	1
1990	1
1991	1
1993	1
1997	3
1998	1
1999	2
2000	1
2001	3
2002	2
2003	5
2004	3
2005	2
2007	3
2008	3
2009	1
2010	1
2011	1
2024	0

1

Pediatric radiological diagnostic procedures in cases of suspected child abuse.

Erfurt C, Hahn G, Roesner D, Schmidt U. Erfurt C, et al. Among authors: roesner d. Forensic Sci Med Pathol. 2011 Mar;7(1):65-74. doi: 10.1007/s12024-010-9148-y. Epub 2010 Feb 27. Forensic Sci Med Pathol. 2011. PMID: 20195804 Review.

2

[Definition of shock types].

Adams HA, Baumann G, Gänsslen A, Janssens U, Knoefel W, Koch T, Marx G, Müller-Werdan U, Pape HC, Prange W, Roesner D, Standl T, Teske W, Werner G, Zander R; I.A.G.-Schock. Adams HA, et al. Among authors: roesner d. Anasthesiol Intensivmed Notfallmed Schmerzther. 2001 Nov;36 Suppl 2:S140-3. doi: 10.1055/s-2001-18174. Anasthesiol Intensivmed Notfallmed Schmerzther. 2001. PMID: 11753724 German.

3

Rare occurrence of PHOX2b mutations in sporadic neuroblastomas.

Serra A, Häberle B, König IR, Kappler R, Suttorp M, Schackert HK, Roesner D, Fitze G. Serra A, et al. Among authors: roesner d. J Pediatr Hematol Oncol. 2008 Oct;30(10):728-32. doi: 10.1097/MPH.0b013e3181772141. J Pediatr Hematol Oncol. 2008. PMID: 19011468

4

Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease.

Fitze G, Schierz M, Kuhlisch E, Schreiber M, Ziegler A, Roesner D, Schackert HK. Fitze G, et al. Among authors: roesner d. Hum Mutat. 2003 Aug;22(2):177. doi: 10.1002/humu.9161. Hum Mutat. 2003. PMID: 12872262

5

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.

Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E, Roesner D, Schackert HK. Fitze G, et al. Among authors: roesner d. Lancet. 2002 Apr 6;359(9313):1200-5. doi: 10.1016/S0140-6736(02)08218-1. Lancet. 2002. PMID: 11955539

6

Association of germline mutations and polymorphisms of the RET proto-oncogene with idiopathic congenital central hypoventilation syndrome in 33 patients.

Fitze G, Paditz E, Schläfke M, Kuhlisch E, Roesner D, Schackert HK. Fitze G, et al. Among authors: roesner d. J Med Genet. 2003 Feb;40(2):E10. doi: 10.1136/jmg.40.2.e10. J Med Genet. 2003. PMID: 12566528 Free PMC article. No abstract available.

7

[Accidents in children and adolescents. Analysis of the accident event].

Schneiders W, Rollow A, Rammelt S, Reuter M, Holch M, Richter S, Gruner EM, Schlag B, Roesner D, Zwipp H. Schneiders W, et al. Among authors: roesner d. Unfallchirurg. 2005 Nov;108(11):920-2, 924-6. doi: 10.1007/s00113-005-0973-5. Unfallchirurg. 2005. PMID: 16059729 German.

8

Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease.

Fitze G, König IR, Paditz E, Serra A, Schläfke M, Roesner D, Ziegler A, Schackert HK. Fitze G, et al. Among authors: roesner d. Am J Med Genet A. 2008 Jun 1;146A(11):1486-9. doi: 10.1002/ajmg.a.32300. Am J Med Genet A. 2008. PMID: 18438890 No abstract available.

9

[Pediatric radiological diagnostics in suspected child abuse].

Erfurt C, Hahn G, Roesner D, Schmidt U. Erfurt C, et al. Among authors: roesner d. Radiologe. 2009 Oct;49(10):932, 934-41. doi: 10.1007/s00117-009-1840-0. Radiologe. 2009. PMID: 19838747 German.

10

[The reconstruction of rectal atresia. Diagnostics, therapy and prognosis of anorectal malformations].

Roesner D. Roesner D. Zentralbl Chir. 2001;126 Suppl 1:50-4. doi: 10.1055/s-2001-19200. Zentralbl Chir. 2001. PMID: 11819173 German.

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