Reutter H - Search Results

1

Isolated cytokine-enriched pericardial effusion: A likely key feature for Aymé-Gripp syndrome.

König AL, Sabir H, Strizek B, Gembruch U, Herberg U, Bertrand M, Grasshoff U, Wiegand G, Wiechers C, Bernis E, Reutter H, Müller A. König AL, et al. Among authors: reutter h. Am J Med Genet A. 2022 Feb;188(2):624-627. doi: 10.1002/ajmg.a.62540. Epub 2021 Oct 12. Am J Med Genet A. 2022. PMID: 34643041

2

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H. Engels H, et al. Among authors: reutter h. Am J Med Genet. 2002 Aug 1;111(2):205-9. doi: 10.1002/ajmg.10560. Am J Med Genet. 2002. PMID: 12210352 Review.

3

Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature.

Bağci S, Müller A, Franz A, Heydweiller A, Berg C, Nöthen MM, Bartmann P, Reutter H. Bağci S, et al. Among authors: reutter h. Fetal Diagn Ther. 2010;27(2):113-7. doi: 10.1159/000284929. Epub 2010 Feb 16. Fetal Diagn Ther. 2010. PMID: 20160426 Review.

4

Primary pulmonary hypertension, congenital heart defect, central nervous system malformations, hypo- and aplastic toes: another case of Yunis-Varón syndrome or report of a new entity.

Reutter H, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Eggermann T, Spengler S, Bartmann P, Rudnik-Schöneborn S. Reutter H, et al. Eur J Med Genet. 2012 Jan;55(1):27-31. doi: 10.1016/j.ejmg.2011.09.002. Epub 2011 Oct 11. Eur J Med Genet. 2012. PMID: 22044576

5

Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.

Schulz AC, Bartels E, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Heydweiller A, Bachour H, Schumacher J, Bartmann P, Nöthen MM, Reutter H. Schulz AC, et al. Among authors: reutter h. Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):182-6. doi: 10.1002/bdra.22879. Epub 2012 Jan 30. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22287212 Review.

6

A classic twin study of isolated gastroschisis.

Schulz AC, Stressig R, Ritgen J, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Reutter HM. Schulz AC, et al. Fetal Pediatr Pathol. 2012 Oct;31(5):324-30. doi: 10.3109/15513815.2012.659393. Epub 2012 Mar 20. Fetal Pediatr Pathol. 2012. PMID: 22433012 Review.

7

Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.

Berner AL, Bağci S, Wohlleber E, Engels E, Müller A, Bartmann P, Weber RG, Reutter H. Berner AL, et al. Among authors: reutter h. Cytogenet Genome Res. 2012;136(4):308-13. doi: 10.1159/000337019. Epub 2012 Mar 17. Cytogenet Genome Res. 2012. PMID: 22433391 Free article. Review.

8

VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis.

Bartels E, Schulz AC, Mora NW, Pineda-Alvarez DE, Wijers CHW, Marcelis CM, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Hoffmann P, Hilger AC, Dworschak GC, Baudisch F, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Nöthen MM, van Rooij IALM, Solomon BD, Reutter HM. Bartels E, et al. Among authors: reutter hm. Clin Dysmorphol. 2012 Oct;21(4):191-195. doi: 10.1097/MCD.0b013e328358243c. Clin Dysmorphol. 2012. PMID: 22895008 Free PMC article. Review.

9

Early prenatal diagnosis of the OEIS complex with different appearance in early compared with late pregnancy before spontaneous rupture of the cloacal membrane.

Mallmann MR, Reutter H, Geipel A, Berg C, Gembruch U. Mallmann MR, et al. Among authors: reutter h. Prenat Diagn. 2014 Aug;34(8):803-5. doi: 10.1002/pd.4355. Epub 2014 May 26. Prenat Diagn. 2014. PMID: 24623061 No abstract available.

10

Scimitar syndrome in a case with VACTERL association.

Fritz CJ, Reutter HM, Herberg U. Fritz CJ, et al. Cardiol Young. 2015 Mar;25(3):606-9. doi: 10.1017/S1047951114000924. Epub 2014 Jun 6. Cardiol Young. 2015. PMID: 24905790

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