Reutter HM - Search Results

1

Successful ECMO therapy in a child with COVID-19-associated ARDS and acute lymphoblastic leukemia.

Ebach F, Hainmann I, Eis-Hübinger AM, Escherisch G, Dilloo D, Reutter HM, Müller A. Ebach F, et al. Among authors: reutter hm. Pediatr Blood Cancer. 2021 Sep;68(9):e29100. doi: 10.1002/pbc.29100. Epub 2021 May 22. Pediatr Blood Cancer. 2021. PMID: 34022118 Free PMC article. No abstract available.

2

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. Fetal Diagn Ther. 2010;27(2):113-7. doi: 10.1159/000284929. Epub 2010 Feb 16. Fetal Diagn Ther. 2010. PMID: 20160426 Review.

3

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

4

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. 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.

5

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. Among authors: reutter hm. 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.

6

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. 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.

7

Prenatal diagnosis of covered cloacal exstrophy.

Mallmann MR, Reutter H, Müller A, Boemers TM, Geipel A, Berg C, Gembruch U. Mallmann MR, et al. Fetal Diagn Ther. 2014;36(4):333-6. doi: 10.1159/000360418. Epub 2014 Aug 1. Fetal Diagn Ther. 2014. PMID: 25096248

8

Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouse.

Gurung N, Grosse G, Draaken M, Hilger AC, Nauman N, Müller A, Gembruch U, Merz WM, Reutter H, Ludwig M. Gurung N, et al. Mol Med Rep. 2015 Jul;12(1):1579-83. doi: 10.3892/mmr.2015.3486. Epub 2015 Mar 13. Mol Med Rep. 2015. PMID: 25775927

9

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.

Bogs T, Kipfmüller F, Kohlschmidt N, Gembruch U, Müller A, Reutter H. Bogs T, et al. J Med Case Rep. 2016 Mar 30;10:76. doi: 10.1186/s13256-016-0855-1. J Med Case Rep. 2016. PMID: 27036947 Free PMC article.

10

Evaluation of two commercially available ELISA kits for the determination of melatonin concentrations in amniotic fluid throughout pregnancy.

Bagci S, Altuntas Ö, Katzer D, Berg C, Willruth A, Reutter H, Bartmann P, Müller A, Zur B. Bagci S, et al. Ann Clin Biochem. 2017 Jan;54(1):107-112. doi: 10.1177/0004563216645123. Epub 2016 Sep 28. Ann Clin Biochem. 2017. PMID: 27166310

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