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Page 1
Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one case.
Pfeifer M, Rehder H, Gerykova Bujalkova M, Bartsch C, Fritz B, Knopp C, Beckers B, Dohle F, Meyer-Wittkopf M, Axt-Fliedner R, Beribisky AV, Hofer M, Laccone F, Schoner K. Pfeifer M, et al. Among authors: meyer wittkopf m. Orphanet J Rare Dis. 2024 Mar 12;19(1):114. doi: 10.1186/s13023-024-03106-z. Orphanet J Rare Dis. 2024. PMID: 38475835 Free PMC article.
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.
Bedei I, Gehrke T, Gloning KP, Meyer-Wittkopf M, Willner D, Krapp M, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns KM, Geipel A, Baumüller JE, Wilhelm L, Gottschalk I, Schröer A, Graf A, Wolter A, Schenk J, Weber A, Van den Veyver IB, Axt-Fliedner R. Bedei I, et al. Among authors: meyer wittkopf m. Prenat Diagn. 2023 Feb;43(2):192-206. doi: 10.1002/pd.6320. Epub 2023 Feb 9. Prenat Diagn. 2023. PMID: 36726284
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.
Bedei I, Gloning KP, Joyeux L, Meyer-Wittkopf M, Willner D, Krapp M, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns KM, Geipel A, Tekesin I, Elsässer M, Wilhelm L, Gottschalk I, Baumüller JE, Birdir C, Schröer A, Zöllner F, Wolter A, Schenk J, Gehrke T, Spaeth A, Axt-Fliedner R. Bedei I, et al. Among authors: meyer wittkopf m. Prenat Diagn. 2023 Feb;43(2):183-191. doi: 10.1002/pd.6302. Epub 2023 Jan 31. Prenat Diagn. 2023. PMID: 36600414
Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report.
Willy D, Schmitz R, Möllers M, Heitplatz B, Kuntze A, Stratis Y, Bahlke K, Röpke A, Meyer-Wittkopf M, Oelmeier K. Willy D, et al. Among authors: meyer wittkopf m. Front Med (Lausanne). 2024 Feb 13;11:1340905. doi: 10.3389/fmed.2024.1340905. eCollection 2024. Front Med (Lausanne). 2024. PMID: 38414622 Free PMC article.
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?
Bedei IA, Graf A, Gloning KP, Meyer-Wittkopf M, Willner D, Krapp M, Hentze S, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns K, Geipel A, Tekesin I, Elsässer M, Wilhelm L, Gottschalk I, Baumüller JE, Birdir C, Zöllner F, Wolter A, Schenk J, Gehrke T, Keil C, Espinosa J, Axt-Fliedner R. Bedei IA, et al. Among authors: meyer wittkopf m. J Clin Med. 2022 Aug 5;11(15):4588. doi: 10.3390/jcm11154588. J Clin Med. 2022. PMID: 35956203 Free PMC article.
Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.
Schoner K, Witsch-Baumgartner M, Behunova J, Petrovic R, Bald R, Kircher SG, Ramaswamy A, Kluge B, Meyer-Wittkopf M, Schmitz R, Fritz B, Zschocke J, Laccone F, Rehder H. Schoner K, et al. Among authors: meyer wittkopf m. Birth Defects Res. 2020 Jan 15;112(2):175-185. doi: 10.1002/bdr2.1620. Epub 2019 Dec 16. Birth Defects Res. 2020. PMID: 31840946 Free PMC article.
Absent pulmonary valve syndrome - diagnosis, associations, and outcome in 71 prenatally diagnosed cases.
Axt-Fliedner R, Kurkevych A, Slodki M, Respondek-Liberska M, Zych-Krekora K, Stressig R, Ritgen J, Rizzo G, Krapp M, de Catte L, Mielke G, Bosselmann S, Meyer-Wittkopf M, Kawecki A, Wolter A, Mamalis M, Enzensberger C; International Prenatal Cardiology Collaboration Group. Axt-Fliedner R, et al. Among authors: meyer wittkopf m. Prenat Diagn. 2017 Aug;37(8):812-819. doi: 10.1002/pd.5094. Epub 2017 Jul 12. Prenat Diagn. 2017. PMID: 28621803
Primary Human Cytomegalovirus (HCMV) Infection in Pregnancy.
Buxmann H, Hamprecht K, Meyer-Wittkopf M, Friese K. Buxmann H, et al. Among authors: meyer wittkopf m. Dtsch Arztebl Int. 2017 Jan 27;114(4):45-52. doi: 10.3238/arztebl.2017.0045. Dtsch Arztebl Int. 2017. PMID: 28211317 Free PMC article. Review.
33 results