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[Quality of Life and Experienced Distress of Patients Suspected of having a Rare (Chronic) Health Condition - Initial Findings from the ZSE-DUO Study].
Witt S, Kristensen K, Blömeke J, Hebestreit H, Wocker M, Pfister L, Bullinger M, Tüscher O, Deckert J, Graessner H, Lapstich AM, Zwaan M, Mundlos C, Quitmann JH. Witt S, et al. Among authors: mundlos c. Psychother Psychosom Med Psychol. 2023 Jan;73(1):9-15. doi: 10.1055/a-1814-3998. Epub 2022 Jul 6. Psychother Psychosom Med Psychol. 2023. PMID: 35793670 German.
[se-atlas.de-Medical care atlas for people with rare diseases].
Neff M, Schaaf J, Tegtbauer N, Schäfer J, Till M, Wagner TOF, Graeßner H, Mundlos C, Storf H. Neff M, et al. Among authors: mundlos c. Internist (Berl). 2021 Oct;62(10):1115-1122. doi: 10.1007/s00108-021-01085-y. Epub 2021 Jul 20. Internist (Berl). 2021. PMID: 34283250 Free PMC article. Review. German.
Dual guidance structure for evaluation of patients with unclear diagnosis in centers for rare diseases (ZSE-DUO): study protocol for a controlled multi-center cohort study.
Hebestreit H, Zeidler C, Schippers C, de Zwaan M, Deckert J, Heuschmann P, Krauth C, Bullinger M, Berger A, Berneburg M, Brandstetter L, Deibele A, Dieris-Hirche J, Graessner H, Gündel H, Herpertz S, Heuft G, Lapstich AM, Lücke T, Maisch T, Mundlos C, Petermann-Meyer A, Müller S, Ott S, Pfister L, Quitmann J, Romanos M, Rutsch F, Schaubert K, Schubert K, Schulz JB, Schweiger S, Tüscher O, Ungethüm K, Wagner TOF, Haas K; ZSE-DUO working group. Hebestreit H, et al. Among authors: mundlos c. Orphanet J Rare Dis. 2022 Feb 14;17(1):47. doi: 10.1186/s13023-022-02176-1. Orphanet J Rare Dis. 2022. PMID: 35164804 Free PMC article.
Effect of the addition of a mental health specialist for evaluation of undiagnosed patients in centres for rare diseases (ZSE-DUO): a prospective, controlled trial with a two-phase cohort design.
Hebestreit H, Lapstich AM, Brandstetter L, Krauth C, Deckert J, Haas K, Pfister L, Witt S, Schippers C, Dieris-Hirche J, Maisch T, Tüscher O, Bârlescu L, Berger A, Berneburg M, Britz V, Deibele A, Graeßner H, Gündel H, Heuft G, Lücke T, Mundlos C, Quitmann J, Rutsch F, Schubert K, Schulz JB, Schweiger S, Zeidler C, Zeltner L, de Zwaan M; ZSE-DUO Working Group. Hebestreit H, et al. Among authors: mundlos c. EClinicalMedicine. 2023 Oct 6;65:102260. doi: 10.1016/j.eclinm.2023.102260. eCollection 2023 Nov. EClinicalMedicine. 2023. PMID: 37855024 Free PMC article.
Introduction of ICD-11 in Germany: Seizing opportunities together.
Broich K, Callhoff J, Kaskel P, Kowalski C, Malzahn J, Mundlos C, Schöbel C. Broich K, et al. Among authors: mundlos c. Gesundheitswesen. 2024 Sep;86(S 04):S290-S298. doi: 10.1055/a-2342-4453. Epub 2024 Jun 11. Gesundheitswesen. 2024. PMID: 38863176 Free article. English, German.
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR. Mundlos S, et al. Among authors: mundlos c. Cell. 1997 May 30;89(5):773-9. doi: 10.1016/s0092-8674(00)80260-3. Cell. 1997. PMID: 9182765 Free article.
Firsttrimester Diagnosis and Therapy @ 11 - 13 +6 Weeks of Gestation - Part 1 : Guideline of the DEGUM, ÖGUM, SGUMGG, DGGG, ÖGG, Gynecologie Suisse, DGPM, DGPGM, BVF, ACHSE (AWMF S2e LL 085-002 1.1.2024) (https://register.awmf.org/de/leitlinien/detail/085-002).
von Kaisenberg C, Kozlowski P, Kagan KO, Hoopmann M, Heling KS, Chaoui R, Klaritsch P, Pertl B, Burkhardt T, Tercanli S, Frenzel J, Mundlos C. von Kaisenberg C, et al. Among authors: mundlos c. Geburtshilfe Frauenheilkd. 2024 Oct 1;84(10):928-941. doi: 10.1055/a-2280-8772. eCollection 2024 Oct. Geburtshilfe Frauenheilkd. 2024. PMID: 39359546 Free PMC article.
14 results