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Page 1
Standardization of Light Transmission Aggregometry for Diagnosis of Platelet Disorders: An Inter-Laboratory External Quality Assessment.
Althaus K, Zieger B, Bakchoul T, Jurk K; THROMKID-Plus Studiengruppe der Gesellschaft für Thrombose- und Hämostaseforschung (GTH) und der Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH). Althaus K, et al. Among authors: zieger b. Thromb Haemost. 2019 Jul;119(7):1154-1161. doi: 10.1055/s-0039-1688791. Epub 2019 Jun 2. Thromb Haemost. 2019. PMID: 31154663
The novel human platelet septin SEPT8 is an interaction partner of SEPT4.
Bläser S, Horn J, Würmell P, Bauer H, Strümpell S, Nurden P, Pagenstecher A, Busse A, Wunderle D, Hainmann I, Zieger B. Bläser S, et al. Among authors: zieger b. Thromb Haemost. 2004 May;91(5):959-66. doi: 10.1160/TH03-09-0578. Thromb Haemost. 2004. PMID: 15116257
Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.
Bartsch I, Sandrock K, Lanza F, Nurden P, Hainmann I, Pavlova A, Greinacher A, Tacke U, Barth M, Busse A, Oldenburg J, Bommer M, Strahm B, Superti-Furga A, Zieger B. Bartsch I, et al. Among authors: zieger b. Thromb Haemost. 2011 Sep;106(3):475-83. doi: 10.1160/TH11-05-0305. Epub 2011 Jul 28. Thromb Haemost. 2011. PMID: 21800012
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)].
Knöfler R, Eberl W, Schulze H, Bakchoul T, Bergmann F, Gehrisch S, Geisen C, Gottstein S, Halimeh S, Harbrecht U, Kappert G, Kirchmaier C, Kehrel B, Lösche W, Krause M, Mahnel R, Meyer O, Pilgrimm AK, Pillitteri D, Rott H, Santoso S, Siegemund A, Schambeck C, Scheer M, Schmugge M, Scholl T, Strauss G, Zieger B, Zotz R, Hermann M, Streif W. Knöfler R, et al. Among authors: zieger b. Hamostaseologie. 2014;34(3):201-12. doi: 10.5482/HAMO-13-04-0024. Epub 2014 Jun 6. Hamostaseologie. 2014. PMID: 24903476 German.
Identification of platelet function defects by multi-parameter assessment of thrombus formation.
de Witt SM, Swieringa F, Cavill R, Lamers MM, van Kruchten R, Mastenbroek T, Baaten C, Coort S, Pugh N, Schulz A, Scharrer I, Jurk K, Zieger B, Clemetson KJ, Farndale RW, Heemskerk JW, Cosemans JM. de Witt SM, et al. Among authors: zieger b. Nat Commun. 2014 Jul 16;5:4257. doi: 10.1038/ncomms5257. Nat Commun. 2014. PMID: 25027852 Free PMC article.
Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations.
Sandrock-Lang K, Oldenburg J, Wiegering V, Halimeh S, Santoso S, Kurnik K, Fischer L, Tsakiris DA, Sigl-Kraetzig M, Brand B, Bührlen M, Kraetzer K, Deeg N, Hund M, Busse E, Kahle A, Zieger B. Sandrock-Lang K, et al. Among authors: zieger b. Thromb Haemost. 2015 Apr;113(4):782-91. doi: 10.1160/TH14-05-0479. Epub 2014 Nov 6. Thromb Haemost. 2015. PMID: 25373348
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC.
Gresele P, Orsini S, Noris P, Falcinelli E, Alessi MC, Bury L, Borhany M, Santoro C, Glembotsky AC, Cid AR, Tosetto A, De Candia E, Fontana P, Guglielmini G, Pecci A; BAT-VAL study investigators. Gresele P, et al. J Thromb Haemost. 2020 Mar;18(3):732-739. doi: 10.1111/jth.14683. Epub 2019 Dec 16. J Thromb Haemost. 2020. PMID: 31750621 Free article.
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
Barco S, Sollfrank S, Trinchero A, Adenaeuer A, Abolghasemi H, Conti L, Häuser F, Kremer Hovinga JA, Lackner KJ, Loewecke F, Miloni E, Vazifeh Shiran N, Tomao L, Wuillemin WA, Zieger B, Lämmle B, Rossmann H. Barco S, et al. Among authors: zieger b. J Thromb Haemost. 2020 Jul;18(7):1598-1617. doi: 10.1111/jth.14805. Epub 2020 May 15. J Thromb Haemost. 2020. PMID: 32202057 Free article.
220 results