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Items: 1 to 50 of 141

1.

Treatment of pregnancy-associated venous thromboembolism - position paper from the Working Group in Women's Health of the Society of Thrombosis and Haemostasis (GTH).

Linnemann B, Scholz U, Rott H, Halimeh S, Zotz R, Gerhardt A, Toth B, Bauersachs R; Working Group in Women's Health of the Society of Thrombosis and Hemostasis.

Vasa. 2016;45(2):103-18. doi: 10.1024/0301-1526/a000504. Review.

PMID:
27058796
2.

Diagnosis of pregnancy-associated venous thromboembolism - position paper of the Working Group in Women's Health of the Society of Thrombosis and Haemostasis (GTH).

Linnemann B, Bauersachs R, Rott H, Halimeh S, Zotz R, Gerhardt A, Boddenberg-Pätzold B, Toth B, Scholz U; Working Group in Women's Health of the Society of Thrombosis and Haemostasis.

Vasa. 2016;45(2):87-101. doi: 10.1024/0301-1526/a000503. Review.

PMID:
27058795
3.

PBAC score: an easy-to-use tool to predict coagulation disorders in women with idiopathic heavy menstrual bleeding.

Halimeh S, Rott H, Kappert G.

Haemophilia. 2016 May;22(3):e217-20. doi: 10.1111/hae.12886. Epub 2016 Mar 29. No abstract available.

PMID:
27028334
4.

[Therapy 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.)].

Streif W, Knöfler R, Eberl W, Andres O, Bakchoul T, Bergmann F, Beutel K, Dittmer R, Gehrisch S, Gottstein S, Halimeh S, Haselböck J, Hassenpflug WA, Heine S, Holzhauer S, King S, Kirchmaier CM, Krause M, Kreuz W, Lösche W, Mahnel R, Maurer M, Nimtz-Talaska A, Olivieri M, Rott H, Schambeck ChM, Schedel A, Schilling FH, Schmugge M, Schneppenheim R, Scholz U, Scholz T, Schulze H, Siegemund A, Strauß G, Sykora KW, Wermes C, Wiegering V, Wieland I, Zieger B, Zotz RB; Paediatric Committee of the Society of Thrombosis and Haemostasis Research.

Hamostaseologie. 2014;34(4):269-75, quiz 276. doi: 10.5482/HAMO-2014040001. German.

PMID:
25370176
5.

Prevention and treatment of venous thromboembolism during HRT: current perspectives.

Rott H.

Int J Gen Med. 2014 Sep 1;7:433-40. doi: 10.2147/IJGM.S46310. eCollection 2014. Review.

6.

[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.

Hamostaseologie. 2014;34(3):201-12. doi: 10.5482/HAMO-13-04-0024. Epub 2014 Jun 6. German.

PMID:
24903476
7.

Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

Biswas A, Ivaskevicius V, Thomas A, Varvenne M, Brand B, Rott H, Haussels I, Ruehl H, Scholz U, Klamroth R, Oldenburg J.

Ann Hematol. 2014 Oct;93(10):1665-76. doi: 10.1007/s00277-014-2102-4. Epub 2014 Jun 3.

PMID:
24889649
8.

Age--an independent prognostic factor of clinical outcome in renal malignancies: results of a large study over two decades.

Hupe MC, Merseburger AS, Lokeshwar VB, Eggers H, Rott H, Wegener G, Abbas M, Kuczyk MA, Herrmann TR.

World J Urol. 2014 Feb;32(1):115-21. doi: 10.1007/s00345-013-1164-6. Epub 2013 Oct 2.

PMID:
24085371
9.

Contraception, venous thrombosis and biological plausability.

Rott H.

Minerva Med. 2013 Apr;104(2):161-7. Review.

PMID:
23514992
10.

A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population.

Ivaskevicius V, Biswas A, Thomas A, Lyonga S, Rott H, Halimeh S, Kappert G, Klammroth R, Scholz U, Eberl W, Harbrecht U, Gnida C, Hertfelder HJ, Marquardt N, Oldenburg J.

Ann Hematol. 2013 Jul;92(7):975-9. doi: 10.1007/s00277-013-1724-2. Epub 2013 Mar 19.

PMID:
23508224
11.

A reconciled estimate of ice-sheet mass balance.

Shepherd A, Ivins ER, A G, Barletta VR, Bentley MJ, Bettadpur S, Briggs KH, Bromwich DH, Forsberg R, Galin N, Horwath M, Jacobs S, Joughin I, King MA, Lenaerts JT, Li J, Ligtenberg SR, Luckman A, Luthcke SB, McMillan M, Meister R, Milne G, Mouginot J, Muir A, Nicolas JP, Paden J, Payne AJ, Pritchard H, Rignot E, Rott H, Sørensen LS, Scambos TA, Scheuchl B, Schrama EJ, Smith B, Sundal AV, van Angelen JH, van de Berg WJ, van den Broeke MR, Vaughan DG, Velicogna I, Wahr J, Whitehouse PL, Wingham DJ, Yi D, Young D, Zwally HJ.

Science. 2012 Nov 30;338(6111):1183-9. doi: 10.1126/science.1228102. Erratum in: Science. 2012 Dec 21;338(6114):1539.

12.

[Treatment of haemophilia with an integrated therapeutical concept--Duisburg model].

Halimeh S, Rott H, Kappert G.

Hamostaseologie. 2012;32 Suppl 1:S25-8. German.

PMID:
22961178
13.

Thrombotic risks of oral contraceptives.

Rott H.

Curr Opin Obstet Gynecol. 2012 Aug;24(4):235-40. doi: 10.1097/GCO.0b013e328355871d. Review.

PMID:
22729096
14.

Ejaculate in differential diagnosis.

Rott HD.

Dtsch Arztebl Int. 2012 Apr;109(17):315; author reply 315. doi: 10.3238/arztebl.2012.0315a. Epub 2012 Apr 27. No abstract available.

15.

Hormonal contraception in thrombophilic adolescents: risk of thrombosis and recommendations.

Rott H.

Hamostaseologie. 2012;32(1):15-21. doi: 10.5482/ha-1177. Epub 2011 Oct 18.

PMID:
22009044
16.

Cardiovascular diseases in pregnancy. Not helpful.

Rott H.

Dtsch Arztebl Int. 2011 Sep;108(37):621; author reply 621-2. doi: 10.3238/arztebl.2011.0621a. Epub 2011 Sep 16. No abstract available.

17.

Does male sex influence the prognosis of patients with renal cancer?

Waalkes S, Rott H, Herrmann TR, Wegener G, Kramer MW, Merseburger AS, Schrader M, Hofmann R, Kuczyk MA, Schrader AJ.

Onkologie. 2011;34(1-2):24-8. doi: 10.1159/000323379. Epub 2011 Jan 24.

PMID:
21346381
18.

Long-term secondary prophylaxis in children, adolescents and young adults with von Willebrand disease. Results of a cohort study.

Halimeh S, Krümpel A, Rott H, Bogdanova N, Budde U, Manner D, Faeser B, Mesters R, Nowak-Göttl U.

Thromb Haemost. 2011 Apr;105(4):597-604. doi: 10.1160/TH10-09-0616. Epub 2011 Feb 8.

PMID:
21301780
19.

Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents.

Halimeh S, Angelis Gd, Sander A, Edelbusch C, Rott H, Thedieck S, Mesters R, Schlegel N, Nowak-Göttl U.

Klin Padiatr. 2010 May;222(3):158-63. doi: 10.1055/s-0030-1249081. Epub 2010 May 31.

PMID:
20514620
20.

Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency.

Ivaskevicius V, Biswas A, Loreth R, Schroeder V, Ohlenforst S, Rott H, Krause M, Kohler HP, Scharrer I, Oldenburg J.

Haemophilia. 2010 Jul 1;16(4):675-82. doi: 10.1111/j.1365-2516.2010.02207.x. Epub 2010 Mar 10.

PMID:
20331752
21.

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

Ivaskevicius V, Biswas A, Bevans C, Schroeder V, Kohler HP, Rott H, Halimeh S, Petrides PE, Lenk H, Krause M, Miterski B, Harbrecht U, Oldenburg J.

Haematologica. 2010 Jun;95(6):956-62. doi: 10.3324/haematol.2009.017210. Epub 2010 Feb 23.

22.

[Contraception and thrombophilia].

Rott H, Kruempel A, Kappert G, Nowak-Göttl U, Halimeh S.

Hamostaseologie. 2009 May;29(2):193-6. German.

PMID:
19404523
23.

Recombinant factor VIIa for long-term replacement therapy in patients with congenital factor VII deficiency.

Huth-Kühne A, Rott H, Zimmermann R, Halimeh S.

Thromb Haemost. 2007 Oct;98(4):912-5. No abstract available.

PMID:
17938823
24.

Use of recombinant factor VIIa, Novo Seven, in the management of acute haemorrhage.

Rott H, Trobisch H, Kretzschmar E.

Curr Opin Anaesthesiol. 2004 Apr;17(2):159-63.

PMID:
17021545
25.

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.

Teber OA, Gillessen-Kaesbach G, Fischer S, Böhringer S, Albrecht B, Albert A, Arslan-Kirchner M, Haan E, Hagedorn-Greiwe M, Hammans C, Henn W, Hinkel GK, König R, Kunstmann E, Kunze J, Neumann LM, Prott EC, Rauch A, Rott HD, Seidel H, Spranger S, Sprengel M, Zoll B, Lohmann DR, Wieczorek D.

Eur J Hum Genet. 2004 Nov;12(11):879-90.

26.

[Detection by ultrasonic computed tomography].

Rott HD.

Ultraschall Med. 2004 Apr;25(2):105. German. No abstract available.

PMID:
15146861
27.

Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis.

Mayer K, Goedbloed M, van Zijl K, Nellist M, Rott HD.

J Med Genet. 2004 May;41(5):e64. No abstract available.

28.

Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.

Shoichet SA, Hoffmann K, Menzel C, Trautmann U, Moser B, Hoeltzenbein M, Echenne B, Partington M, Van Bokhoven H, Moraine C, Fryns JP, Chelly J, Rott HD, Ropers HH, Kalscheuer VM.

Am J Hum Genet. 2003 Dec;73(6):1341-54. Epub 2003 Nov 18.

29.

Multiple malformations in a male and maternal osteopathia strata with cranial sclerosis (OSCS).

Rott HD, Krieg P, Rütschle H, Kraus C.

Genet Couns. 2003;14(3):281-8. Review.

PMID:
14577672
30.

Comments on "osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritance".

Kraus C, König R, Rott HD.

Am J Med Genet A. 2003 Jun 15;119A(3):400. No abstract available.

PMID:
12784316
31.

Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.

Huehne K, Benes V, Thiel C, Kraus C, Kress W, Hoeltzenbein M, Ploner CJ, Kotzian J, Reis A, Rott HD, Rautenstrauss BW.

Hum Mutat. 2003 Jan;21(1):100.

PMID:
12497641
32.

Cyst-like cerebral lesions in tuberous sclerosis.

Rott HD, Lemcke B, Zenker M, Huk W, Horst J, Mayer K.

Am J Med Genet. 2002 Sep 1;111(4):435-9.

PMID:
12210306
33.

"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.

Zweier C, Albrecht B, Mitulla B, Behrens R, Beese M, Gillessen-Kaesbach G, Rott HD, Rauch A.

Am J Med Genet. 2002 Mar 15;108(3):177-81.

PMID:
11891681
34.

[Forms of thrombophilia and their treatment].

Rott H.

Med Monatsschr Pharm. 2001 Jan;24(1):6-14. Review. German. No abstract available.

PMID:
11209733
35.

Gerhard koch 1913-1999

Schwanitz G, Gebhart E, Rott HD.

Am J Med Genet. 2000 Nov 27;95(3):191-2. No abstract available.

PMID:
11102921
36.
37.
38.
39.

International recommendations and guidelines for the safe use of diagnostic ultrasound in medicine.

Barnett SB, Ter Haar GR, Ziskin MC, Rott HD, Duck FA, Maeda K.

Ultrasound Med Biol. 2000 Mar;26(3):355-66. Review.

PMID:
10773365
41.

Safety of ultrasonic contrast agents. European Committee for Medical Ultrasound Safety.

Rott HD.

Eur J Ultrasound. 1999 May;9(2):195-7. Review. No abstract available.

PMID:
10413757
42.

European Committee for Medical Ultrasound Safety (ECMUS).

Rott HD.

Eur J Ultrasound. 1999 May;9(2):191-3. Review. No abstract available.

PMID:
10413756
43.

Extracutaneous analogies of Blaschko lines.

Rott HD.

Am J Med Genet. 1999 Aug 6;85(4):338-41. Review.

PMID:
10398255
44.

[EFSUB statement on clinical safety of ultrasound diagnosis].

Rott HD.

Ultraschall Med. 1998 Aug;19(4):192. German. No abstract available.

PMID:
9816625
45.
46.

A serologic study of organisms possibly associated with pertussis-like coughing.

Wirsing von König CH, Rott H, Bogaerts H, Schmitt HJ.

Pediatr Infect Dis J. 1998 Jul;17(7):645-9.

PMID:
9686733
47.

[EFSUMB tutorial: thermal and mechanical indices].

Rott HD.

Ultraschall Med. 1998 Apr;19(2):92-5. German. No abstract available. Erratum in: Ultraschall Med 1998 Jun;19(3):146.

PMID:
9654677
48.

[EFSUMB Tutorial: Terms in describing ultrasonic exposures].

Rott HD.

Ultraschall Med. 1997 Dec;18(6):280-2. German. No abstract available.

PMID:
9491497
49.

[Lung hemorrhage caused by diagnostic ultrasound. Review of the literature].

Rott HD.

Ultraschall Med. 1997 Oct;18(5):226-8. Review. German.

PMID:
9441391
50.

The sensitivity of biological tissue to ultrasound.

Barnett SB, Rott HD, ter Haar GR, Ziskin MC, Maeda K.

Ultrasound Med Biol. 1997;23(6):805-12. Review.

PMID:
9300983

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