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Items: 15

1.

Transmission of chromosomally integrated human herpes virus-6A via haploidentical stem cell transplantation poses a risk for virus reactivation and associated complications.

Oevermann L, Zimmermann C, Voigt S, Künkele A, Lobitz S, Eggert A, Schulte JH, Kaufer BB, Deubzer HE.

Bone Marrow Transplant. 2019 Apr 15. doi: 10.1038/s41409-019-0530-4. [Epub ahead of print] No abstract available.

PMID:
30988380
2.

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.

Gallon R, Mühlegger B, Wenzel SS, Sheth H, Hayes C, Aretz S, Dahan K, Foulkes W, Kratz CP, Ripperger T, Azizi AA, Baris Feldman H, Chong AL, Demirsoy U, Florkin B, Imschweiler T, Januszkiewicz-Lewandowska D, Lobitz S, Nathrath M, Pander HJ, Perez-Alonso V, Perne C, Ragab I, Rosenbaum T, Rueda D, Seidel MG, Suerink M, Taeubner J, Zimmermann SY, Zschocke J, Borthwick GM, Burn J, Jackson MS, Santibanez-Koref M, Wimmer K.

Hum Mutat. 2019 May;40(5):649-655. doi: 10.1002/humu.23721. Epub 2019 Mar 6.

PMID:
30740824
3.

Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.

Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Backman Johansson C, Badens C, Bento C, Bouva MJ, Canatan D, Charlton M, Coppinger C, Daniel Y, de Montalembert M, Ducoroy P, Dulin E, Fingerhut R, Frömmel C, García-Morin M, Gulbis B, Holtkamp U, Inusa B, James J, Kleanthous M, Klein J, Kunz JB, Langabeer L, Lapouméroulie C, Marcao A, Marín Soria JL, McMahon C, Ohene-Frempong K, Périni JM, Piel FB, Russo G, Sainati L, Schmugge M, Streetly A, Tshilolo L, Turner C, Venturelli D, Vilarinho L, Yahyaoui R, Elion J, Colombatti R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Haematological Diseases.

Br J Haematol. 2018 Nov;183(4):648-660. doi: 10.1111/bjh.15600. Epub 2018 Oct 18.

PMID:
30334577
4.

Newborn screening by tandem mass spectrometry confirms the high prevalence of sickle cell disease among German newborns.

Lobitz S, Klein J, Brose A, Blankenstein O, Frömmel C.

Ann Hematol. 2019 Jan;98(1):47-53. doi: 10.1007/s00277-018-3477-4. Epub 2018 Aug 21.

PMID:
30132072
5.

The epidemiology of sickle cell disease in Germany following recent large-scale immigration.

Kunz JB, Cario H, Grosse R, Jarisch A, Lobitz S, Kulozik AE.

Pediatr Blood Cancer. 2017 Jul;64(7). doi: 10.1002/pbc.26550. Epub 2017 Apr 6.

PMID:
28383793
6.

Cognitive and fine motor deficits in a pediatric sickle cell disease cohort of mixed ethnic origin.

Burkhardt L, Lobitz S, Koustenis E, Rueckriegel SM, Hernáiz Driever P.

Ann Hematol. 2017 Feb;96(2):199-213. doi: 10.1007/s00277-016-2861-1. Epub 2016 Oct 29.

PMID:
27796476
7.

Newborn screening for sickle cell disease: technical and legal aspects of a German pilot study with 38,220 participants.

Frömmel C, Brose A, Klein J, Blankenstein O, Lobitz S.

Biomed Res Int. 2014;2014:695828. doi: 10.1155/2014/695828. Epub 2014 Jul 23.

8.

Incidence of sickle cell disease in an unselected cohort of neonates born in Berlin, Germany.

Lobitz S, Frömmel C, Brose A, Klein J, Blankenstein O.

Eur J Hum Genet. 2014 Aug;22(8):1051-3. doi: 10.1038/ejhg.2013.286. Epub 2014 Jan 8.

9.

Salmonella SL7207 application is the most effective DNA vaccine delivery method for successful tumor eradication in a murine model for neuroblastoma.

Berger E, Soldati R, Huebener N, Hohn O, Stermann A, Durmus T, Lobitz S, Zenclussen AC, Christiansen H, Lode HN, Fest S.

Cancer Lett. 2013 May 1;331(2):167-73. doi: 10.1016/j.canlet.2012.12.026. Epub 2013 Jan 18.

PMID:
23337288
10.

Molecular mechanisms of mistletoe plant extract-induced apoptosis in acute lymphoblastic leukemia in vivo and in vitro.

Seifert G, Jesse P, Laengler A, Reindl T, Lüth M, Lobitz S, Henze G, Prokop A, Lode HN.

Cancer Lett. 2008 Jun 18;264(2):218-28. doi: 10.1016/j.canlet.2008.01.036. Epub 2008 Mar 7.

PMID:
18314258
11.

A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network.

Antonio Casado J, Callén E, Jacome A, Río P, Castella M, Lobitz S, Ferro T, Muñoz A, Sevilla J, Cantalejo A, Cela E, Cervera J, Sánchez-Calero J, Badell I, Estella J, Dasí A, Olivé T, José Ortega J, Rodriguez-Villa A, Tapia M, Molinés A, Madero L, Segovia JC, Neveling K, Kalb R, Schindler D, Hanenberg H, Surrallés J, Bueren JA.

J Med Genet. 2007 Apr;44(4):241-9. Epub 2006 Nov 14.

12.

Guido Fanconi (1892-1979): a jack of all trades.

Lobitz S, Velleuer E.

Nat Rev Cancer. 2006 Nov;6(11):893-8. Epub 2006 Oct 12. Review.

PMID:
17036037
13.

Fatal course after administration of rituximab in a boy with relapsed all: a case report and review of literature.

Seifert G, Reindl T, Lobitz S, Seeger K, Henze G.

Haematologica. 2006 Jun;91(6 Suppl):ECR23. Review.

14.

An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.

Demuth I, Frappart PO, Hildebrand G, Melchers A, Lobitz S, Stöckl L, Varon R, Herceg Z, Sperling K, Wang ZQ, Digweed M.

Hum Mol Genet. 2004 Oct 15;13(20):2385-97. Epub 2004 Aug 27.

PMID:
15333589
15.

Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.

Hanenberg H, Batish SD, Pollok KE, Vieten L, Verlander PC, Leurs C, Cooper RJ, Göttsche K, Haneline L, Clapp DW, Lobitz S, Williams DA, Auerbach AD.

Exp Hematol. 2002 May;30(5):410-20.

PMID:
12031647

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