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Items: 1 to 20 of 25

1.

Lack of Association of CD55 Receptor Genetic Variants and Severe Malaria in Ghanaian Children.

Schuldt K, Ehmen C, Sievertsen J, Evans J, May J, Ansong D, Muntau B, Ruge G, Timmann C, Agbenyega T, Horstmann RD, Thye T.

G3 (Bethesda). 2017 Mar 10;7(3):859-864. doi: 10.1534/g3.116.036475.

2.

The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area).

Grosse R, Lukacs Z, Cobos PN, Oyen F, Ehmen C, Muntau B, Timmann C, Noack B.

Pediatr Blood Cancer. 2016 Jan;63(1):168-70. doi: 10.1002/pbc.25706. Epub 2015 Aug 14.

PMID:
26275168
3.

CCN1 mutation is associated with atrial septal defect.

Perrot A, Schmitt KR, Roth EM, Stiller B, Posch MG, Browne EN, Timmann C, Horstmann RD, Berger F, Özcelik C.

Pediatr Cardiol. 2015 Feb;36(2):295-9. doi: 10.1007/s00246-014-1001-8. Epub 2014 Aug 19.

PMID:
25135600
4.

The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.

Sirdah MM, Sievertsen J, Al-Yazji MS, Tarazi IS, Al-Haddad RM, Horstmann RD, Timmann C.

Blood Cells Mol Dis. 2013 Apr;50(4):247-51. doi: 10.1016/j.bcmd.2012.12.004. Epub 2013 Jan 12.

PMID:
23321370
5.

Genome-wide association study indicates two novel resistance loci for severe malaria.

Timmann C, Thye T, Vens M, Evans J, May J, Ehmen C, Sievertsen J, Muntau B, Ruge G, Loag W, Ansong D, Antwi S, Asafo-Adjei E, Nguah SB, Kwakye KO, Akoto AO, Sylverken J, Brendel M, Schuldt K, Loley C, Franke A, Meyer CG, Agbenyega T, Ziegler A, Horstmann RD.

Nature. 2012 Sep 20;489(7416):443-6. doi: 10.1038/nature11334. Epub 2012 Aug 15.

PMID:
22895189
6.

A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria.

Schuldt K, Kretz CC, Timmann C, Sievertsen J, Ehmen C, Esser C, Loag W, Ansong D, Dering C, Evans J, Ziegler A, May J, Krammer PH, Agbenyega T, Horstmann RD.

PLoS Genet. 2011 May;7(5):e1002066. doi: 10.1371/journal.pgen.1002066. Epub 2011 May 19.

7.

The new Powerplex® ESX17 and ESI17 kits in paternity and maternity analyses involving people from Africa--including allele frequencies for three African populations.

Poetsch M, Ergin Z, Bayer K, El-Mostaqim D, Rakotomavo N, Browne EN, Timmann C, Horstmann RD, Schwark T, von Wurmb-Schwark N.

Int J Legal Med. 2011 Jan;125(1):149-54. doi: 10.1007/s00414-010-0502-0. Epub 2010 Sep 9.

PMID:
20827485
8.

Malaria, mummies, mutations: Tutankhamun's archaeological autopsy.

Timmann C, Meyer CG.

Trop Med Int Health. 2010 Nov;15(11):1278-80. doi: 10.1111/j.1365-3156.2010.02614.x.

9.

King Tutankhamun's family and demise.

Timmann C, Meyer CG.

JAMA. 2010 Jun 23;303(24):2473; author reply 2473-5. doi: 10.1001/jama.2010.822. No abstract available.

PMID:
20571010
10.

Genetic predisposition (NLRP3 V198M mutation) for IL-1-mediated inflammation in a patient with Schnitzler syndrome.

Loock J, Lamprecht P, Timmann C, Mrowietz U, Csernok E, Gross WL.

J Allergy Clin Immunol. 2010 Feb;125(2):500-2. doi: 10.1016/j.jaci.2009.10.066. No abstract available.

PMID:
20159265
11.

FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian children.

Schuldt K, Esser C, Evans J, May J, Timmann C, Ehmen C, Loag W, Ansong D, Ziegler A, Agbenyega T, Meyer CG, Horstmann RD.

J Med Genet. 2010 Jul;47(7):471-5. doi: 10.1136/jmg.2009.073643. Epub 2009 Dec 3.

PMID:
19965803
12.

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics.

Lainka E, Neudorf U, Lohse P, Timmann C, Stojanov S, Huss K, von Kries R, Niehues T.

Rheumatology (Oxford). 2009 Aug;48(8):987-91. doi: 10.1093/rheumatology/kep140. Epub 2009 Jun 18.

PMID:
19541728
13.

Allele frequencies of 11 X-chromosomal loci in a population sample from Ghana.

Poetsch M, El-Mostaqim D, Tschentscher F, Browne EN, Timmann C, Horstmann RD, von Wurmb-Schwark N.

Int J Legal Med. 2009 Jan;123(1):81-3. doi: 10.1007/s00414-008-0251-5. Epub 2008 Jul 8.

PMID:
18607615
14.

Human genetic resistance to Onchocerca volvulus: evidence for linkage to chromosome 2p from an autosome-wide scan.

Timmann C, van der Kamp E, Kleensang A, König IR, Thye T, Büttner DW, Hamelmann C, Marfo Y, Vens M, Brattig N, Ziegler A, Horstmann RD.

J Infect Dis. 2008 Aug 1;198(3):427-33. doi: 10.1086/589720.

PMID:
18558870
15.

Hemoglobin variants and disease manifestations in severe falciparum malaria.

May J, Evans JA, Timmann C, Ehmen C, Busch W, Thye T, Agbenyega T, Horstmann RD.

JAMA. 2007 May 23;297(20):2220-6.

PMID:
17519411
16.

Genome-wide linkage analysis of malaria infection intensity and mild disease.

Timmann C, Evans JA, König IR, Kleensang A, Rüschendorf F, Lenzen J, Sievertsen J, Becker C, Enuameh Y, Kwakye KO, Opoku E, Browne EN, Ziegler A, Nürnberg P, Horstmann RD.

PLoS Genet. 2007 Mar 23;3(3):e48.

17.

Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement.

Kallinich T, Haffner D, Niehues T, Huss K, Lainka E, Neudorf U, Schaefer C, Stojanov S, Timmann C, Keitzer R, Ozdogan H, Ozen S.

Pediatrics. 2007 Feb;119(2):e474-83. Epub 2007 Jan 22. Review.

PMID:
17242135
18.

Capillary refill time as an independent prognostic indicator in severe and complicated malaria.

Evans JA, May J, Ansong D, Antwi S, Asafo-Adjei E, Nguah SB, Osei-Kwakye K, Akoto AO, Ofori AO, Sambian D, Sylverken J, Busch W, Timmann C, Agbenyega T, Horstmann RD.

J Pediatr. 2006 Nov;149(5):676-81.

PMID:
17095342
19.

Promoter polymorphism of the anion-exchange protein 1 associated with severe malarial anemia and fatality.

von Kalckreuth V, Evans JA, Timmann C, Kuhn D, Agbenyega T, Horstmann RD, May J.

J Infect Dis. 2006 Oct 1;194(7):949-57. Epub 2006 Aug 30.

PMID:
16960783
20.

Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease?

Siewert R, Ferber J, Horstmann RD, Specker C, Heering PJ, Timmann C.

Am J Kidney Dis. 2006 Sep;48(3):e41-5.

PMID:
16931207

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