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Items: 1 to 50 of 133

1.

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C, Tarnok Z, Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ, McMahon WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee PC, Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A, Hoekstra PJ, Kuperman S, Zinner SH, Luðvigsson P, Sæmundsen E, Thorarensen Ó, Atzmon G, Barzilai N, Wagner M, Moessner R, Ophoff R, Pato CN, Pato MT, Knowles JA, Roffman JL, Smoller JW, Buckner RL, Willsey AJ, Tischfield JA, Heiman GA, Stefansson H, Stefansson K, Posthuma D, Cox NJ, Pauls DL, Freimer NB, Neale BM, Davis LK, Paschou P, Coppola G, Mathews CA, Scharf JM; Tourette Association of America International Consortium for Genetics, the Gilles de la Tourette GWAS Replication Initiative, the Tourette International Collaborative Genetics Study, and the Psychiatric Genomics Consortium Tourette Syndrome Working Group.

Am J Psychiatry. 2019 Mar 1;176(3):217-227. doi: 10.1176/appi.ajp.2018.18070857.

PMID:
30818990
2.

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.

Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL, Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H, Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C, Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G; Tourette Syndrome Association International Consortium for Genetics (TSAICG); Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI).

Neuron. 2017 Jun 21;94(6):1101-1111.e7. doi: 10.1016/j.neuron.2017.06.010.

3.

NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?

Scholz C, Steinemann D, Mälzer M, Roy M, Arslan-Kirchner M, Illig T, Schmidtke J, Stuhrmann M.

Eur J Med Genet. 2016 Oct;59(10):493-8. doi: 10.1016/j.ejmg.2016.08.006. Epub 2016 Sep 2.

PMID:
27596683
4.

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort.

Bertelsen B, Stefánsson H, Riff Jensen L, Melchior L, Mol Debes N, Groth C, Skov L, Werge T, Karagiannidis I, Tarnok Z, Barta C, Nagy P, Farkas L, Brøndum-Nielsen K, Rizzo R, Gulisano M, Rujescu D, Kiemeney LA, Tosato S, Nawaz MS, Ingason A, Unnsteinsdottir U, Steinberg S, Ludvigsson P, Stefansson K, Kuss AW, Paschou P, Cath D, Hoekstra PJ, Müller-Vahl K, Stuhrmann M, Silahtaroglu A, Pfundt R, Tümer Z.

Biol Psychiatry. 2016 Mar 1;79(5):383-391. doi: 10.1016/j.biopsych.2015.08.027. Epub 2015 Sep 3.

PMID:
26444075
5.

Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy.

Derda AA, Thum S, Lorenzen JM, Bavendiek U, Heineke J, Keyser B, Stuhrmann M, Givens RC, Kennel PJ, Schulze PC, Widder JD, Bauersachs J, Thum T.

Int J Cardiol. 2015 Oct 1;196:115-22. doi: 10.1016/j.ijcard.2015.05.185. Epub 2015 Jun 5.

6.

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.

Schubert S, Haas C, Bartsch C, Mirshekarnejad M, Kohrs S, Roettinger I, Grosshennig A, Stuhrmann M, Scholz C, Schmidtke J.

Mol Cell Probes. 2015 Feb;29(1):31-4. doi: 10.1016/j.mcp.2014.10.006. Epub 2014 Nov 4.

PMID:
25449952
7.

Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipients.

Alkharsah KR, Alzahrani AJ, Obeid OE, El-Harith EH, Guella A, Mohamed EA, Haykal AH, Stuhrmann M, Al-Ali AK.

Transpl Infect Dis. 2014 Oct;16(5):783-9. doi: 10.1111/tid.12277. Epub 2014 Aug 14.

PMID:
25124076
8.

Genetic association signal near NTN4 in Tourette syndrome.

Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, Nagy P, Barta C, Tarnok Z, Rizzo R, Depienne C, Worbe Y, Hartmann A, Cath DC, Budman CL, Sandor P, Barr C, Wolanczyk T, Singer H, Chou IC, Grados M, Posthuma D, Rouleau GA, Aschauer H, Freimer NB, Pauls DL, Cox NJ, Mathews CA, Scharf JM.

Ann Neurol. 2014 Aug;76(2):310-5. doi: 10.1002/ana.24215. Epub 2014 Jul 21.

9.

CFTR, SPINK1, PRSS1, and CTRC mutations are not associated with pancreatic cancer in German patients.

Schubert S, Traub F, Brakensiek K, von Kopylow K, Marohn B, Maelzer M, Gaedcke J, Kreipe H, Stuhrmann M.

Pancreas. 2014 Oct;43(7):1078-82. doi: 10.1097/MPA.0000000000000166.

PMID:
25003218
10.

1,25-Dihydroxyvitamin D decreases HTRA1 promoter activity in the rhesus monkey--a plausible explanation for the influence of vitamin D on age-related macular degeneration?

Pahl L, Schubert S, Skawran B, Sandbothe M, Schmidtke J, Stuhrmann M.

Exp Eye Res. 2013 Nov;116:234-9. doi: 10.1016/j.exer.2013.09.012. Epub 2013 Sep 27.

PMID:
24076413
11.

Association of TNF-α polymorphism rs1800629 with multisomatoform disorder in a group of German patients and healthy controls: an explorative study.

Harms KC, Kapitza KP, Pahl L, Tran AT, Volkmann L, Buers D, Karst M, Stuhrmann M, Bernateck M.

Cytokine. 2013 Feb;61(2):389-93. doi: 10.1016/j.cyto.2012.12.004. Epub 2013 Jan 5.

PMID:
23294973
12.

High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.

Kathiravel U, Keyser B, Hoffjan S, Kötting J, Müller M, Sivalingam S, Bonin M, Arslan-Kirchner M, von Kodolitsch Y, Binner P, Scheffold T, Stuhrmann M, Waldmüller S.

Mol Cell Probes. 2013 Apr;27(2):103-8. doi: 10.1016/j.mcp.2012.10.002. Epub 2012 Nov 6.

PMID:
23142374
13.

Interaction of the dopaminergic and serotonergic systems significantly influences the risk for multisomatoform disorder: a controlled pilot study.

Pahl L, Bernateck M, Jakobi J, Tran AT, Volkmann L, Buers D, Lehmann U, Karst M, Stuhrmann M.

Genet Test Mol Biomarkers. 2012 Aug;16(8):892-6. doi: 10.1089/gtmb.2011.0329. Epub 2012 Jul 11.

PMID:
22784335
14.

Improvement of interpretation in cystic fibrosis clinical laboratory reports: longitudinal analysis of external quality assessment data.

Berwouts S, Girodon E, Schwarz M, Stuhrmann M, Morris MA, Dequeker E.

Eur J Hum Genet. 2012 Dec;20(12):1209-15. doi: 10.1038/ejhg.2012.131. Epub 2012 Jun 20.

15.

Diagnosis of hereditary hemochromatosis in the era of genetic testing.

Trieß C, von Figura G, Stuhrmann M, Butzeck B, Krayenbuehl PA, Strnad P, Kulaksiz H.

Dig Dis Sci. 2012 Nov;57(11):2988-94. doi: 10.1007/s10620-012-2243-z. Epub 2012 Jun 7.

PMID:
22674401
16.

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

Yalcinkaya C, Erturk O, Tuysuz B, Yesil G, Verbeke JI, Keyser B, Stuhrmann M, Steinemann D, Sistermans EA, van der Knaap MS.

Neuropediatrics. 2012 Jun;43(3):159-61. doi: 10.1055/s-0032-1313912. Epub 2012 May 19.

PMID:
22610664
17.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1.

Pahl L, Spangenberg A, Schubert S, Schönmann U, Schmidtke J, Stuhrmann M.

Exp Eye Res. 2012 May;98:75-8. doi: 10.1016/j.exer.2012.03.007. Epub 2012 Mar 21.

PMID:
22465519
18.

Homozygous CFTR mutation M348K in a boy with respiratory symptoms and failure to thrive. Disease-causing mutation or benign alteration?

Hentschel J, Riesener G, Nelle H, Stuhrmann M, Schöner A, Sommerburg O, Fritzsching E, Mall MA, von Eggeling F, Mainz JG.

Eur J Pediatr. 2012 Jul;171(7):1039-46. doi: 10.1007/s00431-012-1672-1. Epub 2012 Jan 25.

PMID:
22274833
19.

Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?

Javaher P, Stuhrmann M, Wilke C, Frenzel E, Manukjan G, Grosshenig A, Dechend F, Schwaab E, Schmidtke J, Schubert S.

Fertil Steril. 2012 Feb;97(2):402-6. doi: 10.1016/j.fertnstert.2011.11.002. Epub 2011 Dec 2.

PMID:
22137496
20.

Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.

Sheikhzadeh S, Kade C, Keyser B, Stuhrmann M, Arslan-Kirchner M, Rybczynski M, Bernhardt AM, Habermann CR, Hillebrand M, Mir T, Robinson PN, Berger J, Detter C, Blankenberg S, Schmidtke J, von Kodolitsch Y.

Clin Genet. 2012 Sep;82(3):240-7. doi: 10.1111/j.1399-0004.2011.01771.x. Epub 2011 Oct 5.

PMID:
21883168
21.

Mutation nomenclature in practice: findings and recommendations from the cystic fibrosis external quality assessment scheme.

Berwouts S, Morris MA, Girodon E, Schwarz M, Stuhrmann M, Dequeker E.

Hum Mutat. 2011 Nov;32(11):1197-203. doi: 10.1002/humu.21569. Epub 2011 Aug 17.

PMID:
21796730
22.

Aortic dissecting aneurysms--histopathological findings.

Bode-Jänisch S, Schmidt A, Günther D, Stuhrmann M, Fieguth A.

Forensic Sci Int. 2012 Jan 10;214(1-3):13-7. doi: 10.1016/j.forsciint.2011.07.006. Epub 2011 Jul 26.

PMID:
21794994
23.

Recommendations for the classification of diseases as CFTR-related disorders.

Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E, Sermet I, Schwarz M, Tzetis M, Wilschanski M, Bareil C, Bilton D, Castellani C, Cuppens H, Cutting GR, Drevínek P, Farrell P, Elborn JS, Jarvi K, Kerem B, Kerem E, Knowles M, Macek M Jr, Munck A, Radojkovic D, Seia M, Sheppard DN, Southern KW, Stuhrmann M, Tullis E, Zielenski J, Pignatti PF, Ferec C.

J Cyst Fibros. 2011 Jun;10 Suppl 2:S86-102. doi: 10.1016/S1569-1993(11)60014-3.

24.

Are polymorphisms of molecules involved in bone healing correlated to aseptic femoral and tibial shaft non-unions?

Zeckey C, Hildebrand F, Glaubitz LM, Jürgens S, Ludwig T, Andruszkow H, Hüfner T, Krettek C, Stuhrmann M.

J Orthop Res. 2011 Nov;29(11):1724-31. doi: 10.1002/jor.21443. Epub 2011 Apr 28.

25.

Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome.

Wessels K, Bohnhorst B, Luhmer I, Morlot S, Bohring A, Jonasson J, Epplen JT, Gadzicki D, Glaser S, Göhring G, Mälzer M, Hein A, Arslan-Kirchner M, Stuhrmann M, Schmidtke J, Pabst B.

Eur J Med Genet. 2010 Sep-Oct;53(5):280-5. doi: 10.1016/j.ejmg.2010.07.002. Epub 2010 Jul 30.

PMID:
20624498
26.

Neonatal Marfan syndrome: unusually large deletion of exons 24-26 of FBN1 associated with poor prognosis.

Apitz C, Mackensen-Haen S, Girisch M, Kerst G, Wiegand G, Stuhrmann M, Niethammer K, Behrwind G, Hofbeck M.

Klin Padiatr. 2010 Jul;222(4):261-3. doi: 10.1055/s-0030-1247510. Epub 2010 May 7.

PMID:
20455198
27.

Augmentation index and the evolution of aortic disease in marfan-like syndromes.

Mortensen K, Baulmann J, Rybczynski M, Sheikhzadeh S, Aydin MA, Treede H, Dombrowski E, Kühne K, Peitsmeier P, Habermann CR, Robinson PN, Stuhrmann M, Berger J, Meinertz T, von Kodolitsch Y.

Am J Hypertens. 2010 Jul;23(7):716-24. doi: 10.1038/ajh.2010.78. Epub 2010 Apr 15.

PMID:
20395939
28.

Catechol-O-methyltransferase gene polymorphisms are not associated with multisomatoform disorder in a group of German multisomatoform disorder patients and healthy controls.

Jakobi J, Bernateck M, Tran AT, Holm L, Volkmann L, Buers D, Karst M, Stuhrmann M.

Genet Test Mol Biomarkers. 2010 Jun;14(3):293-7. doi: 10.1089/gtmb.2009.0142.

PMID:
20373853
29.

Digenic mutations in severe congenital neutropenia.

Germeshausen M, Zeidler C, Stuhrmann M, Lanciotti M, Ballmaier M, Welte K.

Haematologica. 2010 Jul;95(7):1207-10. doi: 10.3324/haematol.2009.017665. Epub 2010 Mar 10.

30.

Clinical utility gene card for: Haemochromatosis [HFE].

Stuhrmann M, Gabriel H, Keeney S.

Eur J Hum Genet. 2010 Sep;18(9). doi: 10.1038/ejhg.2009.245. Epub 2010 Feb 3. No abstract available.

31.

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1.

Steinemann D, Arning L, Praulich I, Stuhrmann M, Hasle H, Stary J, Schlegelberger B, Niemeyer CM, Flotho C.

Haematologica. 2010 Feb;95(2):320-3. doi: 10.3324/haematol.2009.010355. Epub 2009 Dec 16.

32.

Juvenile hemochromatosis due to homozygosity for the G320V mutation in the HJV gene with fatal outcome.

Brakensiek K, Fegbeutel C, Mälzer M, Strüber M, Kreipe H, Stuhrmann M.

Clin Genet. 2009 Nov;76(5):493-5. doi: 10.1111/j.1399-0004.2009.01261.x. Epub 2009 Sep 30. No abstract available.

PMID:
19796184
33.

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease.

Azad AK, Rauh R, Vermeulen F, Jaspers M, Korbmacher J, Boissier B, Bassinet L, Fichou Y, des Georges M, Stanke F, De Boeck K, Dupont L, Balascáková M, Hjelte L, Lebecque P, Radojkovic D, Castellani C, Schwartz M, Stuhrmann M, Schwarz M, Skalicka V, de Monestrol I, Girodon E, Férec C, Claustres M, Tümmler B, Cassiman JJ, Korbmacher C, Cuppens H.

Hum Mutat. 2009 Jul;30(7):1093-103. doi: 10.1002/humu.21011.

PMID:
19462466
34.

No association between CALCA polymorphisms and clinical outcome or serum procalcitonin levels in German polytrauma patients.

Hildebrand F, Kalmbach M, Kaapke A, Krettek C, Stuhrmann M.

Cytokine. 2009 Jul;47(1):30-6. doi: 10.1016/j.cyto.2009.04.002. Epub 2009 May 15.

PMID:
19447044
35.

A novel approach to CFTR mutation testing by pyrosequencing-based assay panels adapted to ethnicities.

Bickmann JK, Kamin W, Wiebel M, Häuser F, Wenzel JJ, Neukirch C, Stuhrmann M, Lackner KJ, Rossmann H.

Clin Chem. 2009 Jun;55(6):1083-91. doi: 10.1373/clinchem.2008.120220. Epub 2009 Apr 16.

36.

Testing the parents to confirm genotypes of CF patients is highly recommended: report of two cases.

Stuhrmann M, Brakensiek K, Argyriou L, Boehm I, Hinderhofer K, Bauer I, Rhode BM, Maelzer M, Zuehlke C, Krueger G, Schmidtke J.

Eur J Hum Genet. 2009 Apr;17(4):417-9. doi: 10.1038/ejhg.2008.190. Epub 2008 Dec 3. No abstract available.

37.

Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL gene.

El-Harith el-HA, Roesl C, Ballmaier M, Germeshausen M, Frye-Boukhriss H, von Neuhoff N, Becker C, Nürnberg G, Nürnberg P, Ahmed MA, Hübener J, Schmidtke J, Welte K, Stuhrmann M.

Br J Haematol. 2009 Jan;144(2):185-94. doi: 10.1111/j.1365-2141.2008.07430.x. Epub 2008 Nov 19.

PMID:
19036112
38.

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.

Dequeker E, Stuhrmann M, Morris MA, Casals T, Castellani C, Claustres M, Cuppens H, des Georges M, Ferec C, Macek M, Pignatti PF, Scheffer H, Schwartz M, Witt M, Schwarz M, Girodon E.

Eur J Hum Genet. 2009 Jan;17(1):51-65. doi: 10.1038/ejhg.2008.136. Epub 2008 Aug 6.

39.

Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia.

Brakensiek K, Frye-Boukhriss H, Mälzer M, Abramowicz M, Bahr MJ, von Beckerath N, Bergmann C, Caselitz M, Holinski-Feder E, Muschke P, Oexle K, Strobl-Wildemann G, Wolff G, El-Harith EA, Stuhrmann M.

Clin Genet. 2008 Aug;74(2):171-7. doi: 10.1111/j.1399-0004.2008.01029.x. Epub 2008 May 21.

PMID:
18498373
40.

Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.

Stuhrmann M, Hennies HC, Bukhari IA, Brakensiek K, Nürnberg G, Becker C, Huebener J, Miranda MC, Frye-Boukhriss H, Knothe S, Schmidtke J, El-Harith EH.

Clin Genet. 2008 Jun;73(6):566-72. doi: 10.1111/j.1399-0004.2008.01000.x. Epub 2008 May 6.

PMID:
18462451
41.

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Castellani C, Cuppens H, Macek M Jr, Cassiman JJ, Kerem E, Durie P, Tullis E, Assael BM, Bombieri C, Brown A, Casals T, Claustres M, Cutting GR, Dequeker E, Dodge J, Doull I, Farrell P, Ferec C, Girodon E, Johannesson M, Kerem B, Knowles M, Munck A, Pignatti PF, Radojkovic D, Rizzotti P, Schwarz M, Stuhrmann M, Tzetis M, Zielenski J, Elborn JS.

J Cyst Fibros. 2008 May;7(3):179-96. doi: 10.1016/j.jcf.2008.03.009. Review.

42.

No association of CNR1 gene variations with susceptibility to schizophrenia.

Seifert J, Ossege S, Emrich HM, Schneider U, Stuhrmann M.

Neurosci Lett. 2007 Oct 9;426(1):29-33. Epub 2007 Aug 10.

PMID:
17881126
43.

Prenatal diagnosis of the Rhesus D fetal blood type on amniotic fluid in daily practice.

Goebel JC, Soergel P, Pruggmayer M, Mühlhaus K, Stuhrmann M, Scharf A.

Arch Gynecol Obstet. 2008 Feb;277(2):155-60. Epub 2007 Aug 15.

PMID:
17701192
44.

Role of the novel tryptophan hydroxylase-2 gene in Tourette syndrome.

Mössner R, Müller-Vahl KR, Döring N, Stuhrmann M.

Mol Psychiatry. 2007 Jul;12(7):617-9. No abstract available.

PMID:
17592484
45.

Association of IL-8-251A/T polymorphism with incidence of Acute Respiratory Distress Syndrome (ARDS) and IL-8 synthesis after multiple trauma.

Hildebrand F, Stuhrmann M, van Griensven M, Meier S, Hasenkamp S, Krettek C, Pape HC.

Cytokine. 2007 Mar;37(3):192-9. Epub 2007 May 10.

PMID:
17498967
46.

Hereditary hemorrhagic telangiectasia. Genetics, pathogenesis, clinical manifestation and management.

Stuhrmann M, El-Harith el-HA.

Saudi Med J. 2007 Jan;28(1):11-21. Review.

PMID:
17206283
47.

Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.

Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Mariotti C, Lange HW, Weirich-Schwaiger H, Wenning GK, Seppi K, Melegh B, Havasi V, Balikó L, Wieczorek S, Zaremba J, Hoffman-Zacharska D, Sulek A, Basak AN, Soydan E, Zidovska J, Kebrdlova V, Pandolfo M, Ribaï P, Kadasi L, Kvasnicova M, Weber BH, Kreuz F, Dose M, Stuhrmann M, Riess O.

Hum Genet. 2006 Sep;120(2):285-92. Epub 2006 Jul 18.

PMID:
16847693
48.

Hereditary hemorrhagic telangiectasia is caused by the Q490X mutation of the ACVRL1 gene in a large Arab family: support of homozygous lethality.

El-Harith el-HA, Kühnau W, Schmidtke J, Gadzicki D, Ahmed M, Krawczak M, Stuhrmann M.

Eur J Med Genet. 2006 Jul-Aug;49(4):323-30. Epub 2005 Oct 25.

PMID:
16829353
49.

Genetic knowledge among participants of a German pilot study on hemochromatosis screening.

Stuhrmann M, Nippert I, Hoy L, Schmidtke J.

Clin Genet. 2006 Jul;70(1):73-7. No abstract available.

PMID:
16813609
50.

Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family.

Bukhari IA, El-Harith EA, Stuhrmann M.

J Eur Acad Dermatol Venereol. 2006 May;20(5):628-9. No abstract available.

PMID:
16684309

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