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Items: 1 to 50 of 238

1.

Ein Fall von Muckle-Wells-Syndrom mit einer neuen NLRP3-Mutation.

Yuksel S, Metz M, Lohse P, Krause K.

J Dtsch Dermatol Ges. 2018 Oct;16(10):1250-1252. doi: 10.1111/ddg.13640_g. No abstract available.

PMID:
30300484
2.

A Case of Muckle-Wells Syndrome due to novel NLRP3 mutation.

Yuksel S, Metz M, Lohse P, Krause K.

J Dtsch Dermatol Ges. 2018 Oct;16(10):1250-1252. doi: 10.1111/ddg.13640. Epub 2018 Aug 29. No abstract available.

PMID:
30157308
3.

TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.

Blaschek A, V Kries R, Lohse P, Huss K, Vill K, Belohradsky BH, Heinen F, Müller-Felber W, Kümpfel T.

Eur J Paediatr Neurol. 2018 Jan;22(1):72-81. doi: 10.1016/j.ejpn.2017.08.007. Epub 2017 Sep 1.

PMID:
28927886
4.

Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges.

Kuemmerle-Deschner JB, Verma D, Endres T, Broderick L, de Jesus AA, Hofer F, Blank N, Krause K, Rietschel C, Horneff G, Aksentijevich I, Lohse P, Goldbach-Mansky R, Hoffman HM, Benseler SM.

Arthritis Rheumatol. 2017 Nov;69(11):2233-2240. doi: 10.1002/art.40208. Epub 2017 Oct 17.

5.

Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts.

Löffler W, Lohse P, Weihmayr T, Widenmayer W.

Infection. 2017 Aug;45(4):395-402. doi: 10.1007/s15010-017-0996-1. Epub 2017 Mar 1. Review.

PMID:
28251506
6.

[Genetics of cryopyrin-associated periodic syndrome].

Kümmerle-Deschner JB, Lohse P.

Z Rheumatol. 2017 May;76(4):313-321. doi: 10.1007/s00393-017-0271-y. Review. German.

PMID:
28197772
7.

Hearing preservation in acoustic neuroma resection: Analysis of petrous bone measurement and intraoperative application.

Tanrikulu L, Lohse P, Fahlbusch R, Naraghi R.

Surg Neurol Int. 2016 Dec 12;7(Suppl 40):S980-S988. doi: 10.4103/2152-7806.195572. eCollection 2016.

8.

Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.

Schlabe S, Schwarze-Zander C, Lohse P, Rockstroh JK.

BMJ Case Rep. 2016 Nov 29;2016. pii: bcr2016217616. doi: 10.1136/bcr-2016-217616.

9.

Peripheral Hole Acceptor Moieties on an Organic Dye Improve Dye-Sensitized Solar Cell Performance.

Hao Y, Gabrielsson E, Lohse PW, Yang W, Johansson EM, Hagfeldt A, Sun L, Boschloo G.

Adv Sci (Weinh). 2015 Sep 1;2(11):1500174. eCollection 2015 Nov.

10.

Lung disease caused by ABCA3 mutations.

Kröner C, Wittmann T, Reu S, Teusch V, Klemme M, Rauch D, Hengst M, Kappler M, Cobanoglu N, Sismanlar T, Aslan AT, Campo I, Proesmans M, Schaible T, Terheggen-Lagro S, Regamey N, Eber E, Seidenberg J, Schwerk N, Aslanidis C, Lohse P, Brasch F, Zarbock R, Griese M.

Thorax. 2017 Mar;72(3):213-220. doi: 10.1136/thoraxjnl-2016-208649. Epub 2016 Aug 11.

PMID:
27516224
11.

Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean Fever.

Gohar F, Orak B, Kallinich T, Jeske M, Lieber M, von Bernuth H, Giese A, Weissbarth-Riedel E, Haas JP, Dressler F, Holzinger D, Lohse P, Neudorf U, Lainka E, Hinze C, Masjosthusmann K, Kessel C, Weinhage T, Foell D, Wittkowski H.

Arthritis Rheumatol. 2016 Dec;68(12):3010-3022. doi: 10.1002/art.39784.

12.

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.

Sadovnick AD, Traboulsee AL, Bernales CQ, Ross JP, Forwell AL, Yee IM, Guillot-Noel L, Fontaine B, Cournu-Rebeix I, Alcina A, Fedetz M, Izquierdo G, Matesanz F, Hilven K, Dubois B, Goris A, Astobiza I, Alloza I, Antigüedad A, Vandenbroeck K, Akkad DA, Aktas O, Blaschke P, Buttmann M, Chan A, Epplen JT, Gerdes LA, Kroner A, Kubisch C, Kümpfel T, Lohse P, Rieckmann P, Zettl UK, Zipp F, Bertram L, Lill CM, Fernandez O, Urbaneja P, Leyva L, Alvarez-Cermeño JC, Arroyo R, Garagorri AM, García-Martínez A, Villar LM, Urcelay E, Malhotra S, Montalban X, Comabella M, Berger T, Fazekas F, Reindl M, Schmied MC, Zimprich A, Vilariño-Güell C.

G3 (Bethesda). 2016 Jul 7;6(7):2073-9. doi: 10.1534/g3.116.030841.

13.

Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.

Wittmann T, Frixel S, Höppner S, Schindlbeck U, Schams A, Kappler M, Hegermann J, Wrede C, Liebisch G, Vierzig A, Zacharasiewicz A, Kopp MV, Poets CF, Baden W, Hartl D, van Kaam AH, Lohse P, Aslanidis C, Zarbock R, Griese M.

Mol Med. 2016 Sep;22:183-191. doi: 10.2119/molmed.2015.00244. Epub 2016 Feb 26.

14.

Early detection of sensorineural hearing loss in Muckle-Wells-syndrome.

Kuemmerle-Deschner JB, Koitschev A, Tyrrell PN, Plontke SK, Deschner N, Hansmann S, Ummenhofer K, Lohse P, Koitschev C, Benseler SM.

Pediatr Rheumatol Online J. 2015 Nov 4;13(1):43. doi: 10.1186/s12969-015-0041-9.

15.

Increased serum concentrations of neutrophil-derived protein S100A12 in heterozygous carriers of MEFV mutations.

Lieber M, Kallinich T, Lohse P, Klotsche J, Holzinger D, Foell D, Wittkowski H.

Clin Exp Rheumatol. 2015 Nov-Dec;33(6 Suppl 94):S113-6. Epub 2015 Oct 19.

PMID:
26486615
16.

Genome-wide significant association with seven novel multiple sclerosis risk loci.

Lill CM, Luessi F, Alcina A, Sokolova EA, Ugidos N, de la Hera B, Guillot-Noël L, Malhotra S, Reinthaler E, Schjeide BM, Mescheriakova JY, Mashychev A, Wohlers I, Akkad DA, Aktas O, Alloza I, Antigüedad A, Arroyo R, Astobiza I, Blaschke P, Boyko AN, Buttmann M, Chan A, Dörner T, Epplen JT, Favorova OO, Fedetz M, Fernández O, García-Martínez A, Gerdes LA, Graetz C, Hartung HP, Hoffjan S, Izquierdo G, Korobko DS, Kroner A, Kubisch C, Kümpfel T, Leyva L, Lohse P, Malkova NA, Montalban X, Popova EV, Rieckmann P, Rozhdestvenskii AS, Schmied C, Smagina IV, Tsareva EY, Winkelmann A, Zettl UK, Binder H, Cournu-Rebeix I, Hintzen R, Zimprich A, Comabella M, Fontaine B, Urcelay E, Vandenbroeck K, Filipenko M, Matesanz F, Zipp F, Bertram L.

J Med Genet. 2015 Dec;52(12):848-55. doi: 10.1136/jmedgenet-2015-103442. Epub 2015 Oct 16.

PMID:
26475045
17.

Categorizing diffuse parenchymal lung disease in children.

Griese M, Irnstetter A, Hengst M, Burmester H, Nagel F, Ripper J, Feilcke M, Pawlita I, Gothe F, Kappler M, Schams A, Wesselak T, Rauch D, Wittmann T, Lohse P, Brasch F, Kröner C.

Orphanet J Rare Dis. 2015 Sep 25;10:122. doi: 10.1186/s13023-015-0339-1.

18.

Surfactant proteins in pediatric interstitial lung disease.

Griese M, Lorenz E, Hengst M, Schams A, Wesselak T, Rauch D, Wittmann T, Kirchberger V, Escribano A, Schaible T, Baden W, Schulze J, Krude H, Aslanidis C, Schwerk N, Kappler M, Hartl D, Lohse P, Zarbock R.

Pediatr Res. 2016 Jan;79(1-1):34-41. doi: 10.1038/pr.2015.173. Epub 2015 Sep 16.

PMID:
26375475
19.

Lipocalin-2 Is a Disease Activity Marker in Inflammatory Bowel Disease Regulated by IL-17A, IL-22, and TNF-α and Modulated by IL23R Genotype Status.

Stallhofer J, Friedrich M, Konrad-Zerna A, Wetzke M, Lohse P, Glas J, Tillack-Schreiber C, Schnitzler F, Beigel F, Brand S.

Inflamm Bowel Dis. 2015 Oct;21(10):2327-40. doi: 10.1097/MIB.0000000000000515.

PMID:
26263469
20.

The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations.

Schnitzler F, Friedrich M, Wolf C, Stallhofer J, Angelberger M, Diegelmann J, Olszak T, Tillack C, Beigel F, Göke B, Glas J, Lohse P, Brand S.

PLoS One. 2015 Jul 6;10(7):e0116044. doi: 10.1371/journal.pone.0116044. eCollection 2015.

21.

Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases.

Holzinger D, Fassl SK, de Jager W, Lohse P, Röhrig UF, Gattorno M, Omenetti A, Chiesa S, Schena F, Austermann J, Vogl T, Kuhns DB, Holland SM, Rodríguez-Gallego C, López-Almaraz R, Arostegui JI, Colino E, Roldan R, Fessatou S, Isidor B, Poignant S, Ito K, Epple HJ, Bernstein JA, Jeng M, Frankovich J, Lionetti G, Church JA, Ong PY, LaPlant M, Abinun M, Skinner R, Bigley V, Sachs UJ, Hinze C, Hoppenreijs E, Ehrchen J, Foell D, Chae JJ, Ombrello A, Aksentijevich I, Sunderkoetter C, Roth J.

J Allergy Clin Immunol. 2015 Nov;136(5):1337-45. doi: 10.1016/j.jaci.2015.04.016. Epub 2015 May 27.

22.

Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations.

Schuh E, Lohse P, Ertl-Wagner B, Witt M, Krumbholz M, Frankenberger M, Gerdes LA, Hohlfeld R, Kümpfel T.

Neurol Neuroimmunol Neuroinflamm. 2015 May 14;2(4):e109. doi: 10.1212/NXI.0000000000000109. eCollection 2015 Aug.

23.

Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.

Kröner C, Reu S, Teusch V, Schams A, Grimmelt AC, Barker M, Brand J, Gappa M, Kitz R, Kramer BW, Lange L, Lau S, Pfannenstiel C, Proesmans M, Seidenberg J, Sismanlar T, Aslan AT, Werner C, Zielen S, Zarbock R, Brasch F, Lohse P, Griese M.

Eur Respir J. 2015 Jul;46(1):197-206. doi: 10.1183/09031936.00129414. Epub 2015 Feb 5.

24.

Multiple sclerosis-like lesions and type I interferon signature in a patient with RVCL.

Schuh E, Ertl-Wagner B, Lohse P, Wolf W, Mann JF, Lee-Kirsch MA, Hohlfeld R, Kümpfel T.

Neurol Neuroimmunol Neuroinflamm. 2014 Dec 23;2(1):e55. doi: 10.1212/NXI.0000000000000055. eCollection 2015 Feb. No abstract available.

25.

Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.

Hildebrandt J, Yalcin E, Bresser HG, Cinel G, Gappa M, Haghighi A, Kiper N, Khalilzadeh S, Reiter K, Sayer J, Schwerk N, Sibbersen A, Van Daele S, Nübling G, Lohse P, Griese M.

Orphanet J Rare Dis. 2014 Nov 26;9:171. doi: 10.1186/s13023-014-0171-z.

26.

Risk factors for AA amyloidosis in Germany.

Blank N, Hegenbart U, Lohse P, Beimler J, Röcken C, Ho AD, Lorenz HM, Schönland SO.

Amyloid. 2015 Mar;22(1):1-7. doi: 10.3109/13506129.2014.980942. Epub 2014 Nov 7.

PMID:
25376380
27.

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

Schnitzler F, Friedrich M, Wolf C, Angelberger M, Diegelmann J, Olszak T, Beigel F, Tillack C, Stallhofer J, Göke B, Glas J, Lohse P, Brand S.

PLoS One. 2014 Nov 3;9(11):e108503. doi: 10.1371/journal.pone.0108503. eCollection 2014.

28.

Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone.

Staub J, Pfannschmidt N, Strohal R, Braun-Falco M, Lohse P, Goerdt S, Leverkus M.

J Eur Acad Dermatol Venereol. 2015 Nov;29(11):2243-7. doi: 10.1111/jdv.12765. Epub 2014 Oct 28. Review.

PMID:
25352307
29.

[Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)].

Muehlenberg K, Faltermeier N, Lohse P, Tannapfel A, Pech O.

Z Gastroenterol. 2014 Sep;52(9):1075-80. doi: 10.1055/s-0034-1366809. Epub 2014 Sep 8. German.

PMID:
25198087
30.

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor.

Bork K, Wulff K, Hardt J, Witzke G, Lohse P.

Haemophilia. 2014 Sep;20(5):e372-5. doi: 10.1111/hae.12519. Epub 2014 Aug 12. No abstract available.

PMID:
25113305
31.

Urticaria, fever, and hypofibrinogenemia.

Mohr V, Schulz A, Lohse P, Schumann C, Debatin KM, Schuetz C.

Arthritis Rheumatol. 2014 May;66(5):1377. doi: 10.1002/art.38345. No abstract available.

32.

The effect of dye coverage on the performance of dye-sensitized solar cells with a cobalt-based electrolyte.

Pazoki M, Lohse PW, Taghavinia N, Hagfeldt A, Boschloo G.

Phys Chem Chem Phys. 2014 May 14;16(18):8503-8. doi: 10.1039/c4cp00335g.

PMID:
24668285
33.

Electron and hole transfer dynamics of a triarylamine-based dye with peripheral hole acceptors on TiO2 in the absence and presence of solvent.

Oum K, Flender O, Lohse PW, Scholz M, Hagfeldt A, Boschloo G, Lenzer T.

Phys Chem Chem Phys. 2014 May 7;16(17):8019-29. doi: 10.1039/c3cp55298e.

PMID:
24647655
34.

Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis.

Lill CM, Schilling M, Ansaloni S, Schröder J, Jaedicke M, Luessi F, Schjeide BM, Mashychev A, Graetz C, Akkad DA, Gerdes LA, Kroner A, Blaschke P, Hoffjan S, Winkelmann A, Dörner T, Rieckmann P, Steinhagen-Thiessen E, Lindenberger U, Chan A, Hartung HP, Aktas O, Lohse P, Buttmann M, Kümpfel T, Kubisch C, Zettl UK, Epplen JT, Zipp F, Bertram L.

Neurogenetics. 2014 May;15(2):129-34. doi: 10.1007/s10048-014-0396-y. Epub 2014 Mar 18.

PMID:
24638856
35.

Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infant.

Albers K, Schlein C, Wenner K, Lohse P, Bartelt A, Heeren J, Santer R, Merkel M.

Atherosclerosis. 2014 Mar;233(1):97-103. doi: 10.1016/j.atherosclerosis.2013.12.009. Epub 2014 Jan 8.

36.

Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations.

Bork K, Wulff K, Witzke G, Stanger C, Lohse P, Hardt J.

Am J Med. 2013 Dec;126(12):1142.e9-14. doi: 10.1016/j.amjmed.2013.05.017.

PMID:
24262729
37.

Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net study.

Jeske M, Lohse P, Kallinich T, Berger T, Rietschel C, Holzinger D, Kamlah C, Lankisch P, Berendes R, Dueckers G, Horneff G, Lilienthal E, Haas JP, Giese A, Dressler F, Berrang J, Braunewell L, Neudorf U, Niehues T, Föll D, Lainka E.

Klin Padiatr. 2013 Nov;225(6):325-30. doi: 10.1055/s-0033-1355372. Epub 2013 Oct 24.

PMID:
24158885
38.

Macrophage activation syndrome as the initial manifestation of tumour necrosis factor receptor 1-associated periodic syndrome (TRAPS).

Horneff G, Rhouma A, Weber C, Lohse P.

Clin Exp Rheumatol. 2013 May-Jun;31(3 Suppl 77):99-102. Epub 2013 Sep 9.

PMID:
24064022
39.

Cholesteryl ester storage disease: an easily missed diagnosis in oligosymptomatic children.

Freudenberg F, Bufler P, Ensenauer R, Lohse P, Koletzko S.

Z Gastroenterol. 2013 Oct;51(10):1184-7. doi: 10.1055/s-0033-1350463. Epub 2013 Oct 11.

PMID:
24122380
40.

Involvement of the same TNFR1 residue in mendelian and multifactorial inflammatory disorders.

Jéru I, Charmion S, Cochet E, Copin B, Duquesnoy P, Garcia MT, Le Borgne G, Cathebras P, Gaillat J, Karabina S, Dodé C, Lohse P, Hentgen V, Amselem S.

PLoS One. 2013 Jul 24;8(7):e69757. doi: 10.1371/journal.pone.0069757. Print 2013.

41.

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.

International Multiple Sclerosis Genetics Consortium, Lill CM, Schjeide BM, Graetz C, Ban M, Alcina A, Ortiz MA, Pérez J, Damotte V, Booth D, Lopez de Lapuente A, Broer L, Schilling M, Akkad DA, Aktas O, Alloza I, Antigüedad A, Arroyo R, Blaschke P, Buttmann M, Chan A, Compston A, Cournu-Rebeix I, Dörner T, Epplen JT, Fernández Ó, Gerdes LA, Guillot-Noël L, Hartung HP, Hoffjan S, Izquierdo G, Kemppinen A, Kroner A, Kubisch C, Kümpfel T, Li SC, Lindenberger U, Lohse P, Lubetzki C, Luessi F, Malhotra S, Mescheriakova J, Montalban X, Papeix C, Paredes LF, Rieckmann P, Steinhagen-Thiessen E, Winkelmann A, Zettl UK, Hintzen R, Vandenbroeck K, Stewart G, Fontaine B, Comabella M, Urcelay E, Matesanz F, Sawcer S, Bertram L, Zipp F.

Brain. 2013 Jun;136(Pt 6):1778-82. doi: 10.1093/brain/awt101.

42.

Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine.

Hepping N, Griese M, Lohse P, Garbe W, Lange L.

J Perinatol. 2013 Jun;33(6):492-4. doi: 10.1038/jp.2012.131.

PMID:
23719253
43.

Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens.

Kuemmerle-Deschner JB, Wittkowski H, Tyrrell PN, Koetter I, Lohse P, Ummenhofer K, Reess F, Hansmann S, Koitschev A, Deuter C, Bialkowski A, Foell D, Benseler SM.

Arthritis Res Ther. 2013;15(3):R64.

44.

Regeneration and recombination kinetics in cobalt polypyridine based dye-sensitized solar cells, explained using Marcus theory.

Feldt SM, Lohse PW, Kessler F, Nazeeruddin MK, Grätzel M, Boschloo G, Hagfeldt A.

Phys Chem Chem Phys. 2013 May 21;15(19):7087-97. doi: 10.1039/c3cp50997d.

PMID:
23552732
45.

Recurrent multiple spinal paragangliomas as a manifestation of a metastatic composite paraganglioma-ganglioneuroblastoma.

Gempt J, Baldawa SS, Weirich G, Delbridge C, Hempel M, Lohse P, Meyer B, Ringel F.

Acta Neurochir (Wien). 2013 Jul;155(7):1241-2. doi: 10.1007/s00701-013-1678-0. Epub 2013 Mar 27. No abstract available.

PMID:
23532344
46.

Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.

Bonfig W, Salem NJ, Heiliger K, Hempel M, Lederer G, Bornkamm M, Wieland K, Lohse P, Burdach S, Oexle K.

J Pediatr Endocrinol Metab. 2012;25(9-10):991-5. doi: 10.1515/jpem-2012-0103.

PMID:
23426831
47.

Photoinduced ultrafast dynamics of the triphenylamine-based organic sensitizer D35 on TiO2, ZrO2 and in acetonitrile.

Oum K, Lohse PW, Klein JR, Flender O, Scholz M, Hagfeldt A, Boschloo G, Lenzer T.

Phys Chem Chem Phys. 2013 Mar 21;15(11):3906-16. doi: 10.1039/c3cp44095h.

PMID:
23403702
48.

Homozygosity for piebaldism with a proven KIT mutation resulting in depigmentation of the skin and hair, deafness, developmental delay and autism spectrum disorder.

Kilsby AJ, Cruwys M, Kukendrajah C, Russell-Eggitt I, Raglan E, Rajput K, Lohse P, Brady AF.

Clin Dysmorphol. 2013 Apr;22(2):64-7. doi: 10.1097/MCD.0b013e32835e8ce5. No abstract available. Erratum in: Clin Dysmorphol. 2014 Oct;23(4):158. Loshe, Peter [corrected to Lohse, Peter].

PMID:
23399981
49.
50.

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.

Lill CM, Schjeide BM, Graetz C, Liu T, Damotte V, Akkad DA, Blaschke P, Gerdes LA, Kroner A, Luessi F, Cournu-Rebeix I, Hoffjan S, Winkelmann A, Touze E, Pico F, Corcia P, Otaegui D, Antigüedad A, Alcina A, Comabella M, Montalban X, Olascoaga J, Matesanz F, Dörner T, Li SC, Steinhagen-Thiessen E, Lindenberger U, Chan A, Rieckmann P, Hartung HP, Aktas O, Lohse P, Buttmann M, Kümpfel T, Kubisch C, Zettl UK, Epplen JT, Fontaine B, Zipp F, Vandenbroeck K, Bertram L.

J Med Genet. 2013 Mar;50(3):140-3. doi: 10.1136/jmedgenet-2012-101411. Epub 2013 Jan 12. No abstract available.

PMID:
23315543

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