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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 3
1994 2
1995 2
1996 1
1997 3
1998 1
1999 3
2000 3
2001 3
2002 1
2003 2
2004 4
2005 7
2006 1
2007 1
2008 3
2009 2
2010 1
2011 3
2012 5
2013 4
2014 5
2015 2
2016 4
2017 2
2019 2
2020 2
2021 3
2022 2
2023 3
2024 0

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72 results

Results by year

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Page 1
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.
Ripperger T, Bielack SS, Borkhardt A, Brecht IB, Burkhardt B, Calaminus G, Debatin KM, Deubzer H, Dirksen U, Eckert C, Eggert A, Erlacher M, Fleischhack G, Frühwald MC, Gnekow A, Goehring G, Graf N, Hanenberg H, Hauer J, Hero B, Hettmer S, von Hoff K, Horstmann M, Hoyer J, Illig T, Kaatsch P, Kappler R, Kerl K, Klingebiel T, Kontny U, Kordes U, Körholz D, Koscielniak E, Kramm CM, Kuhlen M, Kulozik AE, Lamottke B, Leuschner I, Lohmann DR, Meinhardt A, Metzler M, Meyer LH, Moser O, Nathrath M, Niemeyer CM, Nustede R, Pajtler KW, Paret C, Rasche M, Reinhardt D, Rieß O, Russo A, Rutkowski S, Schlegelberger B, Schneider D, Schneppenheim R, Schrappe M, Schroeder C, von Schweinitz D, Simon T, Sparber-Sauer M, Spix C, Stanulla M, Steinemann D, Strahm B, Temming P, Thomay K, von Bueren AO, Vorwerk P, Witt O, Wlodarski M, Wössmann W, Zenker M, Zimmermann S, Pfister SM, Kratz CP. Ripperger T, et al. Among authors: lohmann dr. Am J Med Genet A. 2017 Apr;173(4):1017-1037. doi: 10.1002/ajmg.a.38142. Epub 2017 Feb 7. Am J Med Genet A. 2017. PMID: 28168833 Review.
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders.
Di Donato N, Guerrini R, Billington CJ, Barkovich AJ, Dinkel P, Freri E, Heide M, Gershon ES, Gertler TS, Hopkin RJ, Jacob S, Keedy SK, Kooshavar D, Lockhart PJ, Lohmann DR, Mahmoud IG, Parrini E, Schrock E, Severi G, Timms AE, Webster RI, Willis MJH, Zaki MS, Gleeson JG, Leventer RJ, Dobyns WB. Di Donato N, et al. Among authors: lohmann dr. Brain. 2022 Sep 14;145(9):3274-3287. doi: 10.1093/brain/awac164. Brain. 2022. PMID: 35769015 Free PMC article.
Retinoblastoma.
Lohmann DR, Gallie BL. Lohmann DR, et al. 2000 Jul 18 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Jul 18 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301625 Free Books & Documents. Review.
RB1 gene mutations in retinoblastoma.
Lohmann DR. Lohmann DR. Hum Mutat. 1999;14(4):283-8. doi: 10.1002/(SICI)1098-1004(199910)14:4<283::AID-HUMU2>3.0.CO;2-J. Hum Mutat. 1999. PMID: 10502774 Review.
Hereditary Diffuse Infiltrating Retinoblastoma.
Schedler KJ, Traine PG, Lohmann DR, Haritoglou C, Metz KA, Rodrigues EB. Schedler KJ, et al. Among authors: lohmann dr. Ophthalmic Genet. 2016;37(1):95-7. doi: 10.3109/13816810.2014.921315. Epub 2014 Jun 3. Ophthalmic Genet. 2016. PMID: 24892564
Pediatric second primary malignancies after retinoblastoma treatment.
Temming P, Viehmann A, Arendt M, Eisele L, Spix C, Bornfeld N, Sauerwein W, Jöckel KH, Lohmann DR. Temming P, et al. Among authors: lohmann dr. Pediatr Blood Cancer. 2015 Oct;62(10):1799-804. doi: 10.1002/pbc.25576. Epub 2015 May 13. Pediatr Blood Cancer. 2015. PMID: 25970657
72 results