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Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?
JIMD Rep. 2017;37:49-54. doi: 10.1007/8904_2017_14. Epub 2017 Mar 9.
JIMD Rep. 2017.
PMID: 28275972
Free PMC article.
Atypical Clinical Presentations of TAZ Mutations: An Underdiagnosed Cause of Growth Retardation?
Thiels C, Fleger M, Huemer M, Rodenburg RJ, Vaz FM, Houtkooper RH, Haack TB, Prokisch H, Feichtinger RG, Lücke T, Mayr JA, Wortmann SB.
Thiels C, et al. Among authors: fleger m.
JIMD Rep. 2016;29:89-93. doi: 10.1007/8904_2015_525. Epub 2016 Jan 3.
JIMD Rep. 2016.
PMID: 26724946
Free PMC article.
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Impaired glucose-1,6-biphosphate production due to bi-allelic PGM2L1 mutations is associated with a neurodevelopmental disorder.
Morava E, Schatz UA, Torring PM, Abbott MA, Baumann M, Brasch-Andersen C, Chevalier N, Dunkhase-Heinl U, Fleger M, Haack TB, Nelson S, Potelle S, Radenkovic S, Bommer GT, Van Schaftingen E, Veiga-da-Cunha M.
Morava E, et al. Among authors: fleger m.
Am J Hum Genet. 2021 Jun 3;108(6):1151-1160. doi: 10.1016/j.ajhg.2021.04.017. Epub 2021 May 11.
Am J Hum Genet. 2021.
PMID: 33979636
Free PMC article.
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Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder.
Hengel H, Hannan SB, Dyack S, MacKay SB, Schatz U, Fleger M, Kurringer A, Balousha G, Ghanim Z, Alkuraya FS, Alzaidan H, Alsaif HS, Mitani T, Bozdogan S, Pehlivan D, Lupski JR, Gleeson JJ, Dehghani M, Mehrjardi MYV, Sherr EH, Parks KC, Argilli E, Begtrup A, Galehdari H, Balousha O, Shariati G, Mazaheri N, Malamiri RA, Pagnamenta AT, Kingston H, Banka S, Jackson A, Osmond M; Care4Rare Canada Consortium; Genomics England Research Consortium; Rieß A, Haack TB, Nägele T, Schuster S, Hauser S, Admard J, Casadei N, Velic A, Macek B, Ossowski S, Houlden H, Maroofian R, Schöls L.
Hengel H, et al. Among authors: fleger m.
Am J Hum Genet. 2021 Jun 3;108(6):1069-1082. doi: 10.1016/j.ajhg.2021.04.024. Epub 2021 May 21.
Am J Hum Genet. 2021.
PMID: 34022130
Free PMC article.
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Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiences.
Biró A, Stephani U, Tarallo T, Bast T, Schlachter K, Fleger M, Kurlemann G, Fiedler B, Leiz S, Nikanorova M, Wolff M, Müller A, Selch C, Staudt M, Kluger G.
Biró A, et al. Among authors: fleger m.
Neuropediatrics. 2015 Apr;46(2):110-6. doi: 10.1055/s-0035-1546276. Epub 2015 Mar 2.
Neuropediatrics. 2015.
PMID: 25730374
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Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.
Schwartz O, Vill K, Pfaffenlehner M, Behrens M, Weiß C, Johannsen J, Friese J, Hahn A, Ziegler A, Illsinger S, Smitka M, von Moers A, Kölbel H, Schreiber G, Kaiser N, Wilichowski E, Flotats-Bastardas M, Husain RA, Baumann M, Köhler C, Trollmann R, Schwerin-Nagel A, Eisenkölbl A, Schimmel M, Fleger M, Kauffmann B, Wiegand G, Baumgartner M, Rauscher C, Cirak S, Gläser D, Bernert G, Hagenacker T, Goldbach S, Probst-Schendzielorz K, Lochmüller H, Müller-Felber W, Schara-Schmidt U, Walter MC, Kirschner J, Pechmann A; SMARTCARE study group.
Schwartz O, et al. Among authors: fleger m.
JAMA Pediatr. 2024 Jun 1;178(6):540-547. doi: 10.1001/jamapediatrics.2024.0492.
JAMA Pediatr. 2024.
PMID: 38587854
Clinical Trial.
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Addressable microfluidic polymer chip for DNA-directed immobilization of oligonucleotide-tagged compounds.
Schröder H, Hoffmann L, Müller J, Alhorn P, Fleger M, Neyer A, Niemeyer CM.
Schröder H, et al. Among authors: fleger m.
Small. 2009 Jul;5(13):1547-52. doi: 10.1002/smll.200801016.
Small. 2009.
PMID: 19326353
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Microfabricated polymer analysis chip for optical detection.
Fleger M, Siepe D, Neyer A.
Fleger M, et al.
IEE Proc Nanobiotechnol. 2004 Aug;151(4):159-61. doi: 10.1049/ip-nbt:20040402.
IEE Proc Nanobiotechnol. 2004.
PMID: 16475861
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