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Richard Koch

university of southern california

45H指数
762论文数
6.8K被引数
收录论文 28
发表时间
An epigenetic memory of inflammation controls context-dependent lineage plasticity in the pancreas
err2022-11-15
err0
PREAI
errFalvo, David J.; Grimont, Adrien; Zumbo, Paul; Yang, Julie L.; Osterhoudt, Alexa; Pan, Grace; Rendeiro, Andre F.; Wilkinson, John E.; Dundar, Friederike; Elemento, Olivier; Yantiss, Rhonda K.; Betel, Doron; Koch, Richard; Chandwani, Rohit
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Increased Cardiovascular Risk in Psoriatic Arthritis: Results From a Case-Control Monocentric Study
err2022-05-19
err8
errOAAI
errDegboe, Yannick; Koch, Richard; Zabraniecki, Laurent; Jamard, Benedicte; Couture, Guillaume; Ruidavets, Jean Bernard; Ferrieres, Jean; Ruyssen-Witrand, Adeline; Constantin, Arnaud
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Suboptimal outcomes in patients with PKU treated early with diet alone: Revisiting the evidence
err2010-10-01
err153
PREAI
errEnns, G. M.; Koch, R.; Brumm, V.; Blakely, E.; Suter, R.; Jurecki, E.
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Psychosocial issues and outcomes in maternal PKU
err2010-01-01
err29
PREAI
errKoch, Richard; Trefz, Friedrich; Waisbren, Susan
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Mutations in the phenflalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles
err2007-07-01
err48
PREAI
errDobrowolski, Steven F.; Ellingson, Clinton; Coyne, Thomas; Grey, Jesse; Martin, Ranae; Naylor, Edwin W.; Koch, Richard; Levy, Harvey L.
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Response of patients with phenylketonuria in the US to tetrahydrobiopterin
err2005-12-01
err35
PREAI
errMatalon, R; Michals-Matalon, K; Koch, R; Grady, J; Tyring, S; Stevens, RC
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Pitfalls in newborn screening
err2005-07-01
err1
PREAI
errCrombez, E; Koch, R; Cederbaum, S
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Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations
err2004-11-19
err168
errOAAI
errErlandsen, H; Pey, AL; Gámez, A; Pérez, B; Desviat, LR; Aguado, C; Koch, R; Surendran, S; Tyring, S; Matalon, R; Scriver, CR; Ugarte, M; Martínez, A; Stevens, RC
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Biopterin responsive phenylalanine hydroxylase deficiency
err2004-01-01
err54
errOAAI
errMatalon, R; Koch, R; Michals-Matalon, K; Moseley, K; Surendran, S; Tyring, S; Erlandsen, H; Gamez, A; Stevens, RC; Romstad, A; Moller, LB; Guttler, F
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Congenital heart disease in maternal phenylketonuria:: Report from the Maternal PKU Collaborative Study
err2001-05-01
err69
errOAAI
errLevy, HL; Guldberg, P; Güttler, F; Hanley, WB; Matalon, R; Rouse, BM; Trefz, E; Azen, C; Allred, EN; de la Cruz, F; Koch, R
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Blood-brain phenylalanine relationships in persons with phenylketonuria
err2000-11-01
err62
PREAI
errKoch, R; Moats, R; Guttler, F; Guldberg, P; Nelson, M
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Maternal phenylketonuria: An international study
err2000-09-01
err42
PREAI
errKoch, R; Hanley, W; Levy, H; Matalon, R; Rouse, B; Trefz, F; Guttler, F; Azen, C; Friedman, E; Platt, L; de la Cruz, F
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The International Study of Pregnancy Outcome in Women with Maternal Phenylketonuria:: Report of a 12-year study
err2000-02-01
err61
PREAI
errPlatt, LD; Koch, R; Hanley, WB; Levy, HL; Matalon, R; Rouse, B; Trefz, F; de la Cruz, F; Güttler, F; Azen, C; Friedman, EG
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Maternal phenylketonuria syndrome: Congenital heart defects, microcephaly, and developmental outcomes
err2000-01-01
err49
PREAI
errRouse, B; Matalon, R; Koch, R; Azen, C; Levy, H; Hanley, W; Trefz, F; de la Cruz, F
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Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency:: Report from the Maternal Phenylketonuria Collaborative Study
err1999-08-01
err53
PREAI
errGüttler, F; Azen, C; Guldberg, P; Romstad, A; Hanley, WB; Levy, HL; Matalon, R; Rouse, BM; Trefz, F; de la Cruz, F; Koch, R
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