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6. Corrigendum to "Pyridoxine-5'-phosphate oxidase (Pnpo) deficiency: Clinical and biochemical alterations associated with the C.347g>A (P.·Arg116gln) mutation" [Mol. Genet. Metab. 122/1-2 (2017) 135-142]. di Salvo ML; Mastrangelo M; Nogués I; Tolve M; Paiardini A; Carducci C; Mei D; Montomoli M; Tramonti A; Guerrini R; Contestabile R; Leuzzi V Mol Genet Metab; 2018 Dec; 125(4):359. PubMed ID: 29548777 [No Abstract] [Full Text] [Related]
7. Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213]. Cassiman D; Packman S; Bembi B; Turkia HB; Al-Sayed M; Schiff M; Imrie J; Mabe P; Takahashi T; Mengel KE; Giugliani R; Cox GF Mol Genet Metab; 2018 Dec; 125(4):360. PubMed ID: 29129654 [No Abstract] [Full Text] [Related]
8. Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]. Morey M; Fernández-Marmiesse A; Castiñeiras D; Fraga JM; Couce ML; Cocho JA Mol Genet Metab; 2015 Mar; 114(3):484. PubMed ID: 25877474 [No Abstract] [Full Text] [Related]
9. Corrigendum to "Risk factors for developing mineral bone disease in phenylketonuric patients" [Mol. Genet. Metab. 108 (2013) 149-154]. Mirás A; Dolores Bóveda M; Leis MR; Mera A; Aldámiz-Echevarría L; Fernández-Lorenzo JR; Fraga JM; Couce ML Mol Genet Metab; 2015 Mar; 114(3):483. PubMed ID: 25877473 [No Abstract] [Full Text] [Related]
11. Corrigendum to "Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: impact on growth in PKU" [Mol. Genet. Metab. 109 (2013) 331-338]. Aldámiz-Echevarría L; Bueno MA; Couce ML; Lage S; Dalmau J; Vitoria I; Andrade F; Llarena M; Blasco J; Alcalde C; Gil D; García MC; González-Lamuño D; Ruiz M; Ruiz MA; González D; Sánchez-Valverde F Mol Genet Metab; 2015 Mar; 114(3):485. PubMed ID: 25877475 [No Abstract] [Full Text] [Related]
12. Corrigendum to "Retinal thinning in Gaucher disease patients and carriers: Results of a pilot study" [Mol. Genet. Metab. 109 (2013) 221-223]. McNeill A; Roberti G; Lascaratos G; Hughes D; Mehta A; Garway-Heath DF; Schapira AHV Mol Genet Metab; 2014 Mar; 111(3):408. PubMed ID: 28843379 [No Abstract] [Full Text] [Related]
13. Corrigendum to "Development of hypomelanotic macules is associated with constitutive activated mTORC1 in tuberous sclerosis complex" [Mol. Genet. Metab. 120(4) (Apr 2017) 384-391]. Møller LB; Schönewolf-Greulich B; Rosengren T; Larsen LJ; Ostergaard JR; Sommerlund M; Ostenfeldt C; Stausbøl-Grøn B; Linnet KM; Gregersen PA; Jensen UB Mol Genet Metab; 2018 Dec; 125(4):361. PubMed ID: 29325814 [No Abstract] [Full Text] [Related]
14. Corrigendum to "In vitro evaluation of 2-hydroxyalkylated β-cyclodextrins as potential therapeutic agents for Niemann-pick type C disease" [Mol. Genet. Metab. (2016) 214-219]. Kondo Y; Tokumaru H; Ishitsuka Y; Matsumoto T; Taguchi M; Motoyama K; Higashi T; Arima H; Matsuo M; Higaki K; Ohno K; Irie T Mol Genet Metab; 2017 Mar; 120(3):296-297. PubMed ID: 27733311 [No Abstract] [Full Text] [Related]
15. Corrigendum to "Development of a neurologic severity scale for Aicardi Goutières Syndrome" [Mol Genet Metab. 2020 Jun;130(2):153-160. PMID: 32279991]. Adang LA; Gavazzi F; Jawad AF; Cusack SV; Kopin K; Peer K; Besnier C; De Simone M; De Giorgis V; Orcesi S; Fazzi E; Galli J; Shults J; Vanderver A Mol Genet Metab; 2022 May; 136(1):81. PubMed ID: 35422341 [No Abstract] [Full Text] [Related]
16. Corrigendum to "The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII" [Mol Genet Metab 2020 Mar;129(3):219-227]. Wang RY; da Silva Franco JF; López-Valdez J; Martins E; Sutton VR; Whitley CB; Zhang L; Cimms T; Marsden D; Jurecka A; Harmatz P Mol Genet Metab; 2020; 131(1-2):285. PubMed ID: 32843286 [No Abstract] [Full Text] [Related]
17. Corrigendum to "Interactions between metabolism and chromatin in plant models" [Mol Metab 38 (Aug 2020) 100951]. Lindermayr C; Rudolf EE; Durner J; Groth M Mol Metab; 2020 Nov; 41():101069. PubMed ID: 32891669 [No Abstract] [Full Text] [Related]
18. Corrigendum to "Digenic variants of planar cell polarity genes in human neural tube defect patients." Mol Genet Metab. 2018 May;124(1):94-100. doi:10.1016/j.ymgme.2018.03.005. Epub 2018 Mar 18. https://pubmed.ncbi.nlm.nih.gov/29573971/. Wang L; Xiao Y; Tian T; Jin L; Lei Y; Finnell RH; Ren A Mol Genet Metab; 2021 Mar; 132(3):211. PubMed ID: 33582009 [No Abstract] [Full Text] [Related]
19. A response to Germain, et al. The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts. Gurevich A; Schenk J; Wellhoefer H; Kalampoki V Mol Genet Metab Rep; 2019 Jun; 19():100471. PubMed ID: 31011537 [No Abstract] [Full Text] [Related]
20. Corrigendum to "Molecular regulation of urea cycle function by the liver glucocorticoid receptor" [Mol Metab 4 (10) (2015 Oct) 732-740]. Okun JG; Conway S; Schmidt KV; Schumacher J; Wang X; de Guia R; Zota A; Klement J; Seibert O; Peters A; Maida A; Herzig S; Rose AJ Mol Metab; 2020 Nov; 41():101068. PubMed ID: 32896509 [No Abstract] [Full Text] [Related] [Next] [New Search]