首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
fetal inherited metabolic disorder相关文献:
Fetal anemia: Diagnosis and management.
Prefumo F, Fichera A, Fratelli N, Sartori E.
Best Pract Res Clin Obstet Gynaecol. 2019 Jul;58:2-14. doi: 10.1016/j.bpobgyn.2019.01.001. Epub 2019 Jan 9.
PMID:30718211
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.
Warrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S, Hao K, Feenstra B, Wood AR, Mahajan A, Tyrrell J, Robertson NR, Rayner NW, Qiao Z, Moen GH, Vaudel M, Marsit CJ, Chen J, Nodzenski M, Schnurr TM, Zafarmand MH, Bradfield JP, Grarup N, Kooijman MN, Li-Gao R, Geller F, Ahluwalia TS, Paternoster L, Rueedi R, Huikari V, Hottenga JJ, Lyytikäinen LP, Cavadino A, Metrustry S, Cousminer DL, Wu Y, Thiering E, Wang CA, Have CT, Vilor-Tejedor N, Joshi PK, Painter JN, Ntalla I, Myhre R, Pitkänen N, van Leeuwen EM, Joro R, Lagou V, Richmond RC, Espinosa A, Barton SJ, Inskip HM, Holloway JW, Santa-Marina L, Estivill X, Ang W, Marsh JA, Reichetzeder C, Marullo L, Hocher B, Lunetta KL, Murabito JM, Relton CL, Kogevinas M, Chatzi L, Allard C, Bouchard L, Hivert MF, Zhang G, Muglia LJ, Heikkinen J; EGG Consortium; Morgen CS, van Kampen AHC, van Schaik BDC, Mentch FD, Langenberg C, Luan J, Scott RA, Zhao JH, Hemani G, Ring SM, Bennett AJ, Gaulton KJ, Fernandez-Tajes J, van Zuydam NR, Medina-Gomez C, de Haan HG, Rosendaal FR, Kutalik Z, Marques-Vidal P, Das S, Willemsen G, Mbarek H, Müller-Nurasyid M, Standl M, Appel EVR, Fonvig CE, Trier C, van Beijsterveldt C…
Nat Genet. 2019 May;51(5):804-814. doi: 10.1038/s41588-019-0403-1. Epub 2019 May 1.
PMID:31043758
Anemia in Pregnancy: Screening and Clinical Management Strategies.
Stanley AY, Wallace JB, Hernandez AM, Spell JL.
MCN Am J Matern Child Nurs. 2022 Jan-Feb 01;47(1):25-32. doi: 10.1097/NMC.0000000000000787.
PMID:34860784
Galactose metabolism and health.
Coelho AI, Berry GT, Rubio-Gozalbo ME.
Curr Opin Clin Nutr Metab Care. 2015 Jul;18(4):422-7. doi: 10.1097/MCO.0000000000000189.
PMID:26001656
Blood type biochemistry and human disease.
Ewald DR, Sumner SC.
Wiley Interdiscip Rev Syst Biol Med. 2016 Nov;8(6):517-535. doi: 10.1002/wsbm.1355. Epub 2016 Sep 7.
PMID:27599872
Iron deficiency anemia in pregnancy.
Di Renzo GC, Spano F, Giardina I, Brillo E, Clerici G, Roura LC.
Womens Health (Lond). 2015 Nov;11(6):891-900. doi: 10.2217/whe.15.35. Epub 2015 Oct 16.
PMID:26472066
Inherited Metabolic Disorders: Implications for the Obstetrician-Gynecologist.
Hopkins MK, Dugoff L, Kuller JA.
Obstet Gynecol Surv. 2018 Jun;73(6):361-367. doi: 10.1097/OGX.0000000000000566.
PMID:29955896
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders.
Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, Capasso G, Emma F, Schlingmann KP, Singh M, Trepiccione F, Walsh SB, Whitton K, Vargas-Poussou R, Bockenhauer D.
Kidney Int. 2021 Feb;99(2):324-335. doi: 10.1016/j.kint.2020.10.035.
PMID:33509356
CRISPR/Cas9-based functional genomics strategy to decipher the pathogenicity of genetic variants in inherited metabolic disorders.
Muñoz-Pujol G, Ugarteburu O, Segur-Bailach E, Moliner S, Jurado S, Garrabou G, Guitart-Mampel M, García-Villoria J, Artuch R, Fons C, Ribes A, Tort F.
J Inherit Metab Dis. 2023 Nov;46(6):1029-1042. doi: 10.1002/jimd.12681. Epub 2023 Oct 3.
PMID:37718653
Clinical implications of the glucokinase impaired function - GCK MODY today.
Hulín J, Škopková M, Valkovičová T, Mikulajová S, Rosoľanková M, Papcun P, Gašperíková D, Staník J.
Physiol Res. 2020 Dec 22;69(6):995-1011. doi: 10.33549/physiolres.934487. Epub 2020 Nov 2.
PMID:33129248
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3