Newborn screening [NEW TOPIC PAGE]

PubMed Clinical Queries



From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Newborn screening" 

Results: 5 of 4950

• Subcutaneous fat necrosis of the newborn and associated hypercalcemia: A systematic review of the literature.
  Stefanko NS, Drolet BA.Pediatr Dermatol. 2018 Sep 6; . Epub 2018 Sep 6.
• Screening for gestational diabetes mellitus: one step versus two step approach. A meta-analysis of randomized trials.
  Saccone G, Khalifeh A, Al-Kouatly HB, Sendek K, Berghella V.J Matern Fetal Neonatal Med. 2018 Sep 3; :1-231. Epub 2018 Sep 3.
• Estimating glomerular filtration rate in children: evaluation of creatinine- and cystatin C-based equations.
  Salvador CL, Tøndel C, Rowe AD, Bjerre A, Brun A, Brackman D, Mørkrid L.Pediatr Nephrol. 2018 Aug 31; . Epub 2018 Aug 31.
• Quantitative chest computerized tomography and FEV₁ equally identify pulmonary exacerbation risk in children with cystic fibrosis.
  Sanders DB, Li Z, Parker-McGill K, Farrell P, Brody AS.Pediatr Pulmonol. 2018 Aug 29; . Epub 2018 Aug 29.
• Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for <i>in vivo</i> screening of candidate therapeutic compounds.
  Tseng WC, Loeb HE, Pei W, Tsai-Morris CH, Xu L, Cluzeau CV, Wassif CA, Feldman B, Burgess SM, Pavan WJ, et al.Dis Model Mech. 2018 Aug 15; 11(9). Epub 2018 Aug 15.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 1126

• Subcutaneous fat necrosis of the newborn and associated hypercalcemia: A systematic review of the literature.
  Stefanko NS, Drolet BA.Pediatr Dermatol. 2018 Sep 6; . Epub 2018 Sep 6.
• Screening for gestational diabetes mellitus: one step versus two step approach. A meta-analysis of randomized trials.
  Saccone G, Khalifeh A, Al-Kouatly HB, Sendek K, Berghella V.J Matern Fetal Neonatal Med. 2018 Sep 3; :1-231. Epub 2018 Sep 3.
• Can untreated PKU patients escape from intellectual disability? A systematic review.
  van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Blau N, Bulut FD, Casas K, Didycz B, Djordjevic M, Federico A, et al.Orphanet J Rare Dis. 2018 Aug 29; 13(1):149. Epub 2018 Aug 29.
• Newborn screening in the developing countries.
  Therrell BL Jr, Padilla CD.Curr Opin Pediatr. 2018 Aug 16; . Epub 2018 Aug 16.
• Prevalence of Autism Spectrum Disorder in Preterm Infants: A Meta-analysis.
  Agrawal S, Rao SC, Bulsara MK, Patole SK.Pediatrics. 2018 Sep; 142(3). Epub 2018 Aug 3.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 7499

• Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency.
  Kohn DB, Hershfield MS, Puck JM, Aiuti A, Blincoe A, Gaspar HB, Notarangelo LD, Grunebaum E.J Allergy Clin Immunol. 2018 Sep 5; . Epub 2018 Sep 5.
• The diagnostic challenge in very-long chain acyl-CoA dehydrogenase deficiency (VLCADD).
  Hesse J, Braun C, Behringer S, Matysiak U, Spiekerkoetter U, Tucci S.J Inherit Metab Dis. 2018 Sep 7; . Epub 2018 Sep 7.
• Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Syndrome Causing Severe Neonatal Hyperammonemia.
  Wild KT, Ganetzky RD, Yudkoff M, Ierardi-Curto L.JIMD Rep. 2018 Sep 6; . Epub 2018 Sep 6.
• Generation of iPSC-Derived Human Peripheral Sensory Neurons Releasing Substance P Elicited by TRPV1 Agonists.
  Guimarães MZP, De Vecchi R, Vitória G, Sochacki JK, Paulsen BS, Lima I, Rodrigues da Silva F, da Costa RFM, Castro NG, Breton L, et al.Front Mol Neurosci. 2018; 11:277. Epub 2018 Aug 22.
• Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong Kong.
  Chong SC, Lo P, Chow CW, Yuen L, Chu WCW, Leung TY, Hui J, Scaglia F.Mol Genet Metab Rep. 2018 Dec; 17:3-8. Epub 2018 Sep 1.

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This column displays citations pertaining to topics in medical genetics. See more filter information.