These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
269 related articles for article (PubMed ID: 34097229)
61. Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for clinicians. Saudubray JM; Mochel F; Lamari F; Garcia-Cazorla A J Inherit Metab Dis; 2019 Jul; 42(4):706-727. PubMed ID: 30883825 [TBL] [Abstract][Full Text] [Related]
62. Impact of pregnancy on inborn errors of metabolism. Wilcox G Rev Endocr Metab Disord; 2018 Mar; 19(1):13-33. PubMed ID: 30198059 [TBL] [Abstract][Full Text] [Related]
63. [Diagnosis and acute treatment of inborn metabolic diseases in infants]. Lund AM; Christensen E; Skovby F Ugeskr Laeger; 2002 Nov; 164(48):5613-9. PubMed ID: 12523004 [TBL] [Abstract][Full Text] [Related]
64. Untargeted Metabolomics for Metabolic Diagnostic Screening with Automated Data Interpretation Using a Knowledge-Based Algorithm. Haijes HA; van der Ham M; Prinsen HCMT; Broeks MH; van Hasselt PM; de Sain-van der Velden MGM; Verhoeven-Duif NM; Jans JJM Int J Mol Sci; 2020 Feb; 21(3):. PubMed ID: 32024143 [TBL] [Abstract][Full Text] [Related]
65. Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China. Jiang M; Liu L; Mei H; Li X; Cheng J; Cai Y J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):375-80. PubMed ID: 25781538 [TBL] [Abstract][Full Text] [Related]
66. Newborn screening of inherited metabolic disorders: the Italian situation. Focardi M; Pinchi V; Defraia B; Gualco B; Varvara G; Norelli GA J Biol Regul Homeost Agents; 2016; 30(3):909-914. PubMed ID: 27655520 [TBL] [Abstract][Full Text] [Related]
67. New Advances for Newborn Screening of Inborn Errors of Metabolism by Capillary Electrophoresis-Mass Spectrometry (CE-MS). Shanmuganathan M; Britz-McKibbin P Methods Mol Biol; 2019; 1972():139-163. PubMed ID: 30847789 [TBL] [Abstract][Full Text] [Related]
68. Clinical biochemical genetics in the twenty-first century. Rinaldo P; Hahn S; Matern D Acta Paediatr Suppl; 2004 May; 93(445):22-6; discussion 27. PubMed ID: 15176715 [TBL] [Abstract][Full Text] [Related]
69. Outcome of Inherited Metabolic Disorders Presenting in the Neonatal Period. Balakrishnan U; Chandrasekaran A; Amboiram P; Ninan B; Ignatious S Indian J Pediatr; 2021 May; 88(5):455-462. PubMed ID: 33051787 [TBL] [Abstract][Full Text] [Related]
70. Diagnosis and monitoring of inborn errors of metabolism using urease-pretreatment of urine, isotope dilution, and gas chromatography-mass spectrometry. Kuhara T J Chromatogr B Analyt Technol Biomed Life Sci; 2002 Dec; 781(1-2):497-517. PubMed ID: 12450676 [TBL] [Abstract][Full Text] [Related]
71. Pilot study of newborn screening of inborn error of metabolism using tandem mass spectrometry in Malaysia: outcome and challenges. Yunus ZM; Rahman SA; Choy YS; Keng WT; Ngu LH J Pediatr Endocrinol Metab; 2016 Sep; 29(9):1031-9. PubMed ID: 27544719 [TBL] [Abstract][Full Text] [Related]
72. High Risk Stratified Neonatal Screening. ICMR Task Force on Inherited Metabolic Disorders Indian J Pediatr; 2018 Dec; 85(12):1050-1054. PubMed ID: 29542068 [TBL] [Abstract][Full Text] [Related]
73. [Inborn errors of metabolism: new developments and challenges]. De Laet C; Carlier C; Robert M; Thiebaut I; Prové G; Sergooris R; Goyens P Rev Med Brux; 2006; 27 Spec No():Sp74-7. PubMed ID: 21818897 [TBL] [Abstract][Full Text] [Related]
74. Gas chromatography/mass spectrometry-based urine metabolome study in children for inborn errors of metabolism: An Indian experience. Hampe MH; Panaskar SN; Yadav AA; Ingale PW Clin Biochem; 2017 Feb; 50(3):121-126. PubMed ID: 27784639 [TBL] [Abstract][Full Text] [Related]
75. Acute management of sick infants with suspected inborn errors of metabolism. Gupta N; Kabra M Indian J Pediatr; 2011 Jul; 78(7):854-9. PubMed ID: 21681651 [TBL] [Abstract][Full Text] [Related]
76. [Selective screening of inborn errors of metabolism by using the tandem mass spectrometry: pilot study of 552 children at high risk]. Lou Y; Yin N; Chen FQ; Cheng YY; Xu LJ; Dai F; Song XT Zhongguo Dang Dai Er Ke Za Zhi; 2011 Apr; 13(4):296-9. PubMed ID: 21507298 [TBL] [Abstract][Full Text] [Related]
77. Transplantation in inborn errors of metabolism: current considerations and future perspectives. Boelens JJ; Orchard PJ; Wynn RF Br J Haematol; 2014 Nov; 167(3):293-303. PubMed ID: 25074667 [TBL] [Abstract][Full Text] [Related]
78. The utility of EEG monitoring in neonates with hyperammonemia due to inborn errors of metabolism. Wiwattanadittakul N; Prust M; Gaillard WD; Massaro A; Vezina G; Tsuchida TN; Gropman AL Mol Genet Metab; 2018 Nov; 125(3):235-240. PubMed ID: 30197275 [TBL] [Abstract][Full Text] [Related]
79. Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemia. Deodato F; Boenzi S; Rizzo C; Abeni D; Caviglia S; Picca S; Bartuli A; Dionisi-Vici C Acta Paediatr Suppl; 2004 May; 93(445):18-21. PubMed ID: 15176714 [TBL] [Abstract][Full Text] [Related]
80. [Tandem mass spectrometry as screening for inborn errors of metabolism]. Campos H D Rev Med Chil; 2011 Oct; 139(10):1356-64. PubMed ID: 22286738 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]