Sir Archibald Garrod by K Varadaraj Shenoy, P Thara, M Sharmila

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Frequency inborn error of mitochondrial function in Mosul and Kurdistan region by Ashwaq N. Abbas, Mwafak K. Hasan, Muhammad A. Ahmed

Subjects: “…keywords: mitochondria, an inborn error of metabolism, carnitine, mosul…”
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Congenital hyperinsulinism in clinical practice: From biochemical pathophysiology to new monitoring techniques by Mariangela Martino, Jacopo Sartorelli, Vincenza Gragnaniello, Alberto Burlina

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Isovaleric Acidemia as a Rare Cause for Bad Obstetric History by Sailatha Ramanujam, Shery Angel, Anuradha Coimbatore Ramachandran, Anu Bhargavi Basker

Subjects: “…inborn error of metabolism…”
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Frequency inborn error of mitochondrial function in Mosul and Kurdistan region by Ashwaq N. Abbas, Mwafak K. Hasan, Muhammad A. Ahmed

Subjects: “…Keywords: mitochondria, an inborn error of metabolism, carnitine, Mosul…”
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Neural correlates of working memory and its association with metabolic parameters in early-treated adults with phenylketonuria by Stephanie Abgottspon, Raphaela Muri, Shawn E. Christ, Michel Hochuli, Piotr Radojewski, Roman Trepp, Regula Everts

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A Proposed Diagnostic Algorithm for Inborn Errors of Metabolism Presenting With Movements Disorders by Juan Darío Ortigoza-Escobar

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Renal replacement therapy in neonates with an inborn error of metabolism by Heeyeon Cho

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Vaccination strategies for people living with inborn errors of metabolism in Brazil by Barbara C.F. Ramos, Carolina S. Aranda, Rita S.B. Cardona, Ana Maria Martins, Dirceu Solé, Sue Ann C. Clemens, Ralf Clemens

Subjects: “…Inborn error of metabolism…”
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Transient Hyperammonemia of the Newborn: A Case Study by Amir Kamal Hardani, Majid Aminzadeh

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Do early‐treated adults with phenylketonuria sense high phenylalanine levels? by Laura Hauri, Raphaela Muri, Regula Everts, Roman Trepp

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Parkinson’s Disease and Metal Storage Disorders: A Systematic Review by Edward Botsford, Jayan George, Ellen E. Buckley

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A rare case of fructose-1, 6-bisphosphatase deficiency: Clinical features in a pediatric patient by Shami Pokhrel, Subha Sainju, Prasanna Lamsal, Uma Devi Chhetri

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Development of a robust 30-minute reverse-phase high pressure liquid chromatography method to measure amino acids using widely available equipment and its comparison to current cli... by G. Cunningham, Yun Zhou, M. Summar

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Toxic Metabolites and Inborn Errors of Amino Acid Metabolism: What One Informs about the Other by Namgyu Lee, Dohoon Kim

Subjects: “…inborn error of metabolism (IEM)…”
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Propionic Acidemia diagnosed in Amish adults and pregnancy outcomes: A case series by Ethan M. Scott, Brandon Smith, Joseph Liu, Karlee Hoffman, Jennifer Hershberger, Andew Crosby, Emma L. Baple, Olivia K. Wenger

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A novel, high throughput, and low-cost method for the detection of 40 amines relevant to inborn errors of metabolism, in under 60 min, using reverse phase high performance liquid c... by Kirkland A. Wilson, Yun Zhou, Gary Cunningham, Kimberly Chapman, Marshall Summar, Debra Regier

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Risk of Developing Insulin Resistance in Adult Subjects with Phenylketonuria: Machine Learning Model Reveals an Association with Phenylalanine Concentrations in Dried Blood Spots by María Jesús Leal-Witt, Eugenia Rojas-Agurto, Manuel Muñoz-González, Felipe Peñaloza, Carolina Arias, Karen Fuenzalida, Daniel Bunout, Verónica Cornejo, Alejandro Acevedo

Subjects: “…inborn error of metabolism…”
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Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and Management by Brahim Tabarki, Wejdan Hakami, Nader Alkhuraish, Kalthoum Graies-Tlili, Marwan Nashabat, Majid Alfadhel, Majid Alfadhel

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The rs2229611 (G6PC:c.*23 T>C) is associated with glycogen storage disease type Ia in Brazilian patients by Franciele Cabral Pinheiro, Fernanda Sperb-Ludwig, Juliana Maria Fagundes Verch, Bruna Bento dos Santos, Carolina Fischinger Moura de Souza, Ida Vanessa Doederlein Schwartz

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