Anesthetic Management of a Pediatric Patient with Arginase Deficiency by Abdulkadir Atım, Hüseyin Oğuz Yılmaz, Tuncer Çaycı, Mehmet Emin Orhan

Subjects: “…Arginase deficiency…”
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Phenotypic pleiotropy in arginase deficiency: A single center cohort by Narmadham K Bharathi, Maya Mary Thomas, Sangeetha Yoganathan, Mahalakshmi Chandran, Rekha Aaron, Sumita Danda

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A Rare Cause of Spasticity and Microcephaly: Argininemia by Pembe Soylu Üstkoyuncu, Mustafa Kendirci, Songül Gökay, Fatih Kardaş, Hakan Gümüş, Hüseyin Per, Hatice Gamze Poyrazoğlu, Ayşe Kaçar Bayram, Mehmet Canpolat, Sefer Kumandaş

Subjects: “…arginase deficiency…”
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Plasma arginine levels in arginase deficiency in the “real world” by Pranoot Tanpaiboon, Yue Huang, Judy Z. Louie, Rajesh Sharma, Stephen Cederbaum, Denise Salazar

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Late onset arginase deficiency presenting with encephalopathy and midbrain hyperintensity by Boby Varkey Maramattom, Rajat Raja, Anuroop Balagopal

Subjects: “…Arginase deficiency…”
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Creatine metabolism in patients with urea cycle disorders by Filippo Ingoglia, Jean-Leon Chong, Marzia Pasquali, Nicola Longo

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Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia by Yue Huang, Rajesh Sharma, Annette Feigenbaum, Chung Lee, Inderneel Sahai, Rossana Sanchez Russo, Juanita Neira, Susan Sklower Brooks, Kelly E. Jackson, Derek Wong, Stephen Cederbaum, Felicitas L. Lacbawan, Charles M. Rowland, Pranoot Tanpaiboon, Denise Salazar

Subjects: “…Arginase deficiency…”
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Arginase deficiency masked by cerebral palsy and coagulopathy—Three varied presentations of Latin American origin by Shelby L. Mills, Paige Roberts, Myla Ashfaq, Kathryn Leal, Hope Northrup, Deborah L. Brown, David Rodriguez‐Buritica, Laura S. Farach

Subjects: “…arginase deficiency…”
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A Case with Autism Spectrum Disorder and Concomitant Arginase Deficiency by Rabia Eren, Buket Canlan Özaydın, Emine Göksoy, Zehra Manav Yiğit, Börte Gürbüz Özgür

Subjects: “…arginase deficiency disorder…”
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ACMG/AMP variant classification framework in arginase 1 deficiency: Implications for birth prevalence estimates and diagnostics by Jessie M. Cameron, Mayowa Azeez Osundiji, Rory J. Olson, Bukola A. Olarewaju, Andreas Schulze

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Intermittent lipid nanoparticle mRNA administration prevents cortical dysmyelination associated with arginase deficiency by Suhail Khoja, Xiao-Bo Liu, Brian Truong, Matthew Nitzahn, Jenna Lambert, Adam Eliav, Eram Nasser, Emma Randolph, Kristine E. Burke, Rebecca White, Xuling Zhu, Paolo G.V. Martini, Itzhak Nissim, Stephen D. Cederbaum, Gerald S. Lipshutz

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Review of Multi-Modal Imaging in Urea Cycle Disorders: The Old, the New, the Borrowed, and the Blue by Kuntal Sen, Afrouz A. Anderson, Matthew T. Whitehead, Andrea L. Gropman

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Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Inte... by Emanuele Panza, Diego Martinelli, Pamela Magini, Carlo Dionisi Vici, Marco Seri

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