Newborn screening for guanidinoacetate methyl transferase deficiency (original) (raw)

Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiency

Andreas Schulze

Neurology, 2006

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Elevation of guanidinoacetate in newborn dried blood spots and impact of early treatment in GAMT deficiency

Areeg El-gharbawy

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Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism

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Prenatal Diagnosis of Guanidinoacetate Methyltransferase Deficiency: Increased Guanidinoacetate Concentrations in Amniotic Fluid

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Selective screening in neonates suspected to have inborn errors of metabolism

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Incidence of Inborn Errors of Metabolism in Sick Neonates in a Tertiary Care Hospital in Developing Country

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Guanidinoacetate methyltransferase deficiency identified in adults and a child with mental retardation

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Diagnoses of newborns and mothers with carnitine uptake defects through newborn screening

Chun-an Chen

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Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme

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Guanidinoacetate methyltransferase deficiency: New clinical features

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Evidence-based neonatal screening for inborn errors of metabolism

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Creatine Deficiency Syndrome could be Missed Easily: A Case Report of Guanidinoacetate Methyltransferase Deficiency Presented with Neurodevelopmental Delay, Seizures, and Behavioral Changes, but Normal Structural MRI

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Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: Early treatment can prevent phenotypic expression of the disease

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Screening for inborn errors of metabolism among newborns with metabolic disturbance and/or neurological manifestations without determined cause

Vânia D'Almeida

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Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: Diagnostic tools for a new inborn error of metabolism

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The Journal of Pediatrics, 1997

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Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemia

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Acta Paediatrica, 2004

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Creatine and guanidinoacetate: diagnostic markers for inborn errors in creatine biosynthesis and transport

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Amino Acid and Acylcarnitine Profiles in Premature Neonates: A Pilot Study

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Neonates with inborn errors of metabolism: spectrum and short-term outcomes at a tertiary care hospital

mehmet can gündüz

The Turkish journal of pediatrics

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A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism

Mike Addison

Journal of Public Health, 1998

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Guanidinoacetate Methyltransferase (GAMT) Deficiency in Two Tunisian Siblings: Clinical and Biochemical Features

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Selective Screening for Inborn Errors of Metabolism: A Report of Six Years Experience

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Iranian Journal of Pediatrics, 2017

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Neonatal screening for glutaryl-CoA dehydrogenase deficiency

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Journal of Inherited Metabolic Disease, 2000

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Neonatal Screening for Congenital Metabolic and Endocrine Disorders

Oliver Blankenstein

Deutsches Ärzteblatt international, 2021

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Inborn errors of metabolism in a neonatology unit: Impact and long-term results

jose m fraga

Pediatrics International, 2011

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