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Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patients

Molecular genetics and metabolism, 2018-03, Vol.123 (3), p.357-363

2018

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Evaluating psychosocial stressors in families of children with inborn errors of metabolism

Molecular genetics and metabolism reports, 2021-06, Vol.27, p.100740-100740, Article 100740

2021

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Cardiac Disease in Methylmalonic Acidemia

The Journal of pediatrics, 2011-11, Vol.159 (5), p.862-864

2011

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Acute Progression of Neuromuscular Findings in Infantile Pompe Disease

Pediatric neurology, 2010-06, Vol.42 (6), p.455-458

2010

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Whither design space?

AI EDAM, 2006-05, Vol.20 (2), p.63-82

2006

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THE OXFORD HANDBOOK OF NEW TESTAMENT, GENDER, AND SEXUALITY Edited by Benjamin H.DunningOxford: Oxford University Press, 2019. Pp. xxv+706. US $150

Religious studies review, 2020-12, Vol.46 (4), p.489-490

Burrow, Andrew

2020

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Eliglustat compared with imiglucerase in patients with Gaucher's disease type 1 stabilised on enzyme replacement therapy: a phase 3, randomised, open-label, non-inferiority trial

The Lancet (British edition), 2015-06, Vol.385 (9985), p.2355-2362

2015

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Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children’s Hospital

Journal of personalized medicine, 2021-05, Vol.11 (5), p.394

2021

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The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?

Molecular genetics and metabolism, 2022-05, Vol.136 (1), p.4-21

2022

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Gaucher disease and SARS-CoV-2 infection: Emerging management challenges

Molecular genetics and metabolism, 2020-07, Vol.130 (3), p.164-169

2020

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Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource

Molecular genetics and metabolism, 2023-03, Vol.138 (3), p.107525-107525, Article 107525

2023

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GALATIANS AND THE RHETORIC OF CRISIS: DEMOSTHENES–CICERO–PAUL. By Nina E.Livesey. Farmington, MN: Polebridge Press, 2016. Pp. x + 273. $26.00

Religious studies review, 2018-09, Vol.44 (3), p.340-340

Burrow, Andrew

2018

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PAUL BEHAVING BADLY: WAS THE APOSTLE PAUL A RACIST, CHAUVINIST JERK? By Brandon J.O’Brien and E.Randolph Richards. Downers Grove, IL: InterVarsity Press, 2016. Pp. 224. $16.00

Religious studies review, 2018-09, Vol.44 (3), p.338-339

Burrow, Andrew

2018

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Bargaining with Jesus: Irony in Mark 5:1-20

Biblical interpretation, 2017-01, Vol.25 (2), p.234-251

Burrow, Andrew

2017

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Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis

American journal of human genetics, 2018-07, Vol.103 (1), p.125-130

2018

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O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV

Genetics in Medicine Open, 2023, Vol.1 (1), p.100114, Article 100114

2023

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CNTNAP1-Related Congenital Hypomyelinating Neuropathy

Pediatric neurology, 2019-04, Vol.93, p.43-49

2019

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Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly

American journal of medical genetics. Part A, 2022-11, Vol.188 (11), p.3364-3368

2022

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Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1

Blood cells, molecules, & diseases, 2018-07, Vol.71, p.71-74

2018

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Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi

Journal of investigative dermatology, 2014-04, Vol.134 (4), p.1149-1152

2014

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Bradycardia and Acidosis in a Term Newborn

Neoreviews (Elk Grove Village, Ill.), 2024-03, Vol.25 (3), p.e166-e168

2024

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Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy

The Journal of pediatrics, 2007-02, Vol.150 (2), p.202-206

2007

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Home infusion of intravenous velaglucerase alfa: Experience from pooled clinical studies in 104 patients with type 1 Gaucher disease

Molecular genetics and metabolism, 2017-01, Vol.120 (1-2), p.111-115

2017

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Could it be something else? Patients with Gaucher disease, chronic pain, and fatigue found to also meet diagnostic criteria for another inherited condition, Ehlers-Danlos syndrome, hypermobility type

Molecular genetics and metabolism, 2017-01, Vol.120 (1-2), p.S24

2017

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'Telcordia Technologies Inc. V. Telkom SA Ltd': A fresh start for international arbitration in South Africa?

Arbitration international, 2008-06, Vol.24 (2), p.337-343

Burrow, A.

2008

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Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patients

Evaluating psychosocial stressors in families of children with inborn errors of metabolism

Cardiac Disease in Methylmalonic Acidemia

Acute Progression of Neuromuscular Findings in Infantile Pompe Disease

Whither design space?

THE OXFORD HANDBOOK OF NEW TESTAMENT, GENDER, AND SEXUALITY Edited by Benjamin H.DunningOxford: Oxford University Press, 2019. Pp. xxv+706. US $150

Eliglustat compared with imiglucerase in patients with Gaucher's disease type 1 stabilised on enzyme replacement therapy: a phase 3, randomised, open-label, non-inferiority trial

Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children’s Hospital

The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?

Gaucher disease and SARS-CoV-2 infection: Emerging management challenges

Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource

GALATIANS AND THE RHETORIC OF CRISIS: DEMOSTHENES–CICERO–PAUL. By Nina E.Livesey. Farmington, MN: Polebridge Press, 2016. Pp. x + 273. $26.00

PAUL BEHAVING BADLY: WAS THE APOSTLE PAUL A RACIST, CHAUVINIST JERK? By Brandon J.O’Brien and E.Randolph Richards. Downers Grove, IL: InterVarsity Press, 2016. Pp. 224. $16.00

Bargaining with Jesus: Irony in Mark 5:1-20

Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis

O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV

CNTNAP1-Related Congenital Hypomyelinating Neuropathy

Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly

Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1

Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi

Bradycardia and Acidosis in a Term Newborn

Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy

Home infusion of intravenous velaglucerase alfa: Experience from pooled clinical studies in 104 patients with type 1 Gaucher disease

Could it be something else? Patients with Gaucher disease, chronic pain, and fatigue found to also meet diagnostic criteria for another inherited condition, Ehlers-Danlos syndrome, hypermobility type

'Telcordia Technologies Inc. V. Telkom SA Ltd': A fresh start for international arbitration in South Africa?

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