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James E. Davison

7PUBLICATIONS

23CO-AUTHORS

NeonatologyPharmacogenomicsGene expression (incl. microarray and other genome-wide approaches)OptometryDevelopmental genetics (incl. sex determination)

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Publications (7)

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|Jan 19, 2026

Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non-Finnish Patients.

Isaac Bernhardt, Polona Le Quesne Stabej, Claire Hart

|Feb 08, 2021

Advances in diagnosis and management of Pompe disease.

James E Davison

|Jan 22, 2021

Neuroradiologic Phenotyping of Galactosemia: From the Neonatal Form to the Chronic Stage.

M C Rossi-Espagnet, S Sudhakar, E Fontana

|Jan 15, 2021

Eye involvement in inherited metabolic disorders.

James E Davison

|May 13, 2020

Adrenoleukodystrophy in the Differential Diagnosis of Boys Presenting with Primary Adrenal Insufficiency without Adrenal Antibodies

Michael R. Ryalls, Hoong-Wei Gan, James E. Davison

|Aug 28, 2019

Free urinary glycosylated hydroxylysine as an indicator of altered collagen degradation in the mucopolysaccharidoses.

Nina Patel, Philippa Mills, James Davison

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Frequent Collaborators

1 joint publications

M C Rossi-Espagnet

1 joint publications

S Sudhakar

1 joint publications

E Fontana

1 joint publications

D Longo

1 joint publications

A L Petengill

1 joint publications

E Bevivino

1 joint publications

F T Pacheco

1 joint publications

A J da Rocha

1 joint publications

P Hanagandi

1 joint publications

M Soldatelli

Frequent Collaborators

1 joint publications

M C Rossi-Espagnet

1 joint publications

S Sudhakar

1 joint publications

E Fontana

1 joint publications

D Longo

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