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List of works by William J Craigen

Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disorders ⬇️

scientific article published on 06 July 2012

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

scientific article published on 20 November 2017

Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review ⬇️

scientific article published on 02 February 2012

Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation

scientific article

Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementation

scientific article published on 27 January 2016

MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations.

scientific article

Mitochondria: role of citrulline and arginine supplementation in MELAS syndrome

scientific article published on 08 January 2014

Mitochondrial DNA maintenance defects

scientific article published on 16 February 2017

Molecular findings among patients referred for clinical whole-exome sequencing

scientific article

OEIS complex associated with chromosome 1p36 deletion: a case report and review.

scientific article published in February 2010

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

scientific article (publication date: 12 November 2009)

Restoration of impaired nitric oxide production in MELAS syndrome with citrulline and arginine supplementation.

scientific article

Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes ⬇️

scientific article published on December 20, 2010

The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndrome

scientific article

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