(Q34172908)

31 July 2017

3 references

24 March 2019

22 April 2019

25 April 2019

Diagnosis and management of glutaric aciduria type I--revised recommendations (English)

1 reference

amino acid metabolic disorder

31 July 2017

main subject

3 references

24 March 2019

22 April 2019

25 April 2019

1 reference

ChEBI release 2020-05-28

1 reference

Stefan Kölker

1

1 reference

31 July 2017

Ernst Christensen

2

1 reference

31 July 2017

James V Leonard

3

1 reference

31 July 2017

Cheryl R Greenberg

4

1 reference

31 July 2017

Avihu Boneh

5

1 reference

31 July 2017

Alberto B Burlina

6

1 reference

31 July 2017

Alessandro P Burlina

7

1 reference

31 July 2017

Marjorie Dixon

8

1 reference

31 July 2017

Marinus Duran

9

1 reference

31 July 2017

Angels García Cazorla

10

1 reference

31 July 2017

Stephen I Goodman

11

1 reference

31 July 2017

David M Koeller

12

1 reference

31 July 2017

Mårten Kyllerman

13

1 reference

31 July 2017

Chris Mühlhausen

14

1 reference

31 July 2017

Edith Müller

15

1 reference

31 July 2017

Jürgen G Okun

16

1 reference

31 July 2017

Bridget Wilcken

17

1 reference

31 July 2017

Georg F Hoffmann

18

1 reference

31 July 2017

Peter Burgard

19

1 reference

31 July 2017

publication date

23 March 2011

1 reference

Journal of Inherited Metabolic Disease

31 July 2017

1 June 2011

3 references

24 March 2019

22 April 2019

25 April 2019

4 references

31 July 2017

24 March 2019

22 April 2019

25 April 2019

34

1 reference

31 July 2017

issue

3

1 reference

31 July 2017

page(s)

677-694

1 reference

Use of guidelines improves the neurological outcome in glutaric aciduria type I.

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Cognitive, behavioural and adaptive profiles of children with glutaric aciduria type I detected through newborn screening

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Carnitine supplementation for inborn errors of metabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Maternal glutaric acidemia, type I identified by newborn screening

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Prospective open-label clinical trial of trihexyphenidyl in children with secondary dystonia due to cerebral palsy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Neonatal screening for glutaric aciduria type I: strategies to proceed

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Quantification of glutaric and 3-hydroxyglutaric acids in urine of glutaric acidemia type I patients by HPLC with intramolecular excimer-forming fluorescence derivatization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Cascade screening: whose information is it anyway?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Reduction of lysine intake while avoiding malnutrition--major goals and major problems in dietary treatment of glutaryl-CoA dehydrogenase deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Maintenance treatment of glutaryl-CoA dehydrogenase deficiency.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Neuroradiological findings in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Neonatal screening for glutaryl-CoA dehydrogenase deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Crystal structures of human glutaryl-CoA dehydrogenase with and without an alternate substrate: structural bases of dehydrogenation and decarboxylation reactions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Long-term follow-up, neurological outcome and survival rate in 28 Nordic patients with glutaric aciduria type 1.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Neuroimaging findings in glutaric aciduria type 1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Type I glutaric aciduria, part 1: natural history of 77 patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Magnetic resonance imaging of the brain in glutaric acidemia type I: a review of the literature and a report of four new cases with attention to the basal ganglia and imaging technique

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Emergency management of inherited metabolic diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Age at symptom onset predicts severity of motor impairment and clinical outcome of glutaric acidemia type 1.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Mutation analysis in glutaric aciduria type I.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type I

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Glutaric aciduria type I: ultrasonographic demonstration of early signs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Neonatal screening for inborn errors of metabolism: cost, yield and outcome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Protein requirements of infants and children

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Nutrition support for glutaric acidemia type I.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

CT and MR of the brain in glutaric acidemia type I: a review of 59 published cases and a report of 5 new patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

L-carnitine treatment in glutaric aciduria type I.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Intercurrent illness in inborn errors of intermediary metabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria). Experience with diet, riboflavin, and GABA analogue

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Adult onset glutaric aciduria type I presenting with a leukoencephalopathy.

5 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric acidemia type 1 in patients of Lumbee heritage from North Carolina

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria type I: outcome following detection by newborn screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Newborn screening for glutaric aciduria type I in Victoria: treatment and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic options

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Seizures versus dystonia in encephalopathic crisis of glutaric aciduria type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria type I: value of diffusion-weighted magnetic resonance imaging for diagnosing acute striatal necrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaryl-CoA dehydrogenase deficiency and newborn screening: retrospective analysis of a low excretor provides further evidence that some cases may be missed

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Outcome of three cases of untreated maternal glutaric aciduria type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria type 1 and nonaccidental head injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Breastfeeding experience in inborn errors of metabolism other than phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Novel mutation and prenatal sonographic findings of glutaric aciduria (type I) in two Taiwanese families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria type 1 presenting with epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Prenatal cerebral ultrasound and MRI findings in glutaric aciduria Type 1: a de novo case

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Rating scales for dystonia in cerebral palsy: reliability and validity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria and suspected child abuse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Pseudo-glutarylcarnitinaemia in medium-chain acyl-CoA dehydrogenase deficiency detected by tandem mass spectrometry newborn screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric aciduria type I: outcome in the Republic of Ireland

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Diffusion-weighted MR imaging and MR spectroscopy in glutaric aciduria type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Bilateral pallidotomy for severe dystonia in an 18-month-old child with glutaric aciduria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Pilot study on trihexyphenidyl in the treatment of dystonia in children with cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Glutaric acidemia, type I, missed by newborn screening in an infant with dystonia following promethazine administration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

L-carnitine in inborn errors of metabolism: what is the evidence?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Screening newborns for inborn errors of metabolism by tandem mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9289-5

Therapeutic modulation of cerebral l-lysine metabolism in a mouse model for glutaric aciduria type I

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Protein and amino acid requirements in human nutrition.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Riboflavin-responsive glutaryl CoA dehydrogenase deficiency

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

A different approach to breast-feeding of the infant with phenylketonuria

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

More rapid method for simultaneous measurement of tryptophan and kynurenine by HPLC.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109243

Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I

28 October 2018

1 reference

12 December 2020

A case of glutaric acidemia type I: effect of riboflavin and carnitine

1 reference

12 December 2020

Bilateral arachnoid cysts of the temporal fossa in four children with glutaric aciduria type I

1 reference

12 December 2020

Breast feeding in IMD

1 reference

12 December 2020

Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

1 reference

12 December 2020

Children with bilateral temporal arachnoid cysts may have glutaric aciduria type 1 (GAT1); operation without knowing that may be harmful

1 reference

12 December 2020

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)

1 reference

12 December 2020

Bilateral arachnoid cysts of the sylvian region in female siblings with glutaric aciduria type I. Report of two cases

1 reference

12 December 2020

A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I

1 reference

12 December 2020

Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Subdural haematoma in a child with glutaric aciduria type I

1 reference

12 December 2020

Reliability and responsiveness of the Barry-Albright Dystonia Scale

1 reference

12 December 2020

Glutaric aciduria; A “new” disorder of amino acid metabolism

1 reference

12 December 2020

High-performance liquid-chromatographic analysis for tryptophan in serum

1 reference

12 December 2020

10.1007/S10545-011-9289-5

Identifiers

DOI

1 reference

Dimensions Publication ID

31 July 2017

0 references

1 reference

31 July 2017

1 reference