(Q26862930)

Frédéric Sedel

series ordinal

2

1 reference

language of work or name

1 reference

2014

1 reference

Annals of General Psychiatry

published in

1 reference

volume

13

1 reference

page(s)

27

1 reference

Creative Commons Attribution 4.0 International

copyright license

start time

24 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/s12991-014-0027-x

0 references

cites work

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Acute intermittent porphyria presenting solely with psychosis: a case report and discussion.

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Treatable metabolic psychoses that go undetected: what Niemann-Pick type C can teach us.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Bipolar disorders and Wilson's disease.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Recommendations for the diagnosis and management of Niemann-Pick disease type C: an update

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Schizoaffective disorder with missed diagnosis of acute porphyria: a case report and overview

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

A review of the clinical presentation, natural history and inheritance of variegate porphyria: its implausibility as the source of the 'Royal Malady'.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Diagnosis, symptoms, frequency and mortality of 260 patients with urea cycle disorders from a 21-year, multicentre study of acute hyperammonaemic episodes.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Neurocognitive testing in late-onset Tay-Sachs disease: a pilot study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

The adult form of Niemann-Pick disease type C.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Creatine deficiency syndromes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Niemann-Pick disease type C.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Psychiatric symptoms of inherited metabolic disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

The neuropsychiatry of adult-onset adrenoleukodystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

The little imitator--porphyria: a neuropsychiatric disorder

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Psychosis as the initial manifestation of adult-onset Niemann-Pick disease type C.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsiveness

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Cerebrotendinous xanthomatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Adult Forms of Metachromatic Leukodystrophy: Clinical and Biochemical Approach

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Wilson's disease: Current status

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Wilson's disease: the problem of delayed diagnosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Physical Illness Presenting as Psychiatric Disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Mismanagement of Wilson's disease as psychotic disorder

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

High prevalence of intermittent acute porphyria in a psychiatric patient population

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Adult adrenoleukodystrophy: a sporadic case?

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Molecular and clinical heterogeneity of adult GM2 gangliosidosis

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

The psychiatric presentations of Wilson's disease

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Medical and developmental risk factors of catatonia in children and adolescents: a prospective case-control study.

19 June 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Postpartum "psychosis" in mild argininosuccinate synthetase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Neuropsychiatric aspects of treated Wilson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Acute, progressive akinetic-rigid syndrome induced by neuroleptics in a case of Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Niemann-Pick disease type C in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Recommendations on the diagnosis and management of Niemann-Pick disease type C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Homocystinuria presenting as psychosis in an adolescent

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: a case report and phenotypic comparison with a previously reported case.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Late-onset Tay-Sachs disease: phenotypic characterization and genotypic correlations in 21 affected patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Miglustat in late-onset Tay-Sachs disease: a 12-month, randomized, controlled clinical study with 24 months of extended treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Eighty-six cases of Addison's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

[Psychiatric and cognitive signs associated with inborn errors of metabolism].

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12991-014-0027-X

Cerebrotendinous xanthomatosis presenting with severe externalized disorder: improvement after one year of treatment with chenodeoxycholic Acid.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4255667

Bipolar Disorder and Niemann-Pick Disease Type C

28 November 2018

1 reference

12 December 2020

Phenomenology of organic and functional psychoses and the overlap between them

1 reference

12 December 2020

Coma in a young anorexic woman

1 reference

12 December 2020

Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma

1 reference

12 December 2020

Low ceruloplasmin in a patient with Niemann-Pick Type C disease

1 reference

12 December 2020

Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation

1 reference

12 December 2020

Potential confusion of neuroleptic malignant syndrome and Wilson's disease

1 reference

12 December 2020

[Presenting psychiatric and cognitive disorders in adult neurolipidoses]

1 reference

12 December 2020

10.1186/S12991-014-0027-X

Identifiers

DOI

1 reference

Dimensions Publication ID

5034917

1028830360

0 references

5034917

1 reference

1 reference

1 reference