Psychiatric manifestations of treatable hereditary metabolic disorders in adults
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Psychiatric manifestations of treatable hereditary metabolic disorders in adults
Authors
Keywords
Inherited metabolic diseases, Psychiatric disorders, Neurological signs, Diagnosis, Treatment, Adults
Journal
Annals of General Psychiatry
Volume 13, Issue 1, Pages -
Publisher
Springer Nature
Online
2014-09-23
DOI
10.1186/s12991-014-0027-x
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Cerebrotendinous Xanthomatosis Presenting with Severe Externalized Disorder: Improvement After One Year of Treatment with Chenodeoxycholic Acid.
- (2017) Olivier Bonnot et al. CNS SPECTRUMS
- Treatable metabolic psychoses that go undetected: What Niemann-Pick type C can teach us
- (2012) Hans-Hermann Klünemann et al. INTERNATIONAL JOURNAL OF PSYCHIATRY IN CLINICAL PRACTICE
- Low ceruloplasmin in a patient with Niemann-Pick Type C disease
- (2012) Bernhard J. Connemann et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Recommendations for the diagnosis and management of Niemann–Pick disease type C: An update
- (2012) Marc C. Patterson et al. MOLECULAR GENETICS AND METABOLISM
- Acute Intermittent Porphyria Presenting Solely with Psychosis: A Case Report and Discussion
- (2012) Bharat Kumar PSYCHOSOMATICS
- Medical and developmental risk factors of catatonia in children and adolescents: A prospective case–control study
- (2012) Angèle Consoli et al. SCHIZOPHRENIA RESEARCH
- A review of the clinical presentation, natural history and inheritance of variegate porphyria: its implausibility as the source of the ‘Royal Malady’
- (2011) Richard J Hift et al. JOURNAL OF CLINICAL PATHOLOGY
- Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case
- (2011) Takehiro Hayashi et al. PSYCHIATRY AND CLINICAL NEUROSCIENCES
- Troubles psychiatriques et cognitifs associées aux maladies neurométaboliques
- (2011) O. Bonnot et al. REVUE NEUROLOGIQUE
- Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation
- (2010) Radan Bruha et al. LIVER INTERNATIONAL
- Miglustat in late-onset Tay-Sachs disease: a 12-month, randomized, controlled clinical study with 24 months of extended treatment
- (2009) Barbara E Shapiro et al. GENETICS IN MEDICINE
- Recommendations on the diagnosis and management of Niemann-Pick disease type C
- (2009) James E. Wraith et al. MOLECULAR GENETICS AND METABOLISM
- Miglustat in patients with Niemann-Pick disease Type C (NP-C): A multicenter observational retrospective cohort study
- (2009) M. Pineda et al. MOLECULAR GENETICS AND METABOLISM
- A revisit to the natural history of homocystinuria due to cystathionine β-synthase deficiency
- (2009) Flemming Skovby et al. MOLECULAR GENETICS AND METABOLISM
- Neuropsychiatric aspects of treated Wilson's disease
- (2009) Marina Svetel et al. PARKINSONISM & RELATED DISORDERS
- Diagnosis, symptoms, frequency and mortality of 260 patients with urea cycle disorders from a 21-year, multicentre study of acute hyperammonaemic episodes
- (2008) Marshall L Summar et al. ACTA PAEDIATRICA
- Neurocognitive testing in late-onset Tay–Sachs disease: A pilot study
- (2008) D. Elstein et al. JOURNAL OF INHERITED METABOLIC DISEASE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started