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JIMD Podcasts Journal of Inherited Metabolic Disease
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- 科學
A fortnightly podcast from the Journal of Inherited Metabolic Disease, where authors discuss recent publications from the journal. The podcast is intended for specialists and interested clinicians but is also intended to increase the accessibility of this work for patients and families. Supported by Wiley.
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Acute liver failure? Think metabolic
When might acute liver failure have a metabolic cause? Dr Robert Hegarty tries to answer this question and more following his recent review article on Genetic aetiologies of acute liver failure.
Genetic aetiologies of acute liver failure
Robert Hegarty, Richard J. Thompson
https://doi.org/10.1002/jimd.12733 -
Aicardi-Goutières syndrome
Dr Mariko Bennett and Dr Laura Adang discuss the precarious balance between a protective and a destructive immune response, as is seen in inborn errors in nucleotide metabolism. Our discussion focuses on the most common of these disorders: Aicardi Goutières syndrome (AGS). Sadly, despite the many gains in understanding about AGS, there remain many gaps in our understanding of this condition.
Nucleotide metabolism, leukodystrophies, and CNS pathology
Francesco Gavazzi, et al
https://doi.org/10.1002/jimd.12721 -
Shortcast: Pediatric palliative care for IMD: 20-year survey of outpatients at a Brazilian hospital
Dr Gustavo Spolador discusses the paucity of data around palliative care in Inherited Metabolic Disease and some of his own observations in a Brazilian quaternary hospital.
Pediatric palliative care for metabolic diseases: 20-year epidemiological survey of outpatients at a Brazilian quaternary hospital
Gustavo Marquezani Spolador, et al
https://doi.org/10.1002/jmd2.12417 -
Pregnancy in Urea Cycle Disorders
This episode brings together two popular podcast topics, pregnancy and urea cycle disorders. Dr Margreet Wagenmakers and Dr Karolina Stepien share recent insights from a literature review and international survey exploring the experiences of mothers with urea cycle disorders.
The management and clinical outcomes of pregnancies in women with urea cycle disorders: A review of the literature and results of an international survey
Karolina M. Stepien, et al
https://doi.org/10.1002/jimd.12695 -
Shortcast: Clinical experience with glycerol phenylbutyrate in 20 patients with UCDs
Mel McSweeney and Dr Mildrid Yeo briefly outline the approach to urea cycle disorder management and the Gt Ormond Street experience using glycerol phenylbutyrate as a nitrogen scavenger.
Clinical experience with glycerol phenylbutyrate in 20 patients with urea cycle disorders at a UK paediatric centre
Mildrid Yeo, et al
https://doi.org/10.1002/jmd2.12386 -
Liver directed gene therapy
The podcast returns to the subject of gene therapy, with Julien Baruteau, Nicola Brunetti-Pierri, and Paul Gissen discussing the potential of liver directed therapies with an emphasis on Wilson disease, Crigler-Najjar syndrome and PKU.
Liver-directed gene therapy for inherited metabolic diseases
Julien Baruteau, Nicola Brunetti-Pierri, Paul Gissen
https://doi.org/10.1002/jimd.12709