164本のエピソード

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.

JIMD Podcasts Journal of Inherited Metabolic Disease

    • 科学

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.

    Pregnancy in phenylketonuria

    Pregnancy in phenylketonuria

    Dr Maja Risager Nielsen and Dr François Feillet discuss pregnancy in PKU and two different papers looking at the outcomes in pregnancies with and without BH4 treatment.

    The impact of phenylalanine levels during pregnancy on birth weight and later development in children born to women with phenylketonuria
    Maja Risager Nielsen, et al
    https://doi.org/10.1002/jimd.12600

    Efficacy and safety of sapropterin before and during pregnancy: Final analysis of the Kuvan® Adult Maternal Paediatric European Registry (KAMPER) maternal and Phenylketonuria Developmental Outcomes and Safety (PKUDOS) PKU-MOMs sub-registries
    François Feillet, et al
    https://doi.org/10.1002/jimd.12724

    • 30分
    Acute liver failure? Think metabolic

    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

    • 10分
    Aicardi-Goutières syndrome

    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

    • 32分
    Shortcast: Pediatric palliative care for IMD: 20-year survey of outpatients at a Brazilian hospital

    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

    • 4分
    Pregnancy in Urea Cycle Disorders

    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

    • 17分
    Shortcast: Clinical experience with glycerol phenylbutyrate in 20 patients with UCDs

    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

    • 9分

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