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JIMD Podcasts is home to the Journal of Inherited Metabolic Disease podcast and the JIMD Shortcast. We're also proud to showcase Metabolic Mysteries and the new Footprints in IMD podcast.

JIMD Podcasts Journal of Inherited Metabolic Disease

    • Vetenskap

JIMD Podcasts is home to the Journal of Inherited Metabolic Disease podcast and the JIMD Shortcast. We're also proud to showcase Metabolic Mysteries and the new Footprints in IMD podcast.

    Footprints of IMD: the IEMbase and Cerebral Palsy... with Gabriella Horvath

    Footprints of IMD: the IEMbase and Cerebral Palsy... with Gabriella Horvath

    Eva Morava discusses the creation of the IEMbase with Nenad Blau before the pair welcome Gabriella Horvath to discuss metabolic mimics of cerebral palsy in the first episode of the footprints series.

    Read the referenced paper here: https://doi.org/10.1016/j.ymgme.2021.03.008

    Find all the metabolic mimics of CP at http://iembase.org/gamuts/store/docs/Metabolic_mimics_of_cerebral_palsy.pdf

    • 18 min
    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 min
    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 min
    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 min
    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 min
    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 min

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