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  1. 1
    The Further Adventures of Newborn Screening for Biotinidase Deficiency: Where It Is at and What We Still Need to Know

    The Further Adventures of Newborn Screening for Biotinidase Deficiency: Where It Is at and What We Still Need to Know by Barry Wolf

    Published 2016-10-01
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  2. 2
    Biotinidase deficiency is a rare, potentially treatable cause of peripheral neuropathy with or without optic neuropathy in adults

    Biotinidase deficiency is a rare, potentially treatable cause of peripheral neuropathy with or without optic neuropathy in adults by Elizabeth Kellom, Kimberly Stepien, Gregory Rice, Barry Wolf

    Published 2021-03-01
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  3. 3
    Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin Therapy

    Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin Therapy by Géraldine Van Winckel, Diana Ballhausen, Barry Wolf, Barry Wolf, Melinda Procter, Rong Mao, Rong Mao, Patricie Burda, Davide Strambo, Thierry Kuntzer, Christel Tran

    Published 2020-10-01
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  4. 4
    Neurological deficits in mice with profound biotinidase deficiency are associated with demylination and axonal degeneration

    Neurological deficits in mice with profound biotinidase deficiency are associated with demylination and axonal degeneration by Kirit Pindolia, Jieli Chen, Cisley Cardwell, Xu Cui, Michael Chopp, Barry Wolf

    Published 2012-09-01
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  5. 5
    First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children

    First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children by Danika Nadeen Senanayake, Eresha. A. Jasinge, Kirit Pindolia, Jithangi Wanigasinghe, Kristin Monaghan, Sharon F. Suchy, Sainan Wei, Subashini Jaysena, Barry Wolf

    Published 2015-03-01
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  6. 6
    Corrigendum to “First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children” [Mol. Genet. Metab. Rep. 2 (2016) 81–84]

    Corrigendum to “First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children” [Mol. Genet. Metab. Rep. 2 (2016) 81–84] by Danika Nadeen Senanayake, Eresha A. Jasinge, Kirit Pindolia, Jithangi Wanigasinghe, Kristin Monaghan, Sharon F. Suchy, Sainan Wei, Subashini Jaysena, Barry Wolf

    Published 2017-06-01
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