Orphanet Journal of Rare Diseases

Published by: Biomed Central Ltd  

People

  1. Boelens
    Boelens
  2. Abdel-Wahab
    Abdel-Wahab
  3. Diamond
    Diamond
  4. Hatzoglou
    Hatzoglou
  5. Healey
    Healey
  6. Holodny
    Holodny
  7. Rampal
    Rampal

Groups

  1. Tow Center for Developmental Oncology (TCDO) (3)
  2. Pediatrics, Department of (2)
  3. Stem Cell Transplantation and Cellular Therapy Service (2)
  4. Adult Leukemia (1)
  5. Center for Hematologic Malignancies (1)
  6. Department of Medicine (1)
  7. Early Drug Development Service (1)
  8. Executive Committee, Center for Hematologic Malignancies (1)
  9. GSK Faculty (1)
  10. Hematologic Malignancies, Division of (1)
Search Within
  1. "Journal article"
Formats
  1. Journal Article (4)
Groups
  1. Tow Center for Developmental Oncology (TCDO) (3)
  2. Pediatrics, Department of (2)
  3. Stem Cell Transplantation and Cellular Therapy Service (2)
  4. Adult Leukemia (1)
  5. Center for Hematologic Malignancies (1)
  6. Department of Medicine (1)

More Groups

People
  1. Jaap Jan Boelens (2)
  2. Andrei Holodny (1)
  3. David Hyman (1)
  4. Eli Diamond (1)
  5. John Healey (1)
  6. Omar Abdel-Wahab (1)

More People

Years
  1. 2024 (1)
  2. 2022 (1)
  3. 2021 (1)
  4. 2016 (1)
Publishers
  1. Biomed Central Ltd (4)

Results (4)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries
    Journal Article

    Schoenmakers, D. H.; Mochel, F.; Adang, L. A.; Boelens, J. J.; Calbi, V.; Eklund, E. A.; Grønborg, S. W.; Fumagalli, F.; Groeschel, S.; Lindemans, C.; more...
    Orphanet Journal of Rare Diseases (2024)

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  • Modified Delphi procedure-based expert consensus on endpoints for an international disease registry for metachromatic leukodystrophy: The European Metachromatic Leukodystrophy initiative (MLDi)
    Journal Article

    Schoenmakers, D. H.; Beerepoot, S.; van den Berg, S.; Adang, L.; Bley, A.; Boelens, J. J.; Fumagalli, F.; Goettsch, W. G.; Grønborg, S.; Groeschel, S.; more...
    Orphanet Journal of Rare Diseases (2022)

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  • The diffuse-type tenosynovial giant cell tumor (dt-TGCT) patient journey: A prospective multicenter study
    Journal Article

    Bernthal, N. M.; Spierenburg, G.; Healey, J. H.; Palmerini, E.; Bauer, S.; Topp Study Group; Gelderblom, H.; Staals, E. L.; Lopez-Bastida, J.; Fronk, E. M.; more...
    Orphanet Journal of Rare Diseases (2021)

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  • Diffuse reduction of cerebral grey matter volumes in Erdheim-Chester disease
    Journal Article

    Diamond, E. L.; Hatzoglou, V.; Patel, S.; Abdel-Wahab, O.; Rampal, R.; Hyman, D. M.; Holodny, A. I.; Raj, A.
    Orphanet Journal of Rare Diseases (2016)

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    • Orphanet Journal of Rare Diseases – authorized name for:

    Name ISSN / ISBN Publisher
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 1750-1172 Unknown
    Orphanet Journal of Rare Diseases 17501172 2022, The Author(s)
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 17501172 The Author(s) 2024
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 17501172 Unknown
    Orphanet Journal of Rare Diseases 17501172 The Author(s) 2025
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd
    Orphanet Journal of Rare Diseases 1750-1172 Biomed Central Ltd