Hereditary Coproporphyria

Hereditary Coproporphyria is a rare autosomal dominant metabolic disorder of the heme biosynthesis pathway characterized by a partial deficiency of coproporphyrinogen oxidase, leading to the accumulation and excretion of coproporphyrin III and clinical manifestations such as neurovisceral attacks and photosensitivity.

99

Publications

4K

Citations

317

Authors

129

Institutions

Publications per year

2017–2026

2

Variants

Hcp

Authors

317

  1. YN
    Y Nordmann

    Hôpital Louis-Mourier, France

    10 publications · 495 citations

    10

    h-index

  2. MM
    Michael Moore

    Stobhill Hospital, United Kingdom

    8 publications · 348 citations

    8

    h-index

  3. JD
    Jean‐Charles Deybach

    Hôpital Louis-Mourier, France

    8 publications · 592 citations

    8

    h-index

  4. BG
    Bernard Grandchamp

    Inserm, France

    8 publications · 582 citations

    8

    h-index

  5. AG
    A. Goldberg

    Western Infirmary, United Kingdom

    7 publications · 338 citations

    7

    h-index

1–5 of 317

Venues

  1. Archives of Dermatology

    8 publications · 345 citations

    8

    h-index

  2. PubMed

    Repository · 6 publications · 126 citations

    6

    h-index

  3. Journal of Inherited Metabolic Disease

    JIMD · 5 publications · 389 citations

    5

    h-index

  4. Human Molecular Genetics

    5 publications · 269 citations

    5

    h-index

  5. New England Journal of Medicine

    NEJM · 4 publications · 267 citations

    4

    h-index

1–5