Showing 1 - 14 results of 14 for search 'Rudolf Happle', query time: 0.10s Refine Results
  1. 1
    An unusual case of segmental hailey-Hailey disease developing in a 1.5-year-old child: A proposed diagnosis

    An unusual case of segmental hailey-Hailey disease developing in a 1.5-year-old child: A proposed diagnosis by Rudolf Happle

    Published 2022
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  2. 2
    RASA1 Variants in Capillary Malformations of Children: A Comment to Maruani A et al.

    RASA1 Variants in Capillary Malformations of Children: A Comment to Maruani A et al. by Rudolf Happle

    Published 2018
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  3. 3
    Progressive osseous heteroplasia is not an autosomal dominant trait but reflects superimposed mosaicism in different GNAS inactivation disorders

    Progressive osseous heteroplasia is not an autosomal dominant trait but reflects superimposed mosaicism in different GNAS inactivation disorders by Rudolf Happle

    Published 2021
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  4. 4
    An Early Description of a "Human Mosaic" Involving the Skin: A Story from 1945

    An Early Description of a "Human Mosaic" Involving the Skin: A Story from 1945 by Rudolf Happle

    Published 2020
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  5. 5
    Skin Lesions Suggesting Type 2 Segmental Mosaicism in Noonan Syndrome

    Skin Lesions Suggesting Type 2 Segmental Mosaicism in Noonan Syndrome by Rudolf Happle

    Published 2018
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  6. 6
    More about Zlotnikov, the Man Who Explained Blaschko's Lines to be a Mosaic

    More about Zlotnikov, the Man Who Explained Blaschko's Lines to be a Mosaic by Rudolf Happle, Eckart Haneke

    Published 2021
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  7. 7
    Macrodactyly with skin hypertrophy: a minimal form of the Proteus syndrome Macrodactilia com hipertrofia da pele: uma forma mínima da síndrome de Proteu

    Macrodactyly with skin hypertrophy: a minimal form of the Proteus syndrome Macrodactilia com hipertrofia da pele: uma forma mínima da síndrome de Proteu by Hiram Larangeira de Almeida Jr, Roberto Coswig Fiss, Rudolf Happle

    Published 2011
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  8. 8
    A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert Syndrome

    A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert Syndrome by Martin Zenker, Sigrid Tinschert, Ilse Wieland, Denny Schanze, Rudolf Happle

    Published 2018
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  9. 9
    Phacomatosis cesioflammea with cutis marmorata-like lesions and unusual extracutaneous abnormalities: Is it a distinct disorder?

    Phacomatosis cesioflammea with cutis marmorata-like lesions and unusual extracutaneous abnormalities: Is it a distinct disorder? by Shyam B Verma, Hitesh K Desai, Vishal N Shah, Rudolf Happle

    Published 2017
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  10. 10
    Superimposed segmental manifestation of juvenile amyopathic dermatomyositis in a 9-year-old boy

    Superimposed segmental manifestation of juvenile amyopathic dermatomyositis in a 9-year-old boy by Isil Bulur, Hilal Kaya Erdogan, Zeynep Nurhan Saracoglu, Rudolf Happle, Funda Canaz

    Published 2017
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  11. 11
    A Family with Palmar and Plantar Hyperkeratosis: A Quiz

    A Family with Palmar and Plantar Hyperkeratosis: A Quiz by Hazem A. Juratli, Sabine Jägle, Rudolf Happle, Pinar Avci, Dario Didona, Judith Fischer

    Published 2020
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  12. 12
    A Case of Linear Porokeratosis Superimposed on Disseminated Superficial Actinic Porokeratosis

    A Case of Linear Porokeratosis Superimposed on Disseminated Superficial Actinic Porokeratosis by Rebecca Löhrer, Aysegül Neumann-Acikel, Rüdiger Eming, Karin Hartmann, Heinrich Rasokat, Thomas Krieg, Rudolf Happle, Sabine Eming

    Published 2010
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  13. 13
    Pseudodidymosis aplasticosebacea: Binary phenomenon of congenital aplasia cutis congenita and nevus sebaceus

    Pseudodidymosis aplasticosebacea: Binary phenomenon of congenital aplasia cutis congenita and nevus sebaceus by Retno Danarti, MD, Rudolf Happle, MD, Ani Rifko, MD, Agnes Rosarina Prita Sari, MSc, WenChieh Chen, MD

    Published 2024
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  14. 14
    Porokeratosis Plantaris, Palmaris et Disseminata Caused by Con- genital Pathogenic Variants in the MVD Gene and Loss of Hetero­zygosity in Affected Skin

    Porokeratosis Plantaris, Palmaris et Disseminata Caused by Con- genital Pathogenic Variants in the MVD Gene and Loss of Hetero­zygosity in Affected Skin by Sabine Jägle, Hazem A. Juratli, Geoffroy Hickman, Kira Süssmuth, Maria C. Boente, Julia Kopp, Peter Kirchmeier, Andreas Zimmer, Rudolf Happle, Emmanuelle Bourrat, Henning Hamm, Judith Fischer

    Published 2021
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