Publications by authors named "Happle Rudolf"

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

JAAD Case Rep· June 2024

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Pioneers in Dermatology and Venereology: An interview with Professor Rudolf Happle.
Rudolf Happle

J Eur Acad Dermatol Venereol· May 2024

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What is in a name-Perifollicular fibroma or fibrofolliculoma?
Eckart Haneke, Rudolf Happle

J Cutan Pathol· February 2024

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Incontinentia pigmenti Stage 1 is not simply vesiculo-bullous but vesiculo-pustular.
Tubanur Çetinarslan, Regina Fölster-Holst, Dirk Van Gysel, Matthias Buchner, Rudolf Happle

Pediatr Dermatol· January 2024

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Phacomatosis spilosebacea: A new name for a distinctive binary genodermatosis.
Daniele Torchia, Rudolf Happle

J Am Acad Dermatol· October 2023

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Superimposed Mosaicism in the Form of Extremely Extended Segmental Plexiform Neurofibroma Caused by a Novel Pathogenic Variant in the NF1 Gene.
Klára Veres, Judit Bene, Kinga Hadzsiev, Miklós Garami, Sára Pálla, Rudolf Happle

Int J Mol Sci· July 2023

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PTPN11 Mosaicism Causes a Spectrum of Pigmentary and Vascular Neurocutaneous Disorders and Predisposes to Melanoma.
Satyamaanasa Polubothu, Nicole Bender, Siobhan Muthiah, Davide Zecchin, Charalambos Demetriou, Rudolf Happle

J Invest Dermatol· June 2023

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Autosomal dominant genodermatoses in adults being heralded by superimposed skin lesions in children.
Rudolf Happle

Am J Med Genet C Semin Med Genet· June 2023

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[Update on nevi and nevoid skin disorders].
Rudolf Happle

Dermatologie (Heidelb)· May 2023

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Superimposed mosaicism in cutaneous sarcoidosis: A hypothesis.
Rudolf Happle, Martin Wetzke

Am J Med Genet A· March 2023

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Autosomal dominant inheritance with sex-limited manifestation: An unusual mode of transmission in humans and animals.
Rudolf Happle, Kilian Eyerich

Am J Med Genet A· March 2023

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The Bork-Baykal phenomenon and umbilical sparing in large and giant congenital melanocytic nevus: A 21-case series.
Ethel Nunes de Sousa Fernandes, Rudolf Happle, Bernardo Gontijo, Joao Renato Vianna Gontijo, Flávia Vasques Bittencourt

J Eur Acad Dermatol Venereol· January 2023

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Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations.
Claudia Schuart, Andrea Bassi, Friedrich Kapp, Ilse Wieland, Angelica Pagliazzi, Rudolf Happle

Eur J Med Genet· May 2022

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Three novel pathogenic NEK9 variants in patients with nevus comedonicus: A case series.
Hazem A Juratli, Sabine Jägle, Martin Theiler, Dario Didona, Rudolf Happle

J Am Acad Dermatol· April 2022

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An unusual Case of Segmental Hailey-Hailey Disease Developing in a 1.5-Year-Old Child: A Proposed Diagnosis.
Rudolf Happle

Indian J Dermatol· January 2022

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Conradi-Hünermann-Happle syndrome with minimal signs.
Manuel Agud-Dios, Nelmar Valentina Ortiz Cabrera, Lucero Noguera-Morel, Angela Hernández-Martín, Isabel Colmenero, Rudolf Happle

Pediatr Dermatol· November 2021

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

Acta Derm Venereol· August 2021

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Can Waardenburg syndrome type 2 be explained by epigenetic mosaicism?
Rudolf Happle

Am J Med Genet A· April 2021

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Progressive Osseous Heteroplasia is not an Autosomal Dominant Trait but Reflects Superimposed Mosaicism in Different Inactivation Disorders.
Rudolf Happle

Indian Dermatol Online J· March 2021

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Porokeratosis Plantaris, Palmaris et Disseminata Caused by Con- genital Pathogenic Variants in the MVD Gene and Loss of Hetero-zygosity in Affected Skin.
Sabine Jägle, Hazem A Juratli, Geoffroy Hickman, Kira Süssmuth, Maria C Boente, Rudolf Happle

Acta Derm Venereol· February 2021

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The PORCN non-Goltz spectrum (PONGOS): A new group of genetic disorders.
Rudolf Happle

Am J Med Genet A· January 2021

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A six-attribute classification of genetic mosaicism.
Víctor Martínez-Glez, Jair Tenorio, Julián Nevado, Gema Gordo, Lara Rodríguez-Laguna, Rudolf Happle

Genet Med· November 2020

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Verrucous hyperkeratosis with predominant involvement of the left side of the body and concomitant onychodystrophy in a 17-year-old girl.
Schulte Armina, Traupe Heiko, Happle Rudolf, Fischer Judith, Kiritsi Dimitra

J Dtsch Dermatol Ges· September 2020

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[Not Available].
Armina Schulte, Heiko Traupe, Rudolf Happle, Judith Fischer, Dimitra Kiritsi

J Dtsch Dermatol Ges· September 2020

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Papular nevus spilus syndrome: a further three cases.
Daniele Torchia, Rudolf Happle

Eur J Dermatol· August 2020

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