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Capillary malformations: a classification using specific names for specific skin disorders

Journal of the European Academy of Dermatology and Venereology, 2015-12, Vol.29 (12), p.2295-2305

Happle, R.

2015

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White lentiginosis of Grosshans: which mode of inheritance?

Journal of the European Academy of Dermatology and Venereology, 2022-04, Vol.36 (4), p.e290-e291

Happle, R.

2022

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Hornstein–Knickenberg syndrome vs. Birt–Hogg–Dubé syndrome: a critical review of an unjustified designation

Journal of the European Academy of Dermatology and Venereology, 2020-04, Vol.34 (4), p.885-887

Happle, R.

2020

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Korean gender differences in hidradenitis suppuratva: nature or nurture?

Journal of the European Academy of Dermatology and Venereology, 2019-07, Vol.33 (7), p.e256-e256

Happle, R.

2019

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The concept of type 2 segmental mosaicism, expanding from dermatology to general medicine

Journal of the European Academy of Dermatology and Venereology, 2018-07, Vol.32 (7), p.1075-1088

Happle, R.

2018

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Diphencyprone: the career of a strong contact sensitizer in clinical dermatology

Journal of the European Academy of Dermatology and Venereology, 2019-11, Vol.33 (11), p.2012-2013

Happle, R.

2019

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Lessons to be learned from type 1 segmental Gorlin syndrome

British journal of dermatology (1951), 2017-07, Vol.177 (1), p.20-21

Happle, R.

2017

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The Bork–Baykal phenomenon: a revised eponymic designation for the sparing of nipple and areola in large melanocytic nevi involving the breast

Journal of the European Academy of Dermatology and Venereology, 2017-04, Vol.31 (4), p.e214-e214

Happle, R.

2017

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The Baykal phenomenon: large congenital melanocytic nevi involving the breast tend to spare the nipple and areola

Journal of the European Academy of Dermatology and Venereology, 2016-12, Vol.30 (12), p.e181-e183

Happle, R.

2016

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Sparing of the nipple‐areola complex in segmental dermal melanocytosis involving the breast

Journal of the European Academy of Dermatology and Venereology, 2017-01, Vol.31 (1), p.e26-e27

Happle, R.

2017

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An unusual linear hypermelanosis reflecting lyonization in women with Börjeson-Forssman-Lehmann syndrome

Journal of the European Academy of Dermatology and Venereology, 2016-02, Vol.30 (2), p.323-324

Happle, R.

2016

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Superimposed mosaicism in tuberous sclerosis complex: a key to understanding all of the manifold manifestations?

Journal of the European Academy of Dermatology and Venereology, 2020-11, Vol.34 (11), p.2511-2517

2020

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Mosaicism in Human Skin: Understanding Nevi, Nevoid Skin Disorders, and Cutaneous Neoplasia

Second revised and updated edition, 2022

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Koebner's sheep in Wolf's clothing: does the isotopic response exist as a distinct phenomenon?

Journal of the European Academy of Dermatology and Venereology, 2018-04, Vol.32 (4), p.542-543

2018

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A proposed new category of cutaneous segmental mosaicism: Isolated segmental biallelic monoclonal mosaicism

Journal of the European Academy of Dermatology and Venereology, 2021-04, Vol.35 (4), p.e265-e267

2021

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Happle-Tinschert syndrome can be caused by a mosaic SMO mutation and is suggested to be a variant of Curry-Jones syndrome

British journal of dermatology (1951), 2016-11, Vol.175 (5), p.1108-1108

2016

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Superimposed segmental dermatosis papulosa nigra

Clinical and experimental dermatology, 2020-06, Vol.45 (4), p.521-523

2020

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Two examples of Renbök phenomenon in dermatophytosis sparing congenital nevi

Journal of the European Academy of Dermatology and Venereology, 2021-10, Vol.35 (10), p.e695-e697

2021

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What is paradominant inheritance?

Journal of medical genetics, 2009-09, Vol.46 (9), p.648-648

Happle, R

2009

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Type 2 segmental Cowden disease vs. Proteus syndrome

British journal of dermatology (1951), 2007-05, Vol.156 (5), p.1089-1090

Happle, R.

2007

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Porokeratosis palmaris, plantaris et disseminata vs. porokeratosis of Mibelli

British journal of dermatology (1951), 2012-03, Vol.166 (3), p.681-682

Happle, R.

2012

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Flag‐like hypermelanosis with superimposed lichen sclerosus et atrophicus: an unusual Koebner phenomenon?

Journal of the European Academy of Dermatology and Venereology, 2021-02, Vol.35 (2), p.e147-e149

2021

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Answer to Tatu AL, Nwabudike LC: Koebner's sheep in Wolf's clothing – does the isotopic response exist as a distinct phenomenon?

Journal of the European Academy of Dermatology and Venereology, 2018-08, Vol.32 (8), p.e337-e337

2018

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Loss of heterozygosity in human skin

Journal of the American Academy of Dermatology, 1999-08, Vol.41 (2), p.143-161

Happle, Rudolf

1999

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Segmental hypomelanosis and hypermelanosis arranged in a checkerboard pattern are distinct naevi: flag-like hypomelanotic naevus and flag-like hypermelanotic naevus

Journal of the European Academy of Dermatology and Venereology, 2015-11, Vol.29 (11), p.2088-2099

2015

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Capillary malformations: a classification using specific names for specific skin disorders

White lentiginosis of Grosshans: which mode of inheritance?

Hornstein–Knickenberg syndrome vs. Birt–Hogg–Dubé syndrome: a critical review of an unjustified designation

Korean gender differences in hidradenitis suppuratva: nature or nurture?

The concept of type 2 segmental mosaicism, expanding from dermatology to general medicine

Diphencyprone: the career of a strong contact sensitizer in clinical dermatology

Lessons to be learned from type 1 segmental Gorlin syndrome

The Bork–Baykal phenomenon: a revised eponymic designation for the sparing of nipple and areola in large melanocytic nevi involving the breast

The Baykal phenomenon: large congenital melanocytic nevi involving the breast tend to spare the nipple and areola

Sparing of the nipple‐areola complex in segmental dermal melanocytosis involving the breast

An unusual linear hypermelanosis reflecting lyonization in women with Börjeson-Forssman-Lehmann syndrome

Superimposed mosaicism in tuberous sclerosis complex: a key to understanding all of the manifold manifestations?

Mosaicism in Human Skin: Understanding Nevi, Nevoid Skin Disorders, and Cutaneous Neoplasia

Koebner's sheep in Wolf's clothing: does the isotopic response exist as a distinct phenomenon?

A proposed new category of cutaneous segmental mosaicism: Isolated segmental biallelic monoclonal mosaicism

Happle-Tinschert syndrome can be caused by a mosaic SMO mutation and is suggested to be a variant of Curry-Jones syndrome

Superimposed segmental dermatosis papulosa nigra

Two examples of Renbök phenomenon in dermatophytosis sparing congenital nevi

What is paradominant inheritance?

Type 2 segmental Cowden disease vs. Proteus syndrome

Porokeratosis palmaris, plantaris et disseminata vs. porokeratosis of Mibelli

Flag‐like hypermelanosis with superimposed lichen sclerosus et atrophicus: an unusual Koebner phenomenon?

Answer to Tatu AL, Nwabudike LC: Koebner's sheep in Wolf's clothing – does the isotopic response exist as a distinct phenomenon?

Loss of heterozygosity in human skin

Segmental hypomelanosis and hypermelanosis arranged in a checkerboard pattern are distinct naevi: flag-like hypomelanotic naevus and flag-like hypermelanotic naevus

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