Ruhong Cheng

1665 Kongjiang Road
Shanghai, 200092, China

Last Updated: 09/26/2026

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Found 35 publications

Arcuate Proliferative Red Nodules on the Scalp: A Case of Syringocystadenoma Papilliferum.

Arcuate Proliferative Red Nodules on the Scalp: A Case of Syringocystadenoma Papilliferum.

Journal: International journal of dermatology

Published: December 17, 2025

Widespread erythematous scaly eruption in an infant with phenylketonuria.

Widespread erythematous scaly eruption in an infant with phenylketonuria.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: July 28, 2025

Case Report: Pediatric palisaded neutrophilic and granulomatous dermatitis without systemic diseases treated with sulfasalazine.

Case Report: Pediatric palisaded neutrophilic and granulomatous dermatitis without systemic diseases treated with sulfasalazine.

Journal: Frontiers in medicine

Published: July 21, 2025

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report.

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report.

Journal: Frontiers in immunology

Published: April 18, 2024

Successful treatment of infantile refractory bullous pemphigoid with baricitinib.

Successful treatment of infantile refractory bullous pemphigoid with baricitinib.

Journal: The Australasian journal of dermatology

Published: March 08, 2024

ADAM17 variant causes hair loss via ubiquitin ligase TRIM47-mediated degradation.

ADAM17 variant causes hair loss via ubiquitin ligase TRIM47-mediated degradation.

Journal: JCI insight

Published: November 14, 2023

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

Journal: EMBO molecular medicine

Published: September 02, 2021

The first case of Chinese phacomatosis pigmentokeratotica diagnosed by a missense HRAS mosaicism.

The first case of Chinese phacomatosis pigmentokeratotica diagnosed by a missense HRAS mosaicism.

Journal: The Journal of dermatology

Published: August 10, 2021

Factors associated with persistence of early-onset atopic dermatitis up to the age of 12 years: a prospective cohort study in China.

Factors associated with persistence of early-onset atopic dermatitis up to the age of 12 years: a prospective cohort study in China.

Journal: European journal of dermatology : EJD

Published: July 26, 2021

Deep-intronic and frameshift DSG1 variants associated with atypical severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome in a Chinese family.

Deep-intronic and frameshift DSG1 variants associated with atypical severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome in a Chinese family.

Journal: European journal of dermatology : EJD

Published: April 05, 2021

Additional causal SNRPE mutations in hereditary hypotrichosis simplex.

Additional causal SNRPE mutations in hereditary hypotrichosis simplex.

Journal: The British journal of dermatology

Published: December 14, 2020

The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra-Deep Sequence.

The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra-Deep Sequence.

Journal: Molecular genetics & genomic medicine

Published: April 14, 2020

Showing 1-12 of 35

Last Updated: 09/26/2026