Suchergebnisse - "Estébanez, Andrea"

PubPharm (22)

1

Anti-Mi-2 dermatomyositis with ulcerative plaques

enthalten in: Rheumatology (Oxford, England) | 2022

von Palacios-Diaz, R. | Abril-Pérez, C. | Estebanez, A. | +3

2

Pinhole amniotic membrane for peripheral corneal defects in patients with a single eye or low vision

enthalten in: International ophthalmology | 2022

von San Román Llorens, J. | Estébanez Corrales, N. | Estébanez, A. | +2

3

Pinhole amniotic membrane for peripheral corneal defects in patients with a single eye or low vision

enthalten in: International ophthalmology | 2022

von San Román Llorens, J. | Estébanez Corrales, N. | Estébanez, A. | +2

4

Characteristics of mucocutaneous vascular malformations drawn from a decade of a multidisciplinary committee experience

enthalten in: Dermatologic therapy | 2021

von Estébanez, A. | Puche-Torres, M. | Sanchis García, J. | +6

5

Morpheaform Plaques and an Infiltrated Scar : Answer

enthalten in: The American Journal of dermatopathology | 2021

von García-Vázquez, A. | Guillen-Climent, S. | Silva, E. | +2

6

Morpheaform Plaques and an Infiltrated Scar : Challenge

enthalten in: The American Journal of dermatopathology | 2021

von García-Vázquez, A. | Guillen-Climent, S. | Silva, E. | +2

7

A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome

enthalten in: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG | 2021

von Estébanez, A. | Verdú-Amorós, J. | Silva, E. | +4

8

enthalten in: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG | 2021

von Estébanez, A. | Verdú-Amorós, J. | Silva, E. | +4

9

Pseudoxanthoma elasticum-like syndrome with coagulation deficiency associated with carotid artery hypoplasia and a novel gamma-glutamyl carboxylase gene mutation

enthalten in: International journal of dermatology | 2021

von Guillen-Climent, S. | García-Vázquez, A. | Silva, E. | +5

10

A heterozygous mutation in the RAG2 gene with cutaneous and systemic manifestations partially resembling Omenn syndrome

enthalten in: JDDG: Journal der Deutschen Dermatologischen Gesellschaft | 2021

von Estébanez, A. | Verdú‐Amorós, J. | Silva, E. | +4