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Dive into the research topics where Julio César Salas Alanís is active.

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Featured researches published by Julio César Salas Alanís.


Anais Brasileiros De Dermatologia | 2015

Coccidioidomycosis and the skin: a comprehensive review

Sandra Cecilia García García; Julio César Salas Alanís; Minerva Gómez Flores; Sergio E González González; Lucio Vera Cabrera; Jorge Ocampo Candiani

Coccidioidomycosis is a highly prevalent disease in the Western hemisphere. It is considered one of the most virulent primary fungal infections. Coccidioides species live in arid and semi-arid regions, causing mainly pulmonary infection through inhalation of arthroconidia although many other organs can be affected. Primary inoculation is rare. Since the first case of coccidioidomycosis was reported in 1892, the skin has been identified as an important target of this disease. Knowledge of cutaneous clinical forms of this infection is important and very useful for establishing prompt diagnosis and treatment. The purpose of this article is to provide a review of this infection, emphasizing its cutaneous manifestations, diagnostic methods and current treatment.


Journal of The American Academy of Dermatology | 2013

Measuring quality of life in epidermolysis bullosa in Mexico: Cross-cultural validation of the Hispanic version of the Quality of Life in Epidermolysis Bullosa questionnaire

John W. Frew; Rodrigo Cepeda Valdés; Giulio Fortuna; Dédée F. Murrell; Julio César Salas Alanís

To the Editor: The Quality of Life in Epidermolysis Bullosa (QOLEB) questionnaire is a valid and reliable epidermolysis bullosa (EB)-specific quality-ofLife (QOL) measurement tool. It aims to reflect clinically significant changes in disease status and well-being as opposed to purely physical attributes such as new blister formation, which may improve with interventions but have no clinically significant impact upon function, emotional status, or survival. Cross-cultural validation of questionnaires enable the use of questionnaires in international multicenter clinical research, allow comparison of burden of disease, and encourage much-needed funding, particularly in regions or population groups where health care is not widely accessible or affordable. This study aims to develop a valid, culturally appropriate translation of the QOLEB questionnaire for use in Hispanic populations. The validated, guideline-based methodology of this study comprised 5 separate steps: ethical approval, forward and backward translation, expert committee review, pretesting, and statistical analysis. The final Hispanic translation of the QOLEB questionnaire is available directly from the corresponding author. Patient burden was low, the average time being 4.6 minutes to complete the questionnaire. Of patients, 100% completed the QOLEB questionnaire and the accompanying Skindex-29 questionnaire. Four patients only partially completed the ShortForm 36 (SF-36) questionnaire and these incomplete questionnaires were excluded from analysis.


Anais Brasileiros De Dermatologia | 2016

Cutaneous graft-versus-host disease after hematopoietic stem cell transplant - a review.

Cesar Daniel Villarreal Villarreal; Julio César Salas Alanís; José Carlos Jaime Pérez; Jorge Ocampo Candiani

Graft-versus-host disease (GVHD) is a major complication of allogeneic hematopoietic stem cell transplants (allo-HSCT) associated with significant morbidity and mortality. The earliest and most common manifestation is cutaneous graft-versus-host disease. This review focuses on the pathophysiology, clinical features, prevention and treatment of cutaneous graft-versus-host disease. We discuss various insights into the diseases mechanisms and the different treatments for acute and chronic skin graft-versus-host disease.


Archive | 2015

Monitoring to Prevent Complications: Anemia, Infections, Osteopenia, Failure to Thrive, Renal Disease, Squamous Cell Carcinoma, Cardiomyopathy

Irene Lara-Corrales; Anna L. Bruckner; Julio César Salas Alanís; Jemma E. Mellerio; Francis Pallison; Dédée F. Murrell

There have been many comorbidities identified in EB patients; the most commonly seen are anemia, infections, osteopenia, failure to thrive, renal disease, squamous cell carcinoma, and cardiomyopathy. Physicians caring for EB patients should be aware of all these complications, initially to prevent some of these from developing by establishing preventive measures and secondly to monitor closely and identify early signs and symptoms of these complications for better clinical outcomes.


Gaceta Medica De Mexico | 2014

Enfermedad de Lyme: actualizaciones

Martha Elena García Meléndez; Cassandra Michele Skinner Taylor; Julio César Salas Alanís; Jorge Ocampo Candiani


Revista De Investigacion Clinica | 2014

BRAF mutations among patients from the Northeast of México with malignant melanoma

Oscar Raúl Fajardo Ramírez; Julio César Salas Alanís; Eduardo Guzmán Huerta; Ubaldo Martínez; Alvaro Barbosa; Sean Scott; José A Hernández Hernández; Luis Villela


Archive | 2017

DESIGN AND USE OF PROBES TO DETECT AND DIAGNOSE THE RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA.

Julio César Salas Alanís; María Guadalupe Moreno Treviño; Rafael Baltazar Reyes León Cachón; Oscar Raúl Fajardo Ramírez


Gaceta Medica De Mexico | 2016

Síndrome de Sjögren (SS), revisión del tema y saliva como método diagnóstico

Janett Carmen Luzmila Riega Torres; Antonio Jaime Villarreal Gonzalez; Luis Angel Ceceñas Falcón; Julio César Salas Alanís


Dermatología cosmética, médica y quirúrgica | 2016

La era del diagnóstico molecular para las enfermedades hereditarias de la piel

Francisco co Guajardo; Julio César Salas Alanís; John A. McGrath


Dermatología cosmética, médica y quirúrgica | 2016

Fístula dental intraoral: reporte de caso

juan de Dios Garza Gallardo; Alfredo Salinas Noyola; Julio César Salas Alanís; Sonia Toussaint Caire

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Jorge Ocampo Candiani

Universidad Autónoma de Nuevo León

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Dédée F. Murrell

University of New South Wales

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Anna L. Bruckner

University of Colorado Denver

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Giulio Fortuna

Carolinas Medical Center

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