I. Fuentes

发表

Cells from discarded dressings differentiate chronic from acute wounds in patients with Epidermolysis Bullosa

R. Cho, B. Rebolledo-Jaramillo, M. Prisco, 2020, Scientific Reports.

Thrombospondin-1 Is a Major Activator of TGF-β Signaling in Recessive Dystrophic Epidermolysis Bullosa Fibroblasts.

J. McGrath, A. Fertala, A. South, 2019, The Journal of investigative dermatology.

APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa

E. Purdom, K. Tsai, E. Collisson, 2018, Science Translational Medicine.

Recessive dystrophic epidermolysis bullosa results in painful small fibre neuropathy

D. Bennett, F. Palisson, J. Idiaquez, 2017, Brain : a journal of neurology.

Reduced Microbial Diversity Is a Feature of Recessive Dystrophic Epidermolysis Bullosa-Involved Skin and Wounds.

A. Tay, J. Reichelt, S. Denil, 2018, The Journal of investigative dermatology.

Epithelial HMGB1 Delays Skin Wound Healing and Drives Tumor Initiation by Priming Neutrophils for NET Formation.

R. Schwabe, Y. Saeys, L. Boon, 2019, Cell reports.

Collagen VII maintains proteostasis in dermal fibroblasts by scaffolding TANGO1 cargo

J. McGrath, Mei Chen, A. South, 2022, Matrix biology : journal of the International Society for Matrix Biology.

Clinical Practice Guidelines for Epidermolysis Bullosa Laboratory Diagnosis

C. Has, G. Zambruno, M. Escámez, 2019 .

Identification of Rigosertib for the Treatment of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma

J. McGrath, A. Hovnanian, M. Prisco, 2019, Clinical Cancer Research.

Extracellular Vesicles as Biomarkers for the Detection of a Tumor Marker Gene in Epidermolysis Bullosa-Associated Squamous Cell Carcinoma.

J. Reichelt, J. Mellerio, J. Bauer, 2017, The Journal of investigative dermatology.

Collagen VII maintains proteostasis in dermal fibroblasts by scaffolding TANGO1 cargo

J. McGrath, Mei Chen, A. South, 2022, Matrix biology : journal of the International Society for Matrix Biology.

Renal involvement in epidermolysis bullosa patients: a case series study

F. Palisson, F. Cavagnaro, I. Fuentes, 2018, Journal of Pediatrics & Neonatal Care.

Ophthalmologic Approach in Epidermolysis Bullosa: A Cross-Sectional Study With Phenotype–Genotype Correlations

F. Palisson, I. Fuentes, A. Kantor, 2018, Cornea.

Longitudinal study of wound healing status and bacterial colonisation of Staphylococcus aureus and Corynebacterium diphtheriae in epidermolysis bullosa patients

Karen Y. Oróstica, B. Rebolledo-Jaramillo, Francisco Acevedo, 2022, International wound journal.

Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

Christopher R. Gignoux, F. Montinaro, M. Metspalu, 2021, American journal of medical genetics. Part A.

Early teeth extraction in patients with generalized recessive dystrophic epidermolysis bullosa: A case series.

H. Huber, I. Fuentes, M. J. Yubero, 2020, Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry.

Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa

C. Has, G. Zambruno, P. Akker, 2019, The British journal of dermatology.

Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated Cardiomyopathy.

B. Rebolledo-Jaramillo, A. Paller, S. Duchatelet, 2019, The Journal of investigative dermatology.

Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids

C. Mummery, X. Gidrol, S. M. Chuva de Sousa Lopes, 2022, Stem cell reports.

Epidermolysis bullosa simplex–generalized severe type due to keratin 5 p.Glu477Lys mutation: Genotype‐phenotype correlation and in silico modeling analysis

A. Hovnanian, Leah Lalor, K. Tasanen, 2018, Pediatric dermatology.

Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance

G. Repetto, S. González, A. Klausegger, 2017, The British journal of dermatology.

Case Report: Crown Resorption in a Patient With Junctional Epidermolysis Bullosa and Amelogenesis Imperfecta With LAMB3 Gene Mutations

I. Morales-Bozo, F. Palisson, B. Urzúa, 2021, Frontiers in Dental Medicine.

Maintenance of chronicity signatures in fibroblasts isolated from recessive dystrophic epidermolysis bullosa chronic wound dressings under culture conditions

F. Altermatt, M. Ezquer, A. South, 2023, Biological Research.

Outcomes and Predictors for Re-stenosis of Esophageal Stricture in Epidermolysis Bullosa: A Multicenter Cohort Study.

D. Murrell, J. Mellerio, A. Lucky, 2020, Journal of pediatric gastroenterology and nutrition.

Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24.

C. Mummery, H. Mikkers, C. Freund, 2021, Stem cell research.