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Pediatric Dermatology
|
January 11, 2024
Osteoporosis and bone health in pediatric patients with epidermolysis bullosa: A scoping review
Andie Kwon, Austin Hwang, Corinne H Miller, et al.
Orphanet Journal of Rare Diseases
|
May 20, 2024
Therapies for cutaneous squamous cell carcinoma in recessive dystrophic epidermolysis bullosa: a systematic review of 157 cases
Austin Hwang, Andie Kwon, Corinne H Miller, et al.
Acta Dermato-Venereologica
|
December 16, 2017
The Position of Targeted Next-generation Sequencing in Epidermolysis Bullosa Diagnosis
Cristina Has, Julia Küsel, Antonia Reimer, et al.
Acta Dermato-Venereologica
|
July 3, 2018
Successful Multidisciplinary Treatment of Chronic Facial Wounds in Junctional Epidermolysis Bullosa
Antonia Reimer, Roland Laszig, Jens Pfeiffer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
March 12, 2025
Pathophysiological insights into the successful treatment of EBV-positive hydroa vacciniforme lymphoproliferative disorder with hydroxychloroquine
Christina Bürgler, Lukas Meyer-Landolt, Stefanie Häfliger, et al.
The Journal of Investigative Dermatology
|
February 12, 2022
Predominance of Staphylococcus Correlates with Wound Burden and Disease Activity in Dystrophic Epidermolysis Bullosa: A Prospective Case-Control Study
Antonia Reimer-Taschenbrecker, Axel Künstner, Misa Hirose, et al.
Pediatric Dermatology
|
December 3, 2022
Gastrostomy tube feeding in epidermolysis bullosa: A multi-center assessment of caregiver satisfaction
Elana P Kleinman, Antonia Reimer-Taschenbrecker, Courtney N Haller, et al.
Clinical Immunology (Orlando, Fla.)
|
June 14, 2019
Profound immunodeficiency with severe skin disease explained by concomitant novel CARMIL2 and PLEC1 loss-of-function mutations
Maria E Maccari, Carsten Speckmann, Maximilian Heeg, et al.
The British Journal of Dermatology
|
February 10, 2023
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings
Mingfeng Li, Kenneth Lay, Andreas Zimmer, et al.
Eclinicalmedicine
|
November 14, 2024
Safety and tolerability of losartan to treat recessive dystrophic epidermolysis bullosa in children (REFLECT): an open-label, single-arm, phase 1/2 trial
Dimitra Kiritsi, Franziska Schauer, Stella Gewert, et al.
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Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Pediatric Dermatology
|
January 11, 2024
Osteoporosis and bone health in pediatric patients with epidermolysis bullosa: A scoping review
Andie Kwon, Austin Hwang, Corinne H Miller, et al.
Orphanet Journal of Rare Diseases
|
May 20, 2024
Therapies for cutaneous squamous cell carcinoma in recessive dystrophic epidermolysis bullosa: a systematic review of 157 cases
Austin Hwang, Andie Kwon, Corinne H Miller, et al.
Acta Dermato-Venereologica
|
December 16, 2017
The Position of Targeted Next-generation Sequencing in Epidermolysis Bullosa Diagnosis
Cristina Has, Julia Küsel, Antonia Reimer, et al.
Acta Dermato-Venereologica
|
July 3, 2018
Successful Multidisciplinary Treatment of Chronic Facial Wounds in Junctional Epidermolysis Bullosa
Antonia Reimer, Roland Laszig, Jens Pfeiffer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
March 12, 2025
Pathophysiological insights into the successful treatment of EBV-positive hydroa vacciniforme lymphoproliferative disorder with hydroxychloroquine
Christina Bürgler, Lukas Meyer-Landolt, Stefanie Häfliger, et al.
The Journal of Investigative Dermatology
|
February 12, 2022
Predominance of Staphylococcus Correlates with Wound Burden and Disease Activity in Dystrophic Epidermolysis Bullosa: A Prospective Case-Control Study
Antonia Reimer-Taschenbrecker, Axel Künstner, Misa Hirose, et al.
Pediatric Dermatology
|
December 3, 2022
Gastrostomy tube feeding in epidermolysis bullosa: A multi-center assessment of caregiver satisfaction
Elana P Kleinman, Antonia Reimer-Taschenbrecker, Courtney N Haller, et al.
Clinical Immunology (Orlando, Fla.)
|
June 14, 2019
Profound immunodeficiency with severe skin disease explained by concomitant novel CARMIL2 and PLEC1 loss-of-function mutations
Maria E Maccari, Carsten Speckmann, Maximilian Heeg, et al.
The British Journal of Dermatology
|
February 10, 2023
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings
Mingfeng Li, Kenneth Lay, Andreas Zimmer, et al.
Eclinicalmedicine
|
November 14, 2024
Safety and tolerability of losartan to treat recessive dystrophic epidermolysis bullosa in children (REFLECT): an open-label, single-arm, phase 1/2 trial
Dimitra Kiritsi, Franziska Schauer, Stella Gewert, et al.
Page
of 3