Works matching DE "EPIDERMOLYSIS bullosa"
Results: 2859
Molecular insights into genodermatoses: Genetic findings from 43 patients.
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- Archives of Dermatological Research, 2025, v. 317, n. 1, p. 1, doi. 10.1007/s00403-025-04056-7
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- Article
An Intriguing Case of Anti-p 200 Pemphigoid Revealing String of Pearl Appearance.
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- Indian Dermatology Online Journal, 2025, v. 16, n. 2, p. 294, doi. 10.4103/idoj.idoj_51_24
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- Article
Survey of skin disorders in newborns: clinical observation in an Egyptian medical centre nursery.
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- Eastern Mediterranean Health Journal, 2012, v. 18, n. 1, p. 49, doi. 10.26719/2012.18.1.49
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- Article
Raising money for DebRA.
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- Practice Nursing, 2010, v. 21, n. 1, p. 46
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- Article
Charity trek for DebRA.
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- Practice Nursing, 2009, v. 20, n. 9, p. 472
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- Article
Combined Digital/Conventional Technique for Rehabilitation of a Patient With Epidermolysis Bullosa: A Case Letter.
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- Journal of Oral Implantology, 2017, v. 43, n. 5, p. 387, doi. 10.1563/aaid-joi-D-17-00103
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- Article
Fixed Implant-Supported Full-Arch Prosthesis in Epidermolysis Bullosa With Severe Symptoms.
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- Journal of Oral Implantology, 2016, v. 42, n. 6, p. 498, doi. 10.1563/aaid-joi-D-14-00104
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- Article
Epidermolysis Bullosa Acquisita: A Rare Challenge in Dental Management.
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- Compendium of Continuing Education in Dentistry (15488578), 2012, v. 33, n. 4, p. 238
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- Article
Dental and craniofacial defects in the Crtap<sup>−/−</sup> mouse model of osteogenesis imperfecta type VII.
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- Developmental Dynamics, 2020, v. 249, n. 7, p. 884, doi. 10.1002/dvdy.166
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Congenital Cerebellar Malignant Rhabdoid Tumor in an Infant with Junctional Epidermolysis Bullosa.
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- 2007
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- Case Study
Treatment of feet deformities in epidermolysis bullosa.
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- 2016
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- journal article
Plectin tethers desmin intermediate filaments onto subsarcolemmal dense plaques containing dystrophin and vinculin.
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- Histochemistry & Cell Biology, 2003, v. 119, n. 2, p. 109, doi. 10.1007/s00418-003-0496-5
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- Article
Cutaneous gene therapy – an update.
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- Histochemistry & Cell Biology, 2001, v. 115, n. 1, p. 73, doi. 10.1007/s004180000210
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- Article
Keratin gene mutations influence the keratinocyte response to DNA damage and cytokine induced apoptosis.
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- Archives of Dermatological Research, 2017, v. 309, n. 7, p. 587, doi. 10.1007/s00403-017-1757-9
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- Article
The use of Biochip immunofluorescence microscopy for the serological diagnosis of epidermolysis bullosa acquisita.
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- Archives of Dermatological Research, 2016, v. 308, n. 4, p. 273, doi. 10.1007/s00403-016-1632-0
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- Article
Apocytolysis, a proposed mechanism of blister formation in epidermolysis bullosa simplex.
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- Archives of Dermatological Research, 2015, v. 307, n. 4, p. 371, doi. 10.1007/s00403-015-1560-4
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- Article
Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.
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- Archives of Dermatological Research, 2014, v. 306, n. 4, p. 405, doi. 10.1007/s00403-013-1421-y
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- Article
Keratinocyte-based cell assays: their potential pitfalls.
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- Archives of Dermatological Research, 2012, v. 304, n. 9, p. 765, doi. 10.1007/s00403-012-1285-6
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- Article
Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's disease.
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- Archives of Dermatological Research, 2011, v. 303, n. 5, p. 371, doi. 10.1007/s00403-011-1148-6
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- Article
A novel splice-site mutation of ATP2A2 gene in a Chinese family with Darier disease.
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- Archives of Dermatological Research, 2010, v. 302, n. 10, p. 769, doi. 10.1007/s00403-010-1081-0
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- Article
Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis.
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- Archives of Dermatological Research, 2008, v. 300, n. 7, p. 365, doi. 10.1007/s00403-008-0861-2
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- Article
Intraperitoneal injection of pemphigus vulgaris-IgG into mouse depletes epidermal keratinocytes of desmoglein 3 associated with generation of acantholysis.
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- Archives of Dermatological Research, 2007, v. 299, n. 3, p. 165, doi. 10.1007/s00403-007-0754-9
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- Article
Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland.
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- Archives of Dermatological Research, 2005, v. 296, n. 12, p. 577, doi. 10.1007/s00403-005-0560-1
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- Article
Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations.
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- Archives of Dermatological Research, 2004, v. 295, n. 10, p. 442, doi. 10.1007/s00403-003-0444-1
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- Article
Genetic abnormalities and clinical classification of epidermolysis bullosa.
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- Archives of Dermatological Research, 2003, v. 295, p. S29, doi. 10.1007/s00403-002-0369-0
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- Article
Epidermolysis bullosa: directions for future research and new challenges for treatment.
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- Archives of Dermatological Research, 2003, v. 295, p. S34, doi. 10.1007/s00403-002-0370-7
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- Article
Japanese guidelines for diagnosis and treatment of junctional and dystrophic epidermolysis bullosa.
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- Archives of Dermatological Research, 2003, v. 295, p. S24, doi. 10.1007/s00403-002-0379-y
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- Article
Cell-cell junctions in acantholytic diseases : Junction proteins in nonimmune and autoimmune acantholysis.
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- Archives of Dermatological Research, 2001, v. 293, n. 1/2, p. 1, doi. 10.1007/s004030000190
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- Article
Glycine substitution mutations by different amino acids in the same codon of COL7A1 lead to heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa.
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- Archives of Dermatological Research, 2000, v. 292, n. 10, p. 477, doi. 10.1007/s004030000162
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- Article
LAMB3 gene transfection into SV40-transformed keratinocytes from patient with Herlitz junctional epidermolysis bullosa.
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- Archives of Dermatological Research, 2000, v. 292, n. 4, p. 195, doi. 10.1007/s004030050477
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- Article
A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosa.
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- Archives of Dermatological Research, 2000, v. 292, n. 4, p. 159, doi. 10.1007/s004030050472
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- Article
Consumer and Materials-Science Characteristics of Clothes for Children with Epidermolysis Bullosa.
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- Fibre Chemistry, 2021, v. 52, n. 5, p. 371, doi. 10.1007/s10692-021-10215-z
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- Article
Rejuvenation of the ageing face and the role of orthodontics: Guidelines for management.
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- Journal of Orthodontics, 2022, v. 49, n. 4, p. 463, doi. 10.1177/14653125221093390
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- Article
Outcomes and Predictors for Re-stenosis of Esophageal Stricture in Epidermolysis Bullosa: A Multicenter Cohort Study.
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- 2020
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- journal article
Approach and Safety of Esophageal Dilation for Treatment of Strictures in Children With Epidermolysis Bullosa.
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- 2018
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- journal article
Pyloric atresia and Down's syndrome: prenatal double bubble false sign.
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- Cirugía Pediátrica (English Edition), 2021, v. 34, n. 4, p. 211
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- Article
Epidermolisys bullosa: facts for the anesthesiologists.
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- 2016
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- Case Study
Suppression of TGFβ and Angiogenesis by Type VII Collagen in Cutaneous SCC.
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- 2016
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- journal article
Effectiveness and safety of mexiletine versus placebo in patients with myotonia: a systematic review and meta-analysis.
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- Neurological Sciences, 2024, v. 45, n. 8, p. 3989, doi. 10.1007/s10072-024-07412-z
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- Article
Hereditary oral anomalies - a child diagnosed with epidermolysis bullosa.
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- ORL.ro, 2018, n. 41, p. 48, doi. 10.26416/orl.41.4.2018.2122
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- Article
Oral Prosthetic Rehabilitation in Patients with Epidermolysis Bullosa Hereditaria: A Systematic Review.
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- International Journal of Prosthodontics, 2024, v. 37, n. 6, p. 699, doi. 10.11607/ijp.8791
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- Article
Maxillary Implant Prosthodontic Treatment Using Digital Laboratory Protocol for a Patient with Epidermolysis Bullosa: A Case History Report.
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- 2017
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- journal article
Fixed Full-Arch Implant-Supported Prostheses in a Patient with Epidermolysis Bullosa: A Clinical Case History Report.
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- 2015
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- Publication type:
- Case Study
Implant-Supported Fixed Dental Prostheses in an Edentulous Patient with Dystrophic Epidermolysis Bullosa.
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- International Journal of Prosthodontics, 2010, v. 23, n. 1, p. 42
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- Article
Quality of life in people with epidermolysis bullosa: a systematic review.
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- 2020
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- journal article
Endoscopic balloon dilation of esophageal stricture in dystrophic epidermolysis bullosa patient: challenges faced and safety of procedure.
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- Oxford Medical Case Reports, 2024, v. 2024, n. 7, p. 1, doi. 10.1093/omcr/omae079
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- Article
Infant with a hereditary blistering disorder: an interesting case in the NICU.
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- Oxford Medical Case Reports, 2024, v. 2024, n. 5, p. 1, doi. 10.1093/omcr/omae041
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- Article
Epidermolysis bullosa in a mother-infant dyad.
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- Oxford Medical Case Reports, 2023, v. 2023, n. 11, p. 1, doi. 10.1093/omcr/omad124
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- Article
Demystifying debridement and wound cleansing.
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- Journal of Community Nursing, 2016, v. 30, n. 2, p. 26
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- Article
Reply from David P. Burns, Eric F. Lucking and Ken D. O'Halloran: Auxiliary compensation for diaphragm dysfunction in dystrophic disease.
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- Journal of Physiology, 2019, v. 597, n. 15, p. 4103, doi. 10.1113/JP278371
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- Article