715 related articles for article (PubMed ID: 26220012)
1. Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran.
Barzegar M; Asadi-Kani Z; Mozafari N; Vahidnezhad H; Kariminejad A; Toossi P
Int J Dermatol; 2015 Oct; 54(10):e416-23. PubMed ID: 26220012
[TBL] [Abstract][Full Text] [Related]
2. High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well-matched antibody panel.
Meester I; Igoucheva O; Alexeev V; South A; Moreno-Treviño MG; Salas-Alanis JC
Australas J Dermatol; 2018 Feb; 59(1):73-76. PubMed ID: 28707324
[No Abstract] [Full Text] [Related]
3. Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub-classification of inherited epidermolysis bullosa: a single-centre retrospective comparative study of 87 cases with long-term follow-up.
Rossi S; Castiglia D; Pisaneschi E; Diociaiuti A; Stracuzzi A; Cesario C; Mariani R; Floriddia G; Zambruno G; Boldrini R; Abeni D; Novelli A; Alaggio R; El Hachem M
J Eur Acad Dermatol Venereol; 2021 Apr; 35(4):1007-1016. PubMed ID: 33274474
[TBL] [Abstract][Full Text] [Related]
4. Rapid diagnosis of major variants of congenital epidermolysis bullosa using a monoclonal antibody against collagen type IV.
Bolte C; Gonzalez S
Am J Dermatopathol; 1995 Dec; 17(6):580-3. PubMed ID: 8599472
[TBL] [Abstract][Full Text] [Related]
5. A retrospective analysis of diagnostic testing in a large North American cohort of patients with epidermolysis bullosa.
Phillips GS; Huang A; Augsburger BD; Kaplan L; Peoples K; Bruckner AL; Khuu P; Tang JY; Lara-Corrales I; Pope E; Wiss K; Levin LE; Morel KD; Hook KP; Paller AS; Eichenfield LF; McCuaig CC; Powell J; Castelo-Soccio L; Levy ML; Price HN; Schachner LA; Browning JC; Jahnke M; Shwayder T; Bayliss S; Lucky AW; Glick SA
J Am Acad Dermatol; 2022 May; 86(5):1063-1071. PubMed ID: 34634382
[TBL] [Abstract][Full Text] [Related]
6. A comparative study of immunohistochemistry and electron microscopy used in the diagnosis of epidermolysis bullosa.
Petronius D; Bergman R; Ben Izhak O; Leiba R; Sprecher E
Am J Dermatopathol; 2003 Jun; 25(3):198-203. PubMed ID: 12775981
[TBL] [Abstract][Full Text] [Related]
7. Diagnosis of Inherited Epidermolysis Bullosa in Resource-Limited Settings: Immunohistochemistry Revisited.
Yenamandra VK; Bhari N; Ray SB; Sreenivas V; Dinda AK; Scaria V; Sharma VK; Sethuraman G
Dermatology; 2017; 233(4):326-332. PubMed ID: 29069641
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis and molecular genetics of epidermolysis bullosa.
Pulkkinen L; Uitto J
Matrix Biol; 1999 Feb; 18(1):29-42. PubMed ID: 10367729
[TBL] [Abstract][Full Text] [Related]
9. The Role of Collagen IV and Cytokeratin 5/6 Immunohistochemistry in Identifying Subtypes of Hereditary Epidermolysis Bullosa.
Alhumidi A
Appl Immunohistochem Mol Morphol; 2018 Sep; 26(8):586-590. PubMed ID: 27941563
[TBL] [Abstract][Full Text] [Related]
10. The Position of Targeted Next-generation Sequencing in Epidermolysis Bullosa Diagnosis.
Has C; Küsel J; Reimer A; Hoffmann J; Schauer F; Zimmer A; Fischer J
Acta Derm Venereol; 2018 Apr; 98(4):437-440. PubMed ID: 29242947
[TBL] [Abstract][Full Text] [Related]
11. Pathogenesis of mechanobullous disorders.
Bruckner-Tuderman L
Exp Dermatol; 1992 Oct; 1(3):115-20. PubMed ID: 1365310
[TBL] [Abstract][Full Text] [Related]
12. Granulation tissue in the eyelid margin and conjunctiva in junctional epidermolysis bullosa with features of laryngo-onycho-cutaneous syndrome.
Figueira EC; Crotty A; Challinor CJ; Coroneo MT; Murrell DF
Clin Exp Ophthalmol; 2007 Mar; 35(2):163-6. PubMed ID: 17362460
[TBL] [Abstract][Full Text] [Related]
13. Neonatal epidermolysis bullosa: lessons to learn about genetic counseling.
Chong SC; Hon KL; Yuen LYP; Choi PCL; Ng WGG; Chiu TW
J Dermatolog Treat; 2021 Feb; 32(1):29-32. PubMed ID: 30280950
[TBL] [Abstract][Full Text] [Related]
14. Utility of Immunofluorescence Antigen Mapping in Hereditary Epidermolysis Bullosa.
Rao R; Shetty VM
Indian J Dermatol; 2021; 66(4):360-365. PubMed ID: 34759393
[TBL] [Abstract][Full Text] [Related]
15. Next-generation sequencing through multigene panel testing for the diagnosis of hereditary epidermolysis bullosa in Chinese population.
Chen F; Huang L; Li C; Zhang J; Yang W; Zhang B; Li H; Deng D; Liang J; Shen J; Yao Z; Li M
Clin Genet; 2020 Aug; 98(2):179-184. PubMed ID: 32484238
[TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.
Bergson S; Daniely D; Bomze D; Mohamad J; Malovitski K; Meijers O; Briskin V; Bihari O; Malchin N; Israeli S; Mashiah J; Falik-Zaccai T; Avitan-Hersh E; Eskin-Schwartz M; Allon-Shalev S; Sarig O; Sprecher E; Samuelov L
Pediatr Dermatol; 2023; 40(6):1021-1027. PubMed ID: 37827535
[TBL] [Abstract][Full Text] [Related]
17. Novel ITGB4 mutations in lethal and nonlethal variants of epidermolysis bullosa with pyloric atresia: missense versus nonsense.
Pulkkinen L; Rouan F; Bruckner-Tuderman L; Wallerstein R; Garzon M; Brown T; Smith L; Carter W; Uitto J
Am J Hum Genet; 1998 Nov; 63(5):1376-87. PubMed ID: 9792864
[TBL] [Abstract][Full Text] [Related]
18. LDA-1 monoclonal antibody. An excellent reagent for immunofluorescence mapping studies in patients with epidermolysis bullosa.
Fine JD; Gay S
Arch Dermatol; 1986 Jan; 122(1):48-51. PubMed ID: 3510588
[TBL] [Abstract][Full Text] [Related]
19. Epidermolysis Bullosa: Pediatric Perspectives.
Hon KL; Chu S; Leung AKC
Curr Pediatr Rev; 2022; 18(3):182-190. PubMed ID: 34036913
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis of the dystrophic and junctional forms of epidermolysis bullosa: mutations in the type VII collagen and kalinin (laminin 5) genes.
Uitto J; Pulkkinen L; Christiano AM
J Invest Dermatol; 1994 Nov; 103(5 Suppl):39S-46S. PubMed ID: 7963683
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
