These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 33960018)

  • 1. Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort study.
    Reimer-Taschenbrecker A; Hess M; Hotz A; Fischer J; Bruckner-Tuderman L; Has C
    J Eur Acad Dermatol Venereol; 2021 Oct; 35(10):2097-2104. PubMed ID: 33960018
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A global, cross-sectional survey of patient-reported outcomes, disease burden, and quality of life in epidermolysis bullosa simplex.
    So JY; Fulchand S; Wong CY; Li S; Nazaroff J; Gorell ES; de Souza MP; Murrell DF; Teng JM; Chiou AS; Tang JY
    Orphanet J Rare Dis; 2022 Jul; 17(1):270. PubMed ID: 35841105
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of Epidermolysis Bullosa Simplex With Mottled Pigmentation and EXPH5 Mutations.
    Turcan I; Pasmooij AM; Van den Akker PC; Lemmink H; Sinke RJ; Jonkman MF
    JAMA Dermatol; 2016 Oct; 152(10):1137-1141. PubMed ID: 27384765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment of the Timing of Milestone Clinical Events in Patients With Epidermolysis Bullosa From North America.
    Feinstein JA; Jambal P; Peoples K; Lucky AW; Khuu P; Tang JY; Lara-Corrales I; Pope E; Wiss K; Hook KP; Levin LE; Morel KD; Paller AS; McCuaig CC; Powell J; Eichenfield LF; Price H; Levy ML; Schachner LA; Browning JC; Bayliss S; Jahnke M; Shwayder T; Glick SA; Bruckner AL
    JAMA Dermatol; 2019 Feb; 155(2):196-203. PubMed ID: 30586139
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The clinical spectrum of epidermolysis bullosa simplex.
    Horn HM; Tidman MJ
    Br J Dermatol; 2000 Mar; 142(3):468-72. PubMed ID: 10735952
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.
    García M; Santiago JL; Terrón A; Hernández-Martín A; Vicente A; Fortuny C; De Lucas R; López JC; Cuadrado-Corrales N; Holguín A; Illera N; Duarte B; Sánchez-Jimeno C; Llames S; García E; Ayuso C; Martínez-Santamaría L; Castiglia D; De Luca N; Torrelo A; Mechan D; Baty D; Zambruno G; Escámez MJ; Del Río M
    Br J Dermatol; 2011 Sep; 165(3):683-92. PubMed ID: 21623745
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidermolysis bullosa simplex associated with muscular dystrophy: phenotype-genotype correlations and review of the literature.
    Shimizu H; Takizawa Y; Pulkkinen L; Murata S; Kawai M; Hachisuka H; Udono M; Uitto J; Nishikawa T
    J Am Acad Dermatol; 1999 Dec; 41(6):950-6. PubMed ID: 10570379
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Keratin mutations in patients with epidermolysis bullosa simplex: correlations between phenotype severity and disturbance of intermediate filament molecular structure.
    Jerábková B; Marek J; Bucková H; Kopecková L; Veselý K; Valícková J; Fajkus J; Fajkusová L
    Br J Dermatol; 2010 May; 162(5):1004-13. PubMed ID: 20030639
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ophthalmologic Approach in Epidermolysis Bullosa: A Cross-Sectional Study With Phenotype-Genotype Correlations.
    Mellado F; Fuentes I; Palisson F; I Vergara J; Kantor A
    Cornea; 2018 Apr; 37(4):442-447. PubMed ID: 29384803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newborn.
    Darwich E; Vicente A; Bolling MC; González-Enseñat MA; Cusi V; Fortuny C; Bombí JA; Jonkman MF; Mascaró JM
    Eur J Dermatol; 2011; 21(6):966-71. PubMed ID: 21856558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. "Nails Only" Phenotype and Partial Dominance of p.Glu170Lys Mutation in a Family with Epidermolysis Bullosa Simplex.
    González-Cantero Á; Sánchez-Moya AI; Pérez-Hortet C; Martínez-Lorenzo E; Gómez-Dorado B; Schoendorff-Ortega C
    Pediatr Dermatol; 2017 Jul; 34(4):e205-e206. PubMed ID: 28425111
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epidermolysis bullosa simplex herpetiformis of Dowling-Meara with mottled pigmentation: the relationship between EBS herpetiformis and EBS with mottled pigmentation.
    Tay YK; Weston WL
    Pediatr Dermatol; 1996; 13(4):306-9. PubMed ID: 8844751
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation.
    Irvine AD; Rugg EL; Lane EB; Hoare S; Peret C; Hughes AE; Heagerty AH
    Br J Dermatol; 2001 Jan; 144(1):40-5. PubMed ID: 11167681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygous PLEC mutations in a patient of consanguineous parentage with epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia.
    Yin J; Ren Y; Lin Z; Wang H; Zhou Y; Yang Y
    Int J Dermatol; 2015 Feb; 54(2):185-7. PubMed ID: 25209331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Transcriptomic Repositioning Analysis Identifies mTOR Inhibitor as Potential Therapy for Epidermolysis Bullosa Simplex.
    Lee GH; Lekwuttikarn R; Tafoya E; Martin M; Sarin KY; Teng JM
    J Invest Dermatol; 2022 Feb; 142(2):382-389. PubMed ID: 34536484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.
    Rugg EL; Horn HM; Smith FJ; Wilson NJ; Hill AJ; Magee GJ; Shemanko CS; Baty DU; Tidman MJ; Lane EB
    J Invest Dermatol; 2007 Mar; 127(3):574-80. PubMed ID: 17039244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care.
    Marro M; De Smet S; Caldari D; Lambe C; Leclerc-Mercier S; Chiaverini C
    Orphanet J Rare Dis; 2021 Jun; 16(1):271. PubMed ID: 34116697
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation.
    Irvine AD; McKenna KE; Jenkinson H; Hughes AE
    J Invest Dermatol; 1997 May; 108(5):809-10. PubMed ID: 9129237
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment.
    Castela E; Tulic MK; Rozières A; Bourrat E; Nicolas JF; Kanitakis J; Vabres P; Bessis D; Mazereeuw J; Morice-Picard F; Baty D; Berard F; Lacour JP; Passeron T; Chiaverini C
    Br J Dermatol; 2019 Feb; 180(2):357-364. PubMed ID: 29932457
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The eye in epidermolysis bullosa.
    Tong L; Hodgkins PR; Denyer J; Brosnahan D; Harper J; Russell-Eggitt I; Taylor DS; Atherton D
    Br J Ophthalmol; 1999 Mar; 83(3):323-6. PubMed ID: 10365041
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.