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 *

161 related articles for article (PubMed ID: 38368142)

  • 1. Advantages of whole-exome sequencing over immunomapping in 67 Brazilian patients with epidermolysis bullosa.
    Kelmann SV; Stephan BO; Barbosa SMM; Polastrini RTV; Oliveira ZNP; Rivitti-Machado MC; Spolador GM; Honjo RS; Saida K; Matsumoto N; Kim CA
    An Bras Dermatol; 2024; 99(3):350-356. PubMed ID: 38368142
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.
    Tu WT; Hou PC; Chen PC; Chen WR; Huang HY; Wang JY; Huang YT; Wu YH; Su CL; Tang YA; Iwata H; Natsuga K; Chao SC; Sun HS; Tang MJ; Lee JY; McGrath JA; Hsu CK
    Orphanet J Rare Dis; 2022 Dec; 17(1):451. PubMed ID: 36578049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary epidermolysis bullosa: clinical-epidemiological profile of 278 patients at a tertiary hospital in São Paulo, Brazil.
    Thien CI; Bessa VR; Miotto IZ; Samorano LP; Rivitti-Machado MC; Oliveira ZNP
    An Bras Dermatol; 2024; 99(3):380-390. PubMed ID: 38403552
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel and very rare causative variants in the COL7A1 gene of Vietnamese patients with recessive dystrophic epidermolysis bullosa revealed by whole-exome sequencing.
    Ma THT; Luong TLA; Hoang TL; Nguyen TTH; Vu TH; Tran VK; Nguyen DB; Trieu TS; Nguyen HH; Nong VH; Nguyen DT
    Mol Genet Genomic Med; 2021 Aug; 9(8):e1748. PubMed ID: 34286919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of Novel Biallelic Causative Variants in
    Fozia F; Nazli R; Alrashed MM; Ghneim HK; Haq ZU; Jabeen M; Alam Khan S; Ahmad I; Bourhia M; Aboul-Soud MAM
    Diagnostics (Basel); 2022 Jun; 12(7):. PubMed ID: 35885431
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.
    Chen F; Wei R; Deng D; Zhang X; Cao Y; Pan C; Wang Y; Cao Q; Wang J; Zeng M; Huang L; Gu Y; Yao Z; Li M
    J Eur Acad Dermatol Venereol; 2023 Feb; 37(2):411-419. PubMed ID: 36287101
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification and Computational Analysis of Novel Pathogenic Variants in Pakistani Families with Diverse Epidermolysis Bullosa Phenotypes.
    Khan FF; Khan N; Rehman S; Ejaz A; Ali U; Erfan M; Ahmed ZM; Naeem M
    Biomolecules; 2021 Apr; 11(5):. PubMed ID: 33921969
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait.
    Nanda A; Liu L; Al-Ajmi H; Al-Saleh QA; Al-Fadhli S; Anim JT; Ozoemena L; Mellerio JE; McGrath JA
    Int J Dermatol; 2018 Sep; 57(9):1058-1067. PubMed ID: 30011071
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 "knock-out".
    Vahidnezhad H; Youssefian L; Daneshpazhooh M; Mahmoudi H; Kariminejad A; Fischer J; Christiansen J; Schneider H; Guy A; Liu L; McGrath JA; Has C; Uitto J
    Matrix Biol; 2019 Oct; 83():48-59. PubMed ID: 31302245
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole exome sequencing in a sample of Peruvian patients diagnosed with epidermolysis bullosa.
    Zevallos-Morales A; Iberico RT; Obispo D; Danos P; Sanchez RM; Fujita R; Guevara-Fujita ML
    Dermatol Online J; 2022 Oct; 28(5):. PubMed ID: 36809127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An overview of the genetic basis of epidermolysis bullosa in Brazil: discovery of novel and recurrent disease-causing variants.
    Mariath LM; Santin JT; Frantz JA; Doriqui MJR; Kiszewski AE; Schuler-Faccini L
    Clin Genet; 2019 Sep; 96(3):189-198. PubMed ID: 31001817
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory.
    Takeichi T; Liu L; Fong K; Ozoemena L; McMillan JR; Salam A; Campbell P; Akiyama M; Mellerio JE; McLean WH; Simpson MA; McGrath JA
    Br J Dermatol; 2015 Jan; 172(1):94-100. PubMed ID: 24947307
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Novel pathogenic variants in an Indian cohort with epidermolysis bullosa: Expanding the genotypic spectrum.
    Nilay M; Saxena D; Mandal K; Moirangthem A; Phadke SR
    Eur J Med Genet; 2021 Dec; 64(12):104345. PubMed ID: 34597860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases.
    Yu Y; Wang Z; Mi Z; Sun L; Fu X; Yu G; Pang Z; Liu H; Zhang F
    Acta Derm Venereol; 2021 Jul; 101(7):adv00503. PubMed ID: 34046686
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature.
    Ali FM; Zhou J; Wang M; Wang Q; Sun L; Mshenga MM; Lu H
    BMC Pediatr; 2024 Apr; 24(1):242. PubMed ID: 38580989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.