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 *

154 related articles for article (PubMed ID: 34093240)

  • 1. Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study.
    Fermo E; Vercellati C; Marcello AP; Keskin EY; Perrotta S; Zaninoni A; Brancaleoni V; Zanella A; Giannotta JA; Barcellini W; Bianchi P
    Front Physiol; 2021; 12():684569. PubMed ID: 34093240
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience.
    Agarwal AM; McMurty V; Clayton AL; Bolia A; Reading NS; Mani C; Patel JL; Rets A
    Eur J Haematol; 2023 Jun; 110(6):688-695. PubMed ID: 36825813
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Using target next-generation sequencing assay in diagnosing of 46 patients with suspected congenital anemias].
    Li Y; Peng GX; Gao QY; Li Y; Ye L; Li JP; Song L; Fan HH; Yang Y; Xiong YZ; Wu ZJ; Yang WR; Zhou K; Zhao X; Jing LP; Zhang FK; Zhang L
    Zhonghua Xue Ye Xue Za Zhi; 2018 May; 39(5):414-419. PubMed ID: 29779353
    [No Abstract]   [Full Text] [Related]  

  • 4. Screening tools for hereditary hemolytic anemia: new concepts and strategies.
    Fermo E; Vercellati C; Bianchi P
    Expert Rev Hematol; 2021 Mar; 14(3):281-292. PubMed ID: 33543663
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.
    Kedar PS; Harigae H; Ito E; Muramatsu H; Kojima S; Okuno Y; Fujiwara T; Dongerdiye R; Warang PP; Madkaikar MR
    Int J Hematol; 2019 Nov; 110(5):618-626. PubMed ID: 31401766
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.
    Shefer Averbuch N; Steinberg-Shemer O; Dgany O; Krasnov T; Noy-Lotan S; Yacobovich J; Kuperman AA; Kattamis A; Ben Barak A; Roth-Jelinek B; Chubar E; Shabad E; Dufort G; Ellis M; Wolach O; Pazgal I; Abu Quider A; Miskin H; Tamary H
    Eur J Haematol; 2018 Sep; 101(3):297-304. PubMed ID: 29786897
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
    More TA; Dongerdiye R; Devendra R; Warang PP; Kedar PS
    Ann Hematol; 2020 Apr; 99(4):715-727. PubMed ID: 32112123
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.
    Zaninoni A; Fermo E; Vercellati C; Consonni D; Marcello AP; Zanella A; Cortelezzi A; Barcellini W; Bianchi P
    Front Physiol; 2018; 9():451. PubMed ID: 29755372
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
    Russo R; Andolfo I; Manna F; Gambale A; Marra R; Rosato BE; Caforio P; Pinto V; Pignataro P; Radhakrishnan K; Unal S; Tomaiuolo G; Forni GL; Iolascon A
    Am J Hematol; 2018 May; 93(5):672-682. PubMed ID: 29396846
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis.
    Kristan A; Pajič T; Maver A; Režen T; Kunej T; Količ R; Vuga A; Fink M; Žula Š; Podgornik H; Anžej Doma S; Preložnik Zupan I; Rozman D; Debeljak N
    Front Genet; 2021; 12():689868. PubMed ID: 34349782
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeted Next Generation Sequencing (NGS) to Diagnose Hereditary Hemolytic Anemias.
    Bharadwaj R; Raman T; Thangadorai R; Munirathnam D
    Int J Hematol Oncol Stem Cell Res; 2020 Jul; 14(3):177-180. PubMed ID: 33024524
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.
    Kedar PS; Gupta V; Dongerdiye R; Chiddarwar A; Warang P; Madkaikar MR
    J Clin Pathol; 2019 Jan; 72(1):81-85. PubMed ID: 30337328
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Laboratory Approach to Hemolytic Anemia.
    Jamwal M; Sharma P; Das R
    Indian J Pediatr; 2020 Jan; 87(1):66-74. PubMed ID: 31823208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias.
    Steinberg-Shemer O; Tamary H
    Mol Diagn Ther; 2020 Aug; 24(4):397-407. PubMed ID: 32557003
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
    Hu P; Qiao F; Wang Y; Meng L; Ji X; Luo C; Xu T; Zhou R; Zhang J; Yu B; Wang L; Wang T; Pan Q; Ma D; Liang D; Xu Z
    Ultrasound Obstet Gynecol; 2018 Aug; 52(2):205-211. PubMed ID: 29536580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia.
    Rets A; Clayton AL; Christensen RD; Agarwal AM
    Int J Lab Hematol; 2019 May; 41 Suppl 1():95-101. PubMed ID: 31069991
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.
    Simbolo M; Mafficini A; Agostini M; Pedrazzani C; Bedin C; Urso ED; Nitti D; Turri G; Scardoni M; Fassan M; Scarpa A
    Hered Cancer Clin Pract; 2015; 13(1):18. PubMed ID: 26300997
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity.
    Jamwal M; Aggarwal A; Palodhi A; Sharma P; Bansal D; Trehan A; Malhotra P; Maitra A; Das R
    J Mol Diagn; 2020 Apr; 22(4):579-590. PubMed ID: 32036089
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High performance of targeted next generation sequencing on variance detection in clinical tumor specimens in comparison with current conventional methods.
    Su D; Zhang D; Chen K; Lu J; Wu J; Cao X; Ying L; Jin Q; Ye Y; Xie Z; Xiong L; Mao W; Li F
    J Exp Clin Cancer Res; 2017 Sep; 36(1):121. PubMed ID: 28882180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital Hemolytic Anemias: Is There a Role for the Immune System?
    Zaninoni A; Fermo E; Vercellati C; Marcello AP; Barcellini W; Bianchi P
    Front Immunol; 2020; 11():1309. PubMed ID: 32655575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.