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 *

309 related articles for article (PubMed ID: 26574897)

  • 1. Congenital Methemoglobinemia Type II-Clinical Improvement with Short-Term Methylene Blue Treatment.
    Cooper MS; Randall M; Rowell M; Charlton M; Greenway A; Barnes C
    Pediatr Blood Cancer; 2016 Mar; 63(3):558-60. PubMed ID: 26574897
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long-term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency.
    Jaffey JA; Harmon MR; Villani NA; Creighton EK; Johnson GS; Giger U; Dodam JR
    J Vet Intern Med; 2017 Nov; 31(6):1860-1865. PubMed ID: 28963729
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia.
    Arikoglu T; Yarali N; Kara A; Bay A; Bozkaya IO; Tunc B; Percy MJ
    Pediatr Hematol Oncol; 2009; 26(5):381-5. PubMed ID: 19579085
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels.
    de Geus KF; Anas AA; Franssen R; Duijkers FAM; Bikker H; Linthorst GE
    Neth J Med; 2018 May; 76(4):194-197. PubMed ID: 29845943
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
    Warang PP; Kedar PS; Shanmukaiah C; Ghosh K; Colah RB
    Clin Genet; 2015; 87(1):62-7. PubMed ID: 24266649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
    Kedar PS; Colah RB; Ghosh K; Mohanty D
    Haematologia (Budap); 2002; 32(4):543-9. PubMed ID: 12803131
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.
    Shino H; Otsuka-Yamasaki Y; Sato T; Ooi K; Inanami O; Sato R; Yamasaki M
    J Vet Intern Med; 2018 Jan; 32(1):165-171. PubMed ID: 29356095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes].
    Jabłońska-Skwiecińska E; Wierzbicka M; Kubicka K
    Pediatr Pol; 1989 Jan; 64(1):53-9. PubMed ID: 2812907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Thai boy with hereditary enzymopenic methemoglobinemia type II.
    Shotelersuk V; Tosukhowong P; Chotivitayatarakorn P; Pongpunlert W
    J Med Assoc Thai; 2000 Nov; 83(11):1380-6. PubMed ID: 11215870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Oral Methylene Blue Treatment in A Dog with Cytochrome B
    Jaffey JA; Struthers JD; Yuh EL; Hostnik ET; Runyan RA; Reading NS
    Top Companion Anim Med; 2022; 49():100649. PubMed ID: 35202847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Congenital deficiency of erythrocyte NADH-dependent methemoglobin reductase (diaphorase)].
    Barretto OC; Halsman MW; Nonoyama K; Tamigaki M; Maspes V
    Sangre (Barc); 1984; 29(1):62-6. PubMed ID: 6719320
    [No Abstract]   [Full Text] [Related]  

  • 12. Congenital methemoglobinemia in a dog with a promoter deletion and a nonsynonymous coding variant in the gene encoding cytochrome b₅.
    McKenna JA; Sacco J; Son TT; Trepanier LA; Callan MB; Harvey JW; Arndt JW
    J Vet Intern Med; 2014; 28(5):1626-31. PubMed ID: 25145387
    [No Abstract]   [Full Text] [Related]  

  • 13. Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infant.
    Percy MJ; Crowley LJ; Roper D; Vulliamy TJ; Layton DM; Barber MJ
    Blood Cells Mol Dis; 2006; 36(1):81-90. PubMed ID: 16310381
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Congenital methemoglobinemia of the recessive type. Description of 2 cases].
    Varese LA
    Minerva Pediatr; 1967 Mar; 19(10):439-42. PubMed ID: 5607049
    [No Abstract]   [Full Text] [Related]  

  • 15. Congenital methemoglobinemia: a rare cause of cyanosis in the newborn--a case report.
    Da-Silva SS; Sajan IS; Underwood JP
    Pediatrics; 2003 Aug; 112(2):e158-61. PubMed ID: 12897322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital Recessive Methemoglobinemia Revealed in Adulthood: Description of a New Mutation in Cytochrome b5 Reductase Gene.
    Forestier A; Pissard S; Cretet J; Mambie A; Pascal L; Cliquennois M; Cambier N; Rose C
    Hemoglobin; 2015; 39(6):438-41. PubMed ID: 26291966
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.
    Fermo E; Bianchi P; Vercellati C; Marcello AP; Garatti M; Marangoni O; Barcellini W; Zanella A
    Blood Cells Mol Dis; 2008; 41(1):50-5. PubMed ID: 18343696
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metoclopramide-induced methemoglobinemia in an adult.
    Mary AM; Bhupalam L
    J Ky Med Assoc; 2000 Jun; 98(6):245-7. PubMed ID: 10870338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency: report of a case.
    Cheng NJ; Hsu TS; Dunn P; Hung JS
    Taiwan Yi Xue Hui Za Zhi; 1988 Aug; 87(8):823-7. PubMed ID: 3241162
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report.
    Nakata M; Yokota N; Tabata K; Morikawa T; Shibata H; Kenzaka T
    Medicina (Kaunas); 2023 Mar; 59(3):. PubMed ID: 36984616
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.