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 *

227 related articles for article (PubMed ID: 5747939)

  • 1. [Cyanosis due to hereditary methemoglobinemia].
    Martinez AA; Aggio MC; Vogel N; Albanesi N
    Medicina (B Aires); 1968; 28(4):215-8. PubMed ID: 5747939
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Hereditary methemoglobinemia as a cause of cyanosis during anesthesia.
    Gabel RA; Bunn HF
    Anesthesiology; 1974 May; 40(5):516-8. PubMed ID: 4822398
    [No Abstract]   [Full Text] [Related]  

  • 4. [Recessive congenital methemoglobinemia. Clinical and laboratory study of one case].
    Hermabessiere C; Poisson C; Leveque B; Leroux A; Kaplan JC
    Ann Pediatr (Paris); 1976 Sep; 23(8-9):509-13. PubMed ID: 16104185
    [No Abstract]   [Full Text] [Related]  

  • 5. A case with quadriparetic cerebral palsy and cyanosis: congenital methemoglobinemia.
    Gokalp S; Unuvar E; Oguz F; Kilic A; Sidal M
    Pediatr Neurol; 2005 Aug; 33(2):131-3. PubMed ID: 16087059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetics and biochemistry of NADH-cytochrome b5 reductase].
    Shirabe K
    Nihon Rinsho; 2004 Dec; 62 Suppl 12():765-7. PubMed ID: 15658445
    [No Abstract]   [Full Text] [Related]  

  • 7. [Methemoglobinemia in children as a differential diagnosis of cyanosis].
    Greenberg R; Berkovitch M; Paret G; Atias Y; Barr J
    Harefuah; 2004 Apr; 143(4):261-5, 319. PubMed ID: 15116581
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.
    Ewenczyk C; Leroux A; Roubergue A; Laugel V; Afenjar A; Saudubray JM; Beauvais P; Billette de Villemeur T; Vidailhet M; Roze E
    Brain; 2008 Mar; 131(Pt 3):760-1. PubMed ID: 18202104
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II.
    Yüksel D; Senbil N; Yilmaz D; Yarali N; Gürer YK
    Turk J Pediatr; 2009; 51(2):187-9. PubMed ID: 19480335
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cyanosis, a clinical sign of methemoglobinemia].
    de Rubens-Figueroa J; Jiménez-González ME; Francisco-Revilla EN
    Rev Med Inst Mex Seguro Soc; 2008; 46(4):439-44. PubMed ID: 19213218
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The tale of a blue toddler.
    Sharif F; Hussey S; Gill D
    Ir Med J; 2003 Sep; 96(8):248-9. PubMed ID: 14653384
    [No Abstract]   [Full Text] [Related]  

  • 12. [Cyanosis. Hemoglobin M as the cause in 2 unrelated Norwegian families].
    Finne PH; Stavem P
    Tidsskr Nor Laegeforen; 1973 Jun; 93(16):1226-9. PubMed ID: 4752595
    [No Abstract]   [Full Text] [Related]  

  • 13. The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia.
    Kim DS; Baek HJ; Kim BR; Yoon BA; Lee JH; Kook H
    Yonsei Med J; 2020 Dec; 61(12):1064-1067. PubMed ID: 33251782
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 5-Month-Old Infant with Diffuse Cyanosis and No Other Symptoms.
    Deganello Saccomani M; Cavarzere P; Silvagni D; Dal Corso S; Perlini S; Biban P
    Pediatr Ann; 2016 Apr; 45(4):e116-9. PubMed ID: 27064466
    [No Abstract]   [Full Text] [Related]  

  • 15. Hereditary methemoglobinemia.
    Jamal A
    J Coll Physicians Surg Pak; 2006 Feb; 16(2):157-9. PubMed ID: 16499818
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Blue lips].
    Rantalaiho V; Lehto P; Salonen T
    Duodecim; 1999; 115(19):2117,2119. PubMed ID: 11958167
    [No Abstract]   [Full Text] [Related]  

  • 17. [Congenital methaemoglobinaemia--a rare cause of dyspnoea and cyanosis].
    Rasmussen KB; Gantzhorn EK
    Ugeskr Laeger; 2011 Aug; 173(35):2133-4. PubMed ID: 21884667
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cyanosis in 14-year-old patient. Methemoglobinemia: case report].
    Orlandi M; Amadi MA; Goldaracena PX; Péreza FE
    Arch Argent Pediatr; 2018 Jun; 116(3):e429-e432. PubMed ID: 29756717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Congenital methaemoglobinaemia: a rare cause of cyanosis in an adult patient.
    Londhey V; Khadilkar K; Gad J; Chawla B; Asgaonkar D
    J Assoc Physicians India; 2014 Mar; 62(3):269-71. PubMed ID: 25327075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.