166 related articles for article (PubMed ID: 2779813)
1. [Congenital deficiency of metahemoglobin-reductases (diaphorases). A case of cyanosis during general anesthesia].
Sodano R; Talenti A; Cumani P; Aussello F
Minerva Anestesiol; 1989; 55(1-2):53-6. PubMed ID: 2779813
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [Congenital methemoglobinemia: a rare case of cyanosis in the newborn].
Schwartz L; Franck P; Debruille C; Olivier JL; Vigneron C
Ann Biol Clin (Paris); 2005; 63(3):314-6. PubMed ID: 15951263
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. NADH-diaphorase deficiency identified in a patient with congenital methaemoglobinaemia detected by pulse oximetry.
Sugahara K; Sadohara T; Kawaguchi T; Hirano T
Intensive Care Med; 1998 Jul; 24(7):706-8. PubMed ID: 9722041
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. [Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].
Schmidt K; Faber K; Heni F
Blut; 1974 Jul; 29(1):43-9. PubMed ID: 4367854
[No Abstract] [Full Text] [Related]
9. [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]
10. Leukocyte diaphorase deficiency in congenital methemoglobinemia: a valuable prognostic indicator.
Lawson DL; Miale TD; Harvey JL; Bucciarelli RL; Nelson LS
Biol Neonate; 1977; 32(3-4):193-6. PubMed ID: 603804
[No Abstract] [Full Text] [Related]
11. Anesthesia case of the month. Cyanosis in a dog during anesthesia.
Kushner LI; Mackin AJ
J Am Vet Med Assoc; 1999 Apr; 214(7):1007-9. PubMed ID: 10200793
[No Abstract] [Full Text] [Related]
12. Diaphorase deficiency methaemoglobinaemia mimicking cardiac disease in pregnancy.
Vassallo L; Cauchi M
J Obstet Gynaecol Br Commonw; 1970 Feb; 77(2):178-9. PubMed ID: 5419883
[No Abstract] [Full Text] [Related]
13. 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]
14. Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.
Kaplan JC; Beutler E
Biochem Biophys Res Commun; 1967 Nov; 29(4):605-10. PubMed ID: 16496543
[No Abstract] [Full Text] [Related]
15. Hereditary methemoglobinemia due to diaphorase deficiency. Report of a case of heterozygote presenting with cyanosis after birth.
Lo SS; Hitzig WH; Marti HR
Acta Haematol; 1970; 43(3):177-83. PubMed ID: 4986140
[No Abstract] [Full Text] [Related]
16. [Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis].
Smith B; Pryds OA; Christensen E; Lund AM
Ugeskr Laeger; 2008 Aug; 170(33):2460. PubMed ID: 18761834
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes.
Mast A; Milo R; Junien C; Leroux A; Krishnamoorthy R; Wajcman H; Labie D; Kaplan JC
Acta Haematol; 1976; 56(3):174-82. PubMed ID: 826072
[TBL] [Abstract][Full Text] [Related]
19. Mental retardation in methemoglobinemia due to diaphorase deficiency.
Fialkow PJ; Browder JA; Sparkes RS; Motulsky AG
N Engl J Med; 1965 Oct; 273(16):840-5. PubMed ID: 4378489
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
