PubMed

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 Jul-Aug;26(5):381-5.PMID: 19579085 [PubMed - indexed for MEDLINE]Related articles

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 Mar-Apr;51(2):187-9.PMID: 19480335 [PubMed - indexed for MEDLINE]Related articles

Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M.

Spears F, Banerjee A.

Can J Anaesth. 2008 Jun;55(6):391-2. No abstract available. PMID: 18566207 [PubMed - indexed for MEDLINE]Related articles

Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M.

Melarkode K, Prinzhausen H.

Can J Anaesth. 2008 Feb;55(2):129-30. No abstract available. PMID: 18245076 [PubMed - indexed for MEDLINE]Related articles

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.

Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K.

Blood Cells Mol Dis. 2008 May-Jun;40(3):323-7. Epub 2007 Oct 25.PMID: 17964195 [PubMed - indexed for MEDLINE]Related articles

Expression of a novel P275L variant of NADH:cytochrome b5 reductase gives functional insight into the conserved motif important for pyridine nucleotide binding.

Percy MJ, Crowley LJ, Boudreaux J, Barber MJ.

Arch Biochem Biophys. 2006 Mar 1;447(1):59-67. Epub 2006 Jan 19.PMID: 16469290 [PubMed - indexed for MEDLINE]Related articles

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 Jan-Feb;36(1):81-90. Epub 2005 Nov 28.PMID: 16310381 [PubMed - indexed for MEDLINE]Related articles

Methylene blue in congenital methemoglobinemia: prophylactic or on demand?

Sharma D, Pandia MP, Bithal PK.

Can J Anaesth. 2005 Oct;52(8):884-5; author reply 885. No abstract available. PMID: 16189344 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 16087059 [PubMed - indexed for MEDLINE]Related articles

Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.

Kedar PS, Nadkarni AH, Phanasgoankar S, Madkaikar M, Ghosh K, Gorakshakar AC, Colah RB, Mohanty D.

Am J Hematol. 2005 Jun;79(2):168-70.PMID: 15929117 [PubMed - indexed for MEDLINE]Related articles

Heterogeneity of the molecular biology of methemoglobinemia: a study of eight consecutive patients.

Maran J, Guan Y, Ou CN, Prchal JT.

Haematologica. 2005 May;90(5):687-9.PMID: 15921385 [PubMed - indexed for MEDLINE]Related articlesFree article

Prophylactic methylene blue in a patient with congenital methemoglobinemia.

Baraka AS, Ayoub CM, Yazbeck-Karam V, Kaddoum RN, Gerges FJ, Hadi UM, Dagher CM.

Can J Anaesth. 2005 Mar;52(3):258-61.PMID: 15753496 [PubMed - indexed for MEDLINE]Related articles

Anesthetic management of a patient with congenital methemoglobinemia.

Maurtua MA, Emmerling L, Ebrahim Z.

J Clin Anesth. 2004 Sep;16(6):455-7.PMID: 15567652 [PubMed - indexed for MEDLINE]Related articles

Cytochrome b5 oxidoreductase: expression and characterization of the original familial ideopathic methemoglobinemia mutations E255- and G291D.

Davis CA, Barber MJ.

Arch Biochem Biophys. 2004 May 15;425(2):123-32.PMID: 15111120 [PubMed - indexed for MEDLINE]Related articles

Congenital methemoglobinemia: a rare cause of cyanosis in the newborn--a case report.

Da-Silva SS, Sajan IS, Underwood JP 3rd.

Pediatrics. 2003 Aug;112(2):e158-61.PMID: 12897322 [PubMed - indexed for MEDLINE]Related articlesFree article

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.PMID: 12803131 [PubMed - indexed for MEDLINE]Related articles

Introduction: congenital methemoglobinemia revisited.

Gibson Q.

Blood. 2002 Nov 15;100(10):3445-6. No abstract available. PMID: 12411314 [PubMed - indexed for MEDLINE]Related articlesFree article

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase.

Percy MJ, Gillespie MJ, Savage G, Hughes AE, McMullin MF, Lappin TR.

Blood. 2002 Nov 15;100(10):3447-9. Epub 2002 Jul 5.PMID: 12393396 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular mechanism of recessive congenital methemoglobinemia in Chinese pedigrees.

Wang Y, Huang C, Wu Y, Lan F, Tang Y, Zhu Z.

Chin Med J (Engl). 1999 Nov;112(11):1032-5.PMID: 11721467 [PubMed - indexed for MEDLINE]Related articles

Severe oxyhemoglobin desaturation during induction of anesthesia in a patient with congenital methemoglobinemia.

Baraka AS, Ayoub CM, Kaddoum RN, Maalouli JM, Chehab IR, Hadi UM.

Anesthesiology. 2001 Nov;95(5):1296-7. No abstract available. PMID: 11685006 [PubMed - indexed for MEDLINE]Related articlesFree article