138 related articles for article (PubMed ID: 35104462)
41. A novel mutation in type II methemoglobinemia.
Hudspeth MP; Joseph S; Holden KR
J Child Neurol; 2010 Jan; 25(1):91-3. PubMed ID: 19471045
[TBL] [Abstract][Full Text] [Related]
42. 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]
43. Novel Compound Heterogeneous Mutations in CYB5R3 Gene Leading to Methemoglobinemia (Type I) in a Chinese Boy: Case Report and Relevant Comprehensive Analysis.
Yang Y; Yang Y; Meng Y; Huang L; Yang Z
Acta Haematol; 2024 May; ():1-7. PubMed ID: 38781945
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report.
Shin C; Hong M; Kim M; Lee JH
BMC Pediatr; 2019 Jul; 19(1):221. PubMed ID: 31269924
[TBL] [Abstract][Full Text] [Related]
46. Cyanosis and congenital methemoglobinemia in a puppy.
Fine DM; Eyster GE; Anderson LK; Smitley A
J Am Anim Hosp Assoc; 1999; 35(1):33-5. PubMed ID: 9934925
[TBL] [Abstract][Full Text] [Related]
47. Hemoglobin M Disease as a Cause of Cyanosis in a Newborn.
Alonso-Ojembarrena A; Lubián-López SP
J Pediatr Hematol Oncol; 2016 Apr; 38(3):173-5. PubMed ID: 26694193
[TBL] [Abstract][Full Text] [Related]
48. A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II.
Yilmaz D; Cogulu O; Ozkinay F; Kavakli K; Roos D
Am J Med Genet A; 2005 Feb; 133A(1):101-2. PubMed ID: 15744830
[No Abstract] [Full Text] [Related]
49. Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations.
Kedar PS; Warang P; Ghosh K; Colah RB
Am J Hematol; 2011 Mar; 86(3):327-9. PubMed ID: 21328435
[No Abstract] [Full Text] [Related]
50. Congenital Methemoglobinemia: First Confirmed Case in the Arab Population with a Novel Variant in the
Al-Abdulmalek A; Al-Sulaiman R; Abu-Tineh M; Yassin MA
J Blood Med; 2023; 14():247-251. PubMed ID: 37025988
[TBL] [Abstract][Full Text] [Related]
51. HbM methaemoglobinaemia as a rare case of early neonatal benign cyanosis.
Elboraee MS; Clarke G; Belletrutti MJ; Escoredo S
BMJ Case Rep; 2015 Oct; 2015():. PubMed ID: 26494721
[TBL] [Abstract][Full Text] [Related]
52. 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; 447(1):59-67. PubMed ID: 16469290
[TBL] [Abstract][Full Text] [Related]
53. Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase.
Percy MJ; Crowley LJ; Davis CA; McMullin MF; Savage G; Hughes J; McMahon C; Quinn RJ; Smith O; Barber MJ; Lappin TR
Br J Haematol; 2005 Jun; 129(6):847-53. PubMed ID: 15953014
[TBL] [Abstract][Full Text] [Related]
54. Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family.
Kedar P; Warang P; Ghosh K; Colah R
Ann Hematol; 2012 Dec; 91(12):1985-6. PubMed ID: 22797852
[No Abstract] [Full Text] [Related]
55. 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]
56. [Congenital methemoglobinemia with cytochrome-b5-reductase deficiency: 4th Swiss family].
Bürgi W; Fischer S; Killer D; Kaufmann H; Gnehm H; Fricker HS
Schweiz Med Wochenschr; 1989 Sep; 119(39):1355-7. PubMed ID: 2799343
[TBL] [Abstract][Full Text] [Related]
57. Neurological and Neuroimaging Features of
Nicita F; Sabatini L; Alesi V; Lucignani G; Sallicandro E; Sferra A; Bertini E; Zanni G; Palumbo G
Brain Sci; 2022 Jan; 12(2):. PubMed ID: 35203946
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. 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]
60. Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene.
Kugler W; Pekrun A; Laspe P; Erdlenbruch B; Lakomek M
Hum Mutat; 2001 Apr; 17(4):348. PubMed ID: 11295830
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]