نتائج البحث - "Methemoglobinemia"

1

دورية أكاديمية

Rasburicase causing severe oxidative hemolysis and methemoglobinemia in a patient with previously unrecognized glucose-6-phosphate dehydrogenase deficiency.

المؤلفون: Cheah CY; Department of Haematology, Peter MacCallum Cancer Centre, Melbourne, Vic., Australia., Lew TE, Seymour JF, Burbury K

المصدر: Acta haematologica [Acta Haematol] 2013; Vol. 130 (4), pp. 254-9. Date of Electronic Publication: 2013 Jul 11.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1421-9662 (Electronic) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

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2

دورية أكاديمية

Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I.

المؤلفون: Rawa K; Department of Paediatrics, Haematology and Oncology, Medical University of Warsaw, Warsaw, Poland., Chelmecka-Hanusiewicz L, Plochocka D, Pawinska-Wasikowska K, Balwierz W, Burzynska B

المصدر: Acta haematologica [Acta Haematol] 2013; Vol. 130 (2), pp. 122-5. Date of Electronic Publication: 2013 Apr 13.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1421-9662 (Electronic) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Cytochrome-B(5) Reductase/*genetics , Methemoglobinemia/*diagnosis, Child, Preschool ; Cytochrome-B(5) Reductase/chemistry ; Cytochrome-B(5) Reductase/metabolism ; Homozygote ; Humans ; Male ; Methemoglobinemia/genetics ; Pedigree ; Polymorphism, Single Nucleotide ; Protein Structure, Tertiary

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3

دورية أكاديمية

Determination of concentration of cytosolic NADH-cytochrome b5 reductase in erythrocytes from normal Chinese adults, neonates and patients with hereditary methemoglobinemia by double-antibody sandwich ELISA.

المؤلفون: Lan F; Department of Laboratory Medicine, DongFang Hospital, Fuzhou City, Fujian Province (China)., Tang Y, Huang C, Zhu Z

المصدر: Acta haematologica [Acta Haematol] 1998; Vol. 100 (1), pp. 44-8.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Cytochrome Reductases/*analysis , Erythrocytes/*enzymology , Methemoglobinemia/*blood, Adult ; Animals ; Antibodies, Monoclonal ; China ; Cytochrome-B(5) Reductase ; Cytosol/enzymology ; Enzyme-Linked Immunosorbent Assay/methods ; Erythrocytes/ultrastructure ; Female ; Humans ; Infant, Newborn ; Methemoglobinemia/epidemiology ; Methemoglobinemia/genetics ; Rabbits

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4

دورية أكاديمية

Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes.

المؤلفون: Mast A, Milo R, Junien C, Leroux A, Krishnamoorthy R, Wajcman H, Labie D, Kaplan JC

المصدر: Acta haematologica [Acta Haematol] 1976; Vol. 56 (3), pp. 174-82.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Dihydrolipoamide Dehydrogenase/*deficiency , Methemoglobinemia/*congenital, Adolescent ; Adult ; Erythrocytes/enzymology ; Female ; Hemoglobins/analysis ; Homozygote ; Humans ; Isoelectric Focusing ; Leukocytes/enzymology ; Male ; Methemoglobinemia/blood ; Methemoglobinemia/genetics

5

دورية أكاديمية

Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girl.

المؤلفون: Vives-Corrons JL, Pujades A, Vela E, Corretger JM, Leroux A, Kaplan JC

المصدر: Acta haematologica [Acta Haematol] 1978; Vol. 59 (6), pp. 348-53.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

6

دورية أكاديمية

Hereditary methemoglobinemia due to diaphorase deficiency. Report of a case of heterozygote presenting with cyanosis after birth.

المؤلفون: Lo SS, Hitzig WH, Marti HR

المصدر: Acta haematologica [Acta Haematol] 1970; Vol. 43 (3), pp. 177-83.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Metabolism, Inborn Errors*, Dihydrolipoamide Dehydrogenase/*metabolism , Methemoglobinemia/*genetics, Alkaline Phosphatase/blood ; Blood Glucose/analysis ; Calcium/blood ; Calcium/therapeutic use ; Calcium/urine ; Creatinine/urine ; Cyanosis/etiology ; Electrophoresis ; Female ; Gels ; Glutathione/blood ; Hematocrit ; Hemoglobinometry ; Heterozygote ; Humans ; Hypocalcemia/complications ; Infant, Newborn ; Male ; Methemoglobinemia/complications ; Methemoglobinemia/drug therapy ; Pedigree ; Phosphates/blood ; Phosphates/urine ; Pregnancy ; Spectrum Analysis ; Starch ; Urea/blood ; Vitamin D/therapeutic use

7

دورية أكاديمية

[Formation of Heinz bodies and hemoglobin changes].

المؤلفون: MAGOS L, SZIZA M

المصدر: Acta haematologica [Acta Haematol] 1959 Jul; Vol. 22, pp. 51-7.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: OLDMEDLINE

مواضيع طبية MeSH: Erythrocytes* , Heinz Bodies* , Hematologic Tests* , Hemoglobins* , Methemoglobinemia*, Nitrobenzenes/*toxicity

8

دورية أكاديمية

Associated red cell enzyme deficiencies and their significance in a case of congenital enzymopenic methemoglobinemia.

المؤلفون: Das Gupta A, Vaidya MS, Bapat JP, Pavri RS, Baxi AJ, Advani SH

المصدر: Acta haematologica [Acta Haematol] 1980; Vol. 64 (5), pp. 285-8.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

9

دورية أكاديمية

Congenital methemoglobinemia due to hemoglobin M.

المؤلفون: Ozsoylu S

المصدر: Acta haematologica [Acta Haematol] 1972; Vol. 47 (4), pp. 225-32.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobins, Abnormal*, Methemoglobinemia/*genetics, Adolescent ; Adult ; Blood Protein Electrophoresis ; Cyanosis/etiology ; Erythrocytes/analysis ; Erythrocytes/enzymology ; Female ; Glucosephosphate Dehydrogenase/blood ; Glutathione/blood ; Hemoglobinometry ; Humans ; Male ; Methemoglobin ; Methemoglobinemia/complications ; Oxidoreductases/blood ; Pedigree ; Quinones/urine ; Spectrum Analysis

10

دورية أكاديمية

Hereditary methemoglobinemic cyanosis due to diaphorase deficiency in three successive generations.

المؤلفون: Ozsoylu S

المصدر: Acta haematologica [Acta Haematol] 1967; Vol. 37 (5), pp. 276-83.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0141053 Publication Model: Print Cited Medium: Print ISSN: 0001-5792 (Print) Linking ISSN: 00015792 NLM ISO Abbreviation: Acta Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Dihydrolipoamide Dehydrogenase/*metabolism , Methemoglobinemia/*genetics, Adolescent ; Adult ; Aged ; Blood Protein Electrophoresis ; Child ; Cyanosis/genetics ; Enzyme Repression ; Erythrocytes/enzymology ; Female ; Hematocrit ; Hemoglobinometry ; Humans ; Male ; Methemoglobinemia/drug therapy ; Methylene Blue/therapeutic use ; Middle Aged ; Pedigree ; Turkey

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