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Disruption of PF4/H multimolecular complex formation with a minimally anticoagulant heparin (ODSH). [electronic resource]

By:

Joglekar, M V

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Producer: 20120813Description: 717-25 p. digitalISSN:

2567-689X

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Available from publisher's website

In: Thrombosis and haemostasis vol. 107

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Publication Type: Journal Article; Research Support, N.I.H., Extramural

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61 EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. II. MEASUREMENTS OF ERYTHROCYTE GLUCOSE CONSUMPTION, POTASSIUM FLUX AND ADENOSINE TRIPHOSPHATE STABILITY.
by NATHAN, D G
62 Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.
by Bianchi, Paola
63 A novel PKLR gene mutation identified using advanced molecular techniques.
by He, Yunyan
64 AG-348 enhances pyruvate kinase activity in red blood cells from patients with pyruvate kinase deficiency.
by Kung, Charles
65 The burden of disease in pyruvate kinase deficiency: Patients' perception of the impact on health-related quality of life.
by Grace, Rachael F
66 Rapidly fatal
by Zahid, Mohammad Faizan
67 Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
by Warang, Prashant
68 Coexistence of congenital red cell pyruvate kinase and band 3 deficiency.
by Branca, R
69 [Analysis and prenatal diagnosis of PKLR gene mutations in a family with pyruvate kinase deficiency].
by Li, Dongliang
70 Mutation of the E1 alpha subunit of the pyruvate dehydrogenase complex, in relation to heterogeneity.
by Kitano, A
71 Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia.
by Kager, Leo
72 Determination of [U-13C]glucose turnover into various metabolite pools for the differential diagnosis of lactic acidemias.
by Kassel, D B
73 Introduction of a ketogenic diet in young infants.
by Klepper, J
74 A previously unknown mutation in the pyruvate kinase gene (PKLR) identified from a neonate with severe jaundice.
by Yaish, Hassan M
75 [Disorders of pyruvate metabolism and TCA cycle].
by Kuroda, Y
76 Real-time PCR genotyping assay for feline erythrocyte pyruvate kinase deficiency and mutant allele frequency in purebred cats in Japan.
by Kushida, Kazuya
77 Appraisal of patient-reported outcome measures in analogous diseases and recommendations for use in phase II and III clinical trials of pyruvate kinase deficiency.
by Salek, M S
78 Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
by Manco, Licínio
79 Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats.
by Grahn, Robert A
80 Development of the pyruvate kinase deficiency diary and pyruvate kinase deficiency impact assessment: Disease-specific assessments.
by Salek, Sam