Nagel RL - Search Results

1

Evolution of laboratory parameters during sickle cell painful crisis: evidence compatible with dense red cell sequestration without thrombosis.

Billett HH, Nagel RL, Fabry ME. Billett HH, et al. Among authors: nagel rl. Am J Med Sci. 1988 Nov;296(5):293-8. doi: 10.1097/00000441-198811000-00001. Am J Med Sci. 1988. PMID: 2973751

2

The unique red cell heterogeneity of SC disease: crystal formation, dense reticulocytes, and unusual morphology.

Lawrence C, Fabry ME, Nagel RL. Lawrence C, et al. Among authors: nagel rl. Blood. 1991 Oct 15;78(8):2104-12. Blood. 1991. PMID: 1912587 Free article.

3

The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients.

Nagel RL, Erlingsson S, Fabry ME, Croizat H, Susuka SM, Lachman H, Sutton M, Driscoll C, Bouhassira E, Billett HH. Nagel RL, et al. Blood. 1991 Mar 15;77(6):1371-5. Blood. 1991. PMID: 2001460 Free article.

4

Maternal hemoglobin F levels may have an adverse effect on neonatal birth weight in pregnancies with sickle cell disease.

Anyaegbunam A, Billett HH, Langer O, Brustman L, Berger C, Wyse L, Nagel RL, Merkatz IR. Anyaegbunam A, et al. Among authors: nagel rl. Am J Obstet Gynecol. 1989 Sep;161(3):654-6. doi: 10.1016/0002-9378(89)90372-4. Am J Obstet Gynecol. 1989. PMID: 2476930

5

Erythrocytic and vascular factors influencing the microcirculatory behavior of blood in sickle cell anemia.

Kaul DK, Fabry ME, Nagel RL. Kaul DK, et al. Among authors: nagel rl. Ann N Y Acad Sci. 1989;565:316-26. doi: 10.1111/j.1749-6632.1989.tb24179.x. Ann N Y Acad Sci. 1989. PMID: 2672967 Review. No abstract available.

6

Pentoxifylline (Trental) has no significant effect on laboratory parameters in sickle cell disease.

Billett HH, Kaul DK, Connel MM, Fabry ME, Nagel RL. Billett HH, et al. Among authors: nagel rl. Nouv Rev Fr Hematol (1978). 1989;31(6):403-7. Nouv Rev Fr Hematol (1978). 1989. PMID: 2694097 Clinical Trial.

7

Hemoglobin distribution width: a rapid assessment of dense red cells in the steady state and during painful crisis in sickle cell anemia.

Billett HH, Fabry ME, Nagel RL. Billett HH, et al. Among authors: nagel rl. J Lab Clin Med. 1988 Sep;112(3):339-44. J Lab Clin Med. 1988. PMID: 3411196

8

F reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: a double-blind study.

Nagel RL, Vichinsky E, Shah M, Johnson R, Spadacino E, Fabry ME, Mangahas L, Abel R, Stamatoyannopoulos G. Nagel RL, et al. Blood. 1993 Jan 1;81(1):9-14. Blood. 1993. PMID: 8417806 Free article. Clinical Trial.

9

The pathophysiology of vascular obstruction in the sickle syndromes.

Kaul DK, Fabry ME, Nagel RL. Kaul DK, et al. Among authors: nagel rl. Blood Rev. 1996 Mar;10(1):29-44. doi: 10.1016/s0268-960x(96)90018-1. Blood Rev. 1996. PMID: 8861277 Review.

10

Rapid increase in red blood cell density driven by K:Cl cotransport in a subset of sickle cell anemia reticulocytes and discocytes.

Fabry ME, Romero JR, Buchanan ID, Suzuka SM, Stamatoyannopoulos G, Nagel RL, Canessa M. Fabry ME, et al. Among authors: nagel rl. Blood. 1991 Jul 1;78(1):217-25. Blood. 1991. PMID: 1712642 Free article.

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