1015 Walnut Street
Suite 320
Philadelphia, PA 19107
(215) 955-5266 (Voice box 9-8686)
(215) 955-9170 fax
Suite 320
Philadelphia, PA 19107
(215) 955-5266 (Voice box 9-8686)
(215) 955-9170 fax
Most Recent Peer-reviewed Publications
- Aggregation of normal and sickle hemoglobin in high concentration phosphate buffer
- Gender-specific disease modification by NOS3 (multiple letters)
- Kinetics of increased deformability of deoxygenated sickle cells upon oxygenation
- Hydroxyurea analogues as kinetic and mechanistic probes of the nitric oxide producing reactions of hydroxyurea and oxyhemoglobin
- Urease enhances the formation of iron nitrosyl hemoglobin in the presence of hydroxyurea
- Effects of iron nitrosylation on sickle cell hemoglobin solubility
- Changes in mu opioid receptors and rheological properties of erythrocytes among opioid abusers
- Iron nitrosyl hemoglobin formation from the reactions of hemoglobin and hydroxyurea
- Treatment of painful sickle cell leg ulcers with topical opioids [2]
- In vitro sealing of punctured fetal membranes: Potential treatment for midtrimester premature rupture of membranes
- Granulocytic sarcoma in a patient with hemoglobin sc disease
- Evidence for carbon monoxide binding to sickle cell polymers during melting
- In vitro exposure to hydroxyurea reduces sickle red blood cell deformability
- Sudden unexpected death in a patient with splenic sequestration and sickle cell-β +-thalassemia syndrome
- Determinants of red cell survival and erythropoietic activity in patients with sickle cell anemia in the steady state
- Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24
- Cost-effectiveness of hydroxyurea in sickle cell anemia
- The reactions of myoglobin, normal adult hemoglobin, sickle cell hemoglobin and hemin with hydroxyurea
- The reaction of deoxy-sickle cell hemoglobin with hydroxyurea
- Temperature and domain size dependence of sickle cell hemoglobin polymer melting in high concentration phosphate buffer