Results 91 to 100 of about 17,995 (265)

RIFAMPICIN INDUCED PURE RED CELL APLASIA

Zdravniški Vestnik, 2008
BACKGROUND Pure red cell aplasia (PRCA) is a rare condition of severe anemia characterized by anabsence of erythroid precursor in the bone marrow, severe reticulocytopenia and normalplatelet and leukocyte count.
Marija Čeh
doaj  

Islet isolation assessment in man and large animals [PDF]

, 1990
Recent progress in islet isolation from the pancreas of large mammals including man, accentuated the need for the development of precise and reproducible techniques to assess islet yield.
Alejandro, R, Bretzel, RG, Carlo, VD, Falqui, L, Federlin, K, Gray, DWR, Hering, BJ, James, RFL, Kaufman, DB, Kneteman, NM, Lacy, PE, Lake, SP, London, NJM, Mintz, DH, Morris, PJ, Pozza, G, Rajotte, RV, Ricordi, C, Scharp, DW, Socci, C, Starzl, TE, Sutherland, DER, Tzakis, A, Viviani, G, Warnock, GL, Zeng, Y   +25 more
core   +1 more source

Qualitative and Quantitative Blood Cell Disorders Among High‐Level Antiretroviral Therapy‐Experienced Children in Northwest Ethiopia: A Cross‐Sectional Study

Health Science Reports, Volume 8, Issue 6, June 2025.
ABSTRACT Background and Aims The human immunodeficiency virus (HIV) and its treatment are commonly associated with blood cell morphological and numerical abnormalities. As a result, routine examination of blood disorders among HIV patients is necessary to minimize related complications and improve patients' prognosis.
Dereje Mengesha Berta, Biruk Bayleyegn, Solomon Getawa, Zewudu Mulatie, Tiruneh Adane, Elias Chane, Bisrat Birke Teketelew, Melak Aynalem   +7 more
wiley   +1 more source

Pure Red Cell Aplasia Associated with Thymolipoma: Complete Anaemia Resolution following Thymectomy

Case Reports in Hematology, 2018
Pure red cell aplasia is an uncommon cause of anaemia rarely associated with thymoma. A combination of immunosuppressive therapy and thymectomy offers a potential cure. Thymectomy alone rarely results in anaemia resolution.
David Ferreira, Royston Ponraj, Adrian Yeung, Jillian de Malmanche   +3 more
doaj   +1 more source

Robot‐Assisted Versus Open Surgery for the Resection of Large Thymomas: A Retrospective Cohort Study

Journal of Surgical Oncology, Volume 131, Issue 8, Page 1543-1550, June 2025.
ABSTRACT Background Robot‐assisted thoracic surgery (RATS) is increasingly becoming the preferred surgical method for the resection of thymomas. We initiated the current study to evaluate perioperative outcomes and early recurrence associated with the surgical approach.
Benedikt Niedermaier, Raffaella Griffo, Florian Eichhorn, Laura V. Klotz, Heidrun Grosch, Thomas Muley, Hauke Winter, Martin E. Eichhorn   +7 more
wiley   +1 more source

Clinico-Hematological Features in Pure Red Cell Aplasia Patients Diagnosed at Diagnostic & Research Laboratory, Hyderabad

Liaquat Medical Research Journal, 2020
Pure red-cell aplasia (PRCA) or erythroblastopenia is a rare type of anemia or disorder that can be either idiopathic or associated with certain autoimmune diseases and affect red blood cell (RBC) precursors1,2. The disease is often present at birth, and
Faheem Ahmed Memon
doaj  

Bone marrow examination findings at aga Khan University Hospital, Nairobi [PDF]

, 2010
Objective: To establish the bone marrow examination findings and determine the indication for bone marrow examination. Design: A retrospective audit. Setting: Aga Khan University Hospital, Nairobi.
Malkit, Riyat, Okinda, Nancy
core   +2 more sources

Pure Red Cell Aplasia with Adult Onset Still’s Disease

Case Reports in Medicine, 2013
Adult Onset Still’s Disease (AOSD) is a rare inflammatory syndrome mostly seen in young adults. Known for its wide range of clinical manifestations, AOSD often presents with nonremitting systemic signs and symptoms.
Nicholas Robillard, Paul Van Nguyen, Robert Wistaff, Mikhael Laskine   +3 more
doaj   +1 more source

Pathophysiologic Mechanisms And Management Of Large Granular Lymphocytic Leukemia Associated Pure Red Cell Aplasia

OncoTargets and Therapy, 2019
Large granular lymphocytic leukemia (LGLL) is a chronic clonal lymphoproliferative disease of mature T or NK cells, and produces a variety of hematological abnormalities.
Z. Qiu, Rong Qin, Guang-Yu Tian, Yan Wang, Ye-Qing Zhang   +4 more
semanticscholar   +1 more source

CD34+ enriched donor lymphocyte infusions in a case of pure red cell aplasia and late graft failure after major ABO-incompatible bone marrow transplantation [PDF]

, 1998
A variety of immunohematological complications may occur after ABO-incompatible BMT. We report a CML patient (blood group O) who received a BMT from an HLA-identical sibling (blood group AB).
DE ROSA G., LUCIANO L., PEZZULLO L., PICARDI, MARCO, RAIOLA A., ROTOLI, BRUNO, SELLERI C.   +6 more
core   +1 more source