Results 111 to 120 of about 13,066 (196)

LABRAD : Vol 41, Issue 2 - July 2015 [PDF]

, 2015
An Overview of Immunoglobulin G4-Related Disease Plasma Neutrophil Gelatinase Associated Lipocalin (NGAL) a Marker of Acute Kidney Injury Celiac Disease: Biomarkers for Diagnosis and Monitoring Pathophysiology of Paroxysmal Nocturnal Haemoglobinuria and ...
Aga Khan Universiity Hospital, Karachi
core   +1 more source

Paroxysmal nocturnal hemoglobinuria--hemolysis before and after eculizumab. [PDF]

, 2010
Hill A, Hillmen P., Kelly R, Luzzatto L, Notaro R, RISITANO, ANTONIO MARIA   +5 more
core   +1 more source

Antiphosphatidylserine antibody as a cause of multiple dural venous sinus thromboses and ST-elevation myocardial infarction [PDF]

, 2018
Objective: Rare disease Background: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by antibodies directed against phos-pholipids on plasma membranes. Through unclear mechanisms, APS confers hypercoagulability.
Marquardt, Caillin W., Pickens, Peter V., Varner, Chelsea K.   +2 more
core   +1 more source

Anticomplement therapy

Biologics: Targets & Therapy, 2009
Prathit A Kulkarni1, Vahid Afshar-Kharghan21Baylor College of Medicine, Houston, Texas, USA; 2The University of Texas, M.D. Anderson Cancer Center, Houston, Texas, USAAbstract: The complement system is an important part of innate immunity; however, as ...
Prathit A Kulkarni, Vahid Afshar-Kharghan   +1 more
doaj  

A patient with paroxysmal nocturnal hemoglobinuria being treated with eculizumab who underwent laparoscopic cholecystectomy: report of a case [PDF]

, 2015
Isaku Yoshioka, Isaya Hashimoto, Kazuhiro Tsukada, Koshi Matsui, Makoto Moriyama, Takuya Nagata, Tomoyuki Okumura   +6 more
core   +1 more source

SYNOPSIS IS A RARE CASE OF ORPHAN CO-MORBIDITY. EXPERIENCE IN TREATING A PATIENT WITH APLASTIC AND CLONOXYSMAL NOCTURNAL HEMOGLOBINURIA

Медицина в Кузбассе
Paroxysmal nocturnal hemoglobinuria (APG) is a rare clonal disease, an acquired form of hemolytic anemia from the group of rare (orphan) diseases. A characteristic clinical manifestation with a significant APG clone (usually more than 10 % of the total ...
Дмитрий Михайлович Неверов, Марина Владимировна Косинова, Светлана Ивановна Елгина, Елена Владимировна Рудаева, Кира Борисовна Мозес, Наталья Степановна Черных   +5 more
doaj  

Paroxysmal nocturnal hemoglobinuria pnh

Hematology, Transfusion and Cell Therapy, 2020
Hanan Hamed
doaj   +1 more source

Paroxysmal Cold Hemoglobinuria Associated With Monoclonal B-Cell Lymphocytosis in an Elderly Patient: A Report of a Rare Case. [PDF]

Cureus
Nasim S, Bartock M.
europepmc   +1 more source

Paroxysmal Nocturnal Hemoglobinuria-Driven Hepatic Vein Thrombosis: A Case of Budd-Chiari Syndrome in Disguise. [PDF]

Cureus
Agrawal S, Prasad S, Nagda J, Parmar V, Reddy A.   +4 more
europepmc   +1 more source

Successful Birth After First-Trimester Ravulizumab Exposure in a Patient With Paroxysmal Nocturnal Hemoglobinuria: A Case Report. [PDF]

EJHaem
Morioka T, Arai S, Arai Y, Konno S, Tokuda K, Matsuo T, Matsumoto K, Shirasaki R, Ooi J, Kihira C, Sasamori Y, Nagasaka K, Tashiro H.   +12 more
europepmc   +1 more source