Results 111 to 120 of about 14,442 (233)

Identification of glycoprotein Ib as a target for autoantibody in idiopathic (autoimmune) thrombocytopenic purpura [PDF]

, 1986
NS Szatkowski, TJ Kunicki, RH Aster
openalex   +1 more source

Splenectomy for wandering splenomegaly in a patient with idiopathic thrombocytopenic purpura: A case report of a rare association. [PDF]

Int J Surg Case Rep, 2022
Korbi I, Rabti S, Chaouch MA, Bouchrika A, Zouari K, Noomene F.   +5 more
europepmc   +1 more source

Idiopathic Thrombocytopenic Purpura: A Case of Particular Historic Interest [PDF]

, 1980
B A Bannister, B. Wonke, B. G. Clendinnen   +2 more
openalex   +1 more source

Spontaneous bilateral peripapillary, subhyaloid and vitreous hemorrhage with severe anemia secondary to idiopathic thrombocytopenic purpura

Indian Journal of Ophthalmology, 2010
A 42-year-old female presented to us with a complaint of sudden painless loss of vision in both eyes of three days duration. Visual acuity was 20/100 for distance in both eyes.
Majji Ajit, Bhatia Kapil, Mathai Annie
doaj  

Endothelial nitric oxide synthase Glu298Asp gene polymorphism in the cases of idiopathic thrombocytopenic purpura. [PDF]

Blood Res, 2022
Akarsu S, Arslan FN, Erol D.
europepmc   +1 more source

Bolus Methylprednisolone Therapy in Chronic Idiopathic Thrombocytopenic Purpura in Children [PDF]

, 1984
Şînasi Özsoylu
openalex   +1 more source

Intracranial haemorrhage in a 26 year-old woman with idiopathic thrombocytopenic purpura [PDF]

, 1987
Gavin I. Awerbuch, Reuven Sandyk
openalex   +1 more source

Long-term use of anti-D in chronic idiopathic thrombocytopenic purpura

The Turkish Journal of Pediatrics, 1994
Chronic idiopathic thrombocytopenic purpura is an autoimmune disease characterized by antibody-mediated destruction of platelets. To maintain the platelets above the symptomatic level, we administered anti-D (100 micrograms for 5 consecutive days)
I Yaprak, S Cağlayan, S Kansoy, E Ozdoğru, A R Bakiler, H Aydinlioğlu   +5 more
doaj  

Idiopathic thrombocytopenic purpura in a patient with Laurence-Moon-Bardet-Biedl syndrome [PDF]

, 1988
Don M. Benson, Steven R. Shepherd, Bernard Dash   +2 more
openalex   +1 more source

CIResDiff: A Clinically-Informed Residual Diffusion Model for Predicting Idiopathic Pulmonary Fibrosis Progression [PDF]

arXiv
The progression of Idiopathic Pulmonary Fibrosis (IPF) significantly correlates with higher patient mortality rates. Early detection of IPF progression is critical for initiating timely treatment, which can effectively slow down the advancement of the disease. However, the current clinical criteria define disease progression requiring two CT scans with
arxiv