Results 81 to 90 of about 10,614 (201)

Introducing polyautoimmunity: secondary autoimmune diseases no longer exist [PDF]

open access: yes, 2014
Similar pathophysiological mechanisms within autoimmune diseases have stimulated searches for common genetic roots. Polyautoimmunity is defined as the presence of more than one autoimmune disease in a single patient.
Amaya-Amaya, Jenny-Carolina   +4 more
core   +1 more source

Platelet Responses After Tapering and Discontinuation of Fostamatinib in Patients with Immune Thrombocytopenia: A Continuation of the Fostasur Study [PDF]

open access: yes
Background/objectives: Fostamatinib is a spleen tyrosine kinase (SYK) inhibitor approved for the treatment of adult patients with chronic immune thrombocytopenia (ITP).
Mingot-Castellano, María Eva   +20 more
core   +1 more source

Disease pathogenesis, treatment effectiveness, and co-morbid burden among adult patients with primary immune thrombocytopenia (ITP) [PDF]

open access: yes, 2010
Background Primary immune thrombocytopenia (ITP) is an autoimmune disease involving autoantibody-mediated platelet destruction, suboptimal platelet production, and T-cell-mediated platelet lysis.
Sarpatwari, Ameet Vilas
core   +1 more source

Idiopathic thrombocytopenic purpura. Clinical case

open access: yesZaporožskij Medicinskij Žurnal, 2015
Aim. To draw the attention of physicians - internists to the problem of thrombocytopenia and hemorrhagic vasculitis. To describe the clinical case of idiopathic thrombocytopenic purpura, features of diagnostics and treatment of this disease at various ...
V. V. Syvolap   +2 more
doaj   +1 more source

A Remarkable Improvement of Patients with Idiopathic Thrombocytopenic Purpura after appendectomy including Carcinoid tumor

open access: yesIranian South Medical Journal, 2011
The assistance of chronic idiopathic thrombocytopenic purpura and appendiceal carcinoid tumor is so rare and has not been reported before .we present here in a 11 year old boy that is the known case of chronic idiopathic thrombocytopenic purpura (with ...
Hamidreza Alizadeh-Otaghvar   +5 more
doaj  

Diabetes mellitus de tipo I y púrpura trombocitopénica inmunitaria en una niña

open access: yesMedisan
Se detalla el caso clínico de una paciente de 11 años de edad, con antecedentes de diabetes mellitus de tipo I, que comenzó a presentar manchas de color rojo oscuro en la piel (similares a moretones) en brazos, frente y piernas desde hacía 3 meses.
José Raúl Zaldívar Ochoa   +3 more
doaj   +2 more sources

Smjernice za dijagnostiku i liječenje primarne imunosne trombocitopenije u odraslih [Guidelines for diagnostics and treatment of primary immune thrombocytopenia in adults] [PDF]

open access: yes, 2017
Working Group for Diseases of Hemostasis and Thrombosis of the Croatian Cooperative Group for Hematologic Diseases (CROHEM), Referral Center for Hereditary and Acquired Disorders of Hemostasis of the Croatian Ministry of Health, and Croatian Hematology ...
Nemet, Damir   +5 more
core  

GUIDELINES FOR DIAGNOSTICS AND TREATMENT OF PRIMARY IMMUNE THROMBOCYTOPENIA IN ADULTS [PDF]

open access: yes, 2017
Radna skupina za bolesti hemostaze i tromboze Hrvatske kooperativne grupe za hematološke bolesti (KROHEM), Referentni centar Ministarstva zdravlja Republike Hrvatske za nasljedne i stečene bolesti hemostaze te Hrvatsko hematološko društvo Hrvatskoga ...
Damir Nemet   +5 more
core   +1 more source

Diagnostic specifics of demyelinating optic neuritis on the idiopathic thrombocytopenic purpura

open access: yesРоссийский офтальмологический журнал
A clinical case of optic neuritis in a patient with idiopathic thrombocytopenic purpura is presented. As a result of a comprehensive ophthalmological, clinical, instrumental and laboratory examination, objective signs of unilateral demyelinating damage ...
T. D. Okhotsimskaya, E. K. Eliseeva
doaj   +1 more source

Acute immune thrombocytopenic purpura in childhood Presentation and treatment A Hospital based study

open access: yesمجلة كلية الطب, 2014
Background: Acute idiopathic thrombocytopenic purpura (ITP) is a self – limiting illness, usually occurring after an infectious disease, and it is due to decrease number of circulating platelets manifests as a bleeding tendency, easy bruising (purpura ...
Mahjoob Al-Naddawi   +2 more
doaj   +1 more source

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