Results 11 to 20 of about 1,309,059 (309)

The differential diagnosis of chorea [PDF]

open access: yesPractical Neurology, 2007
Chorea is a hyperkinetic movement disorder characterised by excessive spontaneous movements that are irregularly timed, randomly distributed and abrupt. In this article, the authors discuss the causes of chorea, particularly Huntington's disease and the genetic syndromes that may resemble it, including HDL1-3, inherited prion disease, spinocerebellar ...
Wild, EJ, Tabrizi, SJ
openaire   +6 more sources

Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome [PDF]

open access: yesThe Korean Journal of Internal Medicine, 2020
Thrombotic microangiopathy (TMA) is defined by specific clinical characteristics, including microangiopathic hemolytic anemia, thrombocytopenia, and pathologic evidence of endothelial cell damage, as well as the resulting ischemic end-organ injuries.
Hajeong Lee   +14 more
doaj   +1 more source

Epileptic seizure as the first sign of hypoparathyroidism [PDF]

open access: yesVojnosanitetski Pregled, 2011
Background. Hypoparathyroidism refers to a group of disorders in which extracellular calcium levels cannot be maintained within the normal range due to relative or absolute deficiency of parathyroid hormone (PTH).
Pešić Milica   +4 more
doaj   +1 more source

Тhe value of transbronchial needle aspiration cytology in the diagnosis of stage I and II sarcoidosis [PDF]

open access: yesVojnosanitetski Pregled, 2017
Background/Aim. Sarcoidosis is a multisystem infmammatory disease of unknown etiology, with the lungs and intrathoracic lymph nodes the most commonly involved.
Tatomirović Željka   +8 more
doaj   +1 more source

Differential Diagnosis of Elbow Pain

open access: yesThe Ewha Medical Journal, 2023
Elbow pain is a common symptom encountered in clinical practice. Pathology can arise from any component of the joint, including the bone, tendons, ligament, bursa, or nerves.
Hyung-Jin Chung   +3 more
doaj   +1 more source

Congenital cholesteatoma of mastoid origin: A multicenter case series [PDF]

open access: yesVojnosanitetski Pregled, 2014
Background/Aim. The mastoid is the rarest site for the onset of congenital cholesteatoma (CC). The symptoms are atypical and minimal. The aim of this multicenter retrospective descriptive study was to define this extremely rare condition and its
Čvorović Ljiljana   +5 more
doaj   +1 more source

Let’s Play a Game! Kin-LDD: A Tool for Assisting in the Diagnosis of Children with Learning Difficulties

open access: yesMultimodal Technologies and Interaction, 2019
This paper presents an alternative approach for the diagnosis of learning difficulties in children. A game-based evaluation study, using Kinaesthetic Learning Difficulties Diagnosis (Kin-LDD), was performed during the actual diagnosis procedure for the ...
Eleni Chatzidaki   +2 more
doaj   +1 more source

Large saphenous venous graft aneurysm mimicking atypical mediastinal mass [PDF]

open access: yesVojnosanitetski Pregled, 2009
Background. Saphenous venous graft (SVG) aneurysm is a very rare but potentially fatal complication of the coronary artery bypass surgery. Case report. We reported a case of 72-year-old man admitted to hospital because of atypical chest pain related to ...
Krotin Mirjana   +5 more
doaj   +1 more source

Good’s syndrome with increasing γδ T-lymphocyte subpopulation: A case report [PDF]

open access: yesVojnosanitetski Pregled, 2015
Introduction. Good’s syndrome is a rare cause of adultonset immunodeficiency associated with thymoma. Good’s syndrome should be considered in patients older than 40 years with the history of frequent infections.
Tadić Dragana   +3 more
doaj   +1 more source

Differential diagnosis

open access: yesMiddle East Fertility Society Journal, 2016
Abnormal uterine bleeding may be acute or chronic accounting for up to 30% of outpatient visits to gynecologists. Hyperprolactinemia is one of the most common endocrine disorders associated with ovulatory dysfunction that results in menstrual ...
Abdallah Adra   +13 more
doaj   +1 more source

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