Results 321 to 330 of about 6,717,974 (341)
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Practical Neurology, 2019
A 49-year-old woman presented with an acute intense headache with nausea and vomiting, followed by loss of consciousness. CT scan of head showed diffuse subarachnoid haemorrhage involving the interpeduncular cistern from rupture of a right internal carotid artery aneurysm, which was successfully treated by coil embolisation. On waking in intensive care
Reale, Chiara +4 more
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A 49-year-old woman presented with an acute intense headache with nausea and vomiting, followed by loss of consciousness. CT scan of head showed diffuse subarachnoid haemorrhage involving the interpeduncular cistern from rupture of a right internal carotid artery aneurysm, which was successfully treated by coil embolisation. On waking in intensive care
Reale, Chiara +4 more
openaire +3 more sources
Hematology and Cell Therapy, 1996
The authors review the epidemiological biological, diagnostic, prognostic and therapeutic aspects of myelodysplastic syndromes.
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The authors review the epidemiological biological, diagnostic, prognostic and therapeutic aspects of myelodysplastic syndromes.
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Current Opinion in Neurology, 1995
Rett syndrome is a unique and puzzling disorder noted in females, and is possibly caused by fundamental failures in critical brain connectivity during early infancy. Recent reports expand our understanding of the Rett syndrome phenotype, continue the pattern of inconsistent or inconclusive metabolic and genetic results, and extend observations ...
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Rett syndrome is a unique and puzzling disorder noted in females, and is possibly caused by fundamental failures in critical brain connectivity during early infancy. Recent reports expand our understanding of the Rett syndrome phenotype, continue the pattern of inconsistent or inconclusive metabolic and genetic results, and extend observations ...
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Blood Reviews, 2005
Abstract POEMS syndrome is defined by the presence of a peripheral neuropathy (P), a monoclonal plasma cell disorder (M), and other paraneoplastic features, the most common of which include organomegaly (O), endocrinopathy (E), skin changes (S), papilledema, edema, effusions, ascites, and thrombocytosis.
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Abstract POEMS syndrome is defined by the presence of a peripheral neuropathy (P), a monoclonal plasma cell disorder (M), and other paraneoplastic features, the most common of which include organomegaly (O), endocrinopathy (E), skin changes (S), papilledema, edema, effusions, ascites, and thrombocytosis.
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Rheumatic Disease Clinics of North America, 1992
SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) syndrome put together osteoarticular lesions described separately under numerous denominations, such as multifocal osteomyelitis, pustulotic arthroosteitis, acne rheumatism. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is the cornerstone of this new ...
A M, Chamot, M F, Kahn
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SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) syndrome put together osteoarticular lesions described separately under numerous denominations, such as multifocal osteomyelitis, pustulotic arthroosteitis, acne rheumatism. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is the cornerstone of this new ...
A M, Chamot, M F, Kahn
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Current Opinion in Gastroenterology, 2014
To discuss the advances in the understanding of the pathophysiology of experimental and human hepatopulmonary syndrome (HPS) and in the management of HPS, particularly regarding liver transplantation.Advances have been made in defining the pathophysiology of HPS in experimental models as well as in human disease, including the role of endothelin-1 ...
David G, Koch, Michael B, Fallon
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To discuss the advances in the understanding of the pathophysiology of experimental and human hepatopulmonary syndrome (HPS) and in the management of HPS, particularly regarding liver transplantation.Advances have been made in defining the pathophysiology of HPS in experimental models as well as in human disease, including the role of endothelin-1 ...
David G, Koch, Michael B, Fallon
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Hormone Research, 1993
Using cross-sectional and longitudinal analysis of data from the San Antonio Heart Study, syndrome X (primary insulin resistance syndrome) has been redefined in terms of hyperinsulinaemia combined with changes in glucose tolerance, lipid pattern, blood pressure and body fat distribution.
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Using cross-sectional and longitudinal analysis of data from the San Antonio Heart Study, syndrome X (primary insulin resistance syndrome) has been redefined in terms of hyperinsulinaemia combined with changes in glucose tolerance, lipid pattern, blood pressure and body fat distribution.
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Journal of Craniofacial Surgery, 2014
Eagle syndrome, also known as elongated styloid process, is a condition first described by Watt Eagle in 1937. It occurs when an elongated styloid process or calcified stylohyoid ligament causes recurrent throat pain or foreign body sensation, dysphagia, or facial pain.
Ferreira, Pedro Costa +5 more
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Eagle syndrome, also known as elongated styloid process, is a condition first described by Watt Eagle in 1937. It occurs when an elongated styloid process or calcified stylohyoid ligament causes recurrent throat pain or foreign body sensation, dysphagia, or facial pain.
Ferreira, Pedro Costa +5 more
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Medicina clinica, 1995
This study examines chronic airflow obstruction, characterized by a persistent and irreversible limitation of respiratory flow. It is primarily associated with diseases such as Chronic Obstructive Pulmonary Disease (COPD) and originates from pathological structural changes in the airways, lung parenchyma, and blood vessels.
Sole, Amparo, Cordero, Pedro
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This study examines chronic airflow obstruction, characterized by a persistent and irreversible limitation of respiratory flow. It is primarily associated with diseases such as Chronic Obstructive Pulmonary Disease (COPD) and originates from pathological structural changes in the airways, lung parenchyma, and blood vessels.
Sole, Amparo, Cordero, Pedro
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Endocrinology and Metabolism Clinics of North America, 2008
Cushing's syndrome is a rare endocrine disease characterized by cortisol hypersecretion, induced mainly by a pituitary tumor (Cushing's disease) or, rarely, by an adrenal or an ectopic neuroendocine tumor. Cushing's syndrome is associated with severe morbidities and an increased mortality.
PIVONELLO, ROSARIO +4 more
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Cushing's syndrome is a rare endocrine disease characterized by cortisol hypersecretion, induced mainly by a pituitary tumor (Cushing's disease) or, rarely, by an adrenal or an ectopic neuroendocine tumor. Cushing's syndrome is associated with severe morbidities and an increased mortality.
PIVONELLO, ROSARIO +4 more
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