Results 261 to 270 of about 117,920 (299)
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Rett syndrome

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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Schnitzler-Syndrom

Zeitschrift für Rheumatologie, 2018
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. The main characteristics are generalized exanthema and a monoclonal gammopathy with IgM. Other clinical features include fever, muscle, bone and/or joint pain, and lymphadenopathy.
F F, Gellrich, C, Günther
openaire   +4 more sources

Sagliker Syndrome

Cirugía Española (English Edition), 2020
Carta científica. In Press.
Rubio-Manzanares-Dorado, M.   +4 more
openaire   +3 more sources

Metabolic Syndrome in Men with Klinefelter's Syndrome

Urology, 2008
To investigate the metabolic syndrome and sex hormones in patients with Klinefelter's syndrome (KFS), 46XY men with nonobstructive azoospermia (NOA), and an age-matched obstructive azoospermia (OA) group.We examined 60 patients with KFS, 60 46XY male patients with NOA, and 50 patients with OA.
Tomomoto, Ishikawa   +4 more
openaire   +2 more sources

The Hepatopulmonary Syndrome

Annals of Internal Medicine, 1995
To review current knowledge about the hepatopulmonary syndrome, including definition and clinical features, methods for diagnosing it, pathophysiologic mechanisms of the associated vascular dilatations, and considerations in treatment, with emphasis on potential reversibility of the syndrome after liver transplantation.The MEDLINE database from January
P A, Lange, J K, Stoller
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POEMS syndrome

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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What syndrome is this? Tourniquet syndrome.

Pediatric dermatology, 2002
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CORAZZA, Monica   +3 more
openaire   +2 more sources

Metabolic Syndrome in Cushing's Syndrome Patients

2018
Cushing's syndrome (CS), including visceral obesity, dyslipidemia, hypertension and diabetes among its many manifestations, is "a model" of metabolic syndrome. Glucocorticoid (GC) excess, through a combination of effects on liver, muscle, adipose tissue and pancreas, increases gluconeogenesis and impairs insulin sensitivity, leading to carbohydrate ...
Ferraù, Francesco, Korbonits, Márta
openaire   +4 more sources

The metabolic syndrome: A syndrome and not a disease

Nutrition, 2010
CONTALDO, FRANCO   +2 more
openaire   +3 more sources

The metabolic syndrome, the Guy syndrome and the hypofit syndrome

Journal of Cardiovascular Medicine, 2007
Alessandro, Menotti, Mariapaola, Lanti
openaire   +2 more sources

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