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Titlebook: Integrable Hierarchies and Modern Physical Theories; Henrik Aratyn,Alexander S. Sorin Book 2001 Springer Science+Business Media Dordrecht

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Integrable Hierarchies and Modern Physical Theories978-94-010-0720-7Series ISSN 1568-2609
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A. Marshakovderlying genetic disorders, especially multiple endocrine neoplasia type I and von Hippel-Lindau syndrome, are at an increased risk for developing PNETs. Surgical resection is the primary treatment for functional PNETs. However, the decision for surgery depends on multiple factors, including patient
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J. D. Edelstein,M. Gómez-Reinoderlying genetic disorders, especially multiple endocrine neoplasia type I and von Hippel-Lindau syndrome, are at an increased risk for developing PNETs. Surgical resection is the primary treatment for functional PNETs. However, the decision for surgery depends on multiple factors, including patient
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A. Gorsky,A. Mironova benign monomorphic pituitary corticotroph adenoma that secretes excessive adrenocorticotropic hormone (ACTH). Increased ACTH stimulates secretion of cortisol by the adrenal glands, resulting in supraphysiological levels of endogenous steroid resulting in the combination of symptomatology and findi
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V. A. Fateeveral endogenous conditions that result in cortisol excess. Endogenous etiologies are uncommon, but clinicians must recognize the constellation of signs and symptoms to prevent significant morbidity and mortality from the diseases. Clinical suspicion of endogenous hypercortisolism leads to screening
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Y. Nutkuof intracranial mass such as dulled affect, lethargy, hemiparesis, seizures or failing vision [1]. Their goal of therapy is total removal of the intracranial mass which has arisen from the sellar region and restoration of brain function. Ophthalmologists refer patients with specific visual disturban
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