Titlebook: Hypothalamic-Pituitary Diseases; Felipe F. Casanueva,Ezio Ghigo Living reference work 20200th edition hypothalamic-pituitary unit.hypotha

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Kathleen A. Feeley,Jennifer Frostc amenorrhea, drugs, chronic illnesses, and irreversible causes such as central nervous system insults (trauma, irradiation, and intracranial tumors). Diagnosis should take in consideration the age at the clinical presentation (prepubertal or postpubertal), the physical findings as well as biochemic

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https://doi.org/10.1007/978-1-349-20363-5uding TSH level only, can give misleading conclusion of normal thyroid function or even of hyperthyroidism. In most cases of CoCH, the genetic basis of hypothalamic and/or pituitary pathology is undefined. Among the already known molecular causes of CoCH, rarely occurring isolated TSH deficiency is

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Physiopathology, Diagnosis and Treatment of Inappropriate ADH Secretion and Cerebral Salt Wasting Sonic SIAD recommended by all current guidelines, despite the lack?of good evidence base to support its use in the medical literature. A number of key points relevant to the use of fluid restriction are presented in the manuscript which may be helpful for the physician. In addition, the evidence base

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