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Lymphocytic Infundibuloneurohypophysitis

Known as: Infundibuloneurohypophysitides, Lymphocytic, Infundibuloneurohypophysitis, Lymphocytic, Lymphocytic Infundibuloneurohypophysitides 
 
National Institutes of Health

Papers overview

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2017
2017
Rationale: Lymphocytic hypophysitis is a relatively rare autoimmune disease defined by lymphocytic infiltration to the pituitary… Expand
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2015
2015
Lymphocytic hypophysitis is a neuroendocrine disorder characterized by autoimmune infiammation of the pituitary gland with… Expand
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Review
2014
Review
2014
The pathologic spectrum of diseases that infiltrate the pituitary infundibulum includes a broad variety of clinical entities… Expand
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2009
2009
In pediatric and adolescent patients, the most common causes for a thickened pituitary stalk with central diabetes insipidus are… Expand
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Review
2006
Review
2006
Lymphocytic hypophysitis (LYH) is a neuroendocrine disorder characterized by autoimmune inflammation of the pituitary gland with… Expand
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2004
2004
Acquired idiopathic generalized anhidrosis (AIGA) has an acute or insidious onset without additional symptoms. There may be… Expand
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Review
2003
Review
2003
We report two cases of lymphocytic infundibuloneurohypophysitis (LIH). A 32-year-old male and a 13-year-old male were admitted to… Expand
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2002
2002
Hypophysitis has been histologically classified into five types: lymphocytic hypophysitis (LYH), granulomatous hypophysitis (GRH… Expand
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1997
1997
A 56-year-old Japanese man presented with a 2-month duration of polyuria and polydipsia. The diagnosis of diabetes insipidus was… Expand
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