Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
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Acromegaly
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Pituitary Lymphoma Presenting as Fever of Unknown Origin
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Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
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Twelve Cases of Pituitary Apoplexy
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983
Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
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A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015
A 48-year-old Man with Walking Difficulty
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Clinicopath Conf, Neurosarcoidosis
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Sarcoidosis: Clinical, Hormonal, and Magnetic Resonance Imaging (MRI) Manifestations of Hypothalamic-Pituitary Disease in 9 Patients and Review of the Literature
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Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988
Clinicopath Conf
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Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
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Sphenoid Sinus Mucocele
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Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
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Kearns-Sayre Syndrome with Hypoparathyroidism
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Sudden Onset of Unilateral Third Nerve Paresis in a Patient with Cushing Syndrome
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Spontaneous Infarction in Pituitary Tumors:Neurologic & Therapeutic Aspects
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Neurological Problems in Endocrine Diseases
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Medical Approach to Ophthalmopathy of Graves'Disease
Mayo Clin Proc 47:980, Ivy,H., 1972
Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Ovarian Germ Cell Tumors: Pathology,Clinical Manifestations,and Diagnosis
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Pituitary and Stalk Lesions (Infundibulo-Hypophysitis) Associated with Immunoglobulin G4-related Systemic Disease: an Emerging Clinical Entity
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Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
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Neurologic Improvement After Peripheral Blood Stem Cell Transplantation in POEMS Syndrome
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Phaeochromocytoma
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Acromegaly Caused by Secretion of Growth Hormone by a Non-Hodgkin's Lymphoma
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Neuroendocrine Lung Tumors and Disorders of the Neuromuscular Junction
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The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
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Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996
Acromegaly:Clinical and Biochemical Features in 500 Patients
Medicine 73:233-240, Ezzat,S.,et al, 1994
Central Nervous System Germinomas, A Review
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Craniopharyngyoma in Children
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Acromegaly
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Hyponatremia and Inappropriate Secretion of Vasopressin (Antidiuretic Hormone) in Patients with Hypopituitarism
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Hypoparathyroidism
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Resolution of Stiff-Man Syndrome with Cortisol Replacement with Deficiencies of ACTH, Growth Hormone, & Prolactin
NEJM 310:1511-1513, George,T.M.,et al, 1984
Multiple Endocrine Neoplasia Associated with Von Recklinghausen's Disease
BMJ 287:1341-1343, Griffiths,D.F.R.,et al, 1983
Evaluation Of Acromegaly By Radioimmunoassay Of Somatomedin-C
NEJM 301:1138-1142, Clemmons,D.R.,et al, 1979
Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
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Search for the Uremic Toxin
NEJM 298:1000, 1978, Avram,M.M.,et al, 1978
Visual Dysfunction in Optic Tract Lesions
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The Thyroid Gland:Its Relationship to Neurology
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Neuromuscular Disease in Primary Hyperparathyroidism
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Organic Disease Presenting as a Psychiatric Syndrome
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