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Giant Invasive Prolactinomas
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Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
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An Unusual Presentation of Prolonged Delirium
BMJ 373:N1423, Bume, R.,et al, 2021
Isolated Oculomotor Nerve Palsy due to Pituitary Apoplexy Missed on CT scan
Neurol 94:e1774-e1777, Marzoughi, S.,et al, 2020
A 41-year-old man with Thunderclap Headache
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A 45-year-old Woman with Right Limb Weakness
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A 45 Year Old Patient with Headache, Fever, and Hyponatraemia
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Acute Headache Diagnosis in Pregnant Women
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Making Sense of Sellar Region Pathology:Image-Based Diagnostic Algorighm
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Intracranial Neoplasms and Paraneoplastic Disorders, Skull Base Tumor Syndromes
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Clinical Reasoning: A 42-year-old Man with Severe Headache, Fever, and Acute Coma
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Intracranial Lesions with High Signal Intensity on T1-weighted MR images - Review of Pathologies
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Prolactinomas
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Tuberous Sclerosis
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Clinicopath Conf, Pituitary Adenoma
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Clinicopath Conf, Giant-Cell Arteritis
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Clinicopath Conf, Giant-Cell Arteritis
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Cavernous Sinus Syndrome: A Series of 126 Patients
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Trigeminal Autonomic Cephalgias Due to Structural Lesions: A Review of 31 Cases
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The Tuberous Sclerosis Complex
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Acromegaly
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Magnetic Resonance Imaging of Pituitary Adenomas
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Lymphoma Metastasizing to the Pituitary: An Unusual Presentation of a Treatable Disease
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Apoplexy in Pituitary Macroadenoma: Eight Patients Presenting in 12 Months
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An Unusual Case of Growth Retardation
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MR Imaging Presentation of Intracranial Disease Associated with Langerhans Cell Histiocytosis
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Prolactinoma
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Withdrawal of Long-Term Cabergoline Therapy for Tumoral and Nontumoral Hyperprolactinemia
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Primary Sellar Lymphoma:Radiologic and Pathologic Findings in Two Patients
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SUNCT Syndrome in Two Patient with Prolactinomas and Bromocriptine-Induced Attacks
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Clinicopath Conf., Prolactinoma
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Pituitary Apoplexy Caused by Ruptured Internal Carotid Artery Aneurysm
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Narcolepsy Associated with Other Central Nervous System Disorders
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Precipitating Factors in Pituitary Apoplexy
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Clinicopath Conf, Non-Small-Cell Carcinoma of Lung, Metastatic to Hypothalamus, Pituitary Stalk and Pituitary Gland
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Pituitary Carcinoma as a Cause of Acromegaly
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Long-term Treatment of Acromegaly With Pegvisomant, a Growth Hormone Receptor Antagonist
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Pituitary Lymphoma Presenting as Fever of Unknown Origin
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Primary Lymphoma of the Pituitary: An Emerging Clinical Entity
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National Institutes of Health Consensus Conference: Tuberous Sclerosis Complex
Arch Neurol 57:662-665, Hyman,M.H.&Whittemore,V.H., 2000
Treatment of Acromegaly With the Growth Hormone-Receptor Antagonist Pegvisomant
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Diagnosis, Treatment, and Outcome of Pituitary Tumors and Other Abnormal Intrasellar Masses, Retrospective Analysis of 353 Patients
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Pituitary Surgery for Acromegaly, Should be Done by Specialists
BMJ 319:588-589, Clayton,R.N.,et al, 1999
New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Management of Pituitary Tumors
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