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Jaypee Brothers Medical Publishers Endocrine Surgery Made Easy With Photo Cc Rom by Amit Agarwal
Table of Contents : Solitary Thyroid Nodule, Euthyroid Multinodular Goiter, Toxic Multinodular Goiter, Toxic Adenoma, Thyroid Cyst, Graves’ Disease, Graves’ Ophthalmopathy, Juvenile Graves’ Disease, Graves’ with Periodic Paralysis, Hyperthyroidism in elderly with Heart Disease, Amyloid Goiter, Thyroglossal Cyst,Painful/Nodular Hashimoto’s Thyroiditis, Subacute Thyroiditis or De Quervain’s Thyroiditis, Large Goiter, Marine–Lenhart Syndrome, Linguarl Thyroid, Dyshormonogenetic Goiter, Retrosternal Goiter, Post-thyroidectomy Stridor, Papillary Carcinoma, Papillary Microcarcinoma, Occult Papillary Carcinoma Presenting as Cervical Lymph Node Enlargement, Locally Invasive Papillary Carcinoma, Differentiated Thyroid Carcinoma with Lung Metastases, Tall Cell Variant of Papillary Carcinoma (TCV), Follicular Variant of Papillary Carcinoma,
Completion Thyroidectomy, Thyroid Cancer in Children, Follicular Neoplasm, Hurthle Cell Neoplasm / Carcinoma, Follicular Carcinoma Presenting with Bone Metastases, Sporadic MTC, Multiple Endocrine Neoplasia Type 2A (MEN 2A), Persistent Hypercalcitoninemia, Anaplastic Carcinoma: Diagnostic and Therapeutic Challenge, Thyroid Lymphoma, Primary Hyperparathyroidism, Primary Hyperparathyroidism with Pancreatitis, Familial Isolated Hyperparathyroidism (FIHPT),
Parathyroid Crisis, Persistent Hungry Bone Syndrome Following Parathyroidectomy, Conn’s Syndrome, Occult Ectopic ACTH Syndrome, Overt Ectopic ACTH Syndrome, Benign, Functioning Adrenal Adenoma, Adrenocortical Carcinoma Presenting as Adrenal Incidentaloma, Metastatic Adrenocortical Carcinoma, Functioning Adrenocortical Carcinoma in Children, Adrenocortical Carcinoma Presenting as Cushing’s Syndrome in Adults,
Sporadic Pheochromocytoma, Hereditary Pheochromocytoma: Von Hippel Lindau (VHL) Disease, Unusual Presentation of Pheochromocytoma: Patient Presenting with Hemiparesis, Unusual Presentation of Pheochromocytoma: Fainting during Micturition, Pheochromocytoma Presenting with Glycosuria,