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Tumor Lysis Syndrome in a Patient with Secondary Leukemia FollowingPrimary Mediastinal Germ Cell Tumor
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Atypical Presentations do Exist: A Child with Infantile Nephropathic Cystinosis
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Thyroxine Absorption Test Differentiates Malabsorption from Pseudo-malabsorption: A Case Series
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Hair Depigmentation and Dermatitis: A Rare Presentation of Cystic Fibrosis
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Case Series - Two Children with Self-mutilation Behaviour and Hyperuricemia
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Case Report - Postpartum Bone Crisis in a Mother with Gaucher Disease
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Solitary Bone Plasmacytoma of Appendicular Skeleton
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Elevated CA 125 in a Patient without an Ovarian Pathology; A Diagnostic Dilemma
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A Young Lady with Progressive Weakness, Weight Loss, Shortness of Breath and Polyneuropathy
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Biliary Atresia Biochemically Mimicking Carnitine Palmitoyl Transferase1-A Deficiency
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A Patient with Primary Hyperparathyroidism with Controversial Imaging Findings
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A Patient Diagnosed Multiple Myeloma with Negative Monoclonal Band on Serum Protein Electrophoresis
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Positive Benedict Test in a Patient with Cataract
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Case Report of a Child with Seizures and Skin Lesions; What To Do With Biotin???
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A Young Male with Hypertension; Cushing Disease
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A Case Report of Bisalbuminaemia Associated with Chronic Inflammatory DemyelinatingPolyneuropathy
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Primary Pigmented Nodular Adrenocortical Disease (PPNAD):A Rare Cause of ACTH-independent Cushing Syndrome
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Case Report - A Young Female with Primary Hyperaldosteronism
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Role of Measurement Uncertainty in Clinical Decision Making
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Optimizing the Hypoglycemia Cutoff in Insulin Tolerance Test: A Case Report
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A Rare Case of Severe Ectopic Cushing Syndrome due to a Thymic Carcinoma Recurrence
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Assessment of Insulin Resistance Using Quantitative Insulin Sensitivity Check Index (QUICKI): A Case Report
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Importance of Calculating Measurement Uncertainty (MU) in Intra-operative Parathyroid Sampling: A Case Report _
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A case of unresolved hypercortisolism; A diagnostic dilemma _
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A Case Report: A Woman with Cushing's Disease Presenting with Pulmonary Embolism, Severe Refractory Hypokalemia and Hypercortisolism Induced Secondary Hypopituitarism
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Clinical Presentation and Genetic Heterogeneity Including Two Novel Variants in Sri Lankan Patients with Infantile Sandhoff Disease: A Case Series
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Presence of oxalate crystals in cerebrospinal fluid
a case report _
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