Results 81 to 90 of about 16,980 (220)
Presentation of hypoparathyroidism: Etiologies and clinical features
Context: Understanding the etiology, diagnosis, and symptoms of hypoparathyroidism may help to improve quality of life and long-term disease outcomes.
Peacock, Munro +11 more
core +1 more source
ABSTRACT Sjogren's syndrome (SS) is an autoimmune disorder characterized by inflammation of exocrine glands, often presenting with symptoms such as dry eyes and mouth. Although less common, renal involvement can lead to serious complications like hypokalemic paralysis.
Premendra Vimal +3 more
wiley +1 more source
Psychometric evaluation of the hypoparathyroidism symptom diary
Theresa Coles,1 Kristina Chen,2 Lauren Nelson,1 Nimanee Harris,1 Montserrat Vera-Llonch,2 Alan Krasner,2 Susan Martin3 1RTI Health Solutions, Research Triangle Park, NC, USA; 2Shire Human Genetic Therapies, Lexington, MA, USA; 3RTI Health Solutions, Ann ...
Harris N +6 more
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What's new? Global research has found that for people newly diagnosed with advanced non‐small cell lung cancer (NSCLC), the anti‐PD‐1 monoclonal antibody pembrolizumab on its own often leads to better results than traditional chemotherapy. The present report details long‐term findings of pembrolizumab therapy specifically among Chinese patients.
Yi‐Long Wu +14 more
wiley +1 more source
Ying-hao Wang,* Adheesh Bhandari,* Fan Yang, Wei Zhang, Li-jun Xue, Hai-guang Liu, Xiao-hua Zhang, Cheng-ze Chen Department of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, People ...
Zhang W +7 more
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Idiopathic Hypoparathyroidism Mimicking Diffuse Idiopathic Skeletal Hyperostosis
Idiopathic hypoparathyroidism is an uncommon disease caused by insufficient secretion of parathyroid hormone. Idiopathic hypoparathyroidism may cause various musculoskeletal findings, including diffuse ligamentous and entheseal ossifications.
Selek, Hakan +6 more
core +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source
Treatment of severe idiopathic hypoparathyroidism: a case report
Hypoparathyroidism is a rare disorder characterized by parathyroid hormone (PTH) insufficiency, the development of hypocalcemia and alteration of bone tissue remodeling.
Diliara Sh. Umiarova +3 more
doaj +1 more source
Hypoparathyroidism and Pseudo-hypoparathyroidism [PDF]
R R, DE MOWBRAY +2 more
openaire +2 more sources
Clinical Characteristics of Hypoparathyroidism and Pseudohypoparathyroidism [PDF]
PURPOSE: Insufficient production of the parathyroid hormone (PTH) by the parathyroid glands known as hypoparathyroidism, or a resistance against its action on target organs known as pseudohypoparathyroidism, cause PTH-related hypocalcemia associated with
김호성, 채현욱, 권아름
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