ISSN: 2640-7582 Clinical Group

International Journal of Clinical Endocrinology and Metabolism  Open Access

    Recent articles to be released shortly in Volume-5

    Parathyroid adenoma-An incidental diagnosis CrossMark

    DOI Logo 10.17352/ijcem.000032

    Published On: December 18, 2018 | Pages: 012 - 013

    Author(s): Nandini Chatterjee and Chandan Chatterjee*
    A 50 year old man was referred to us with inadequate control of blood pressure for last few years. He was being treated as a case of essential hypertension on a four drug regime. Subsequent work up led to the diagnosis of primary hyper parathyroidism due to left inferior parathyroid adenoma. ...
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    Closing the Mortality Gap in Diabetic Ketoacidosis and Hyperosmolar Hyperglycemic State: Implications of a Clinical Decision Support App CrossMark

    DOI Logo 10.17352/ijcem.000031

    Published On: December 06, 2018 | Pages: 008 - 011

    Author(s): Yair Saperstein, Joongheum Park and Samy I McFarlane*
    Diabetes is a major public health issue affecting millions of people in the United States and worldwide. In the United States alone, about 30.3 million people (9.4% of the population) have diabetes [1]. Worldwide, a staggering 422 million have diabetes according to 2014 estimates [2]. Diabetes complications over years of exposure include cardiovascular disease -- stro ...
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    Two cases of traumatic isolated ACTH deficiency CrossMark

    DOI Logo 10.17352/ijcem.000030

    Published On: October 30, 2018 | Pages: 004 - 007

    Author(s): Tatsuo Ishizuka*, Motochika Asano, Kei Fujioka, Ichiro Mori, Kazuo Kajita and Hiroyuki Morita
    Case 1: A 65- year-old man was accidentally injured by wooden hammer on his top of head on 34 years before. He was suffered from vomiting, diarrhea and hypotension, and the laboratory examination revealed increased CRP level, hyponatremia and decreased plasma cortisol and ACTH levels, suggesting isolated ACTH deficiency and Crohn disease diagnosed by colonoscopic biop ...
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    Recombinant Growth hormone response in Indian girls with Turner syndrome CrossMark

    DOI Logo 10.17352/ijcem.000029

    Published On: October 29, 2018 | Pages: 001 - 003

    Author(s): Inderpal Singh Kochar*, Smita Ramachandran and Aashish Sethi
    Turner syndrome (TS) is characterized by short statute and ovarian dysgenesis in females with one X chromosome and partial or complete absence of the second X. It has an estimated birth prevalence of 1/2000 to 1/5000 female live births [1]. There is a global growth delay in TS characterized by slight intrauterine growth retardation, delayed growth during infancy and c ...
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    Hyperparathyroidism and Asthenia. A New Deal? CrossMark

    DOI Logo 10.17352/ijcem.000028

    Published On: December 07, 2017 | Pages: 046 - 047

    Author(s): S Li Sun Fui* and P Bonnichon
    The profi le of primary hyperparathyroidism (PHPT) changed profoundly over the course of the twentieth century. The highly symptomatic forms reported in the 1960s have progressively been replaced by forms with few symptoms and in some cases totally asymptomatic forms. ...
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