Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Jessica L Hwang"'
Autor:
Trilok Shrivastava, MD, Jessica L Hwang, MD, Laishiya Munshi, DO, Kumar Kunnal Batra, MD, Kriti Ahuja, MD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 4, Pp 989-993 (2021)
A 46-year-old Asian male with history of atraumatic fracture of femur (requiring the use of a walker), muscle cramps and loosening teeth presents to Endocrine clinic. He had elevated parathyroid hormone, severely low phosphorus, elevated bone-specifi
Externí odkaz:
https://doaj.org/article/2a738053c6e644fbaced1728e55eeb12
Publikováno v:
Radiology Case Reports, Vol 16, Iss 4, Pp 989-993 (2021)
Radiology Case Reports
Radiology Case Reports
A 46-year-old Asian male with history of atraumatic fracture of femur (requiring the use of a walker), muscle cramps and loosening teeth presents to Endocrine clinic. He had elevated parathyroid hormone, severely low phosphorus, elevated bone-specifi
Autor:
Jeronimo Berardo, Jessica L Hwang
Publikováno v:
Journal of the Endocrine Society. 6:A342-A342
Introduction Type B insulin resistance syndrome (TBIRS) is a rare life-threatening disorder caused by autoantibodies to the insulin receptor. Suggestive clinical features include profound insulin resistance, concurrent autoimmune disease, acanthosis
Autor:
Jessica L. Hwang, Shivani Berry, Siri Atma W. Greeley, Rochelle N. Naylor, Charles D. Bell, Jazzmyne T. Montgomery, Elizabeth C. Tadie, Louis H. Philipson, David Carmody
Publikováno v:
Acta Diabetologica. 53:703-708
GCK-MODY leads to mildly elevated blood glucose typically not requiring therapy. It has been described in all ethnicities, but mainly in Caucasian Europeans. Here we describe our US cohort of GCK-MODY. We examined the rates of detection of heterozygo
Publikováno v:
Difficult Decisions in Endocrine Surgery ISBN: 9783319928586
Anaplastic thyroid cancer (ATC) is a highly lethal disease. First-line therapy for a patient diagnosed with this disease includes surgical resection or chemoradiation. Due to variable treatment and its rarity, there is a paucity of prospective and/or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::500857f99e803cf0b4d81f560538f04f
https://doi.org/10.1007/978-3-319-92860-9_12
https://doi.org/10.1007/978-3-319-92860-9_12
Autor:
Craig L. Hanis, Benjamin Glaser, Gil Atzmon, Soo-Young Park, Janna F. Wilson, Jessica L. Hwang, Ashley N. Pastore, Xiaoming Liu, Louis H. Philipson, May Sanyoura, Daniela del Gaudio, Siri Atma W. Greeley, David Carmody, Honggang Ye
Publikováno v:
Pediatric diabetes. 19(3)
Diabetes occurs in 1/90 000 to 1/160 000 births and when diagnosed under 6 months of age is very likely to have a primary genetic cause. FOXP3 encodes a transcription factor critical for T regulatory cell function and mutations are known to cause "im
Autor:
Roy E. Weiss, Jessica L. Hwang
Publikováno v:
Diabetes/Metabolism Research and Reviews. 30:96-102
Since the advent of glucocorticoid therapy for autoimmune disease in the 1940s, their widespread application has led to the concurrent therapy-limiting discovery of many adverse metabolic side effects. Unanticipated hyperglycemia associated with the
Publikováno v:
Journal of Clinical Densitometry. 17:16-24
Although peripheral dual-energy X-ray absorptiometry measurements have been found to predict fractures in population studies of white subjects, little is known about their utility in other races and in patients with greater risk of fracture. In a cro
Autor:
R. Martin, Louis H. Philipson, Jessica L. Hwang, Megan N. Scott, Rochelle N. Naylor, K. A. Landmeier, Siri Atma W. Greeley, David Carmody, Lisa R. Letourneau, Michael E. Msall, Scott J. Hunter, Ashley N. Pastore
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 33(10)
Aims KCNJ11-related diabetes is the most common form of permanent neonatal diabetes and has been associated with a spectrum of neurodevelopmental problems. We compared neurodevelopmental outcomes in patients with KCNJ11 mutations and their sibling co
Autor:
I. Karen Temple, Deborah J G Mackay, Charles D. Bell, Siri Atma W. Greeley, David Carmody, Jazzmyne T. Dickens, Rochelle N. Naylor, Nancy Devine, Flavius A. Beca, Jessica L. Hwang, Lisa R. Hays, Louis H. Philipson
Publikováno v:
Diabetes Care
Chromosome 6q24-related transient neonatal diabetes (6q24-TND) is a rare form of diabetes caused by an overexpression of PLAGL1 and HYMAI (1). After remitting in infancy, diabetes recurs in most patients later in life. While the best treatment remain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd5a8dfb2e16bdffb90d6cd64a8447f8
https://eprints.soton.ac.uk/377538/
https://eprints.soton.ac.uk/377538/