Zobrazeno 1 - 10
of 236
pro vyhledávání: '"Mark A, Sperling"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Background The spectrum of disorders associated with hyperinsulinemic hypoglycemia (HHI) has vastly increased over the past 20 years with identification of molecular, metabolic and cellular pathways involved in the regulation of insulin secr
Externí odkaz:
https://doaj.org/article/8ec2900781b443849b8d986370553da3
Autor:
Mark A, Sperling, Lori M, Laffel
Publikováno v:
New England Journal of Medicine. 386:1155-1164
Publikováno v:
Archives of disease in childhood. 108(1)
Insulin is the key anabolic hormone of metabolism, with clear effects on glycaemia. Near-complete insulin deficiency occurs in type 1 diabetes (T1D), the predominant form affecting children, and uniformly fatal until the discovery of insulin. By the
Autor:
Yong eFan, Xin eFang, Asako eTajima, Xuehui eGeng, Sarangarajan eRanganathan, H. Henry eDong, Massimo eTrucco, Mark Alexander Sperling
Publikováno v:
Frontiers in Endocrinology, Vol 5 (2014)
Background: Non-alcoholic fatty liver disease (NAFLD) is one of the most common forms of chronic liver diseases closely associated with obesity and insulin resistance; deficient growth hormone (GH) action in liver has been implicated as a mechanism.
Externí odkaz:
https://doaj.org/article/dc8c93a97c2f42dfa505075018abaa6e
Autor:
Mark A. Sperling
This chapter provides an overview of the principles of pediatric endocrinology as a distinct specialty, focusing on the historical evolution of this field, the impact of evolving advances in the ability to quantify the concentration and cellular acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635d470e62b4827ba590f40c4ad3bd1b
https://doi.org/10.1016/b978-0-323-62520-3.00001-4
https://doi.org/10.1016/b978-0-323-62520-3.00001-4
Autor:
Heide Aungst, Philippe Backeljauw, Jeffrey Baron, Tadej Battelino, Andrew J. Bauer, David T. Breault, Yee-Ming Chan, Steven D. Chernausek, David W. Cooke, Sarah C. Couch, Stephen R. Daniels, Mehul T. Dattani, Diva D. De Leon, Johnny Deladoey, Leo Dunkel, Brian J. Feldman, Lauren Fishbein, Christa E. Flück, Claus Højbjerg Gravholt, Siri Atma W. Greeley, Adda Grimberg, Michael J. Haller, Joan C. Han, Helen N. Jones, Alexander A.L. Jorge, Paul Kruszka, Bassil Kublaoui, Peter A. Lee, Michael A. Levine, David Maahs, Joseph A. Majzoub, Tani Malhotra, Mary K. McCauley, Ram K. Menon, Sam Mesiano, Walter L. Miller, Louis J. Muglia, Jon Nakamoto, Bimota Nambam, Mark R. Palmert, Louis H. Philipson, Moshe Phillip, Sally Radovick, Scott Rivkees, Allen W. Root, Robert L. Rosenfield, Stephen M. Rosenthal, Desmond Schatz, Mark A. Sperling, Abhinash Srivatsa, Charles A. Stanley, Constantine A. Stratakis, William V. Tamborlane, Paul Thornton, Massimo Trucco, Guy Van Vliet, Julia Elisabeth von Oettingen, Steven G. Waguespack, Ram Weiss, William E. Winter, Amy B. Wisniewski, Selma Feldman Witchel, Joseph I. Wolfsdorf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e34e92fbd66e7932e8217b1d9527cf7d
https://doi.org/10.1016/b978-0-323-62520-3.09993-0
https://doi.org/10.1016/b978-0-323-62520-3.09993-0
Publikováno v:
Sperling Pediatric Endocrinology ISBN: 9780323625203
Pediatric Endocrinology ISBN: 9781455748587
Pediatric Endocrinology ISBN: 9781455748587
A newborn or infant with hypoglycemia presents an urgent diagnostic and therapeutic challenge. The clinical features must be rapidly assessed and a plan of action developed based on the infant’s age, maternal and parturition history, severity and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a3842d871033cc71159b36f3a71387
https://doi.org/10.1016/b978-0-323-62520-3.00007-5
https://doi.org/10.1016/b978-0-323-62520-3.00007-5
Publikováno v:
Pediatric Critical Care ISBN: 9783030533625
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91c60bacbe269faa16468600078168c0
https://doi.org/10.1007/978-3-030-53363-2_43
https://doi.org/10.1007/978-3-030-53363-2_43
Publikováno v:
Sperling Pediatric Endocrinology ISBN: 9780323625203
Monogenic diabetes describes a long list of relatively rare causes of diabetes with a genetic basis caused by highly penetrant mutations or alterations at any one gene or locus. There are many important reasons to distinguish such causes from the mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9911d6e064e8974c067f3687564b8570
https://doi.org/10.1016/b978-0-323-62520-3.00010-5
https://doi.org/10.1016/b978-0-323-62520-3.00010-5