Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Priya S. Srivastava"'
Publikováno v:
Journal of Diabetes Research, Vol 2022 (2022)
Type 1 diabetes is associated with complications affecting muscle and bone, with diabetic bone disease and diabetic myopathy becoming increasingly reported in the past few decades. This review is aimed at succinctly reviewing the literature on the cu
Externí odkaz:
https://doaj.org/article/17dd8cf2c8644ac28eccaf7a674c0ae0
Publikováno v:
Journal of the Endocrine Society
Background: Perinatal Hypophosphatasia (HPP) is a rare and lethal disorder associated with a 50–100% mortality rate, usually due to respiratory complications. HPP occurs due to a loss-of-function mutation in the ALPL gene, responsible for the funct
Autor:
Arun Rangaswami, Doruk Ozgediz, Priya S Srivastava, Maya Lodish, Kevin Yen, Robert A. Lindquist, Erik Nakakura
Publikováno v:
Journal of the Endocrine Society
Background: VIPoma, also known as Watery Diarrhea-Hypokalemia- achlorhydria (WDHA) Syndrome is a rare manifestation of multiple endocrine neoplasia syndrome type 1 (MEN1). Vasoactive intestinal peptide, part of the secretin-glucagon family, may be ov
Autor:
Nicola J. Cadenas, Sanziana A. Roman, Anurag K. Agrawal, Kevin Yen, Kelly Hilk, Priya S Srivastava, Maya Lodish
Publikováno v:
Journal of the Endocrine Society
Background: More than 40% of pediatric pheochromocytoma or paragangliomas have associated underlying genetic germline mutation. (1) Clinical Case: We present an 8-year-old male who arrived the emergency department with hypertension to 170/115. MRI of