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pro vyhledávání: '"Mark, Bechter"'
Autor:
Aseel, Bin Sawad, John, Jackimiec, Mark, Bechter, Allison, Trucillo, Kristina, Lindsley, Anil, Bhagat, Jennifer, Uyei, George A, Diaz
Publikováno v:
Molecular Genetics and Metabolism. 137:153-163
Arginase 1 Deficiency (ARG1-D) is a rare, progressive, metabolic disorder that is characterized by devastating manifestations driven by elevated plasma arginine levels. It typically presents in early childhood with spasticity (predominately affecting
Publikováno v:
European Medical Journal Hepatology, Vol 3, Iss 2, Pp 60-67 (2015)
The Synageva BioPharma-sponsored symposium discussed the differential diagnoses for liver diseases that may be under-recognised in clinical settings, with a focus on lysosomal acid lipase deficiency (LAL D). LAL D is a lysosomal storage disorder caus
Externí odkaz:
https://doaj.org/article/62452729d0394422a6703d4fe6f44c62
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES.
Arginase 1 Deficiency (ARG1-D) is a rare urea cycle disorder that results in persistent hyperargininemia and a distinct, progressive neurologic phenotype involving developmental delay, intellectual disability, and spasticity, predominantly affecting
Autor:
Aseel Bin Sawad, John Jackimiec, Mark Bechter, Michael Hull, Jason Yeaw, Yi Wang, George A. Diaz
Publikováno v:
Journal of medical economics. 25(1)
Arginase 1 Deficiency (ARG1-D) is an inherited metabolic disease that leads to significant morbidity.Despite the recognized burden of disease, information on health care resource utilization (HCRU) among patients with ARG1-D is lacking. We, therefore
Autor:
Audrey Hutchcraft, Kelly Farrell, James L Comadoll, Sangeeta Krishnan, Mark Bechter, Huub T C Kreuwel, Shea Comadoll
Publikováno v:
Orthopedics. 35(6)
Bleeding after total knee arthroplasty increases the risk of pain, delayed rehabilitation, blood transfusion, and transfusion-associated complications. The authors compared pre- and postoperative decreases in hemoglobin as a surrogate for blood loss