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CONSULTATION DIRECTORY 2024 Judith Jebastin Thangaiah, M.B.B.S., M.D. 2 Consultation Directory AUTOPSY BONE, SOFT TISSUE, JOINTS BREAST CARDIOVASCULAR Mariam (Priya) Alexander, M.D. Reade Quinton...

fabry_disease_testing_algorithm.pdf

© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 06/2024 Fabry Disease Diagnostic Testing Algorithm FMTT / Familial Variant, Targeted Testing, Varies Clinical suspicion...

celiac_disease_diagnostic_testing_algorithm.pdf

08/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Celiac Disease Diagnostic Testing Algorithm Testing for selective IgA deficiency IGA / Immunoglobulin A (IgA)...

fabry_disease_newborn_screen-positive_follow-up.pdf

08/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Fabry Disease: Newborn Screen-Positive Follow-up False-positive newborn screen Disease-causing variant identified...

steroid_pathways.pdf

01/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Steroid Pathways Mineralocorticoids CYP17A1 = Cytochrome P450 Family 17 Subfamily A Member 1 HSD3B1/HSD3B2 =...

newborn_screen_follow-up_for_glucose-6-phosphate_dehydrogenase__g-6-pd__deficiency.pdf

© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 03/2024 Decreased glucose-6-phosphate dehydrogenase (G6PD) Not G6PD deficiency. In infants with hyperbilirubinemia,...

von_willebrand_disease_profile.pdf

© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 10/2024 von Willebrand Disease Profile Algorithm AVWPR / von Willebrand Disease Profile, Plasma Testing begins with:...

hyperoxaluria_diagnostic_algorithm.pdf

10/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Adapted from “The Primary Hyperoxalurias: An Algorithm for Diagnosis,” American Journal of Nephrology 2005;25:154-160...

Generating awareness of the laboratory - Insights

Medical Laboratory Professionals Week, an annual celebration held in April, is a great time to raise awareness of the impact the laboratory has on patients and providers in the community. Lab Week is also an opportunity to spotlight the...

A new comprehensive genetic panel redefines Parkinson's disease diagnosis - Insights

Mayo Clinic Laboratories introduces the Inherited Parkinson’s Disease Gene Panel (Mayo ID: PARDP), a collaborative breakthrough poised to transform Parkinson’s disease diagnosis and treatment. Led by Rodolfo Savica, M.D., Ph.D., and Zhiyv...