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Priya S. Kishnani | Researchclopedia

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Priya S. Kishnani

Duke Medical Center ORCID

760

Works

22,614

Citations

75

h-index

341

i10-index

Research Topics

Lysosomal Storage Disorders Research Glycogen Storage Diseases and Myoclonus Carbohydrate Chemistry and Synthesis

Affiliations

Prisma Health2006–2006

Google (United States)2023–2023

Seattle Children's Hospital2016–2016

Defence Research and Development Organisation2000–2000

University of Kentucky2020–2020

Top Works

Recombinant human acid α-glucosidase

Priya S. Kishnani,Deya Corzo,et al.

2006763 citations

Biochemical and Molecular Research

Child Nutrition and Feeding Issues

A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease

Ans T. van der Ploeg,Paula R. Clemens,et al.

2010737 citations

Pompe disease diagnosis and management guideline

Priya S. Kishnani,Robert D. Steiner,et al.

2006620 citations

A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease

Priya S. Kishnani,Wuh‐Liang Hwu,et al.

2006580 citations

Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

Priya S. Kishnani,Stephanie Austin,et al.

2014487 citations

Cross-reactive immunologic material status affects treatment outcomes in Pompe disease infants

Priya S. Kishnani,Paula Goldenberg,et al.

2009376 citations

Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial

Andrea Amalfitano,A. Resai Bengur,et al.

2001347 citations

Whole-brain irradiation and decline in intelligence: the influence of dose and age on IQ score.

Jeffrey H. Silber,Jerilynn Radcliffe,et al.

1992344 citations

Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease

Priya S. Kishnani,Deya Corzo,et al.

2009334 citations