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Molecular Genetics and Metabolism|February 4, 2019
Psychosocial issues in erythropoietic protoporphyria - the perspective of parents, children, and young adults: A qualitative studyHetanshi Naik, Shruti Shenbagam, Allysa Marie Go, et al.Journal of Genetic Counseling|October 1, 2017
Patients' Opinions on Genetic Counseling on the Increased Risk of Parkinson Disease among Gaucher Disease CarriersMaureen Mulhern, Louise Bier, Roy N Alcalay, et al.Molecular Genetics and Metabolism|August 20, 2021
The clinical spectrum of SARS-CoV-2 infection in Gaucher disease: Effect of both a pandemic and a rare disease that disrupts the immune systemPraveena Narayanan, Shiny Nair, Manisha Balwani, et al.Gastroenterology|January 15, 2023
AGA Clinical Practice Update on Diagnosis and Management of Acute Hepatic Porphyrias: Expert ReviewBruce Wang, Herbert L Bonkovsky, Joseph K Lim, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counselingHuma Q Rana, Manisha Balwani, Louise Bier, et al.Canadian Association of Radiologists Journal = Journal L'Association Canadienne Des Radiologistes|June 7, 2008
Ultrasound detection of nonpalpable mammographically occult malignancyWilliam L Simpson, George Hermann, Dana R Rausch, et al.Journal of Genetic Counseling|October 31, 2019
Knowledge and attitudes of Parkinson's disease risk in the Gaucher populationLeah Zaretsky, Natasha Zeid, Hetanshi Naik, et al.Archives of Internal Medicine|September 15, 2010
Type 1 Gaucher disease: significant disease manifestations in "asymptomatic" homozygotesManisha Balwani, Laura Fuerstman, Ruth Kornreich, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2009
Use of complementary and alternative medicine by patients with lysosomal storage diseasesManisha Balwani, Laura Fuerstman, Robert J Desnick, et al.Journal of Hepatology|November 14, 2021
Sebelipase alfa in children and adults with lysosomal acid lipase deficiency: Final results of the ARISE studyBarbara K Burton, François Feillet, Katryn N Furuya, et al.Pageof 13