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Manisha Balwani

Showing results (11-20 of 94) with videos related to

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Skeletal Radiology|June 5, 2014
Painless transient bone marrow edema syndrome in a pediatric patientVivek Joshi, George Hermann, Manisha Balwani, 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.
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.
Molecular Genetics and Metabolism|September 6, 2016
Experiences and concerns of patients with recurrent attacks of acute hepatic porphyria: A qualitative studyHetanshi Naik, Mikayla Stoecker, Saskia C Sanderson, et al.
Pageof 10

Showing results (11-20 of 94) with videos related to

Sort By:
Pageof 10
Skeletal Radiology|June 5, 2014
Painless transient bone marrow edema syndrome in a pediatric patientVivek Joshi, George Hermann, Manisha Balwani, 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.
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.
Molecular Genetics and Metabolism|September 6, 2016
Experiences and concerns of patients with recurrent attacks of acute hepatic porphyria: A qualitative studyHetanshi Naik, Mikayla Stoecker, Saskia C Sanderson, et al.
Pageof 10