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Showing results (171-180 of 237) with videos related to

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Neurology. Genetics|April 29, 2016
Clinical course and prognosis in patients with Gaucher disease and parkinsonismGrisel Lopez, Jenny Kim, Edythe Wiggs, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 18, 2011
Risk factors associated with biliary pancreatitis in childrenMichael H Ma, Harrison X Bai, Alexander J Park, et al.
Cureus|February 23, 2026
The Clinico-Epidemiological Profile and Effectiveness of Codeine and Triprolidine in Dry Cough Patients Not Responding to Non-Opioid-Based Antitussives: Results From a Prospective, Multicenter, Single-Arm, Open-Label Postmarketing Observational StudyDeepak Talwar, Balamurugan Santhalingam, Rajveer Kuldeep, et al.
American Journal of Hematology|March 5, 2009
The underrecognized progressive nature of N370S Gaucher disease and assessment of cancer risk in 403 patientsTamar H Taddei, Katherine A Kacena, Mei Yang, et al.
Indian Pediatrics|November 15, 2011
Recombinant macrophage targeted enzyme replacement therapy for Gaucher disease in IndiaA Nagral, P Mewawalla, S Jagadeesh, et al.
Molecular Genetics and Metabolism|January 2, 2017
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher RegistryAmal El-Beshlawy, Anna Tylki-Szymanska, Ashok Vellodi, et al.
American Journal of Hematology|June 17, 2026
Cumulative Antigen Suppression Reduces Clonal Plasma Cell Evolution in Gaucher DiseaseNoor Ul Ain, Noffar Bar, Lilu Guo, et al.
Molecular Genetics and Metabolism|July 4, 2020
Clinical relevance of endpoints in clinical trials for acid sphingomyelinase deficiency enzyme replacement therapySimon A Jones, Margaret McGovern, Olivier Lidove, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2017
Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiencyMargaret M McGovern, Carlo Dionisi-Vici, Roberto Giugliani, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Enzyme replacement therapy and bony changes in Egyptian paediatric Gaucher disease patientsA El-Beshlawy, L Ragab, I Youssry, et al.
Pageof 24

Showing results (171-180 of 237) with videos related to

Sort By:
Pageof 24
Neurology. Genetics|April 29, 2016
Clinical course and prognosis in patients with Gaucher disease and parkinsonismGrisel Lopez, Jenny Kim, Edythe Wiggs, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 18, 2011
Risk factors associated with biliary pancreatitis in childrenMichael H Ma, Harrison X Bai, Alexander J Park, et al.
Cureus|February 23, 2026
The Clinico-Epidemiological Profile and Effectiveness of Codeine and Triprolidine in Dry Cough Patients Not Responding to Non-Opioid-Based Antitussives: Results From a Prospective, Multicenter, Single-Arm, Open-Label Postmarketing Observational StudyDeepak Talwar, Balamurugan Santhalingam, Rajveer Kuldeep, et al.
American Journal of Hematology|March 5, 2009
The underrecognized progressive nature of N370S Gaucher disease and assessment of cancer risk in 403 patientsTamar H Taddei, Katherine A Kacena, Mei Yang, et al.
Indian Pediatrics|November 15, 2011
Recombinant macrophage targeted enzyme replacement therapy for Gaucher disease in IndiaA Nagral, P Mewawalla, S Jagadeesh, et al.
Molecular Genetics and Metabolism|January 2, 2017
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher RegistryAmal El-Beshlawy, Anna Tylki-Szymanska, Ashok Vellodi, et al.
American Journal of Hematology|June 17, 2026
Cumulative Antigen Suppression Reduces Clonal Plasma Cell Evolution in Gaucher DiseaseNoor Ul Ain, Noffar Bar, Lilu Guo, et al.
Molecular Genetics and Metabolism|July 4, 2020
Clinical relevance of endpoints in clinical trials for acid sphingomyelinase deficiency enzyme replacement therapySimon A Jones, Margaret McGovern, Olivier Lidove, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2017
Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiencyMargaret M McGovern, Carlo Dionisi-Vici, Roberto Giugliani, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Enzyme replacement therapy and bony changes in Egyptian paediatric Gaucher disease patientsA El-Beshlawy, L Ragab, I Youssry, et al.
Pageof 24