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Atul Mehta

Showing results (61-70 of 150) with videos related to

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Oxford Medical Case Reports|February 22, 2021
A Unique Case of Combined Nodular and Tracheobronchial AmyloidosisFeihong Ding, Yun Li, Shailesh Balasubramanian, et al.
Molecular Genetics and Metabolism|August 28, 2017
Corrigendum to "Retinal thinning in Gaucher disease patients and carriers: Results of a pilot study" [Mol. Genet. Metab. 109 (2013) 221-223]Alisdair McNeill, Gloria Roberti, Gerassimos Lascaratos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome SurveyUma Ramaswami, Catharina Whybra, Rosella Parini, et al.
Molecular Genetics and Metabolism|December 3, 2010
Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT)Gabor E Linthorst, Dominique P Germain, Carla E M Hollak, et al.
Molecular Genetics and Metabolism|June 5, 2012
Novel pathogenic mutations in the glucocerebrosidase locusRaquel Duran, Alisdair McNeill, Atul Mehta, et al.
Molecular Genetics and Metabolism|May 4, 2013
Retinal thinning in Gaucher disease patients and carriers: results of a pilot studyAlisdair McNeill, Gloria Roberti, Gerassimos Lascaratos, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 7, 2007
Gastric bezoar after lung transplantation in non-cystic fibrosis patients and review of the literatureErik Folch, Hasan Shakoor, Javier Gomez, et al.
Journal of Clinical Medicine|June 26, 2026
Flexible Bronchoscopy in the Intensive Care Unit: Controversies, Clinical Applications, and the Expanding Role of IntensivistsThushira Weerawarna, Rajesh Mishra, Sumara Tantray, et al.
American Journal of Clinical Pathology|September 15, 2004
Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophagesLeonie A Boven, Marjan van Meurs, Rolf G Boot, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
A charitable access program for patients with lysosomal storage disorders in underserved communities worldwideAtul Mehta, Uma Ramaswami, Joseph Muenzer, et al.
Pageof 15

Showing results (61-70 of 150) with videos related to

Sort By:
Pageof 15
Oxford Medical Case Reports|February 22, 2021
A Unique Case of Combined Nodular and Tracheobronchial AmyloidosisFeihong Ding, Yun Li, Shailesh Balasubramanian, et al.
Molecular Genetics and Metabolism|August 28, 2017
Corrigendum to "Retinal thinning in Gaucher disease patients and carriers: Results of a pilot study" [Mol. Genet. Metab. 109 (2013) 221-223]Alisdair McNeill, Gloria Roberti, Gerassimos Lascaratos, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome SurveyUma Ramaswami, Catharina Whybra, Rosella Parini, et al.
Molecular Genetics and Metabolism|December 3, 2010
Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT)Gabor E Linthorst, Dominique P Germain, Carla E M Hollak, et al.
Molecular Genetics and Metabolism|June 5, 2012
Novel pathogenic mutations in the glucocerebrosidase locusRaquel Duran, Alisdair McNeill, Atul Mehta, et al.
Molecular Genetics and Metabolism|May 4, 2013
Retinal thinning in Gaucher disease patients and carriers: results of a pilot studyAlisdair McNeill, Gloria Roberti, Gerassimos Lascaratos, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 7, 2007
Gastric bezoar after lung transplantation in non-cystic fibrosis patients and review of the literatureErik Folch, Hasan Shakoor, Javier Gomez, et al.
Journal of Clinical Medicine|June 26, 2026
Flexible Bronchoscopy in the Intensive Care Unit: Controversies, Clinical Applications, and the Expanding Role of IntensivistsThushira Weerawarna, Rajesh Mishra, Sumara Tantray, et al.
American Journal of Clinical Pathology|September 15, 2004
Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophagesLeonie A Boven, Marjan van Meurs, Rolf G Boot, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
A charitable access program for patients with lysosomal storage disorders in underserved communities worldwideAtul Mehta, Uma Ramaswami, Joseph Muenzer, et al.
Pageof 15