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Anne Rutkowski

Showing results (1-10 of 27) with videos related to

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Annals of Emergency Medicine|October 26, 2002
Death notification in the emergency departmentAnne Rutkowski
Neuromuscular Disorders : NMD|July 20, 2010
A congenital muscular dystrophy quality of life and caregiver assessment surveyDiane Smith-Hoban, Susan Sklaroff-Van Hook, Anne Rutkowski
ERJ Open Research|June 30, 2017
Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for managementKristin L Fraser, Scott Wong, A Reghan Foley, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2012
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophyC Alexander Valencia, Devin Rhodenizer, Shruti Bhide, et al.
Cardiology in the Young|December 13, 2016
Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for careFelice Heller, Ivana Dabaj, Jean K Mah, et al.
Plos One|January 18, 2013
Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panelC Alexander Valencia, Arunkanth Ankala, Devin Rhodenizer, et al.
Neurology|August 27, 2017
A natural history study of X-linked myotubular myopathyKimberly Amburgey, Etsuko Tsuchiya, Sabine de Chastonay, et al.
Neurology|January 16, 2016
Author responsePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Cancer Research and Treatment|March 18, 2017
Retrospective Molecular Epidemiology Study of PD-L1 Expression in Patients with <i>EGFR</i>-Mutant Non-small Cell Lung CancerJong Ho Cho, Wei Zhou, Yoon-La Choi, et al.
Plos One|June 14, 2013
Omigapil treatment decreases fibrosis and improves respiratory rate in dy(2J) mouse model of congenital muscular dystrophyQing Yu, Arpana Sali, Jack Van der Meulen, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Annals of Emergency Medicine|October 26, 2002
Death notification in the emergency departmentAnne Rutkowski
Neuromuscular Disorders : NMD|July 20, 2010
A congenital muscular dystrophy quality of life and caregiver assessment surveyDiane Smith-Hoban, Susan Sklaroff-Van Hook, Anne Rutkowski
ERJ Open Research|June 30, 2017
Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for managementKristin L Fraser, Scott Wong, A Reghan Foley, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2012
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophyC Alexander Valencia, Devin Rhodenizer, Shruti Bhide, et al.
Cardiology in the Young|December 13, 2016
Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for careFelice Heller, Ivana Dabaj, Jean K Mah, et al.
Plos One|January 18, 2013
Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panelC Alexander Valencia, Arunkanth Ankala, Devin Rhodenizer, et al.
Neurology|August 27, 2017
A natural history study of X-linked myotubular myopathyKimberly Amburgey, Etsuko Tsuchiya, Sabine de Chastonay, et al.
Neurology|January 16, 2016
Author responsePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Cancer Research and Treatment|March 18, 2017
Retrospective Molecular Epidemiology Study of PD-L1 Expression in Patients with <i>EGFR</i>-Mutant Non-small Cell Lung CancerJong Ho Cho, Wei Zhou, Yoon-La Choi, et al.
Plos One|June 14, 2013
Omigapil treatment decreases fibrosis and improves respiratory rate in dy(2J) mouse model of congenital muscular dystrophyQing Yu, Arpana Sali, Jack Van der Meulen, et al.
Pageof 3