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John Wolff

Showing results (1-10 of 16) with videos related to

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Journal of Clinical Microbiology|September 30, 2011
Evaluation of Chlamydia trachomatis and Neisseria gonorrhoeae detection in urine, endocervical, and vaginal specimens by a multiplexed isothermal thermophilic helicase-dependent amplification (tHDA) assayDominic O'Neil, Victoria Doseeva, Thomas Rothmann, et al.
Pulmonary Medicine|October 25, 2012
Positive pressure for obesity hypoventilation syndromeArijit Chanda, Jeff S Kwon, Armand John Wolff, et al.
Diagnostic Microbiology and Infectious Disease|October 18, 2011
Multiplex isothermal helicase-dependent amplification assay for detection of Chlamydia trachomatis and Neisseria gonorrhoeaeVictoria Doseeva, Thomas Forbes, John Wolff, et al.
JMIR Formative Research|November 11, 2024
A Novel Web App for Dietary Weight Management: Development, Implementation, and Usability StudyAshleigh Oliveira, John Wolff, Nouf Alfouzan, et al.
American Journal of Medical Genetics|May 7, 2002
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32Zoran Brkanac, Magali Fernandez, Mark Matsushita, et al.
SLAS Technology|November 2, 2019
A Semi-Automated Tuberculosis Testing Workflow Reduces Manual Hazardous Sample Handling and Hands-On Time: A Proof-of-Concept StudyKevin W P Miller, Neil Grossman, Peter Haviernik, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Archives of Neurology|August 8, 2002
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qterZoran Brkanac, Laura Bylenok, Magali Fernandez, et al.
Muscle & Nerve|December 14, 2017
An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical featuresDong-Hui Chen, Maxwell Ma, Mena Scavina, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Clinical Microbiology|September 30, 2011
Evaluation of Chlamydia trachomatis and Neisseria gonorrhoeae detection in urine, endocervical, and vaginal specimens by a multiplexed isothermal thermophilic helicase-dependent amplification (tHDA) assayDominic O'Neil, Victoria Doseeva, Thomas Rothmann, et al.
Pulmonary Medicine|October 25, 2012
Positive pressure for obesity hypoventilation syndromeArijit Chanda, Jeff S Kwon, Armand John Wolff, et al.
Diagnostic Microbiology and Infectious Disease|October 18, 2011
Multiplex isothermal helicase-dependent amplification assay for detection of Chlamydia trachomatis and Neisseria gonorrhoeaeVictoria Doseeva, Thomas Forbes, John Wolff, et al.
JMIR Formative Research|November 11, 2024
A Novel Web App for Dietary Weight Management: Development, Implementation, and Usability StudyAshleigh Oliveira, John Wolff, Nouf Alfouzan, et al.
American Journal of Medical Genetics|May 7, 2002
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32Zoran Brkanac, Magali Fernandez, Mark Matsushita, et al.
SLAS Technology|November 2, 2019
A Semi-Automated Tuberculosis Testing Workflow Reduces Manual Hazardous Sample Handling and Hands-On Time: A Proof-of-Concept StudyKevin W P Miller, Neil Grossman, Peter Haviernik, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Archives of Neurology|August 8, 2002
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qterZoran Brkanac, Laura Bylenok, Magali Fernandez, et al.
Muscle & Nerve|December 14, 2017
An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical featuresDong-Hui Chen, Maxwell Ma, Mena Scavina, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Pageof 2