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William B Hannah

Showing results (1-10 of 18) with videos related to

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American Journal of Respiratory and Critical Care Medicine|August 16, 2018
Rapid Advances in Primary Ciliary Dyskinesia Research. A Brief Update for PulmonologistsFaiza Khalid, William B Hannah, Benjamin M Gaston
Annals of Neurology|October 4, 2021
"Disappearing Infarct" Is Late-Onset MELASTimothy M Landis, William B Hannah, William J Powers
Journal of Experimental Botany|June 3, 2008
Identification of auxins by a chemical genomics approachMay Christian, William B Hannah, Hartwig Lüthen, et al.
Molecular Genetics and Metabolism Reports|February 25, 2020
Adenotonsillectomy should be avoided whenever possible in infantile-onset Pompe diseaseHarrison N Jones, Samuela Fernandes, William B Hannah, et al.
Genetics in Medicine Open|December 13, 2024
Using genomic databases to determine the frequency and population-based heterogeneity of autosomal recessive conditionsWilliam B Hannah, Mitchell L Drumm, Keith Nykamp, et al.
Molecular Genetics and Metabolism Reports|December 13, 2021
A novel cause of emergent hyperammonemia: <i>Cryptococcal</i> fungemia and meningitisWilliam B Hannah, Gregory Nizialek, Katherine J Dempsey, et al.
Nature Reviews. Disease Primers|September 7, 2023
Glycogen storage diseasesWilliam B Hannah, Terry G J Derks, Mitchell L Drumm, et al.
JIMD Reports|September 13, 2023
Screening data from 19 patients with late-onset Pompe disease for a phase I clinical trial of AAV8 vector-mediated gene therapyWilliam B Hannah, Laura E Case, Edward C Smith, et al.
The Lancet. Respiratory Medicine|January 20, 2022
The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysisWilliam B Hannah, Bryce A Seifert, Rebecca Truty, et al.
Molecular Genetics and Metabolism Reports|March 4, 2022
Very early-onset inflammatory bowel disease: Novel description in glycogen storage disease type IaWilliam B Hannah, Ricardo C Ong, Margarita Nieto Moreno, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
American Journal of Respiratory and Critical Care Medicine|August 16, 2018
Rapid Advances in Primary Ciliary Dyskinesia Research. A Brief Update for PulmonologistsFaiza Khalid, William B Hannah, Benjamin M Gaston
Annals of Neurology|October 4, 2021
"Disappearing Infarct" Is Late-Onset MELASTimothy M Landis, William B Hannah, William J Powers
Journal of Experimental Botany|June 3, 2008
Identification of auxins by a chemical genomics approachMay Christian, William B Hannah, Hartwig Lüthen, et al.
Molecular Genetics and Metabolism Reports|February 25, 2020
Adenotonsillectomy should be avoided whenever possible in infantile-onset Pompe diseaseHarrison N Jones, Samuela Fernandes, William B Hannah, et al.
Genetics in Medicine Open|December 13, 2024
Using genomic databases to determine the frequency and population-based heterogeneity of autosomal recessive conditionsWilliam B Hannah, Mitchell L Drumm, Keith Nykamp, et al.
Molecular Genetics and Metabolism Reports|December 13, 2021
A novel cause of emergent hyperammonemia: <i>Cryptococcal</i> fungemia and meningitisWilliam B Hannah, Gregory Nizialek, Katherine J Dempsey, et al.
Nature Reviews. Disease Primers|September 7, 2023
Glycogen storage diseasesWilliam B Hannah, Terry G J Derks, Mitchell L Drumm, et al.
JIMD Reports|September 13, 2023
Screening data from 19 patients with late-onset Pompe disease for a phase I clinical trial of AAV8 vector-mediated gene therapyWilliam B Hannah, Laura E Case, Edward C Smith, et al.
The Lancet. Respiratory Medicine|January 20, 2022
The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysisWilliam B Hannah, Bryce A Seifert, Rebecca Truty, et al.
Molecular Genetics and Metabolism Reports|March 4, 2022
Very early-onset inflammatory bowel disease: Novel description in glycogen storage disease type IaWilliam B Hannah, Ricardo C Ong, Margarita Nieto Moreno, et al.
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