Implementing Cisco IP Telephony and Video, Part 2 (CIPTV2) Foundation learning guide (CCNP Collaboration exam 300-075 CIPTV2)

por Hannah, William Alexander, Behl, Akhil
Publicado 2016

Identification of auxins by a chemical genomics approach

por Christian, May, Hannah, William B., Lüthen, Hartwig, Jones, Alan M.
Publicado 2008

Adenotonsillectomy should be avoided whenever possible in infantile-onset Pompe disease

por Jones, Harrison N., Fernandes, Samuela, Hannah, William B., Kansagra, Sujay, Raynor, Eileen M., Kishnani, Priya S.
Publicado 2020

Screening data from 19 patients with late‐onset Pompe disease for a phase I clinical trial of AAV8 vector‐mediated gene therapy

por Hannah, William B., Case, Laura E., Smith, Edward C., Walters, Crista, Bali, Deeksha, Kishnani, Priya S., Koeberl, Dwight D.
Publicado 2023

A novel cause of emergent hyperammonemia: Cryptococcal fungemia and meningitis

por Hannah, William B., Nizialek, Gregory, Dempsey, Katherine J., Armitage, Keith B., McCandless, Shawn E., Konczal, Laura L.
Publicado 2021

Utility of the HScore for Predicting COVID-19 Severity

por Hannah, William, Shadiack, Anthony, Markofski, Melissa, Dao, Kevin, Shaw, Eric, Odum, Craig, Parisio-Poldiak, Nayda, Finer, Alexis, Flynn, Mike
Publicado 2022

Myelodysplasia and Mast Cell Leukemia with t(9;22)

por Lago, Kathryn J., Shupe, Matthew P., Hannah, William N., Velagaleti, Gopalrao V. N., Mendiola, Christina, Ortega, Veronica, Haney, Brian R.
Publicado 2017

Very early-onset inflammatory bowel disease: Novel description in glycogen storage disease type Ia

por Hannah, William B., Ong, Ricardo C., Moreno, Margarita Nieto, Pendyal, Surekha, Abdelmalak, Monica, Kelsen, Judith, McGreal, Nancy M., Kishnani, Priya S.
Publicado 2022

Hemophilia A and B mice, but not VWF(−/−)mice, display bone defects in congenital development and remodeling after injury

por Taves, Sarah, Sun, Junjiang, Livingston, Eric W., Chen, Xin, Amiaud, Jerome, Brion, Regis, Hannah, William B., Bateman, Ted A., Heymann, Dominique, Monahan, Paul E.
Publicado 2019

The expanding phenotype of OFD1‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia

por Hannah, William B., DeBrosse, Suzanne, Kinghorn, BreAnna, Strausbaugh, Steven, Aitken, Moira L., Rosenfeld, Margaret, Wolf, Whitney E., Knowles, Michael R., Zariwala, Maimoona A.
Publicado 2019

Life-threatening presentations of propionic acidemia due to the Amish PCCB founder variant

por Hannah, William B., Dempsey, Katherine J., Schillaci, Lori-Anne P., Zacharias, Michael, McCandless, Shawn E., Wynshaw-Boris, Anthony, Konczal, Laura L., Bedoyan, Jirair K.
Publicado 2019

Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibro...

por Polineni, Deepika, Piccorelli, Annalisa V., Hannah, William B., Dalrymple, Sarah N., Pace, Rhonda G., Durie, Peter R., Ling, Simon C., Knowles, Michael R., Stonebraker, Jaclyn R.
Publicado 2018

Employing a Gain-of-Function Factor IX Variant R338L to Advance the Efficacy and Safety of Hemophilia B Human Gene Therapy: Preclinical Evaluation Supporting an Ongoing Adeno-Assoc...

por Monahan, Paul E., Sun, Junjiang, Gui, Tong, Hu, Genlin, Hannah, William B., Wichlan, David G., Wu, Zhijian, Grieger, Joshua C., Li, Chengwen, Suwanmanee, Thipparat, Stafford, Darrel W., Booth, Carmen J., Samulski, Jade J., Kafri, Tal, McPhee, Scott W.J., Samulski, R. Jude
Publicado 2015