Prevention of influenza in the general population: recommendation statement from the Canadian Task Force on Preventive Health Care

Por Langley, Joanne M., Faughnan, Marie E.
Publicado em 2004

Prevention of influenza in the general population

Por Langley, Joanne M., Faughnan, Marie E.
Publicado em 2004

Metabolic Alkalosis in Adults with Stable Cystic Fibrosis

Por Al-Ghimlas, Fahad, Faughnan, Marie E, Tullis, Elizabeth
Publicado em 2012

A novel application of capnography during controlled human exposure to air pollution

Por Lukic, Karl Z, Urch, Bruce, Fila, Michael, Faughnan, Marie E, Silverman, Frances
Publicado em 2006

Targeting under-diagnosis in hereditary hemorrhagic telangiectasia: a model approach for rare diseases?

Por Latino, Giuseppe A, Brown, Dale, Glazier, Richard H, Weyman, Jonathan T, Faughnan, Marie E
Publicado no Orphanet J Rare Dis (2014)

Severity score for hereditary hemorrhagic telangiectasia

Por Latino, Giuseppe A, Kim, Helen, Nelson, Jeffrey, Pawlikowska, Ludmila, Young, William, Faughnan, Marie E
Publicado no Orphanet J Rare Dis (2014)

Predicting the need for supplemental oxygen during airline flight in patients with chronic pulmonary disease: A comparison of predictive equations and altitude simulation

Por Bradi, Ana C, Faughnan, Marie E, Stanbrook, Matthew B, Deschenes-Leek, Eva, Chapman, Kenneth R
Publicado em 2009

Symptomatic Liver Involvement in Neonatal Hereditary Hemorrhagic Telangiectasia

Por Al-Saleh, Suhail, John, Philip R., Letarte, Michelle, Faughnan, Marie E., Belik, Jaques, Ratjen, Felix
Publicado em 2011

The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia

Por Grosse, Scott D., Boulet, Sheree L., Grant, Althea M., Hulihan, Mary M., Faughnan, Marie E.
Publicado no Genet Med (2013)

Potential Role of Modifier Genes Influencing Transforming Growth Factor-β1 Levels in the Development of Vascular Defects in Endoglin Heterozygous Mice with Hereditary Hemorrhagic T...

Por Bourdeau, Annie, Faughnan, Marie E., McDonald, Merry-Lynn, Paterson, Andrew D., Wanless, Ian R., Letarte, Michelle
Publicado em 2001

Sarcoidosis complicated by cirrhosis and hepatopulmonary syndrome

Por Gupta, Samir, Faughnan, Marie E, Prud’homme, Gerald J, Hwang, David M, Munoz, David G, Kopplin, Peter
Publicado em 2008

Circulating Angiogenic Cell Dysfunction in Patients with Hereditary Hemorrhagic Telangiectasia

Por Zucco, Liana, Zhang, Qiuwang, Kuliszewski, Michael A., Kandic, Ivana, Faughnan, Marie E., Stewart, Duncan J., Kutryk, Michael J.
Publicado em 2014

The ACVRL1 c.314-35A>G Polymorphism is Associated with Organ Vascular Malformations in Hereditary Hemorrhagic Telangiectasia Patients with ENG Mutations, but not in Patients with A...

Por Pawlikowska, Ludmila, Nelson, Jeffrey, Guo, Diana E., McCulloch, Charles E., Lawton, Michael T., Young, William L., Kim, Helen, Faughnan, Marie E.
Publicado no Am J Med Genet A (2015)

Hemorrhage Rates From Brain Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia Patients

Por Kim, Helen, Nelson, Jeffrey, Krings, Timo, terBrugge, Karel G., McCulloch, Charles E., Lawton, Michael T., Young, William L., Faughnan, Marie E.
Publicado no Stroke (2015)

Brain arteriovenous malformation multiplicity predicts diagnosis of Hereditary Hemorrhagic Telangiectasia: Quantitative assessment

Por Bharatha, Aditya, Faughnan, Marie E., Kim, Helen, Pourmohamad, Tony, Krings, Timo, Bayrak-Toydemir, Pinar, Pawlikowska, Ludmila, McCulloch, Charles E., Lawton, Michael T., Dowd, Christopher F., Young, William L., Terbrugge, Karel G.
Publicado em 2011

Persistent infiltration and pro-inflammatory differentiation of monocytes cause unresolved inflammation in brain arteriovenous malformation

Por Zhang, Rui, Han, Zhenying, Degos, Vincent, Shen, Fanxia, Choi, Eun-Jung, Sun, Zhengda, Kang, Shuai, Wong, Michael, Zhu, Wan, Zhan, Lei, Arthur, Helen M., Oh, S. Paul, Faughnan, Marie E., Su, Hua
Publicado no Angiogenesis (2016)

Brain Arteriovenous Malformations associated with Hereditary Hemorrhagic Telangiectasia: Gene-Phenotype Correlations

Por Nishida, Takeo, Faughnan, Marie E., Krings, Timo, Chakinala, Murali, Gossage, James R., Young, William L., Kim, Helen, Pourmohamad, Tony, Henderson, Katharine J., Schrum, Stacy D., James, Melissa, Quinnine, Nancy, Bharatha, Aditya, terBrugge, Karel G., White, Robert I.
Publicado em 2012

Histogram flow mapping with optical coherence tomography for in vivo skin angiography of hereditary hemorrhagic telangiectasia

Por Cheng, Kyle H. Y., Mariampillai, Adrian, Lee, Kenneth K. C., Vuong, Barry, Luk, Timothy W. H., Ramjist, Joel, Curtis, Anne, Jakubovic, Henry, Kertes, Peter, Letarte, Michelle, Faughnan, Marie E., HHT Investigator Group, Brain Vascular Malformation Consortium, Yang, Victor X. D.
Publicado no J Biomed Opt (2014)

Brain Vascular Malformation Consortium: Overview, Progress and Future Directions

Por Akers, Amy L., Ball, Karen L., Clancy, Marianne, Comi, Anne M., Faughnan, Marie E., Gopal-Srivastava, Rashmi, Jacobs, Thomas P., Kim, Helen, Krischer, Jeffrey, Marchuk, Douglas A., McCulloch, Charles E., Morrison, Leslie, Moses, Marsha, Moy, Claudia S., Pawlikowska, Ludmilla, Young, William L.
Publicado em 2013