Increased production of IL-4 and IL-12p40 from bronchoalveolar lavage cells are biomarkers of Mycobacterium tuberculosis in the sputum von Nolan, Anna, Fajardo, Elaine, Huie, Maryann L, Condos, Rany, Pooran, Anil, Dawson, Rodney, Dheda, Keertan, Bateman, Eric, Rom, William N, Weiden, Michael D

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Immunomodulation with Recombinant Interferon-γ1b in Pulmonary Tuberculosis von Dawson, Rod, Condos, Rany, Tse, Doris, Huie, Maryann L., Ress, Stanley, Tseng, Chi-Hong, Brauns, Clint, Weiden, Michael, Hoshino, Yoshihiko, Bateman, Eric, Rom, William N.

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SCID in Jack Russell Terriers: A New Animal Model of DNA-PKcs Deficiency von Meek, Katheryn, Kienker, Laura, Dallas, Clarissa, Wang, Wei, Dark, Michael J, Venta, Patrick J, Huie, Maryann L, Hirschhorn, Rochelle, Bell, Tom

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Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency von Hirschhorn, Rochelle, Yang, Diana Ruixi, Puck, Jennifer M, Huie, Maryann L, Jiang, Chuan-Kui, Kurlandsky, Lawrence E

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T1981 Plasma Levels of Insulinotropic and Digestive Hormones Predict the Risk of Colonic Adenomas von Wolff, Martin J, Joseph, Neal, Huie, Maryann L, Quijano, Sergio, Muakkassa, Nora, Martiniuk, Frank, Perez-Perez, Guillermo I, Francois, Fritz

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Homozygosity for Multiple Contiguous Single-Nucleotide Polymorphisms as an Indicator of Large Heterozygous Deletions: Identification of a Novel Heterozygous 8-kb Intragenic Deletio... von Huie, Maryann L., Anyane-Yeboa, Kwame, Guzman, Edwin, Hirschhorn, Rochelle

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Intercellular transfer of the virally derived precursor form of acid α-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy pompe disease von PAULY, Daniel F, FRAITES, Thomas J, TOMA, Catalin, BAYES, Helen S, HUIE, Maryann L, HIRSCHHORN, Rochelle, PLOTZ, Paul H, RABEN, Nina, KESSLER, Paul D, BYRNE, Barry J

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Identification of six novel mutations in the acid alpha-glucosidase gene in three Spanish patients with infantile onset glycogen storage disease type II (Pompe disease) von Fernandez-Hojas, Roberto, Huie, Maryann L., Navarro, Carmen, Dominguez, Carmen, Roig, Manuel, Lopez-Coronas, Diana, Teijeira, Susana, Anyane-Yeboa, Kwame, Hirschhorn, Rochelle

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Murine acid α-glucosidase : Cell-specific mRNA differential expression during development and maturation von PONCE, E, WITTE, D. P, HIRSCHHORN, R, HUIE, M. L, GRABOWSKI, G. A

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Elevated IP-10 and IL-6 from bronchoalveolar lavage cells are biomarkers of non-cavitary tuberculosis von Nolan, A., Condos, R., Huie, M. L., Dawson, R., Dheda, K., Bateman, E., Rom, W. N., Weiden, M. D.

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Immunomodulation with recombinant interferon-gamma1b in pulmonary tuberculosis von Dawson, Rod, Condos, Rany, Tse, Doris, Huie, Maryann L, Ress, Stanley, Tseng, Chi-Hong, Brauns, Clint, Weiden, Michael, Hoshino, Yoshihiko, Bateman, Eric, Rom, William N

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Immunomodulation with Recombinant Interferon-[gamma]1b in Pulmonary Tuberculosis von Dawson, Rod, Condos, Rany, Tse, Doris, Huie, Maryann L, Ress, Stanley, Tseng, Chi-Hong, Brauns, Clint, Weiden, Michael, Hoshino, Yoshihiko, Bateman, Eric, Rom, William N

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Increased Production of IL-4 and IL-12p40 from Bronchoalveolar Lavage Cells Are Biomarkers of Mycobacterium tuberculosis in the Sputum. e59461 von Nolan, Anna, Fajardo, Elaine, Huie, Maryann L, Condos, Rany, Pooran, Anil, Dawson, Rodney, Dheda, Keertan, Bateman, Eric, Rom, William N, Weiden, Michael D

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Frequency of mutations for glycogen storage disease type II in different populations: the Δ525T and Δexon 18 mutations are not generally “common” in white populations von HIRSCHHORN, ROCHELLE, HUIE, MARYANN L

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Frequency of mutations for glycogen storage disease type II in different populations: the [delta]525T and [delta]exon 18 mutations are not generally "common" in white populations von HIRSCHHORN, ROCHELLE, HUIE, MARYANN L

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The African Origin of the Common Mutation in African American Patients with Glycogen-Storage Disease Type II von Becker, Jeffrey A., Vlach, John, Raben, Nina, Nagaraju, Kanneboyina, Adams, Elizabeth M., Hermans, Monique M., Reuser, Arnold J.J., Brooks, Susan Sklower, Tifft, Cynthia J., Hirschhorn, Rochelle, Huie, Maryann L., Nicolino, Marc, Plotz, Paul H.

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Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery von HIRSCHHORN, R, RUIXI YANG, D, AJAY ISRANI, HUIE, M. L, OWNBY, D. R

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Localization and ordering of acid alpha-glucosidase (GAA) and thymidine kinase (TK1) by fluorescence in situ hybridization von KUO, W.-L, HIRSCHHORN, R, HUIE, M. L, HIRSCHHORN, K

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Murine Acid α-Glucosidase von Ponce, Elvira, Witte, David P., Hirschhorn, Rochelle, Huie, Maryann L., Grabowski, Gregory A.

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Mutation at the catalytic site (M519V) in glycogen storage disease type II (Pompe disease) von Huie, Maryann L., Hirschhorn, Rochelle, Chen, Agnes S., Martiniuk, Frank, Zhong, Nan

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