The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?
Weinreb, Neal J., Goker-Alpan, Ozlem, Kishnani, Priya S., Longo, Nicola, Burrow, T. Andrew, Bernat, John A., Gupta, Punita, Henderson, Nadene, Pedro, Helio, Prada, Carlos E., Vats, Divya, Pathak, Ravi R., Wright, Ekaterina, Ficicioglu, Can
Published in Molecular genetics and metabolism (01.05.2022)
Published in Molecular genetics and metabolism (01.05.2022)
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Journal Article
Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patients
Serai, Suraj D., Naidu, Anjani P., Andrew Burrow, T., Prada, Carlos E., Xanthakos, Stavra, Towbin, Alexander J.
Published in Molecular genetics and metabolism (01.03.2018)
Published in Molecular genetics and metabolism (01.03.2018)
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Journal Article
Gaucher disease and SARS-CoV-2 infection: Emerging management challenges
Mistry, Pramod, Balwani, Manisha, Barbouth, Deborah, Burrow, T. Andrew, Ginns, Edward I., Goker-Alpan, Ozlem, Grabowski, Gregory A., Kartha, Reena V., Kishnani, Priya S., Lau, Heather, Lee, Chung U., Lopez, Grisel, Maegawa, Gustavo, Packman, Seymour, Prada, Carlos, Rosenbloom, Barry, Lal, Tamanna Roshan, Schiffmann, Rapheal, Weinreb, Neal, Sidransky, Ellen
Published in Molecular genetics and metabolism (01.07.2020)
Published in Molecular genetics and metabolism (01.07.2020)
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Journal Article
Evaluating psychosocial stressors in families of children with inborn errors of metabolism
Grant, Nathan, Burrow, T. Andrew
Published in Molecular genetics and metabolism reports (01.06.2021)
Published in Molecular genetics and metabolism reports (01.06.2021)
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Journal Article
Cardiac Disease in Methylmalonic Acidemia
Prada, Carlos E., MD, Al Jasmi, Fatma, MD, Kirk, Edwin P., MB BS, Hopp, Maxwell, MB BCh, Jones, Owen, MB BChir, Leslie, Nancy D., MD, Burrow, T. Andrew, MD
Published in The Journal of pediatrics (01.11.2011)
Published in The Journal of pediatrics (01.11.2011)
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Journal Article
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource
Koch, Rebecca L., Soler-Alfonso, Claudia, Kiely, Bridget T., Asai, Akihiro, Smith, Ariana L., Bali, Deeksha S., Kang, Peter B., Landstrom, Andrew P., Akman, H. Orhan, Burrow, T. Andrew, Orthmann-Murphy, Jennifer L., Goldman, Deberah S., Pendyal, Surekha, El-Gharbawy, Areeg H., Austin, Stephanie L., Case, Laura E., Schiffmann, Raphael, Hirano, Michio, Kishnani, Priya S.
Published in Molecular genetics and metabolism (01.03.2023)
Published in Molecular genetics and metabolism (01.03.2023)
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Journal Article
Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis
Coman, David, Vissers, Lisenka E.L.M., Riley, Lisa G., Kwint, Michael P., Hauck, Roxanna, Koster, Janet, Geuer, Sinje, Hopkins, Sarah, Hallinan, Barbra, Sweetman, Larry, Engelke, Udo F.H., Burrow, T. Andrew, Cardinal, John, McGill, James, Inwood, Anita, Gurnsey, Christine, Waterham, Hans R., Christodoulou, John, Wevers, Ron A., Pitt, James
Published in American journal of human genetics (05.07.2018)
Published in American journal of human genetics (05.07.2018)
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Journal Article
CNTNAP1-Related Congenital Hypomyelinating Neuropathy
Lesmana, Harry, Vawter Lee, Marissa, Hosseini, Seyed Ali, Burrow, T. Andrew, Hallinan, Barbara, Bove, Kevin, Schapiro, Mark, Hopkin, Robert J.
Published in Pediatric neurology (01.04.2019)
Published in Pediatric neurology (01.04.2019)
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Journal Article
Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly
Hannah, William B., Ryan, Katherine, Pendyal, Surekha, Burrow, T. Andrew, Harley, Susan E., Cordell, Miranda, McCall, Chad M., Mavis, Alisha M., Tan, Queenie K.‐G., Kishnani, Priya S.
Published in American journal of medical genetics. Part A (01.11.2022)
Published in American journal of medical genetics. Part A (01.11.2022)
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Journal Article
Predictive validity of a non-induced mouse model of compulsive-like behavior
Greene-Schloesser, D.M., Van der Zee, E.A., Sheppard, D.K., Castillo, M.R., Gregg, K.A., Burrow, T., Foltz, H., Slater, M., Bult-Ito, A.
Published in Behavioural brain research (01.08.2011)
Published in Behavioural brain research (01.08.2011)
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Journal Article
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Mistry, Pramod K., Balwani, Manisha, Baris, Hagit N., Turkia, Hadhami Ben, Burrow, T. Andrew, Charrow, Joel, Cox, Gerald F., Danda, Sumita, Dragosky, Marta, Drelichman, Guillermo, El-Beshlawy, Amal, Fraga, Cristina, Freisens, Selena, Gaemers, Sebastiaan, Hadjiev, Evgueniy, Kishnani, Priya S., Lukina, Elena, Maison-Blanche, Pierre, Martins, Ana Maria, Pastores, Gregory, Petakov, Milan, Peterschmitt, M. Judith, Rosenbaum, Hanna, Rosenbloom, Barry, Underhill, Lisa H., Cox, Timothy M.
Published in Blood cells, molecules, & diseases (01.07.2018)
Published in Blood cells, molecules, & diseases (01.07.2018)
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Journal Article
Somatic HRAS p.G12S Mutation Causes Woolly Hair and Epidermal Nevi
Levinsohn, Jonathan L., Teng, Joyce, Craiglow, Brittany G., Loring, Erin C., Burrow, T Andrew, Mane, Shrikant S., Overton, John D., Lifton, Richard P., McNiff, Jennifer M., Lucky, Anne W., Choate, Keith A.
Published in Journal of investigative dermatology (01.04.2014)
Published in Journal of investigative dermatology (01.04.2014)
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Journal Article
Acute Progression of Neuromuscular Findings in Infantile Pompe Disease
Burrow, T. Andrew, MD, Bailey, Laurie A., MS, Kinnett, Douglas G., MD, Hopkin, Robert J., MD
Published in Pediatric neurology (01.06.2010)
Published in Pediatric neurology (01.06.2010)
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Journal Article
Home infusion of intravenous velaglucerase alfa: Experience from pooled clinical studies in 104 patients with type 1 Gaucher disease
Elstein, Deborah, Burrow, T Andrew, Charrow, Joel, Giraldo, Pilar, Mehta, Atul, Pastores, Gregory M, Lee, Hak-Myung, Mellgard, Björn, Zimran, Ari
Published in Molecular genetics and metabolism (01.01.2017)
Published in Molecular genetics and metabolism (01.01.2017)
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Journal Article
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Mistry, Pramod K., Balwani, Manisha, Baris, Hagit N., Turkia, Hadhami Ben, Burrow, T. Andrew, Charrow, Joel, Cox, Gerald F., Danda, Sumita, Dragosky, Marta, Drelichman, Guillermo, El-Beshlawy, Amal, Fraga, Cristina, Freisens, Selena, Gaemers, Sebastiaan, Hadjiev, Evgueniy, Kishnani, Priya S., Lukina, Elena, Maison-Blanche, Pierre, Martins, Ana Maria, Pastores, Gregory, Petakov, Milan, Peterschmitt, M. Judith, Rosenbaum, Hanna, Rosenbloom, Barry, Underhill, Lisa H., Cox, Timothy M.
Published in Blood cells, molecules, & diseases (01.07.2019)
Published in Blood cells, molecules, & diseases (01.07.2019)
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Journal Article
Widespread Vasculopathy in a Patient with Morquio A Syndrome
Powell, Adam W, Taylor, Michael D, Burrow, T Andrew, Hopkin, Robert J, Prada, Carlos E, Jefferies, John L
Published in Texas Heart Institute journal (01.12.2017)
Published in Texas Heart Institute journal (01.12.2017)
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Journal Article
Enzyme reconstitution/replacement therapy for lysosomal storage diseases
Burrow, T Andrew, Hopkin, Robert J, Leslie, Nancy D, Tinkle, Bradley T, Grabowski, Gregory A
Published in Current opinion in pediatrics (01.12.2007)
Published in Current opinion in pediatrics (01.12.2007)
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Journal Article
Engineering innovative interfaces for point-of-care diagnostics
Burrow, Damon T., Heggestad, Jacob T., Kinnamon, David S., Chilkoti, Ashutosh
Published in Current opinion in colloid & interface science (01.08.2023)
Published in Current opinion in colloid & interface science (01.08.2023)
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Journal Article
Stability is maintained in adults with Gaucher disease type 1 switched from velaglucerase alfa to eliglustat or imiglucerase: A sub-analysis of the eliglustat ENCORE trial
Pleat, Rebecca, Cox, Timothy M., Burrow, T. Andrew, Giraldo, Pilar, Goker-Alpan, Ozlem, Rosenbloom, Barry E., Croal, Laura R., Underhill, Lisa H., Gaemers, Sebastiaan J.M., Peterschmitt, M. Judith
Published in Molecular genetics and metabolism reports (01.12.2016)
Published in Molecular genetics and metabolism reports (01.12.2016)
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Journal Article
Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy
Burrow, T. Andrew, MD, Cohen, Mitchell B., MD, Bokulic, Ronald, MD, Deutsch, Gail, MD, Choudhary, Arabinda, MD, Falcone, Richard A., MD, Grabowski, Gregory A., MD
Published in The Journal of pediatrics (01.02.2007)
Published in The Journal of pediatrics (01.02.2007)
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Journal Article