Alagille syndrome: clinical perspectives

Por Saleh, Maha, Kamath, Binita M, Chitayat, David
Publicado no Appl Clin Genet (2016)

Williams syndrome presenting with findings consistent with Alagille syndrome

Por Sakhuja, Pankaj, Whyte, Hilary, Kamath, Binita, Martin, Nicole, Chitayat, David
Publicado no Clin Case Rep (2015)

Glatiramer acetate–induced acute hepatotoxicity in an adolescent with MS

Por Makhani, Naila, Ngan, Bo-yee, Kamath, Binita M., Yeh, E. Ann
Publicado em 2013

Pancreatic Insufficiency is Not a Prevalent Problem in Alagille Syndrome

Por Kamath, Binita M., Piccoli, David A., Magee, John C., Sokol, Ronald J.
Publicado em 2012

Case 2: A teenager with nausea, vomiting and dysarthria

Por Atkinson, Celia, Kamath, Binita M, Mandelcorn, Jeff, Cutz, Ernest, Raiman, Julian AJ
Publicado em 2013

A Longitudinal Study to Identify Laboratory Predictors of Liver Disease Outcome in Alagille Syndrome

Por Kamath, Binita M., Munoz, Pedro S., Bab, Natalie, Baker, Alastair, Chen, Zhongxue, Spinner, Nancy B., Piccoli, David A.
Publicado em 2010

Assessment of School Readiness in Chronic Cholestatic Liver Disease: A Pilot Study Examining Children with and without Liver Transplantation

Por Gold, Anna, Rogers, Alaine, Cruchley, Elizabeth, Rankin, Stephanie, Parmar, Arpita, Kamath, Binita M., Avitzur, Yaron, Ng, Vicky Lee
Publicado no Can J Gastroenterol Hepatol (2017)

Alagille Syndrome in a Vietnamese Cohort: Mutation Analysis and Assessment of Facial Features

Por Lin, Henry C., Le Hoang, Phuc, Hutchinson, Anne, Chao, Grace, Gerfen, Jennifer, Loomes, Kathleen M., Krantz, Ian, Kamath, Binita M., Spinner, Nancy B.
Publicado em 2012

Differing Effects of Rapamycin or Calcineurin Inhibitor on T-Regulatory Cells in Pediatric Liver and Kidney Transplant Recipients

Por Akimova, Tatiana, Kamath, Binita M., Goebel, Jens W., Meyers, Kevin E. C., Rand, Elizabeth B., Hawkins, Andre, Levine, Matthew H., Bucuvalas, John C., Hancock, Wayne W.
Publicado em 2012

Renal Anomalies in Alagille Syndrome: A Disease-Defining Feature

Por Kamath, Binita M., Podkameni, Gisele, Hutchinson, Anne L., Leonard, Laura D., Gerfen, Jennifer, Krantz, Ian D., Piccoli, David A., Spinner, Nancy B., Loomes, Kathleen M., Meyers, Kevin
Publicado no Am J Med Genet A (2011)

Pathologic Lower Extremity Fractures in Children with Alagille Syndrome

Por Bales, Christina B., Kamath, Binita M., Munoz, Pedro S., Nguyen, Alexander, Piccoli, David A., Spinner, Nancy B., Horn, David, Shults, Justine, Leonard, Mary B., Grimberg, Adda, Loomes, Kathleen M.
Publicado em 2010

Health Related Quality of Life in Patients with Biliary Atresia Surviving with their Native Liver

Por Sundaram, Shikha S., Alonso, Estella M., Haber, Barbara, Magee, John C., Fredericks, Emily, Kamath, Binita, Kerkar, Nanda, Rosenthal, Philip, Shepherd, Ross, Limbers, Christine, Varni, James W., Robuck, Patricia, Sokol, Ronald J., Liver, Childhood
Publicado em 2013

Genomic Alterations in Biliary Atresia Suggests Region of Potential Disease Susceptibility in 2q37.3

Por Leyva-Vega, Melissa, Gerfen, Jennifer, Thiel, Brian D., Jurkiewicz, Dorota, Rand, Elizabeth B., Pawlowska, Joanna, Kaminska, Diana, Russo, Pierre, Gai, Xiaowu, Krantz, Ian D., Kamath, Binita M., Hakonarson, Hakon, Haber, Barbara A., Spinner, Nancy B.
Publicado em 2010

THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome

Por Tsai, Ellen A., Gilbert, Melissa A., Grochowski, Christopher M., Underkoffler, Lara A., Meng, He, Zhang, Xiaojie, Wang, Michael M., Shitaye, Hailu, Hankenson, Kurt D., Piccoli, David, Lin, Henry, Kamath, Binita M., Devoto, Marcella, Spinner, Nancy B., Loomes, Kathleen M.
Publicado no Cell Mol Gastroenterol Hepatol (2016)

SNP array mapping of 20p deletions: Genotypes, Phenotypes and Copy Number Variation

Por Kamath, Binita M., Thiel, Brian D., Gai, Xiaowu, Conlin, Laura K., Munoz, Pedro S., Glessner, Joseph, Clark, Dinah, Warthen, Daniel M., Shaikh, Tamim H., Mihci, Ercan, Piccoli, David A., Grant, Struan F.A., Hakonarson, Hakon, Krantz, Ian D., Spinner, Nancy B.
Publicado em 2009

NOTCH2 mutations in Alagille syndrome

Por Kamath, Binita Maya, Bauer, Robert C, Loomes, Kathleen M, Chao, Grace, Gerfen, Jennifer, Hutchinson, Anne, Hardikar, Winita, Hirschfield, Gideon, Jara, Paloma, Krantz, Ian D, Lapunzina, Pablo, Leonard, Laura, Ling, Simon, Ng, Vicky Lee, Hoang, Phuc Le, Piccoli, David A, Spinner, Nancy Bettina
Publicado em 2011

Quality of Life and its Determinants in a Multi-Center Cohort of Children with Alagille Syndrome

Por Kamath, Binita M., Chen, Zhen, Romero, Rene, Fredericks, Emily M., Alonso, Estella M., Arnon, Ronen, Heubi, James, Hertel, Paula M., Karpen, Saul J., Loomes, Kathleen M., Murray, Karen F., Rosenthal, Philip, Schwarz, Kathleen B., Subbarao, Girish, Teckman, Jeffrey H., Turmelle, Yumirle P., Wang, Kasper S., Sherker, Averell H., Sokol, Ronald J., Magee, John C.
Publicado no J Pediatr (2015)

Baseline Analysis of a Young Alpha-1-AT Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension

Por Teckman, Jeffrey H, Rosenthal, Philip, Abel, Robert, Bass, Lee M., Michail, Sonia, Murray, Karen F., Rudnick, David A., Thomas, Daniel W., Spino, Cathie, Arnon, Ronen, Hertel, Paula M., Heubi, James, Kamath, Binita M., Karnsakul, Wikrom, Loomes, Kathleen M., Magee, John C., Molleston, Jean P., Romero, Rene, Shneider, Benjamin L, Sherker, Averell H, Sokol, Ronald J
Publicado no J Pediatr Gastroenterol Nutr (2015)

Mutations in TJP2 cause progressive cholestatic liver disease

Por Sambrotta, Melissa, Strautnieks, Sandra, Papouli, Efterpi, Rushton, Peter, Clark, Barnaby E., Parry, David A., Logan, Clare V., Newbury, Lucy J., Kamath, Binita M., Ling, Simon, Grammatikopoulos, Tassos, Wagner, Bart E., Magee, John C., Sokol, Ronald J., Mieli-Vergani, Giorgina, Smith, Joshua D., Johnson, Colin A., McClean, Patricia, Simpson, Michael A., Knisely, A.S., Bull, Laura N., Thompson, Richard J.
Publicado em 2014

Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasis

Por Wang, Kasper S., Tiao, Greg, Bass, Lee M., Hertel, Paula M., Mogul, Douglas, Kerkar, Nanda, Clifton, Matthew, Azen, Colleen, Bull, Laura, Rosenthal, Philip, Stewart, Dylan, Superina, Riccardo, Arnon, Ronen, Bozic, Molly, Brandt, Mary L., Dillon, Patrick A., Fecteau, Annie, Iyer, Kishore, Kamath, Binita, Karpen, Saul, Karrer, Frederick, Loomes, Kathleen M., Mack, Cara, Mattei, Peter, Miethke, Alexander, Soltys, Kyle, Turmelle, Yumirle P., West, Karen, Zagory, Jessica, Goodhue, Cat, Shneider, Benjamin L.
Publicado no Hepatology (2017)