Search Results - "Gillis, Lynette A"

Population-Based Analysis of Hepatocellular Carcinoma in Children: Identifying Optimal Surgical Treatment by Ziogas, Ioannis A., Ye, Fei, Zhao, Zhiguo, Matsuoka, Lea K., Montenovo, Martin I., Izzy, Manhal, Benedetti, Daniel J., Lovvorn, Harold N., Gillis, Lynette A., Alexopoulos, Sophoclis P.

“…Hepatocellular carcinoma (HCC) constitutes 0.5% of childhood malignancies and exhibits poor prognosis. Complete tumor extirpation either by partial liver…”
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NASPGHAN Guidelines for Training in Pediatric Gastroenterology by Leichtner, Alan M, Gillis, Lynette A, Gupta, Sandeep, Heubi, James, Kay, Marsha, Narkewicz, Michael R, Rider, Elizabeth A, Rufo, Paul A, Sferra, Thomas J, Teitelbaum, Jonathan

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Pediatric Liver Transplant Survival in Alagille Syndrome Is Comparable to Biliary Atresia—A Linked Database Analysis by Black, Katherine, Ziogas, Ioannis A., Thurm, Cary, Hall, Matt, Hafberg, Einar, Alexopoulos, Sophoclis P., Godown, Justin, Gillis, Lynette A.

“…Objectives: This study aims to report liver transplantation (LT) outcomes and cardiac disease manifestations in children with Alagille Syndrome (ALGS) in a…”
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Clinicopathologic Features of Severe Acute Hepatitis Associated With Adenovirus Infection in Children by Liang, Jiancong, Kelly, David R., Pai, Anita, Gillis, Lynette A., Sanchez, Luz Helena Gutierrez, Shiau, Henry H., Wang, Huiying, Correa, Hernan, Mohammad, Saeed, Washington, Kay

“…A recent increase in reports of severe acute hepatitis of unknown etiology in children is under investigation. Although adenovirus has been frequently…”
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Safety and Efficacy of Ledipasvir–Sofosbuvir With or Without Ribavirin for Chronic Hepatitis C in Children Ages 6‐11 by Murray, Karen F., Balistreri, William F., Bansal, Sanjay, Whitworth, Suzanne, Evans, Helen M., Gonzalez‐Peralta, Regino P., Wen, Jessica, Massetto, Benedetta, Kersey, Kathryn, Shao, Jiang, Garrison, Kimberly L., Parhy, Bandita, Brainard, Diana M., Arnon, Ronen, Gillis, Lynette A., Jonas, Maureen M., Lin, Chuan‐Hao, Narkewicz, Michael R., Schwarz, Kathleen, Rosenthal, Philip

“…Currently, there are no interferon‐free treatments available for hepatitis C virus (HCV)–infected patients younger than 12 years. We evaluated the safety and…”
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Sofosbuvir and Ribavirin Therapy for Children Aged 3 to <12 Years With Hepatitis C Virus Genotype 2 or 3 Infection by Rosenthal, Philip, Schwarz, Kathleen B., Gonzalez‐Peralta, Regino P., Lin, Chuan‐Hao, Kelly, Deidre A., Nightingale, Scott, Balistreri, William F., Bansal, Sanjay, Jonas, Maureen M., Massetto, Benedetta, Brainard, Diana M., Hsueh, Chia‐Hsiang, Shao, Jiang, Parhy, Bandita, Davison, Suzanne, Feiterna‐Sperling, Cornelia, Gillis, Lynette A., Indolfi, Giuseppe, Sokal, Etienne M., Murray, Karen F., Wirth, Stefan

“…Currently, the only approved hepatitis C virus (HCV) treatment for children aged <12 years is pegylated interferon plus ribavirin. In an open‐label study, we…”
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Mortality Determinants in Children with Biliary Atresia Awaiting Liver Transplantation by Ziogas, Ioannis A., Ye, Fei, Zhao, Zhiguo, Cao, Shu, Rauf, Muhammad A., Izzy, Manhal, Matsuoka, Lea K., Gillis, Lynette A., Alexopoulos, Sophoclis P.

“…To determine risk factors for waitlist mortality in children with biliary atresia listed for liver transplantation. There were 2704 children with biliary…”
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Liver Transplantation in Children with Urea Cycle Disorders: The Importance of Minimizing Waiting Time by Ziogas, Ioannis A., Wu, W. Kelly, Matsuoka, Lea K., Pai, Anita K., Hafberg, Einar T., Gillis, Lynette A., Morgan, Thomas M., Alexopoulos, Sophoclis P.

“…Liver transplantation (LT) for children with urea cycle disorders (UCDs) is capable of correcting the enzymatic defect and preventing progressive neurologic…”
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Clinical and Histopathologic Characteristics of Acute Severe Hepatitis Associated With Human Herpesvirus 6 Infection by Wang, Huiying, Vannilam, Annette, Hafberg, Einar T, Gillis, Lynette A, Kassardjian, Ari, Naini, Bita V, Prasad, Vinay, Kelly, David R, Mroczek-Musulman, Elizabeth C, Knox, Konstance, Correa, Hernan, Liang, Jiancong

“…Acute severe hepatitis associated with active human herpesvirus 6 (HHV-6) infection is a rare life-threatening condition with unclear clinical course and…”
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Pediatric Liver Transplant Outcomes in Alagille Syndrome: A Linked Database Analysis by Black, Katherine, Ziogas, Ioannis A., Thurm, Cary, Hall, Matt, Thor Hafberg, Einar, Alexopoulos, Sophoclis P., Godown, Justin, Gillis, Lynette A.

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Expanding analytic possibilities in pediatric solid organ transplantation through linkage of administrative and clinical registry databases by Godown, Justin, Hall, Matt, Thompson, Bryn, Thurm, Cary, Jabs, Kathy, Gillis, Lynette A., Hafberg, Einar T., Alexopoulos, Sophoclis, Karp, Seth J., Soslow, Jonathan H.

“…Database linkage is a common strategy to expand analytic possibilities. Our group recently completed a linkage between the SRTR and PHIS databases for…”
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Diagnosis of Muscular Dystrophy in a 6‐Week‐Old With Jaundice by Russell, Alexandra C., Gillis, Lynette A.

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Liver Fibrosis Associated With Crigler–Najjar Syndrome in a Compound Heterozygote: A Case Report by Fata, Cynthia R, Gillis, Lynette A, Pacheco, M Cristina

“…Crigler–Najjar syndrome is a hereditary unconjugated hyperbilirubinemia. Two forms of the disease are recognized. Type I is more severe and results in…”
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Enhancing Recovery After Kasai Portoenterostomy With Epidural Analgesia by Phelps, Hannah M., Robinson, Jamie R., Chen, Heidi, Luckett, Twila R., Conroy, Patricia C., Gillis, Lynette A., Hays, Stephen R., Lovvorn, Harold N.

“…Biliary atresia (BA) is a rare obstructive cholangiopathy that presents in early infancy. The Kasai portoenterostomy (PE) improves survival with the native…”
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Cornelia de Lange syndrome is caused by mutations in NIPBL , the human homolog of Drosophila melanogaster Nipped-B by Rappaport, Eric, Morris, Colleen A, Bamshad, Michael J, Calof, Anne L, Li, Hui-hua, Bottani, Armand, Gillis, Lynette A, Krantz, Ian D, Wasserman, Nora, DeScipio, Cheryl, Nowaczyk, Malgorzata J M, Lander, Arthur D, McCallum, Jennifer, Jukofsky, Lori, Devoto, Marcella, Kaur, Maninder, Kawauchi, Shimako, Yaeger, Dinah, Jackson, Laird G, Carey, John C, Toriello, Helga

“…Cornelia de Lange syndrome (CdLS; OMIM 122470) is a dominantly inherited multisystem developmental disorder characterized by growth and cognitive retardation;…”
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Clinical Practice Approach to Nonalcoholic Fatty Liver Disease by Pediatric Gastroenterologists in the United States by Shapiro, Warren L., Yu, Elizabeth L., Arin, Jennifer C., Murray, Karen F., Ali, Sabina, Desai, Nirav K., Xanthakos, Stavra A., Lin, Henry C., Alkhouri, Naim, Abdou, Reham, Abrams, Stephanie H., Butler, Megan W., Faasse, Sarah A., Gillis, Lynette A., Hadley, Timothy A., Jain, Ajay K., Kavan, Marianne, Kordy, Kattayoun, Lee, Peter, Panganiban, Jennifer, Pohl, John F., Potter, Carol, Rudolph, Bryan, Sundaram, Shikha S., Joshi, Shivali, Proudfoot, James A., Goyal, Nidhi P., Harlow, Kathryn E., Newton, Kimberly P., Schwimmer, Jeffrey B.

“…ABSTRACT Objectives: Nonalcoholic fatty liver disease (NAFLD) is common; however, no information is available on how pediatric gastroenterologists in the…”
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NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations by Gillis, Lynette A., McCallum, Jennifer, Kaur, Maninder, DeScipio, Cheryl, Yaeger, Dinah, Mariani, Allison, Kline, Antonie D., Li, Hui-hua, Devoto, Marcella, Jackson, Laird G., Krantz, Ian D.

“…The Cornelia de Lange syndrome (CdLS) is a multisystem developmental disorder characterized by facial dysmorphia, upper-extremity malformations, hirsutism,…”
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Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum by Sukalo, Maja, Fiedler, Ariane, Guzmán, Celina, Spranger, Stephanie, Addor, Marie-Claude, Mcheik, Jiad N., Oltra Benavent, Manuel, Cobben, Jan M., Gillis, Lynette A., Shealy, Amy G., Deshpande, Charu, Bozorgmehr, Bita, Everman, David B., Stattin, Eva-Lena, Liebelt, Jan, Keller, Klaus-Michael, Bertola, Débora Romeo, van Karnebeek, Clara D.M., Bergmann, Carsten, Liu, Zhifeng, Düker, Gesche, Rezaei, Nima, Alkuraya, Fowzan S., Oğur, Gönül, Alrajoudi, Abdullah, Venegas-Vega, Carlos A., Verbeek, Nienke E., Richmond, Erick J., Kirbiyik, Özgür, Ranganath, Prajnya, Singh, Ankur, Godbole, Koumudi, Ali, Fouad A. M., Alves, Crésio, Mayerle, Julia, Lerch, Markus M., Witt, Heiko, Zenker, Martin

“…ABSTRACT Johanson–Blizzard syndrome (JBS) is a rare, autosomal recessive disorder characterized by exocrine pancreatic insufficiency, typical facial features,…”
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Gastrointestinal manifestations of mitochondrial disease by Gillis, Lynette A, Sokol, Ronald J

“…Although non-specific gastrointestinal and hepatic symptoms are commonly found in most mitochondrial disorders, they are among the cardinal manifestations of…”
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Ciliated hepatic foregut cysts in children by Zaydfudim, Victor, Rosen, Michael J., Gillis, Lynette A., Correa, Hernan, Lovvorn III, Harold N., Wright Pinson, C., Kelly, Burnett S.

“…Ciliated hepatic foregut cyst (CHFC) is a rare foregut developmental malformation usually diagnosed in adulthood; however, rare cases have been reported in the…”
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