Search Results - "MOHAN, Parvathi"

The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration by Deneau, Mark R., El‐Matary, Wael, Valentino, Pamela L., Abdou, Reham, Alqoaer, Khaled, Amin, Mansi, Amir, Achiya Z., Auth, Marcus, Bazerbachi, Fateh, Broderick, Annemarie, Chan, Albert, Cotter, Jillian, Doan, Sylvia, El‐Youssef, Mounif, Ferrari, Federica, Furuya, Katryn N., Gottrand, Madeleine, Gottrand, Frederic, Gupta, Nitika, Homan, Matjaz, Kamath, Binita M., Kim, Kyung Mo, Kolho, Kaija‐Leena, Konidari, Anastasia, Koot, Bart, Iorio, Raffaele, Ledder, Oren, Mack, Cara, Martinez, Mercedes, Miloh, Tamir, Mohan, Parvathi, O'Cathain, Niamh, Papadopoulou, Alexandra, Ricciuto, Amanda, Saubermann, Lawrence, Sathya, Pushpa, Shteyer, Eyal, Smolka, Vratislav, Tanaka, Atushi, Varier, Raghu, Venkat, Veena, Vitola, Bernadette, Vos, Miriam B., Woynarowski, Marek, Yap, Jason, Jensen, M. Kyle

“…There are limited data on the natural history of primary sclerosing cholangitis (PSC) in children. We aimed to describe the disease characteristics and…”
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Ursodeoxycholic Acid Therapy in Pediatric Primary Sclerosing Cholangitis: Predictors of Gamma Glutamyltransferase Normalization and Favorable Clinical Course by Deneau, Mark, Perito, Emily, Ricciuto, Amanda, Gupta, Nitika, Kamath, Binita M., Palle, Sirish, Vitola, Bernadette, Smolka, Vratislav, Ferrari, Federica, Amir, Achiya Z., Miloh, Tamir, Papadopoulou, Alexandra, Mohan, Parvathi, Mack, Cara, Kolho, Kaija-Leena, Iorio, Raffaele, El-Matary, Wael, Venkat, Veena, Chan, Albert, Saubermann, Lawrence, Valentino, Pamela L., Shah, Uzma, Miethke, Alexander, Lin, Henry, Jensen, M.K.

“…To investigate patient factors predictive of gamma glutamyltransferase (GGT) normalization following ursodeoxycholic acid (UDCA) therapy in children with…”
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Pegylated interferon for chronic hepatitis C in children affects growth and body composition: Results from the pediatric study of hepatitis C (PEDS-C) trial by Jonas, Maureen M., Balistreri, William, Gonzalez-Peralta, Regino P., Haber, Barbara, Lobritto, Steven, Mohan, Parvathi, Molleston, Jean P., Murray, Karen F., Narkewicz, Michael R., Rosenthal, Philip, Schwarz, Kathleen B., Barton, Bruce A., Shepherd, John A., Mitchell, Paul D., Duggan, Christopher

“…Weight loss and changes in growth are noted in children treated with interferon alpha (IFN‐α). The aim of this study was to prospectively determine changes in…”
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Pathology of chronic hepatitis C in children: Liver biopsy findings in the Peds‐C Trial by Goodman, Zachary D., Makhlouf, Hala R., Liu, Lea, Balistreri, William, Gonzalez‐Peralta, Regino P., Haber, Barbara, Jonas, Maureen M., Mohan, Parvathi, Molleston, Jean P., Murray, Karen F., Narkewicz, Michael R., Rosenthal, Philip, Smith, Lesley J., Robuck, Patricia R., Schwarz, Kathleen B.

“…There is relatively little information in the literature on the histopathology of chronic hepatitis C in children. The Peds‐C Trial, designed to test the…”
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Phenobarbital-enhanced hepatobiliary scintigraphy in the diagnosis of biliary atresia: two decades of experience at a tertiary center by Kwatra, Neha, Shalaby-Rana, Eglal, Narayanan, Srikala, Mohan, Parvathi, Ghelani, Sunil, Majd, Massoud

“…Background Hepatobiliary scintigraphy is highly sensitive for diagnosing biliary atresia; however, its specificity has varied in the literature from 35% to…”
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Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) by Turkbey, Baris, Ocak, Iclal, Daryanani, Kailash, Font-Montgomery, Esperanza, Lukose, Linda, Bryant, Joy, Tuchman, Maya, Mohan, Parvathi, Heller, Theo, Gahl, William A., Choyke, Peter L., Gunay-Aygun, Meral

“…ARPKD/CHF is an inherited disease characterized by non-obstructive fusiform dilatation of the renal collecting ducts leading to enlarged spongiform kidneys and…”
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Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease by O'Brien, Kevin, Font‐Montgomery, Esperanza, Lukose, Linda, Bryant, Joy, Piwnica‐Worms, Katie, Edwards, Hailey, Riney, Lauren, Garcia, Angelica, Daryanani, Kailash, Choyke, Peter, Mohan, Parvathi, Heller, Theo, Gahl, William A., Gunay‐Aygun, Meral

“…ABSTRACT Objectives: Autosomal dominant (ADPKD) and recessive (ARPKD) polycystic kidney diseases are the most common hepatorenal fibrocystic diseases…”
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Clinical Spectrum and Histopathologic Features of Chronic Hepatitis C Infection in Children by Mohan, Parvathi, MD, Colvin, Camilla, MPH, BS, Glymph, Chevelle, MPH, Chandra, Roma R., MD, Kleiner, David E., MD, Patel, Kantilal M., PhD, Luban, Naomi L.C., MD, Alter, Harvey J., MD

“…Objective To define the natural history and outcomes of children infected with hepatitis C virus (HCV) at birth or in early childhood. Study design This…”
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Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference by Gunay-Aygun, Meral, Avner, Ellis D., Bacallao, Robert L., Choyke, Peter L., Flynn, Joseph T., Germino, Gregory G., Guay-Woodford, Lisa, Harris, Peter, Heller, Theo, Ingelfinger, Julie, Kaskel, Frederick, Kleta, Robert, LaRusso, Nicholas F., Mohan, Parvathi, Pazour, Gregory J., Shneider, Benjamin L., Torres, Vicente E., Wilson, Patricia, Zak, Colleen, Zhou, Jing, Gahl, William A.

“…Researchers and clinicians with expertise in autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) and related fields met…”
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Twelve‐year outcomes of intestinal failure–associated liver disease in children with short‐bowel syndrome: 97% transplant‐free survival and 81% enteral autonomy by Torres, Clarivet, Badalyan, Vahe, Mohan, Parvathi

“…Our aim was to analyze the outcomes in children with short‐bowel syndrome (SBS), parenteral nutrition dependence (PND), and intestinal failure–associated liver…”
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Modulation of the IL-12/IFN-γ axis by IFN-α therapy for hepatitis C by Byrnes, Adriana A., Li, Ding‐You, Park, Kiwon, Thompson, Douglas, Mocilnikar, Cathleen, Mohan, Parvathi, Molleston, Jean P., Narkewicz, Michael, Zhou, Huanfang, Wolf, Stanley F., Schwarz, Kathleen B., Karp, Christopher L.

“…Although IFN‐α forms the foundation of therapy for chronic hepatitis C, only a minority of patients has a sustained response to IFN‐α alone. The antiviral…”
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P4.26: Outcomes of three genetic syndromes with intestinal failure (IF), short bowel syndrome (SBS), intestinal failure associated liver disease (IFALD) and parenteral nutrition (PN) dependency, treated in our Intestinal Rehabilitation Program (IRP). Children’s National Medical Center Washington DC by Torres, Clarivet, Badalyan, Vahe, Mohan, Parvathi

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Tu2008 Severity of Hepatic Fibrosis in Children With Biliary Atresia Using Non Invasive Markers vs Liver Biopsy by Sebastian, Teena, Mohan, Parvathi

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Excellent outcomes of children with short bowel syndrome and intestinal failure associated liver disease (IFALD) at Children’s National Health System (CNHS), Washington DC by Torres, Clarivet, Vahe, Badalyan, Mohan, Parvathi

“…OBJECTIVEWe report the outcomes of short bowel syndrome (SBS) parenteral nutrition (PN) dependent patients with IFALD enrolled in our intestinal rehabilitation…”
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320.3: Ultra-Short Bowel Syndrome (USBS) – Does the lengthening procedures improve the outcomes? Intestinal Rehabilitation Program (IRP) Children’s National Medical Center (CNMC) Washington DC - USA by Torres, Clarivet, Badalyan, Vahe, Mohan, Parvathi, Sandler, Anthony

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CASE REPORT: Application of a Self-Expandable Metal Stent (SEMS) in a Child with Complete Malignant Large Bowel Obstruction by HUSSAIN, Sunny Z., Bashir, R. Martin, Kerzner, Benny, Klugman, Darren, Mohan, Parvathi, Bader, Ali Amjed

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A patient with atypical presentation of chronic hepatosteatosis harboring a novel variant in the CPT1A gene by Boonsimma, Ponghatai, Crosby, Kathleen, Mohan, Parvathi, Puscasiu, Elena, Tanpaiboon, Pranoot

“…Carnitine palmitoyltransferase 1A (CPT1A) deficiency is a rare disorder of hepatic long-chain fatty acid oxidation. Most patients with CPT1A deficiency present…”
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Mo1190 Utilizing Ostomy in Continuity (OIC) in the Management of Children With Short Bowel Syndrome (SBS) at the Intestinal Rehabilitation Program (IRP) at Children's National-Washington D.C by Sehgal, Sona, Mohan, Parvathi, Torres, Clarivet

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Granulocyte-colony stimulating factor GCSF mobilizes hematopoietic stem cells in Kasai patients with biliary atresia in a phase 1 study and improves short term outcome by Holterman, AiXuan, Nguyen, Hoa Pham Anh, Nadler, Evan, Vu, Giap H, Mohan, Parvathi, Vu, Megan, Trinh, Thuy Thi, Bui, Huong Thuy Thi, Nguyen, Binh Thanh, Quynh, Anh Tran, Pham, Hien Duy

“…In RCT of adults with decompensated cirrhosis, GCSF mobilizes hematopoietic stem cells HSC and improves short-term outcome. An FDA-IND for sequential…”
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Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease by Gunay–Aygun, Meral, Font–Montgomery, Esperanza, Lukose, Linda, Tuchman Gerstein, Maya, Piwnica–Worms, Katie, Choyke, Peter, Daryanani, Kailash T, Turkbey, Baris, Fischer, Roxanne, Bernardini, Isa, Sincan, Murat, Zhao, Xiongce, Sandler, Netanya G, Roque, Annelys, Douek, Daniel C, Graf, Jennifer, Huizing, Marjan, Bryant, Joy C, Mohan, Parvathi, Gahl, William A, Heller, Theo

“…Background & Aims Autosomal recessive polycystic kidney disease (ARPKD), the most common ciliopathy of childhood, is characterized by congenital hepatic…”
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