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Items: 1 to 50 of 104

1.

Intrahepatic dynamic contrast MR lymphangiography: initial experience with a new technique for the assessment of liver lymphatics.

Biko DM, Smith CL, Otero HJ, Saul D, White AM, DeWitt A, Glatz AC, Piccoli DA, Mamula P, Rome JJ, Dori Y.

Eur Radiol. 2019 Mar 18. doi: 10.1007/s00330-019-06112-z. [Epub ahead of print]

PMID:
30887210
2.

Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE.

Scheers I, Palermo JJ, Freedman S, Wilschanski M, Shah U, Abu-El-Haija M, Barth B, Fishman DS, Gariepy C, Giefer MJ, Heyman MB, Himes RW, Husain SZ, Lin TK, Liu Q, Lowe M, Mascarenhas M, Morinville V, Ooi CY, Perito ER, Piccoli DA, Pohl JF, Schwarzenberg SJ, Troendle D, Werlin S, Zimmerman B, Uc A, Gonska T.

J Pediatr Gastroenterol Nutr. 2018 Aug;67(2):232-236. doi: 10.1097/MPG.0000000000002028.

PMID:
29746340
3.

Reply: The Need to Define Treatment Goals for Protein-Losing Enteropathy in Fontan Care and Research.

Itkin M, Rychik J, Piccoli DA.

J Am Coll Cardiol. 2017 Nov 14;70(20):2603. doi: 10.1016/j.jacc.2017.08.076. No abstract available.

4.

Histological features of ileitis differentiating pediatric Crohn disease from ulcerative colitis with backwash ileitis.

Sahn B, De Matos V, Stein R, Ruchelli E, Masur S, Klink AJ, Baldassano RN, Piccoli DA, Russo P, Mamula P.

Dig Liver Dis. 2018 Feb;50(2):147-153. doi: 10.1016/j.dld.2017.10.006. Epub 2017 Oct 19.

PMID:
29089273
5.

Protein-Losing Enteropathy in Patients With Congenital Heart Disease.

Itkin M, Piccoli DA, Nadolski G, Rychik J, DeWitt A, Pinto E, Rome J, Dori Y.

J Am Coll Cardiol. 2017 Jun 20;69(24):2929-2937. doi: 10.1016/j.jacc.2017.04.023.

6.

Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management.

Scheers I, Palermo JJ, Freedman S, Wilschanski M, Shah U, Abu-El-Haija M, Barth B, Fishman DS, Gariepy C, Giefer MJ, Heyman MB, Himes RW, Husain SZ, Lin TK, Liu Q, Lowe M, Mascarenhas M, Morinville V, Ooi CY, Perito ER, Piccoli DA, Pohl JF, Schwarzenberg SJ, Troendle D, Werlin S, Zimmerman B, Uc A, Gonska T.

Am J Gastroenterol. 2017 Oct;112(10):1604-1611. doi: 10.1038/ajg.2017.85. Epub 2017 Apr 4. Review.

7.

Anterior Chamber Pathology in Alagille Syndrome.

Ho DK, Levin AV, Anninger WV, Piccoli DA, Eagle RC Jr.

Ocul Oncol Pathol. 2016 Oct;2(4):270-275. Epub 2016 Jul 2.

8.

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease.

Conrad MA, Stein RE, Maxwell EC, Albenberg L, Baldassano RN, Dawany N, Grossman AB, Mamula P, Piccoli DA, Kelsen JR.

Inflamm Bowel Dis. 2016 Oct;22(10):2425-31. doi: 10.1097/MIB.0000000000000918.

PMID:
27598742
9.

Chromosome 10q23 Deletion Syndrome: An Overlap of Bannayan-Riley-Ruvalcaba Syndrome and Juvenile Polyposis Syndrome.

Waisbourd-Zinman O, Mamula P, Piccoli DA.

J Paediatr Child Health. 2016 Aug;52(8):852. doi: 10.1111/jpc.13289. No abstract available.

PMID:
27535890
10.

Severe Eosinophilic Gastroenteritis in a Crohn's Disease Patient Treated With Infliximab and Adalimumab.

Muir A, Surrey L, Kriegermeier A, Shaikhkalil A, Piccoli DA.

Am J Gastroenterol. 2016 Mar;111(3):437-8. doi: 10.1038/ajg.2015.438. No abstract available.

PMID:
27018120
11.

Compound heterozygous mutations in NEK8 in siblings with end-stage renal disease with hepatic and cardiac anomalies.

Rajagopalan R, Grochowski CM, Gilbert MA, Falsey AM, Coleman K, Romero R, Loomes KM, Piccoli DA, Devoto M, Spinner NB.

Am J Med Genet A. 2016 Mar;170(3):750-3. doi: 10.1002/ajmg.a.37512. Epub 2015 Dec 24.

PMID:
26697755
12.

Erratum to: A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.

Kelsen JR, Dawany N, Martinez A, Grochowski CM, Maurer K, Rappaport E, Piccoli DA, Baldassano RN, Mamula P, Sullivan KE, Devoto M.

BMC Gastroenterol. 2015 Dec 18;15:179. doi: 10.1186/s12876-015-0412-1. No abstract available.

13.

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.

Kelsen JR, Dawany N, Martinez A, Grochowski CM, Maurer K, Rappaport E, Piccoli DA, Baldassano RN, Mamula P, Sullivan KE, Devoto M.

BMC Gastroenterol. 2015 Nov 18;15:160. doi: 10.1186/s12876-015-0394-z. Erratum in: BMC Gastroenterol. 2015;15:179. Martinez, Alejuandro [corrected to Martinez, Alejandro].

14.

Early life predictive markers of liver disease outcome in an International, Multicentre Cohort of children with Alagille syndrome.

Mouzaki M, Bass LM, Sokol RJ, Piccoli DA, Quammie C, Loomes KM, Heubi JE, Hertel PM, Scheenstra R, Furuya K, Kutsch E, Spinner NB, Robbins KN, Venkat V, Rosenthal P, Beyene J, Baker A, Kamath BM.

Liver Int. 2016 May;36(5):755-60. doi: 10.1111/liv.12920. Epub 2015 Aug 18.

15.

Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome.

Grochowski CM, Rajagopalan R, Falsey AM, Loomes KM, Piccoli DA, Krantz ID, Devoto M, Spinner NB.

Am J Med Genet A. 2015 Apr;167A(4):891-3. doi: 10.1002/ajmg.a.36946. Epub 2015 Mar 3. No abstract available.

PMID:
25737299
16.

Moyamoya syndrome associated with Alagille syndrome: outcome after surgical revascularization.

Baird LC, Smith ER, Ichord R, Piccoli DA, Bernard TJ, Spinner NB, Scott RM, Kamath BM.

J Pediatr. 2015 Feb;166(2):470-3. doi: 10.1016/j.jpeds.2014.10.067. Epub 2014 Oct 30.

PMID:
25465847
17.

Incidence of perforation in pediatric GI endoscopy and colonoscopy: an 11-year experience.

Hsu EK, Chugh P, Kronman MP, Markowitz JE, Piccoli DA, Mamula P.

Gastrointest Endosc. 2013 Jun;77(6):960-6. doi: 10.1016/j.gie.2012.12.020. Epub 2013 Feb 20. No abstract available.

PMID:
23433599
18.

Pancreatic insufficiency is not a prevalent problem in Alagille syndrome.

Kamath BM, Piccoli DA, Magee JC, Sokol RJ; Childhood Liver Disease Research and Education Network.

J Pediatr Gastroenterol Nutr. 2012 Nov;55(5):612-4. doi: 10.1097/MPG.0b013e31825eff61.

19.

NOTCH2 mutations in Alagille syndrome.

Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, Hardikar W, Hirschfield G, Jara P, Krantz ID, Lapunzina P, Leonard L, Ling S, Ng VL, Hoang PL, Piccoli DA, Spinner NB.

J Med Genet. 2012 Feb;49(2):138-44. doi: 10.1136/jmedgenet-2011-100544. Epub 2011 Dec 29.

20.

Renal anomalies in Alagille syndrome: a disease-defining feature.

Kamath BM, Podkameni G, Hutchinson AL, Leonard LD, Gerfen J, Krantz ID, Piccoli DA, Spinner NB, Loomes KM, Meyers K.

Am J Med Genet A. 2012 Jan;158A(1):85-9. doi: 10.1002/ajmg.a.34369. Epub 2011 Nov 21.

21.

A novel method to enhance informed consent: a prospective and randomised trial of form-based versus electronic assisted informed consent in paediatric endoscopy.

Friedlander JA, Loeben GS, Finnegan PK, Puma AE, Zhang X, de Zoeten EF, Piccoli DA, Mamula P.

J Med Ethics. 2011 Apr;37(4):194-200. doi: 10.1136/jme.2010.037622. Epub 2011 Jan 18.

PMID:
21245476
22.

Medical management of Alagille syndrome.

Kamath BM, Loomes KM, Piccoli DA.

J Pediatr Gastroenterol Nutr. 2010 Jun;50(6):580-6. doi: 10.1097/MPG.0b013e3181d98ea8.

PMID:
20479679
23.

Pathologic lower extremity fractures in children with Alagille syndrome.

Bales CB, Kamath BM, Munoz PS, Nguyen A, Piccoli DA, Spinner NB, Horn D, Shults J, Leonard MB, Grimberg A, Loomes KM.

J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):66-70. doi: 10.1097/MPG.0b013e3181cb9629.

24.

A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndrome.

Kamath BM, Munoz PS, Bab N, Baker A, Chen Z, Spinner NB, Piccoli DA.

J Pediatr Gastroenterol Nutr. 2010 May;50(5):526-30. doi: 10.1097/MPG.0b013e3181cea48d.

25.

SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.

Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB.

Hum Mutat. 2009 Mar;30(3):371-8. doi: 10.1002/humu.20863.

26.

A 9-month-old girl with chronic diarrhea.

de Zoeten EF, Markowitz J, Loomes KM, Mamula P, Piccoli DA.

Medscape J Med. 2008;10(8):195. Epub 2008 Aug 19. No abstract available.

27.

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.

Kugathasan S, Baldassano RN, Bradfield JP, Sleiman PM, Imielinski M, Guthery SL, Cucchiara S, Kim CE, Frackelton EC, Annaiah K, Glessner JT, Santa E, Willson T, Eckert AW, Bonkowski E, Shaner JL, Smith RM, Otieno FG, Peterson N, Abrams DJ, Chiavacci RM, Grundmeier R, Mamula P, Tomer G, Piccoli DA, Monos DS, Annese V, Denson LA, Grant SF, Hakonarson H.

Nat Genet. 2008 Oct;40(10):1211-5. doi: 10.1038/ng.203. Epub 2008 Aug 31.

28.

Frequency and clinical correlations of granulomas in children with Crohn disease.

De Matos V, Russo PA, Cohen AB, Mamula P, Baldassano RN, Piccoli DA.

J Pediatr Gastroenterol Nutr. 2008 Apr;46(4):392-8. doi: 10.1097/MPG.0b013e31812e95e1.

PMID:
18367950
29.

Interlobular bile duct loss in pediatric cholestatic disease is associated with aberrant cytokeratin 7 expression by hepatocytes.

Ernst LM, Spinner NB, Piccoli DA, Mauger J, Russo P.

Pediatr Dev Pathol. 2007 Sep-Oct;10(5):383-90.

PMID:
17929991
30.

Immune response to influenza vaccine in pediatric patients with inflammatory bowel disease.

Mamula P, Markowitz JE, Piccoli DA, Klimov A, Cohen L, Baldassano RN.

Clin Gastroenterol Hepatol. 2007 Jul;5(7):851-6. Epub 2007 Jun 4.

PMID:
17544875
31.

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway.

McDaniell R, Warthen DM, Sanchez-Lara PA, Pai A, Krantz ID, Piccoli DA, Spinner NB.

Am J Hum Genet. 2006 Jul;79(1):169-73. Epub 2006 May 10.

32.

Resting energy expenditure is not increased in prepubertal children with Alagille syndrome.

Rovner AJ, Stallings VA, Piccoli DA, Mulberg AE, Zemel BS.

J Pediatr. 2006 May;148(5):680-2.

PMID:
16737885
33.

Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate.

Warthen DM, Moore EC, Kamath BM, Morrissette JJ, Sanchez-Lara PA, Piccoli DA, Krantz ID, Spinner NB.

Hum Mutat. 2006 May;27(5):436-43. Erratum in: Hum Mutat. 2013 Feb;34(2):408. Sanchez, P [corrected to Sanchez-Lara, P A].

PMID:
16575836
34.

A 2-year-old girl with persistent ascites.

De Matos V, Russo P, Hedrick H, Piccoli DA, Mamula P.

MedGenMed. 2005 Aug 3;7(3):18. No abstract available.

35.

Non-invasive fluorescence imaging of cell death in fresh human colon epithelia treated with 5-Fluorouracil, CPT-11 and/or TRAIL.

Finnberg N, Kim SH, Furth EE, Liu JJ, Russo P, Piccoli DA, Grimberg A, El-Deiry WS.

Cancer Biol Ther. 2005 Sep;4(9):937-42. Epub 2005 Sep 18.

36.

Primary sclerosing cholangitis in children: a histologic follow-up study.

Batres LA, Russo P, Mathews M, Piccoli DA, Chuang E, Ruchelli E.

Pediatr Dev Pathol. 2005 Sep-Oct;8(5):568-76. Epub 2005 Oct 7.

PMID:
16220233
37.

Intracranial vascular abnormalities in patients with Alagille syndrome.

Emerick KM, Krantz ID, Kamath BM, Darling C, Burrowes DM, Spinner NB, Whitington PF, Piccoli DA.

J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):99-107.

PMID:
15990638
38.

Cases in pediatric gastroenterology from the Children's Hospital of Philadelphia: a 14-year-old boy with jaundice and pruritus.

Friedman JR, Russo P, Flick J, Mamula P, Piccoli DA.

MedGenMed. 2004 Jun 25;6(2):61. No abstract available.

39.

A 14-month-old boy with hematochezia.

Kamath BM, Kaye R, Mamula P, Piccoli DA.

MedGenMed. 2004 Dec 28;6(4):8. No abstract available.

40.

Deficits in size-adjusted bone mass in children with Alagille syndrome.

Olsen IE, Ittenbach RF, Rovner AJ, Leonard MB, Mulberg AE, Stallings VA, Piccoli DA, Zemel BS.

J Pediatr Gastroenterol Nutr. 2005 Jan;40(1):76-82.

PMID:
15625431
41.
42.

Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality.

Kamath BM, Spinner NB, Emerick KM, Chudley AE, Booth C, Piccoli DA, Krantz ID.

Circulation. 2004 Mar 23;109(11):1354-8. Epub 2004 Mar 1. Review.

PMID:
14993126
43.

Consequences of JAG1 mutations.

Kamath BM, Bason L, Piccoli DA, Krantz ID, Spinner NB.

J Med Genet. 2003 Dec;40(12):891-5.

44.

Heritable disorders of the bile ducts.

Kamath BM, Piccoli DA.

Gastroenterol Clin North Am. 2003 Sep;32(3):857-75, vi. Review.

PMID:
14562578
45.

Pediatric gastroenterology. Preface.

Piccoli DA.

Gastroenterol Clin North Am. 2003 Sep;32(3):xi-xii. No abstract available.

PMID:
14562573
46.

The utility of ultrasound site selection for pediatric percutaneous liver biopsy.

Kader HA, Bellah R, Maller ES, Mamula P, Piccoli DA, Markowitz JE.

J Pediatr Gastroenterol Nutr. 2003 Mar;36(3):364-7.

PMID:
12604975
47.

Biliary atresia associated with a fatty acid oxidation defect.

Matthews RP, Russo P, Berry GT, Piccoli DA, Rand EB.

J Pediatr Gastroenterol Nutr. 2002 Nov;35(5):624-8. No abstract available.

PMID:
12454576
48.

Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome.

McElhinney DB, Krantz ID, Bason L, Piccoli DA, Emerick KM, Spinner NB, Goldmuntz E.

Circulation. 2002 Nov 12;106(20):2567-74.

PMID:
12427653
49.

Vitamin D status in children, adolescents, and young adults with Crohn disease.

Sentongo TA, Semaeo EJ, Stettler N, Piccoli DA, Stallings VA, Zemel BS.

Am J Clin Nutr. 2002 Nov;76(5):1077-81.

PMID:
12399281
50.

Rethinking growth failure in Alagille syndrome: the role of dietary intake and steatorrhea.

Rovner AJ, Schall JI, Jawad AF, Piccoli DA, Stallings VA, Mulberg AE, Zemel BS.

J Pediatr Gastroenterol Nutr. 2002 Oct;35(4):495-502.

PMID:
12394373

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