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Items: 1 to 50 of 215

1.

Congenital Portosystemic Shunts in Children: Associations, Complications, and Outcomes.

DiPaola F, Trout AT, Walther AE, Gupta A, Sheridan R, Campbell KM, Tiao G, Bezerra JA, Bove KE, Patel M, Nathan JD.

Dig Dis Sci. 2019 Sep 23. doi: 10.1007/s10620-019-05834-w. [Epub ahead of print]

PMID:
31549332
2.

Expanding and Underscoring the Hepato-Encephalopathic Phenotype of QIL1/MIC13.

Russell BE, Whaley KG, Bove KE, Labilloy A, Lombardo RC, Hopkin RJ, Leslie ND, Prada C, Assouline Z, Barcia G, Bouchereau J, Chomton M, Debray D, Dorboz I, Durand P, Gaignard P, Habes D, Jardel C, Labarthe F, Lévy J, Lombès A, Mehler-Jacob C, Melki J, Menvielle L, Munnich A, Mussini C, Pichard S, Rio M, Rötig A, Sissaoui S, Slama A, Miethke AG, Schiff M.

Hepatology. 2019 Sep;70(3):1066-1070. doi: 10.1002/hep.30627. Epub 2019 May 16. No abstract available.

PMID:
30912852
3.

Inborn Errors of Bile Acid Metabolism.

Heubi JE, Setchell KDR, Bove KE.

Clin Liver Dis. 2018 Nov;22(4):671-687. doi: 10.1016/j.cld.2018.06.006. Epub 2018 Aug 22. Review.

PMID:
30266156
4.

Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome.

Bove KE, Thrasher AD, Anders R, Chung CT, Cummings OW, Finegold MJ, Finn L, Ranganathan S, Kim GE, Lovell M, Magid MS, Melin-Aldana H, Russo P, Shehata B, Wang L, White F, Chen Z, Spino C, Magee JC.

Am J Surg Pathol. 2018 Dec;42(12):1625-1635. doi: 10.1097/PAS.0000000000001146.

5.

Long-Term Cholic Acid Therapy in Zellweger Spectrum Disorders.

Heubi JE, Setchell KDR, Bove KE.

Case Rep Gastroenterol. 2018 Jun 28;12(2):360-372. doi: 10.1159/000490095. eCollection 2018 May-Aug.

6.

Large-scale proteomics identifies MMP-7 as a sentinel of epithelial injury and of biliary atresia.

Lertudomphonwanit C, Mourya R, Fei L, Zhang Y, Gutta S, Yang L, Bove KE, Shivakumar P, Bezerra JA.

Sci Transl Med. 2017 Nov 22;9(417). pii: eaan8462. doi: 10.1126/scitranslmed.aan8462.

7.

Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiency.

Ellis JL, Bove KE, Schuetz EG, Leino D, Valencia CA, Schuetz JD, Miethke A, Yin C.

Hepatology. 2018 Apr;67(4):1531-1545. doi: 10.1002/hep.29632. Epub 2018 Feb 23.

8.

Oral Cholic Acid Is Efficacious and Well Tolerated in Patients With Bile Acid Synthesis and Zellweger Spectrum Disorders.

Heubi JE, Bove KE, Setchell KDR.

J Pediatr Gastroenterol Nutr. 2018 Feb;66(2):e57-e59. doi: 10.1097/MPG.0000000000001764. No abstract available.

PMID:
28968290
9.

Association between Testicular Microlithiasis and Testicular Neoplasia: Large Multicenter Study in a Pediatric Population.

Trout AT, Chow J, McNamara ER, Darge K, Ramirez Grueso R, Munden M, Rothan SM, Navarro OM, Tijerín Bueno M, Bove KE, Chikwava KR, Heider A, Hicks MJ, Somers GR, Zhang B, Dillman JR.

Radiology. 2017 Nov;285(2):576-583. doi: 10.1148/radiol.2017162625. Epub 2017 Jul 17.

PMID:
28715257
10.

Oral Cholic Acid Is Efficacious and Well Tolerated in Patients With Bile Acid Synthesis and Zellweger Spectrum Disorders.

Heubi JE, Bove KE, Setchell KDR.

J Pediatr Gastroenterol Nutr. 2017 Sep;65(3):321-326. doi: 10.1097/MPG.0000000000001657.

11.

Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia: Correlations With Age, Outcome, and Histology of Proximal Biliary Remnant.

Bove KE, Sheridan R, Fei L, Anders R, Chung CT, Cummings OW, Finegold MJ, Finn L, Ranganathan S, Kim G, Lovell M, Magid MS, Melin-Aldana H, Russo P, Shehata B, Wang L, White F, Chen Z, Spino C, Magee JC.

Pediatr Dev Pathol. 2018 Jan-Feb;21(1):29-40. doi: 10.1177/1093526617707851. Epub 2017 May 5.

PMID:
28474973
12.

Cystic Biliary Atresia and Choledochal Cysts Are Distinct Histopathologic Entities.

Lobeck IN, Sheridan R, Lovell M, Dupree P, Tiao GM, Bove KE.

Am J Surg Pathol. 2017 Mar;41(3):354-364. doi: 10.1097/PAS.0000000000000805.

PMID:
28079575
13.

Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter Study.

Russo P, Magee JC, Anders RA, Bove KE, Chung C, Cummings OW, Finegold MJ, Finn LS, Kim GE, Lovell MA, Magid MS, Melin-Aldana H, Ranganathan S, Shehata BM, Wang LL, White FV, Chen Z, Spino C; Childhood Liver Disease Research Network (ChiLDReN).

Am J Surg Pathol. 2016 Dec;40(12):1601-1615.

14.

Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism.

Valencia CA, Wang X, Wang J, Peters A, Simmons JR, Moran MC, Mathur A, Husami A, Qian Y, Sheridan R, Bove KE, Witte D, Huang T, Miethke AG.

PLoS One. 2016 Aug 2;11(8):e0156738. doi: 10.1371/journal.pone.0156738. eCollection 2016.

15.

Two Case Reports of FGF23-Induced Hypophosphatemia in Childhood Biliary Atresia.

Wasserman H, Ikomi C, Hafberg ET, Miethke AG, Bove KE, Backeljauw PF.

Pediatrics. 2016 Aug;138(2). pii: e20154453. doi: 10.1542/peds.2015-4453.

16.

Infant Mortality, Cause of Death, and Vital Records Reporting in Ohio, United States.

Seske LM, Muglia LJ, Hall ES, Bove KE, Greenberg JM.

Matern Child Health J. 2017 Apr;21(4):727-733. doi: 10.1007/s10995-016-2159-x.

PMID:
27456308
17.

Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.

Leslie N, Wang X, Peng Y, Valencia CA, Khuchua Z, Hata J, Witte D, Huang T, Bove KE.

Hum Pathol. 2016 Mar;49:27-32. doi: 10.1016/j.humpath.2015.09.039. Epub 2015 Oct 28.

PMID:
26826406
19.

Early-lethal Costello syndrome due to rare HRAS Tandem Base substitution (c.35_36GC>AA; p.G12E)-associated pulmonary vascular disease.

Weaver KN, Wang D, Cnota J, Gardner N, Stabley D, Sol-Church K, Gripp KW, Witte DP, Bove KE, Hopkin RJ.

Pediatr Dev Pathol. 2014 Nov-Dec;17(6):421-30. doi: 10.2350/14-05-1488-OA.1. Epub 2014 Aug 18.

20.

Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease.

Varsani H, Charman SC, Li CK, Marie SK, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith AM, Jacques TS, Lundberg IE, Minetti C, Nennesmo I, Rushing EJ, Sallum AM, Sewry C, Pilkington CA, Holton JL, Wedderburn LR; UK Juvenile Dermatomyositis Research Group.

Ann Rheum Dis. 2015 Jan;74(1):204-10. doi: 10.1136/annrheumdis-2013-203396. Epub 2013 Sep 24.

21.

Multifocal hepatic neoplasia in 3 children with APC gene mutation.

Gupta A, Sheridan RM, Towbin A, Geller JI, Tiao G, Bove KE.

Am J Surg Pathol. 2013 Jul;37(7):1058-66. doi: 10.1097/PAS.0b013e31828aeb18.

PMID:
23715166
22.

Genetic defects in bile acid conjugation cause fat-soluble vitamin deficiency.

Setchell KD, Heubi JE, Shah S, Lavine JE, Suskind D, Al-Edreesi M, Potter C, Russell DW, O'Connell NC, Wolfe B, Jha P, Zhang W, Bove KE, Knisely AS, Hofmann AF, Rosenthal P, Bull LN.

Gastroenterology. 2013 May;144(5):945-955.e6; quiz e14-5. doi: 10.1053/j.gastro.2013.02.004. Epub 2013 Feb 13.

23.

Multiple dysplastic liver nodules in PFIC2 underscore risk for neoplasia associated with functional BSEP deficiency.

Sheridan RM, Gupta A, Miethke A, Knisely AS, Bove KE.

Am J Surg Pathol. 2012 May;36(5):785-6. doi: 10.1097/PAS.0b013e3182500c35. No abstract available.

PMID:
22472955
24.

Importance of muscle light microscopic mitochondrial subsarcolemmal aggregates in the diagnosis of respiratory chain deficiency.

Miles L, Miles MV, Horn PS, Degrauw TJ, Wong BL, Bove KE.

Hum Pathol. 2012 Aug;43(8):1249-57. doi: 10.1016/j.humpath.2011.09.016. Epub 2012 Jan 25.

PMID:
22277918
25.

Rectal biopsy in children with Down syndrome and chronic constipation: Hirschsprung disease vs non-hirschsprung disease.

Yin H, Boyd T, Pacheco MC, Schonfeld D, Bove KE.

Pediatr Dev Pathol. 2012 Mar-Apr;15(2):87-95. doi: 10.2350/11-01-0957-OA.1. Epub 2011 Oct 12.

PMID:
21991983
26.

Juvenile dermatomyositis: correlation of MRI at presentation with clinical outcome.

Ladd PE, Emery KH, Salisbury SR, Laor T, Lovell DJ, Bove KE.

AJR Am J Roentgenol. 2011 Jul;197(1):W153-8. doi: 10.2214/AJR.10.5337.

PMID:
21700978
27.

Morphologic findings in progressive familial intrahepatic cholestasis 2 (PFIC2): correlation with genetic and immunohistochemical studies.

Evason K, Bove KE, Finegold MJ, Knisely AS, Rhee S, Rosenthal P, Miethke AG, Karpen SJ, Ferrell LD, Kim GE.

Am J Surg Pathol. 2011 May;35(5):687-96. doi: 10.1097/PAS.0b013e318212ec87.

28.

Design and validation of the biliary atresia research consortium histologic assessment system for cholestasis in infancy.

Russo P, Magee JC, Boitnott J, Bove KE, Raghunathan T, Finegold M, Haas J, Jaffe R, Kim GE, Magid M, Melin-Aldana H, White F, Whitington PF, Sokol RJ; Biliary Atresia Research Consortium.

Clin Gastroenterol Hepatol. 2011 Apr;9(4):357-362.e2. doi: 10.1016/j.cgh.2011.01.003. Epub 2011 Jan 14.

29.

A welcome surprise: nodular fasciitis presenting as soft tissue sarcoma.

Wagner LM, Gelfand MJ, Laor T, Ryckman FC, Al-Ghawi H, Bove KE.

J Pediatr Hematol Oncol. 2011 May;33(4):316-9. doi: 10.1097/MPH.0b013e3181e88649.

PMID:
20975584
30.

Leukocyte adhesion deficiency type 1 presenting with recurrent pyoderma gangrenosum and flaccid scarring.

Hinze CH, Lucky AW, Bove KE, Marsh RA, Bleesing JH, Passo MH.

Pediatr Dermatol. 2010 Sep-Oct;27(5):500-3. doi: 10.1111/j.1525-1470.2010.01260.x. Epub 2010 Aug 27.

PMID:
20807363
31.

Porcine allograft mandible revitalization using autologous adipose-derived stem cells, bone morphogenetic protein-2, and periosteum.

Runyan CM, Jones DC, Bove KE, Maercks RA, Simpson DS, Taylor JA.

Plast Reconstr Surg. 2010 May;125(5):1372-82. doi: 10.1097/PRS.0b013e3181d7032f.

PMID:
20440157
32.

A fetus with hypertrophic cardiomyopathy, restrictive, and single-ventricle physiology, and a beta-myosin heavy chain mutation.

Hinton RB, Michelfelder EC, Marino BS, Bove KE, Ware SM.

J Pediatr. 2010 Jul;157(1):164-6. doi: 10.1016/j.jpeds.2010.02.044. Epub 2010 Apr 14.

33.

Ductal plate malformation-like arrays in early explants after a Kasai procedure are independent of splenic malformation complex (heterotaxy).

Pacheco MC, Campbell KM, Bove KE.

Pediatr Dev Pathol. 2009 Sep-Oct;12(5):355-60. doi: 10.2350/09-01-0598-OA.1.

PMID:
19883236
34.

Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations.

Collins J, Bove KE, Dimmock D, Morehart P, Wong LJ, Wong B.

Neuromuscul Disord. 2009 Nov;19(11):784-7. doi: 10.1016/j.nmd.2009.08.002. Epub 2009 Sep 6.

PMID:
19736010
35.

Concurrent course of transient neonatal diabetes with cholestasis and paucity of interlobular bile ducts: a case report.

Kenny AP, Crimmins NA, Mackay DJ, Hopkin RJ, Bove KE, Leonis MA.

Pediatr Dev Pathol. 2009 Sep-Oct;12(5):417-20. doi: 10.2350/09-03-0628-CR.1.

36.

Phenotypic and microscopic description of a new case of Ermine phenotype.

Zarate YA, Pacheco MC, Bove KE, Gorlin R, Zhao H, Hopkin RJ.

Am J Med Genet A. 2009 Jun;149A(6):1253-6. doi: 10.1002/ajmg.a.32815.

PMID:
19449401
37.

Segmental testicular infarction in a young man simulating a testicular tumor.

Kim HK, Goske MJ, Bove KE, Minovich E.

Pediatr Radiol. 2009 Apr;39(4):400-2. doi: 10.1007/s00247-009-1148-2. Epub 2009 Feb 12.

PMID:
19214495
38.

Two novel STRA6 mutations in a patient with anophthalmia and diaphragmatic eventration.

West B, Bove KE, Slavotinek AM.

Am J Med Genet A. 2009 Mar;149A(3):539-42. doi: 10.1002/ajmg.a.32682. No abstract available.

39.

Megalencephalic leukoencephalopathy with subcortical cysts: a third confirmed case with literature review.

Miles L, DeGrauw TJ, Dinopoulos A, Cecil KM, van der Knaap MS, Bove KE.

Pediatr Dev Pathol. 2009 May-Jun;12(3):180-6. doi: 10.2350/08-06-0481.1.

PMID:
18821826
40.

Mechanisms of disease: Inborn errors of bile acid synthesis.

Sundaram SS, Bove KE, Lovell MA, Sokol RJ.

Nat Clin Pract Gastroenterol Hepatol. 2008 Aug;5(8):456-68. doi: 10.1038/ncpgasthep1179. Epub 2008 Jun 24. Review.

41.

Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies.

Miles MV, Miles L, Tang PH, Horn PS, Steele PE, DeGrauw AJ, Wong BL, Bove KE.

Mitochondrion. 2008 Mar;8(2):170-80. doi: 10.1016/j.mito.2008.01.003. Epub 2008 Feb 2.

PMID:
18313367
42.

Variability of acetylcholinesterase hyperinnervation patterns in distal rectal suction biopsy specimens in Hirschsprung disease.

Pacheco MC, Bove KE.

Pediatr Dev Pathol. 2008 Jul-Aug;11(4):274-82. Epub 2007 Dec 13.

PMID:
18078369
43.

International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials.

Wedderburn LR, Varsani H, Li CK, Newton KR, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith A, Harding B, Hoogendijk J, Lundberg IE, Marie S, Minetti C, Nennesmo I, Rushing EJ, Sewry C, Charman SC, Pilkington CA, Holton JL; UK Juvenile Dermatomyositis Research Group.

Arthritis Rheum. 2007 Oct 15;57(7):1192-201.

44.

Predictability of the clinical course of juvenile dermatomyositis based on initial muscle biopsy: a retrospective study of 72 patients.

Miles L, Bove KE, Lovell D, Wargula JC, Bukulmez H, Shao M, Salisbury S, Bean JA.

Arthritis Rheum. 2007 Oct 15;57(7):1183-91.

45.

False negative histochemical reaction for myophosphorylase activity in fulminant sepsis due to methicillin resistant Staphylococcus aureus.

Cristina Pacheco M, Miles L, Bove KE.

Neuromuscul Disord. 2007 Dec;17(11-12):983-5. Epub 2007 Aug 24.

PMID:
17719780
46.

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.

Wong LJ, Brunetti-Pierri N, Zhang Q, Yazigi N, Bove KE, Dahms BB, Puchowicz MA, Gonzalez-Gomez I, Schmitt ES, Truong CK, Hoppel CL, Chou PC, Wang J, Baldwin EE, Adams D, Leslie N, Boles RG, Kerr DS, Craigen WJ.

Hepatology. 2007 Oct;46(4):1218-27. Erratum in: Hepatology. 2008 Feb;47(2):768.

PMID:
17694548
47.

Inborn errors of bile acid metabolism.

Heubi JE, Setchell KD, Bove KE.

Semin Liver Dis. 2007 Aug;27(3):282-94. Review.

PMID:
17682975
48.

MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeet.

Boor I, Nagtegaal M, Kamphorst W, van der Valk P, Pronk JC, van Horssen J, Dinopoulos A, Bove KE, Pascual-Castroviejo I, Muntoni F, Estévez R, Scheper GC, van der Knaap MS.

Acta Neuropathol. 2007 Oct;114(4):403-10. Epub 2007 Jul 13.

49.
50.

Combined omphalomesenteric and urachal remnants in an 18-month-old girl.

Kranbuhl KH, Lucky AW, Warner BW, Miles L, Bove KE.

Pediatr Dermatol. 2007 Jan-Feb;24(1):65-8.

PMID:
17300654

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