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Items: 1 to 50 of 69

1.

Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients.

Padidela R, Fiest M, Arya V, Smith VV, Ashworth M, Rampling D, Newbould M, Batra G, James J, Wright NB, Dunne MJ, Clayton PE, Banerjee I, Hussain K.

Eur J Endocrinol. 2014 Apr 10;170(5):741-7. doi: 10.1530/EJE-13-1008. Print 2014 May.

PMID:
24599222
2.

A practical guide for the diagnosis of primary enteric nervous system disorders.

Schäppi MG, Staiano A, Milla PJ, Smith VV, Dias JA, Heuschkel R, Husby S, Mearin ML, Papadopoulou A, Ruemmele FM, Vandenplas Y, Koletzko S.

J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):677-86. doi: 10.1097/MPG.0b013e3182a8bb50. Review.

PMID:
24177787
3.

Amniotic fluid stem cells improve survival and enhance repair of damaged intestine in necrotising enterocolitis via a COX-2 dependent mechanism.

Zani A, Cananzi M, Fascetti-Leon F, Lauriti G, Smith VV, Bollini S, Ghionzoli M, D'Arrigo A, Pozzobon M, Piccoli M, Hicks A, Wells J, Siow B, Sebire NJ, Bishop C, Leon A, Atala A, Lythgoe MF, Pierro A, Eaton S, De Coppi P.

Gut. 2014 Feb;63(2):300-9. doi: 10.1136/gutjnl-2012-303735. Epub 2013 Mar 24.

PMID:
23525603
4.

High-resolution colonic manometry accurately predicts colonic neuromuscular pathological phenotype in pediatric slow transit constipation.

Giorgio V, Borrelli O, Smith VV, Rampling D, Köglmeier J, Shah N, Thapar N, Curry J, Lindley KJ.

Neurogastroenterol Motil. 2013 Jan;25(1):70-8.e8-9. doi: 10.1111/nmo.12016. Epub 2012 Oct 3.

PMID:
23030503
5.

Severe resistance to weight gain, lack of stored triglycerides in adipose tissue, hypoglycaemia, and increased energy expenditure: a novel disorder of energy homeostasis.

Padidela R, Bennett K, Nessa A, Wells J, Aufieri R, James C, Smith VV, Brain C, Eaton S, Hussain K.

Horm Res Paediatr. 2012;77(4):261-8. doi: 10.1159/000337248. Epub 2012 Apr 26.

PMID:
22538517
6.

A rat decellularized small bowel scaffold that preserves villus-crypt architecture for intestinal regeneration.

Totonelli G, Maghsoudlou P, Garriboli M, Riegler J, Orlando G, Burns AJ, Sebire NJ, Smith VV, Fishman JM, Ghionzoli M, Turmaine M, Birchall MA, Atala A, Soker S, Lythgoe MF, Seifalian A, Pierro A, Eaton S, De Coppi P.

Biomaterials. 2012 Apr;33(12):3401-10. doi: 10.1016/j.biomaterials.2012.01.012. Epub 2012 Feb 3.

7.

The heterogeneity of focal forms of congenital hyperinsulinism.

Ismail D, Kapoor RR, Smith VV, Ashworth M, Blankenstein O, Pierro A, Flanagan SE, Ellard S, Hussain K.

J Clin Endocrinol Metab. 2012 Jan;97(1):E94-9. doi: 10.1210/jc.2011-1628. Epub 2011 Oct 26.

PMID:
22031516
8.

The predictive value of preoperative fluorine-18-L-3,4-dihydroxyphenylalanine positron emission tomography-computed tomography scans in children with congenital hyperinsulinism of infancy.

Zani A, Nah SA, Ron O, Totonelli G, Ismail D, Smith VV, Ashworth M, Blankenstein O, Mohnike W, De Coppi P, Eaton S, Hussain K, Pierro A.

J Pediatr Surg. 2011 Jan;46(1):204-8. doi: 10.1016/j.jpedsurg.2010.09.093.

PMID:
21238668
9.

Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic Hypoglycemia.

Flanagan SE, Kapoor RR, Smith VV, Hussain K, Ellard S.

Front Endocrinol (Lausanne). 2011 Nov 2;2:66. doi: 10.3389/fendo.2011.00066. eCollection 2011.

10.

Quantitation of cellular components of the enteric nervous system in the normal human gastrointestinal tract--report on behalf of the Gastro 2009 International Working Group.

Knowles CH, Veress B, Kapur RP, Wedel T, Farrugia G, Vanderwinden JM, Geboes K, Smith VV, Martin JE, Lindberg G, Milla PJ, De Giorgio R.

Neurogastroenterol Motil. 2011 Feb;23(2):115-24. doi: 10.1111/j.1365-2982.2010.01657.x. Epub 2010 Dec 22. Review.

PMID:
21175997
11.

Familial focal congenital hyperinsulinism.

Ismail D, Smith VV, de Lonlay P, Ribeiro MJ, Rahier J, Blankenstein O, Flanagan SE, Bellanné-Chantelot C, Verkarre V, Aigrain Y, Pierro A, Ellard S, Hussain K.

J Clin Endocrinol Metab. 2011 Jan;96(1):24-8. doi: 10.1210/jc.2010-1524. Epub 2010 Oct 13.

12.

The London Classification of gastrointestinal neuromuscular pathology: report on behalf of the Gastro 2009 International Working Group.

Knowles CH, De Giorgio R, Kapur RP, Bruder E, Farrugia G, Geboes K, Lindberg G, Martin JE, Meier-Ruge WA, Milla PJ, Smith VV, Vandervinden JM, Veress B, Wedel T.

Gut. 2010 Jul;59(7):882-7. doi: 10.1136/gut.2009.200444.

PMID:
20581236
13.

Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia.

Flanagan SE, Kapoor RR, Banerjee I, Hall C, Smith VV, Hussain K, Ellard S.

Clin Genet. 2011 Jun;79(6):582-7. doi: 10.1111/j.1399-0004.2010.01476.x.

14.

Enteropathic histopathological features may be associated with Shwachman-Diamond syndrome.

Shah N, Cambrook H, Koglmeier J, Mason C, Ancliff P, Lindley K, Smith VV, Bajaj-Elliott M, Sebire NJ.

J Clin Pathol. 2010 Jul;63(7):592-4. doi: 10.1136/jcp.2010.077677. Epub 2010 May 24.

PMID:
20501449
15.

Does intestinal permeability lead to organ failure in experimental necrotizing enterocolitis?

Zani A, Ghionzoli M, Lauriti G, Cananzi M, Smith VV, Pierro A, De Coppi P, Eaton S.

Pediatr Surg Int. 2010 Jan;26(1):85-9. doi: 10.1007/s00383-009-2507-7.

PMID:
19855983
16.

Lymphocytic leiomyositis and myenteric ganglionitis are intrinsic features of cystic fibrosis: studies in distal intestinal obstruction syndrome and meconium ileus.

Smith VV, Schäppi MG, Bisset WM, Kiparissi F, Jaffe A, Milla PJ, Lindley KJ.

J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):42-51. doi: 10.1097/MPG.0b013e318186d35a.

PMID:
19710558
17.

Gastrointestinal neuromuscular pathology: guidelines for histological techniques and reporting on behalf of the Gastro 2009 International Working Group.

Knowles CH, De Giorgio R, Kapur RP, Bruder E, Farrugia G, Geboes K, Gershon MD, Hutson J, Lindberg G, Martin JE, Meier-Ruge WA, Milla PJ, Smith VV, Vandervinden JM, Veress B, Wedel T.

Acta Neuropathol. 2009 Aug;118(2):271-301. doi: 10.1007/s00401-009-0527-y. Epub 2009 Apr 10.

PMID:
19360428
18.

Assessment of a neonatal rat model of necrotizing enterocolitis.

Zani A, Cordischi L, Cananzi M, De Coppi P, Smith VV, Eaton S, Pierro A.

Eur J Pediatr Surg. 2008 Dec;18(6):423-6. doi: 10.1055/s-2008-1038951. Epub 2008 Nov 14.

PMID:
19012230
19.

Mast cell-nerve interactions in children with functional dyspepsia.

Schäppi MG, Borrelli O, Knafelz D, Williams S, Smith VV, Milla PJ, Lindley KJ.

J Pediatr Gastroenterol Nutr. 2008 Oct;47(4):472-80. doi: 10.1097/MPG.0b013e318186008e.

PMID:
18852640
20.

Moderate hypothermia as a rescue therapy against intestinal ischemia and reperfusion injury in the rat.

Stefanutti G, Pierro A, Parkinson EJ, Smith VV, Eaton S.

Crit Care Med. 2008 May;36(5):1564-72. doi: 10.1097/CCM.0b013e3181709e9f.

PMID:
18434898
21.

Captopril reduces the severity of bowel damage in a neonatal rat model of necrotizing enterocolitis.

Zani A, Eaton S, Leon FF, Malerba A, Hall NJ, De Coppi P, Smith VV, Pierro A.

J Pediatr Surg. 2008 Feb;43(2):308-14. doi: 10.1016/j.jpedsurg.2007.10.022.

PMID:
18280280
22.

Pathology of paediatric gastrointestinal neuromuscular disease.

Smith VV.

J Pediatr Gastroenterol Nutr. 2007 Dec;45 Suppl 2:S93-6. doi: 10.1097/MPG.0b013e31812e650e. Review.

PMID:
18185076
23.

An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism.

Hussain K, Flanagan SE, Smith VV, Ashworth M, Day M, Pierro A, Ellard S.

Diabetes. 2008 Jan;57(1):259-63. Epub 2007 Oct 17.

24.

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome).

Fertleman CR, Ferrie CD, Aicardi J, Bednarek NA, Eeg-Olofsson O, Elmslie FV, Griesemer DA, Goutières F, Kirkpatrick M, Malmros IN, Pollitzer M, Rossiter M, Roulet-Perez E, Schubert R, Smith VV, Testard H, Wong V, Stephenson JB.

Neurology. 2007 Aug 7;69(6):586-95.

PMID:
17679678
25.
26.

Diagnosis of neuronal ceroid lipofuscinosis (Batten disease) by electron microscopy in peripheral blood specimens.

Anderson GW, Smith VV, Brooke I, Malone M, Sebire NJ.

Ultrastruct Pathol. 2006 Sep-Oct;30(5):373-8.

PMID:
17090516
27.

Histopathological features of gastrointestinal mucosal biopsy specimens in children with epidermolysis bullosa.

Shah N, Freeman E, Martinez A, Mellerio J, Smith VV, Lindley KJ, Sebire NJ.

J Clin Pathol. 2007 Jul;60(7):843-4. Epub 2006 Oct 17. No abstract available.

28.

Management of fulminating ulcerative colitis in childhood with chimeric anti-CD25 antibody.

Schwarzer A, Ricciardelli I, Kirkham S, Binnie K, Shah N, Elawad MA, Hill SM, Furman M, Smith VV, Sebire N, Milla PJ, Londei M, Lindley KJ.

J Pediatr Gastroenterol Nutr. 2006 Feb;42(2):245-8.

PMID:
16456427
31.

Histopathological features of chronic granulomatous disease (CGD) in childhood.

Levine S, Smith VV, Malone M, Sebire NJ.

Histopathology. 2005 Nov;47(5):508-16.

PMID:
16241999
32.

P-selectin expression, neutrophil infiltration, and histologic injury in neonates with necrotizing enterocolitis.

Stefanutti G, Lister P, Smith VV, Peters MJ, Klein NJ, Pierro A, Eaton S.

J Pediatr Surg. 2005 Jun;40(6):942-7; discussion 947-8.

PMID:
15991175
33.

Intestinal ischemia-reperfusion injury does not lead to acute central nervous system damage.

Hall NJ, Smith VV, Harding B, Pierro A, Eaton S.

J Surg Res. 2005 Dec;129(2):288-91. Epub 2005 Jun 3.

PMID:
15936774
34.

Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.

Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ.

J Clin Endocrinol Metab. 2005 Jul;90(7):4376-82. Epub 2005 Apr 5.

PMID:
15811927
35.

Hypertrophic eosinophilic gastroenteropathy is associated with reduced enterocyte apoptosis.

Cuperus R, Schäppi MG, Shah N, Lindley KJ, Milla PJ, Smith VV.

Histopathology. 2005 Jan;46(1):73-80.

PMID:
15656889
36.

LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome.

Ong C, O'Toole EA, Ghali L, Malone M, Smith VV, Callard R, Harper JI.

Br J Dermatol. 2004 Dec;151(6):1253-7.

PMID:
15606522
37.

The nature of colitis in chronic granulomatous disease.

Schäppi MG, Klein NJ, Lindley KJ, Rampling D, Smith VV, Goldblatt D, Milla PJ.

J Pediatr Gastroenterol Nutr. 2003 May;36(5):623-31.

PMID:
12717086
38.

Eosinophilic myenteric ganglionitis is associated with functional intestinal obstruction.

Schäppi MG, Smith VV, Milla PJ, Lindley KJ.

Gut. 2003 May;52(5):752-5.

39.

The histological appearances of Nissen-type fundoplication in the ferret.

Richards CA, Smith VV, Milla PJ, Spitz L, Andrews PL.

Neurogastroenterol Motil. 2003 Apr;15(2):121-8.

PMID:
12680911
40.

Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.

Hussain K, Cosgrove KE, Shepherd RM, Chapman JC, Swift SM, Smith VV, Kassem SA, Glaser B, Lindley KJ, Aynsley-Green A, Dunne MJ.

Endocr Relat Cancer. 2002 Dec;9(4):221-6.

PMID:
12542400
41.

Acquired myopathic intestinal pseudo-obstruction may be due to autoimmune enteric leiomyositis.

Ruuska TH, Karikoski R, Smith VV, Milla PJ.

Gastroenterology. 2002 Apr;122(4):1133-9.

PMID:
11910363
42.

Faecal elastase 1 concentration is a marker of duodenal enteropathy.

Schäppi MG, Smith VV, Cubitt D, Milla PJ, Lindley KJ.

Arch Dis Child. 2002 Jan;86(1):50-3.

44.

Symptomatic diffuse colonic lipomatosis in Proteus syndrome.

Bates AW, Smith VV.

Histopathology. 2001 Jul;39(1):103-4. No abstract available.

PMID:
11454051
45.

Paraffin wax embedded muscle is suitable for the diagnosis of muscular dystrophy.

Sheriffs IN, Rampling D, Smith VV.

J Clin Pathol. 2001 Jul;54(7):517-20.

46.

Chronic intestinal pseudo-obstruction: the pathologist's perspective.

Smith VV.

J Pediatr Gastroenterol Nutr. 2001;32 Suppl 1:S23-4. Review. No abstract available.

PMID:
11321413
47.
48.

Colitis in chronic granulomatous disease.

Schäppi MG, Smith VV, Goldblatt D, Lindley KJ, Milla PJ.

Arch Dis Child. 2001 Feb;84(2):147-51.

49.
50.

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.

Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B.

Nat Genet. 2000 Sep;26(1):56-60.

PMID:
10973248

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