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Items: 1 to 50 of 128

1.

Diagnosis of Serrated Polyposis Syndrome in an Adolescent Patient.

Daniel R, Lieb J 2nd, Pascasio J, Pall H.

Clin Pediatr (Phila). 2018 Nov 15:9922818812476. doi: 10.1177/0009922818812476. [Epub ahead of print] No abstract available.

PMID:
30428696
2.

Side-to-side bowel anastomosis mimicking intussusception in a 2-year-old child with Peutz-Jeghers syndrome.

Zacharias SA, Prasad R, Kazmi F, Pall H.

Radiol Case Rep. 2018 Jun 20;13(4):839-842. doi: 10.1016/j.radcr.2018.05.012. eCollection 2018 Aug.

3.

Subthalamic deep brain stimulation under general anesthesia and neurophysiological guidance while on dopaminergic medication: comparative cohort study.

Asha MJ, Fisher B, Kausar J, Garratt H, Krovvidi H, Shirley C, White A, Chelvarajah R, Ughratdar I, Hodson JA, Pall H, Mitchell RD.

Acta Neurochir (Wien). 2018 Apr;160(4):823-829. doi: 10.1007/s00701-018-3473-4. Epub 2018 Feb 2.

4.

N-glycosylation and expression in human tissues of the orphan GPR61 receptor.

Kozielewicz P, Alomar H, Yusof S, Grafton G, Cooper AJ, Curnow SJ, Ironside JW, Pall H, Barnes NM.

FEBS Open Bio. 2017 Nov 20;7(12):1982-1993. doi: 10.1002/2211-5463.12339. eCollection 2017 Dec.

5.

Small Bowel Intussusception in a 16-Month-Old Child With Peutz-Jeghers Syndrome.

Zacharias SA, Prasad R, Ciullo S, Mallon MG, Marinovich A, Pall H.

Clin Pediatr (Phila). 2018 Jun;57(6):745-748. doi: 10.1177/0009922817732148. Epub 2017 Sep 20. No abstract available.

PMID:
28929791
6.

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Meyer E, Carss KJ, Rankin J, Nichols JME, Grozeva D, Joseph AP, Mencacci NE, Papandreou A, Ng J, Barral S, Ngoh A, Ben-Pazi H, Willemsen MA, Arkadir D, Barnicoat A, Bergman H, Bhate S, Boys A, Darin N, Foulds N, Gutowski N, Hills A, Houlden H, Hurst JA, Israel Z, Kaminska M, Limousin P, Lumsden D, McKee S, Misra S, Mohammed SS, Nakou V, Nicolai J, Nilsson M, Pall H, Peall KJ, Peters GB, Prabhakar P, Reuter MS, Rump P, Segel R, Sinnema M, Smith M, Turnpenny P, White SM, Wieczorek D, Wiethoff S, Wilson BT, Winter G, Wragg C, Pope S, Heales SJH, Morrogh D; UK10K Consortium; Deciphering Developmental Disorders Study; NIHR BioResource Rare Diseases Consortium, Pittman A, Carr LJ, Perez-Dueñas B, Lin JP, Reis A, Gahl WA, Toro C, Bhatia KP, Wood NW, Kamsteeg EJ, Chong WK, Gissen P, Topf M, Dale RC, Chubb JR, Raymond FL, Kurian MA.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969b. No abstract available.

PMID:
28546572
7.

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.

Smith BN, Topp SD, Fallini C, Shibata H, Chen HJ, Troakes C, King A, Ticozzi N, Kenna KP, Soragia-Gkazi A, Miller JW, Sato A, Dias DM, Jeon M, Vance C, Wong CH, de Majo M, Kattuah W, Mitchell JC, Scotter EL, Parkin NW, Sapp PC, Nolan M, Nestor PJ, Simpson M, Weale M, Lek M, Baas F, Vianney de Jong JM, Ten Asbroek ALMA, Redondo AG, Esteban-Pérez J, Tiloca C, Verde F, Duga S, Leigh N, Pall H, Morrison KE, Al-Chalabi A, Shaw PJ, Kirby J, Turner MR, Talbot K, Hardiman O, Glass JD, De Belleroche J, Maki M, Moss SE, Miller C, Gellera C, Ratti A, Al-Sarraj S, Brown RH Jr, Silani V, Landers JE, Shaw CE.

Sci Transl Med. 2017 May 3;9(388). pii: eaad9157. doi: 10.1126/scitranslmed.aad9157.

8.

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Meyer E, Carss KJ, Rankin J, Nichols JM, Grozeva D, Joseph AP, Mencacci NE, Papandreou A, Ng J, Barral S, Ngoh A, Ben-Pazi H, Willemsen MA, Arkadir D, Barnicoat A, Bergman H, Bhate S, Boys A, Darin N, Foulds N, Gutowski N, Hills A, Houlden H, Hurst JA, Israel Z, Kaminska M, Limousin P, Lumsden D, McKee S, Misra S, Mohammed SS, Nakou V, Nicolai J, Nilsson M, Pall H, Peall KJ, Peters GB, Prabhakar P, Reuter MS, Rump P, Segel R, Sinnema M, Smith M, Turnpenny P, White SM, Wieczorek D, Wiethoff S, Wilson BT, Winter G, Wragg C, Pope S, Heales SJ, Morrogh D; UK10K Consortium; Deciphering Developmental Disorders Study; NIHR BioResource Rare Diseases Consortium, Pittman A, Carr LJ, Perez-Dueñas B, Lin JP, Reis A, Gahl WA, Toro C, Bhatia KP, Wood NW, Kamsteeg EJ, Chong WK, Gissen P, Topf M, Dale RC, Chubb JR, Raymond FL, Kurian MA.

Nat Genet. 2017 Feb;49(2):223-237. doi: 10.1038/ng.3740. Epub 2016 Dec 19. Erratum in: Nat Genet. 2017 May 26;49(6):969.

PMID:
27992417
9.

NASPGHAN Capsule Endoscopy Clinical Report.

Friedlander JA, Liu QY, Sahn B, Kooros K, Walsh CM, Kramer RE, Lightdale JR, Khlevner J, McOmber M, Kurowski J, Giefer MJ, Pall H, Troendle DM, Utterson EC, Brill H, Zacur GM, Lirio RA, Lerner DG, Reynolds C, Gibbons TE, Wilsey M, Liacouras CA, Fishman DS; Endoscopy Committee.

J Pediatr Gastroenterol Nutr. 2017 Mar;64(3):485-494. doi: 10.1097/MPG.0000000000001413.

PMID:
27642781
10.

Age, Sex, Health Insurance, and Race Associated With Increased Rate of Emergent Pediatric Gastrointestinal Procedures.

Andrews A, Franklin L, Rush N, Witts R, Blanco D, Pall H.

J Pediatr Gastroenterol Nutr. 2017 Jun;64(6):907-910. doi: 10.1097/MPG.0000000000001377.

11.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.

Kenna KP, van Doormaal PT, Dekker AM, Ticozzi N, Kenna BJ, Diekstra FP, van Rheenen W, van Eijk KR, Jones AR, Keagle P, Shatunov A, Sproviero W, Smith BN, van Es MA, Topp SD, Kenna A, Miller JW, Fallini C, Tiloca C, McLaughlin RL, Vance C, Troakes C, Colombrita C, Mora G, Calvo A, Verde F, Al-Sarraj S, King A, Calini D, de Belleroche J, Baas F, van der Kooi AJ, de Visser M, Ten Asbroek AL, Sapp PC, McKenna-Yasek D, Polak M, Asress S, Muñoz-Blanco JL, Strom TM, Meitinger T, Morrison KE; SLAGEN Consortium, Lauria G, Williams KL, Leigh PN, Nicholson GA, Blair IP, Leblond CS, Dion PA, Rouleau GA, Pall H, Shaw PJ, Turner MR, Talbot K, Taroni F, Boylan KB, Van Blitterswijk M, Rademakers R, Esteban-Pérez J, García-Redondo A, Van Damme P, Robberecht W, Chio A, Gellera C, Drepper C, Sendtner M, Ratti A, Glass JD, Mora JS, Basak NA, Hardiman O, Ludolph AC, Andersen PM, Weishaupt JH, Brown RH Jr, Al-Chalabi A, Silani V, Shaw CE, van den Berg LH, Veldink JH, Landers JE.

Nat Genet. 2016 Sep;48(9):1037-42. doi: 10.1038/ng.3626. Epub 2016 Jul 25.

12.

Patients' experiences of deep brain stimulation for Parkinson's disease: a qualitative systematic review and synthesis.

Mathers J, Rick C, Jenkinson C, Garside R, Pall H, Mitchell R, Bayliss S, Jones LL.

BMJ Open. 2016 Jun 23;6(6):e011525. doi: 10.1136/bmjopen-2016-011525. Review.

13.

Apathy in patients with Parkinson's disease following deep brain stimulation of the subthalamic nucleus.

Hindle Fisher I, Pall HS, Mitchell RD, Kausar J, Cavanna AE.

CNS Spectr. 2016 Jun;21(3):258-64. doi: 10.1017/S1092852916000171. Epub 2016 May 6.

PMID:
27151388
14.

Phenotypic insights into ADCY5-associated disease.

Chang FC, Westenberger A, Dale RC, Smith M, Pall HS, Perez-Dueñas B, Grattan-Smith P, Ouvrier RA, Mahant N, Hanna BC, Hunter M, Lawson JA, Max C, Sachdev R, Meyer E, Crimmins D, Pryor D, Morris JG, Münchau A, Grozeva D, Carss KJ, Raymond L, Kurian MA, Klein C, Fung VS.

Mov Disord. 2016 Jul;31(7):1033-40. doi: 10.1002/mds.26598. Epub 2016 Apr 8.

15.

Developing the Pediatric Gastrointestinal Endoscopy Unit: A Clinical Report by the Endoscopy and Procedures Committee.

Pall H, Lerner D, Khlevner J, Reynolds C, Kurowski J, Troendle D, Utterson E, Evans PM, Brill H, Wilsey M, Fishman DS.

J Pediatr Gastroenterol Nutr. 2016 Aug;63(2):295-306. doi: 10.1097/MPG.0000000000001189. Review.

PMID:
26974415
16.

Subthalamic nucleus microelectrode recordings (MER) can be reliably detected despite general anaesthesia and dopaminergic treatment.

Asha M, Kausar J, Krovvidi H, Shirely C, White A, Chelvarajah R, Pall H, Mitchell R.

Acta Neurochir (Wien). 2016 May;158(5):1015-6. doi: 10.1007/s00701-016-2758-8. Epub 2016 Mar 4. No abstract available.

PMID:
26940482
17.

Cost-utility analysis of deep brain stimulation surgery plus best medical therapy versus best medical therapy in patients with Parkinson's: Economic evaluation alongside the PD SURG trial.

McIntosh E, Gray A, Daniels J, Gill S, Ives N, Jenkinson C, Mitchell R, Pall H, Patel S, Quinn N, Rick C, Wheatley K, Williams A; PD SURG Collaborators Group.

Mov Disord. 2016 Aug;31(8):1173-82. doi: 10.1002/mds.26423. Epub 2016 Feb 5.

PMID:
26846185
18.

Setting up the Pediatric Endoscopy Unit.

Lerner DG, Pall H.

Gastrointest Endosc Clin N Am. 2016 Jan;26(1):1-12. doi: 10.1016/j.giec.2015.08.008. Epub 2015 Oct 21.

PMID:
26616893
19.

The effect of dopaminergic therapy on intraoperative microelectrode recordings for subthalamic deep brain stimulation under GA: can we operate on patients 'on medications'?

Asha MJ, Kausar J, Krovvidi H, Shirley C, White A, Chelvarajah R, Hodson JA, Pall H, Mitchell RD.

Acta Neurochir (Wien). 2016 Feb;158(2):387-93. doi: 10.1007/s00701-015-2631-1. Epub 2015 Nov 25.

PMID:
26602236
20.

Results From a Patient Experience Study in Pediatric Gastrointestinal Endoscopy.

Jacob DA, Franklin L, Bernstein B, Pall H.

J Patient Exp. 2015 Nov;2(2):23-28. doi: 10.1177/2374373515615978. Epub 2015 Nov 1.

21.

Management of ingested foreign bodies in children: a clinical report of the NASPGHAN Endoscopy Committee.

Kramer RE, Lerner DG, Lin T, Manfredi M, Shah M, Stephen TC, Gibbons TE, Pall H, Sahn B, McOmber M, Zacur G, Friedlander J, Quiros AJ, Fishman DS, Mamula P; North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition Endoscopy Committee.

J Pediatr Gastroenterol Nutr. 2015 Apr;60(4):562-74. doi: 10.1097/MPG.0000000000000729.

PMID:
25611037
22.

Young Age at Diagnosis of Type 1 Diabetes Is Associated with the Development of Celiac Disease-Associated Antibodies in Children Living in Newfoundland and Labrador, Canada.

Pall H, Newhook LA, Aaron H, Curtis J, Randell E.

Children (Basel). 2015 Oct 14;2(4):403-11. doi: 10.3390/children2040403.

23.

Impact of Pre-Procedure Interventions on No-Show Rate in Pediatric Endoscopy.

Mani J, Franklin L, Pall H.

Children (Basel). 2015 Mar 17;2(1):89-97. doi: 10.3390/children2010089.

24.

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp S, Kenna KP, Scotter EL, Kost J, Keagle P, Miller JW, Calini D, Vance C, Danielson EW, Troakes C, Tiloca C, Al-Sarraj S, Lewis EA, King A, Colombrita C, Pensato V, Castellotti B, de Belleroche J, Baas F, ten Asbroek AL, Sapp PC, McKenna-Yasek D, McLaughlin RL, Polak M, Asress S, Esteban-Pérez J, Muñoz-Blanco JL, Simpson M; SLAGEN Consortium, van Rheenen W, Diekstra FP, Lauria G, Duga S, Corti S, Cereda C, Corrado L, Sorarù G, Morrison KE, Williams KL, Nicholson GA, Blair IP, Dion PA, Leblond CS, Rouleau GA, Hardiman O, Veldink JH, van den Berg LH, Al-Chalabi A, Pall H, Shaw PJ, Turner MR, Talbot K, Taroni F, García-Redondo A, Wu Z, Glass JD, Gellera C, Ratti A, Brown RH Jr, Silani V, Shaw CE, Landers JE.

Neuron. 2014 Oct 22;84(2):324-31. doi: 10.1016/j.neuron.2014.09.027. Epub 2014 Oct 22.

25.

SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.

Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine PE, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR.

J Neurol. 2014 Dec;261(12):2296-304. doi: 10.1007/s00415-014-7488-3. Epub 2014 Sep 11.

26.

Bowel preparation for pediatric colonoscopy: report of the NASPGHAN endoscopy and procedures committee.

Pall H, Zacur GM, Kramer RE, Lirio RA, Manfredi M, Shah M, Stephen TC, Tucker N, Gibbons TE, Sahn B, McOmber M, Friedlander J, Quiros JA, Fishman DS, Mamula P.

J Pediatr Gastroenterol Nutr. 2014 Sep;59(3):409-16. doi: 10.1097/MPG.0000000000000447. Review.

PMID:
24897169
27.

Impact of Educational Cartoon on Pediatric Bowel Preparation Quality at Time of Colonoscopy.

Maxwell E, Simmons M, Franklin L, Arnold J, Pall H.

Glob Pediatr Health. 2014 Aug 12;1:2333794X14548199. doi: 10.1177/2333794X14548199. eCollection 2014.

28.

Deep brain stimulation improves survival in severe Parkinson's disease.

Ngoga D, Mitchell R, Kausar J, Hodson J, Harries A, Pall H.

J Neurol Neurosurg Psychiatry. 2014 Jan;85(1):17-22. doi: 10.1136/jnnp-2012-304715. Epub 2013 Jul 10.

PMID:
23843542
29.

Management of sialorrhoea in motor neuron disease: a survey of current UK practice.

Hobson EV, McGeachan A, Al-Chalabi A, Chandran S, Crawley F, Dick D, Donaghy C, Ealing J, Ellis CM, Gorrie G, Hanemann CO, Harrower T, Jung A, Majeed T, Malaspina A, Morrison K, Orrell RW, Pall H, Pinto A, Talbot K, Turner MR, Williams TL, Young CA, Shaw PJ, McDermott CJ.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):521-7. doi: 10.3109/21678421.2013.790452. Epub 2013 May 7.

PMID:
23647474
30.

SGCE mutations cause psychiatric disorders: clinical and genetic characterization.

Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR.

Brain. 2013 Jan;136(Pt 1):294-303. doi: 10.1093/brain/aws308.

31.

Theory of mind deficits in Parkinson's disease: a product of executive dysfunction?

Eddy CM, Beck SR, Mitchell IJ, Praamstra P, Pall HS.

Neuropsychology. 2013 Jan;27(1):37-47. doi: 10.1037/a0031302.

PMID:
23356595
32.

Health-related quality of life and supportive care in patients with rare long-term neurological conditions.

Calvert M, Pall H, Hoppitt T, Eaton B, Savill E, Sackley C.

Qual Life Res. 2013 Aug;22(6):1231-8. doi: 10.1007/s11136-012-0269-5. Epub 2012 Sep 23.

PMID:
23001492
33.

The role of dopamine replacement on the behavioural phenotype of Parkinson's disease.

Alobaidi H, Pall H.

Behav Neurol. 2013;26(4):225-35. doi: 10.3233/BEN-2012-120265. Review.

34.

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.

Smith BN, Newhouse S, Shatunov A, Vance C, Topp S, Johnson L, Miller J, Lee Y, Troakes C, Scott KM, Jones A, Gray I, Wright J, Hortobágyi T, Al-Sarraj S, Rogelj B, Powell J, Lupton M, Lovestone S, Sapp PC, Weber M, Nestor PJ, Schelhaas HJ, Asbroek AA, Silani V, Gellera C, Taroni F, Ticozzi N, Van den Berg L, Veldink J, Van Damme P, Robberecht W, Shaw PJ, Kirby J, Pall H, Morrison KE, Morris A, de Belleroche J, Vianney de Jong JM, Baas F, Andersen PM, Landers J, Brown RH Jr, Weale ME, Al-Chalabi A, Shaw CE.

Eur J Hum Genet. 2013 Jan;21(1):102-8. doi: 10.1038/ejhg.2012.98. Epub 2012 Jun 13.

35.

Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis.

Ingram CJ, Weale ME, Plaster CA, Morrison KE, Goodall EF, Pall HS, Beck M, Jablonka S, Sendtner M, Fisher EM, Bradman N, Kasperavičiūtė D.

Amyotroph Lateral Scler. 2012 Jun;13(4):341-6. doi: 10.3109/17482968.2012.654394. Epub 2012 Mar 13.

PMID:
22409358
36.

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.

Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, Orrell RW, Mead S, Sidle KC, Houlden H, Rohrer JD, Morrison KE, Pall H, Talbot K, Ansorge O; Chromosome 9-ALS/FTD Consortium; French research network on FTLD/FTLD/ALS; ITALSGEN Consortium, Hernandez DG, Arepalli S, Sabatelli M, Mora G, Corbo M, Giannini F, Calvo A, Englund E, Borghero G, Floris GL, Remes AM, Laaksovirta H, McCluskey L, Trojanowski JQ, Van Deerlin VM, Schellenberg GD, Nalls MA, Drory VE, Lu CS, Yeh TH, Ishiura H, Takahashi Y, Tsuji S, Le Ber I, Brice A, Drepper C, Williams N, Kirby J, Shaw P, Hardy J, Tienari PJ, Heutink P, Morris HR, Pickering-Brown S, Traynor BJ.

Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12)70043-1. Epub 2012 Mar 9.

37.

Huntington's disease: current epidemiology and pharmacological management in UK primary care.

Sackley C, Hoppitt TJ, Calvert M, Gill P, Eaton B, Yao G, Pall H.

Neuroepidemiology. 2011;37(3-4):216-21. doi: 10.1159/000331912. Epub 2011 Dec 1.

PMID:
22133668
38.

Deep brain stimulation of the subthalamic nucleus for advanced Parkinson disease using general anesthesia: long-term results.

Harries AM, Kausar J, Roberts SA, Mocroft AP, Hodson JA, Pall HS, Mitchell RD.

J Neurosurg. 2012 Jan;116(1):107-13. doi: 10.3171/2011.7.JNS11319. Epub 2011 Oct 14.

PMID:
21999316
39.

An approach to deep brain stimulation for severe treatment-refractory Tourette syndrome: the UK perspective.

Cavanna AE, Eddy CM, Mitchell R, Pall H, Mitchell I, Zrinzo L, Foltynie T, Jahanshahi M, Limousin P, Hariz MI, Rickards H.

Br J Neurosurg. 2011 Feb;25(1):38-44. doi: 10.3109/02688697.2010.534200. Epub 2010 Dec 15. Review.

PMID:
21158507
40.

A systematic review of the incidence and prevalence of long-term neurological conditions in the UK.

Hoppitt T, Pall H, Calvert M, Gill P, Yao G, Ramsay J, James G, Conduit J, Sackley C.

Neuroepidemiology. 2011;36(1):19-28. doi: 10.1159/000321712. Epub 2010 Nov 17. Review.

41.

Huntington's disease.

Hoppitt T, Calvert M, Pall H, Rickards H, Sackley C.

Lancet. 2010 Oct 30;376(9751):1463-4. doi: 10.1016/S0140-6736(10)61989-7. No abstract available.

PMID:
21036268
42.

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Shatunov A, Mok K, Newhouse S, Weale ME, Smith B, Vance C, Johnson L, Veldink JH, van Es MA, van den Berg LH, Robberecht W, Van Damme P, Hardiman O, Farmer AE, Lewis CM, Butler AW, Abel O, Andersen PM, Fogh I, Silani V, Chiò A, Traynor BJ, Melki J, Meininger V, Landers JE, McGuffin P, Glass JD, Pall H, Leigh PN, Hardy J, Brown RH Jr, Powell JF, Orrell RW, Morrison KE, Shaw PJ, Shaw CE, Al-Chalabi A.

Lancet Neurol. 2010 Oct;9(10):986-94. doi: 10.1016/S1474-4422(10)70197-6. Erratum in: Lancet Neurol. 2011 Mar;10(3):205.

43.

Reporting end-of-life practice: can we trust doctors to be honest?

Draper H, Ives J, Pall H, Smith S, Damery S, Wilson S.

Palliat Med. 2009 Oct;23(7):673-4. doi: 10.1177/0269216309106874. Epub 2009 Jul 30. No abstract available.

PMID:
19643952
44.

Primary sclerosing cholangitis in childhood is associated with abnormalities in cystic fibrosis-mediated chloride channel function.

Pall H, Zielenski J, Jonas MM, DaSilva DA, Potvin KM, Yuan XW, Huang Q, Freedman SD.

J Pediatr. 2007 Sep;151(3):255-9. Epub 2007 Jul 24.

PMID:
17719933
45.

Large-scale pathways-based association study in amyotrophic lateral sclerosis.

Kasperaviciute D, Weale ME, Shianna KV, Banks GT, Simpson CL, Hansen VK, Turner MR, Shaw CE, Al-Chalabi A, Pall HS, Goodall EF, Morrison KE, Orrell RW, Beck M, Jablonka S, Sendtner M, Brockington A, Ince PG, Hartley J, Nixon H, Shaw PJ, Schiavo G, Wood NW, Goldstein DB, Fisher EM.

Brain. 2007 Sep;130(Pt 9):2292-301. Epub 2007 Apr 17.

PMID:
17439985
46.

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS, Zinman LH, Robertson J, Morrison K, Rogaeva E.

Neurobiol Aging. 2008 Aug;29(8):1279-82. Epub 2007 Mar 23.

PMID:
17383054
47.

Duration of Parkinson disease is associated with an increased propensity for "reinvestment".

Masters RS, Pall HS, MacMahon KM, Eves FF.

Neurorehabil Neural Repair. 2007 Mar-Apr;21(2):123-6.

PMID:
17312087
48.

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).

Parkinson N, Ince PG, Smith MO, Highley R, Skibinski G, Andersen PM, Morrison KE, Pall HS, Hardiman O, Collinge J, Shaw PJ, Fisher EM; MRC Proteomics in ALS Study; FReJA Consortium.

Neurology. 2006 Sep 26;67(6):1074-7. Epub 2006 Jun 28.

PMID:
16807408
49.
50.

Pediatric hepatobiliary disease.

Pall H, Jonas MM.

Curr Opin Gastroenterol. 2005 May;21(3):344-7. Review.

PMID:
15818156

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