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Items: 26


A novel approach to study the morphology and chemistry of pollen in a phylogenetic context, applied to the halophytic taxon Nitraria L.(Nitrariaceae).

Woutersen A, Jardine PE, Bogotá-Angel RG, Zhang HX, Silvestro D, Antonelli A, Gogna E, Erkens RHJ, Gosling WD, Dupont-Nivet G, Hoorn C.

PeerJ. 2018 Jul 19;6:e5055. doi: 10.7717/peerj.5055. eCollection 2018.


Pollen and spores as biological recorders of past ultraviolet irradiance.

Jardine PE, Fraser WT, Lomax BH, Sephton MA, Shanahan TM, Miller CS, Gosling WD.

Sci Rep. 2016 Dec 15;6:39269. doi: 10.1038/srep39269.


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.


Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort.

Hacohen Y, Absoud M, Woodhall M, Cummins C, De Goede CG, Hemingway C, Jardine PE, Kneen R, Pike MG, Whitehouse WP, Wassmer E, Waters P, Vincent A, Lim M; UK & Ireland Childhood CNS Inflammatory Demyelination Working Group.

J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):456-61. doi: 10.1136/jnnp-2013-306411. Epub 2013 Oct 16.


SURF1 deficiency: a multi-centre natural history study.

Wedatilake Y, Brown RM, McFarland R, Yaplito-Lee J, Morris AA, Champion M, Jardine PE, Clarke A, Thorburn DR, Taylor RW, Land JM, Forrest K, Dobbie A, Simmons L, Aasheim ET, Ketteridge D, Hanrahan D, Chakrapani A, Brown GK, Rahman S.

Orphanet J Rare Dis. 2013 Jul 5;8:96. doi: 10.1186/1750-1172-8-96.


Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations.

Silveira-Moriyama L, Gardiner AR, Meyer E, King MD, Smith M, Rakshi K, Parker A, Mallick AA, Brown R, Vassallo G, Jardine PE, Guerreiro MM, Lees AJ, Houlden H, Kurian MA.

Dev Med Child Neurol. 2013 Apr;55(4):327-34. doi: 10.1111/dmcn.12056. Epub 2013 Jan 30.


Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features.

Absoud M, Lim MJ, Chong WK, De Goede CG, Foster K, Gunny R, Hemingway C, Jardine PE, Kneen R, Likeman M, Nischal KK, Pike MG, Sibtain NA, Whitehouse WP, Cummins C, Wassmer E; UK and Ireland Childhood CNS Inflammatory Demyelination Working Group.

Mult Scler. 2013 Jan;19(1):76-86. doi: 10.1177/1352458512445944. Epub 2012 Apr 19.


Optic disc drusen masquerading as papilloedema.

Fong CY, Williams C, Pople IK, Jardine PE.

Arch Dis Child. 2010 Aug;95(8):629. doi: 10.1136/adc.2010.186122. Epub 2010 Jun 3. No abstract available.


Cerebral palsy in siblings caused by compound heterozygous mutations in the gene encoding protein C.

Fong CY, Mumford AD, Likeman MJ, Jardine PE.

Dev Med Child Neurol. 2010 May;52(5):489-93. doi: 10.1111/j.1469-8749.2010.03618.x. Epub 2010 Feb 19.


Cerebral venous sinus thrombosis: a case series including thrombolysis.

Mallick AA, Sharples PM, Calvert SE, Jones RW, Leary M, Lux AL, O'Callaghan FJ, Osborne JP, Patel JS, Prendiville AT, Renowden S, Jardine PE.

Arch Dis Child. 2009 Oct;94(10):790-4. doi: 10.1136/adc.2008.154708. Epub 2009 Jun 24.


Syndrome of fixed dystonia in adolescents--short term outcome in 4 cases.

Majumdar A, López-Casas J, Poo P, Colomer J, Galvan M, Lingappa L, Short C, Jardine PE, Fernández-Alvarez E.

Eur J Paediatr Neurol. 2009 Sep;13(5):466-72. doi: 10.1016/j.ejpn.2008.09.005. Epub 2008 Nov 7.


Progressive late-onset myelopathy and arachnoiditis following neonatal meningitis.

de Goede CG, Jardine PE, Eunson P, Renowden S, Sharples P, Newton RW.

Childs Nerv Syst. 2008 Jun;24(6):675; author reply 677. doi: 10.1007/s00381-008-0610-z. Epub 2008 Mar 26. No abstract available.


Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy.

Garrood P, Eagle M, Jardine PE, Bushby K, Straub V.

Neuromuscul Disord. 2008 Jan;18(1):71-3. Epub 2007 Aug 23.


Severe progressive late onset myelopathy and arachnoiditis following neonatal meningitis.

de Goede CG, Jardine PE, Eunson P, Renowden S, Sharples P, Newton RW.

Eur J Paediatr Neurol. 2006 Jan;10(1):31-6. Epub 2006 Mar 15.


Early onset seizures and Rett-like features associated with mutations in CDKL5.

Evans JC, Archer HL, Colley JP, Ravn K, Nielsen JB, Kerr A, Williams E, Christodoulou J, Gécz J, Jardine PE, Wright MJ, Pilz DT, Lazarou L, Cooper DN, Sampson JR, Butler R, Whatley SD, Clarke AJ.

Eur J Hum Genet. 2005 Oct;13(10):1113-20.


The importance of testing for adrenoleucodystrophy in males with idiopathic Addison's disease.

Ronghe MD, Barton J, Jardine PE, Crowne EC, Webster MH, Armitage M, Allen JT, Steward CG.

Arch Dis Child. 2002 Mar;86(3):185-9.


Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.

Kors EE, Terwindt GM, Vermeulen FL, Fitzsimons RB, Jardine PE, Heywood P, Love S, van den Maagdenberg AM, Haan J, Frants RR, Ferrari MD.

Ann Neurol. 2001 Jun;49(6):753-60.


The scleroatrophic syndrome of Huriez.

Kavanagh GM, Jardine PE, Peachey RD, Murray JC, De Berker D.

Br J Dermatol. 1997 Jul;137(1):114-8.


Familial bilateral periventricular nodular heterotopia mimics tuberous sclerosis.

Jardine PE, Clarke MA, Super M.

Arch Dis Child. 1996 Mar;74(3):244-6. Review.


Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

Lunt PW, Jardine PE, Koch MC, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M.

Hum Mol Genet. 1995 May;4(5):951-8. Erratum in: Hum Mol Genet 1995 Jul;4(7):1243-4.


Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.

Lunt PW, Jardine PE, Koch M, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M.

Muscle Nerve Suppl. 1995;(2):S103-9.


Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.

Lunt PW, Jardine PE, Koch M, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M.

Muscle Nerve Suppl. 1995;2:S103-9.


De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).

Jardine PE, Koch MC, Lunt PW, Maynard J, Bathke KD, Harper PS, Upadhyaya M.

Arch Dis Child. 1994 Sep;71(3):221-7.


A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophy.

Jardine PE, Upadhyaya M, Maynard J, Harper P, Lunt PW.

Neuromuscul Disord. 1994 Sep-Nov;4(5-6):477-82.


Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.

Jardine PE, Cotter PD, Johnson SA, Fitzsimons EJ, Tyfield L, Lunt PW, Bishop DF.

J Med Genet. 1994 Mar;31(3):213-8. Review.


Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.

Jardine PE, Burvill-Holmes LC, Schutt WH, Lunt PW.

Clin Dysmorphol. 1993 Jul;2(3):269-73.


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