Jardine P - Search Results

1

A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly.

Shah S, Kumar Y, McLean B, Churchill A, Stoodley N, Rankin J, Rizzu P, van der Knaap M, Jardine P. Shah S, et al. Among authors: jardine p. Eur J Paediatr Neurol. 2010 Mar;14(2):182-7. doi: 10.1016/j.ejpn.2009.04.010. Epub 2009 May 28. Eur J Paediatr Neurol. 2010. PMID: 19477666

2

Childhood presentation of COL4A1 mutations.

Shah S, Ellard S, Kneen R, Lim M, Osborne N, Rankin J, Stoodley N, van der Knaap M, Whitney A, Jardine P. Shah S, et al. Among authors: jardine p. Dev Med Child Neurol. 2012 Jun;54(6):569-74. doi: 10.1111/j.1469-8749.2011.04198.x. Epub 2012 Jan 16. Dev Med Child Neurol. 2012. PMID: 22574627 Free article. Review.

3

Mesenteric angina complicating a mesodermal anomaly.

Howells R, Curran A, Jardine P, Newbury-Ecob R, Sandhu B. Howells R, et al. Among authors: jardine p. Eur J Paediatr Neurol. 2000;4(4):181-3. doi: 10.1053/ejpn.2000.0297. Eur J Paediatr Neurol. 2000. PMID: 11008262

4

Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C.

Rankin J, Auer-Grumbach M, Bagg W, Colclough K, Nguyen TD, Fenton-May J, Hattersley A, Hudson J, Jardine P, Josifova D, Longman C, McWilliam R, Owen K, Walker M, Wehnert M, Ellard S. Rankin J, et al. Among authors: jardine p. Am J Med Genet A. 2008 Jun 15;146A(12):1530-42. doi: 10.1002/ajmg.a.32331. Am J Med Genet A. 2008. PMID: 18478590

5

Severe progressive late onset myelopathy and arachnoiditis following neonatal meningitis.

de Goede CG, Jardine PE, Eunson P, Renowden S, Sharples P, Newton RW. de Goede CG, et al. Among authors: jardine pe. Eur J Paediatr Neurol. 2006 Jan;10(1):31-6. doi: 10.1016/j.ejpn.2005.10.001. Epub 2006 Mar 15. Eur J Paediatr Neurol. 2006. PMID: 16540357

6

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. Kors EE, et al. Among authors: jardine pe. Ann Neurol. 2001 Jun;49(6):753-60. doi: 10.1002/ana.1031. Ann Neurol. 2001. PMID: 11409427

7

Familial bilateral periventricular nodular heterotopia mimics tuberous sclerosis.

Jardine PE, Clarke MA, Super M. Jardine PE, et al. Arch Dis Child. 1996 Mar;74(3):244-6. doi: 10.1136/adc.74.3.244. Arch Dis Child. 1996. PMID: 8787433 Free PMC article. Review.

8

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

Fong CY, Mumford AD, Likeman MJ, Jardine PE. Fong CY, et al. Dev Med Child Neurol. 2010 May;52(5):489-93. doi: 10.1111/j.1469-8749.2010.03618.x. Epub 2010 Feb 19. Dev Med Child Neurol. 2010. PMID: 20187890 Free article.

9

Very long chain fatty acid levels in patients diagnosed with multiple sclerosis.

Wilkins A, Ingram G, Brown A, Jardine P, Steward CG, Robertson NP, Scolding NJ. Wilkins A, et al. Among authors: jardine p. Mult Scler. 2009 Dec;15(12):1525-7. doi: 10.1177/1352458509351731. Epub 2009 Nov 13. Mult Scler. 2009. PMID: 19965514

10

Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD).

Upadhyaya M, Maynard J, Osborn M, Jardine P, Harper PS, Lunt P. Upadhyaya M, et al. Among authors: jardine p. Muscle Nerve Suppl. 1995;2:S45-9. Muscle Nerve Suppl. 1995. PMID: 7739625

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