Stephenson JB - Search Results

1

Muscle ultrasound in the assessment of suspected neuromuscular disease in childhood.

Zuberi SM, Matta N, Nawaz S, Stephenson JB, McWilliam RC, Hollman A. Zuberi SM, et al. Among authors: stephenson jb. Neuromuscul Disord. 1999 Jun;9(4):203-7. doi: 10.1016/s0960-8966(99)00002-4. Neuromuscul Disord. 1999. PMID: 10399745 Clinical Trial.

2

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome.

Crow YJ, Zuberi SM, McWilliam R, Tolmie JL, Hollman A, Pohl K, Stephenson JB. Crow YJ, et al. Among authors: stephenson jb. J Med Genet. 1998 Feb;35(2):94-8. doi: 10.1136/jmg.35.2.94. J Med Genet. 1998. PMID: 9507386 Free PMC article.

3

Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric reflux.

Zuberi SM, Stephenson JB, Azmy AF, Robinson PH, McWilliam RC. Zuberi SM, et al. Among authors: stephenson jb. Arch Dis Child. 1998 Oct;79(4):363-4. doi: 10.1136/adc.79.4.363. Arch Dis Child. 1998. PMID: 9875052 Free PMC article.

4

Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes.

Horrocks IA, Nechay A, Stephenson JB, Zuberi SM. Horrocks IA, et al. Among authors: stephenson jb. Arch Dis Child. 2005 Dec;90(12):1283-7. doi: 10.1136/adc.2005.075408. Epub 2005 Sep 13. Arch Dis Child. 2005. PMID: 16159903 Free PMC article.

5

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

Zuberi SM, Eunson LH, Spauschus A, De Silva R, Tolmie J, Wood NW, McWilliam RC, Stephenson JB, Kullmann DM, Hanna MG. Zuberi SM, et al. Among authors: stephenson jb. Brain. 1999 May;122 ( Pt 5):817-25. doi: 10.1093/brain/122.5.817. Brain. 1999. PMID: 10355668

6

The movement disorders of Coffin-Lowry syndrome.

Stephenson JB, Hoffman MC, Russell AJ, Falconer J, Beach RC, Tolmie JL, McWilliam RC, Zuberi SM. Stephenson JB, et al. Brain Dev. 2005 Mar;27(2):108-13. doi: 10.1016/j.braindev.2003.11.010. Brain Dev. 2005. PMID: 15668049

7

Porencephaly and optic hypoplasia in neonatal isoimmune thrombocytopenia.

Davidson JE, McWilliam RC, Evans TJ, Stephenson JB. Davidson JE, et al. Among authors: stephenson jb. Arch Dis Child. 1989 Jun;64(6):858-60. doi: 10.1136/adc.64.6.858. Arch Dis Child. 1989. PMID: 2505691 Free PMC article.

8

Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphism.

Macleod S, Mallik A, Tolmie JL, Stephenson JB, O'Regan ME, Zuberi SM. Macleod S, et al. Among authors: stephenson jb. Brain Dev. 2005 Mar;27(2):118-24. doi: 10.1016/j.braindev.2003.10.006. Brain Dev. 2005. PMID: 15668051

9

Anoxic-epileptic seizures: home video recordings of epileptic seizures induced by syncopes.

Stephenson J, Breningstall G, Steer C, Kirkpatrick M, Horrocks I, Nechay A, Zuberi S. Stephenson J, et al. Epileptic Disord. 2004 Mar;6(1):15-9. Epileptic Disord. 2004. PMID: 15075063 Free article.

10

Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.

Crow YJ, McMenamin J, Haenggeli CA, Hadley DM, Tirupathi S, Treacy EP, Zuberi SM, Browne BH, Tolmie JL, Stephenson JB. Crow YJ, et al. Among authors: stephenson jb. Neuropediatrics. 2004 Feb;35(1):10-9. doi: 10.1055/s-2003-43552. Neuropediatrics. 2004. PMID: 15002047

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