Pitt MC - Search Results

1

Early detection of abnormalities in partial epilepsy using magnetic resonance.

Cross JH, Jackson GD, Neville BG, Connelly A, Kirkham FJ, Boyd SG, Pitt MC, Gadian DG. Cross JH, et al. Among authors: pitt mc. Arch Dis Child. 1993 Jul;69(1):104-9. doi: 10.1136/adc.69.1.104. Arch Dis Child. 1993. PMID: 8024290 Free PMC article.

2

Cortical dysgenesis: serial EEG findings in children and adults.

Raymond AA, Fish DR, Boyd SG, Smith SJ, Pitt MC, Kendall B. Raymond AA, et al. Among authors: pitt mc. Electroencephalogr Clin Neurophysiol. 1995 Jun;94(6):389-97. doi: 10.1016/0013-4694(94)00335-i. Electroencephalogr Clin Neurophysiol. 1995. PMID: 7607092

3

EEG features of cortical dysplasia in children.

Quirk JA, Kendall B, Kingsley DP, Boyd SG, Pitt MC. Quirk JA, et al. Among authors: pitt mc. Neuropediatrics. 1993 Aug;24(4):193-9. doi: 10.1055/s-2008-1071538. Neuropediatrics. 1993. PMID: 8232776

4

EEG findings in hypomelanosis of Ito.

Esquivel EE, Pitt MC, Boyd SG. Esquivel EE, et al. Among authors: pitt mc. Neuropediatrics. 1991 Nov;22(4):216-9. doi: 10.1055/s-2008-1071444. Neuropediatrics. 1991. PMID: 1775218

5

Lower motor neuron involvement in perisylvian polymicrogyria.

Clark M, Pitt M, Neville BG. Clark M, et al. Dev Med Child Neurol. 2006 Oct;48(10):842-6. doi: 10.1017/S0012162206001800. Dev Med Child Neurol. 2006. PMID: 16978465 Free article.

6

Peripheral neuropathy and neuromuscular blockade presenting as prolonged respiratory paralysis following critical illness.

Heckmatt JZ, Pitt MC, Kirkham F. Heckmatt JZ, et al. Among authors: pitt mc. Neuropediatrics. 1993 Jun;24(3):123-5. doi: 10.1055/s-2008-1071527. Neuropediatrics. 1993. PMID: 8395027

7

Disordered peripheral nerve conduction in DOOR(S) syndrome.

Reardon W, Boyd S, Pitt MC, Wilson J, Winter RM. Reardon W, et al. Among authors: pitt mc. Neuropediatrics. 1994 Feb;25(1):33-5. doi: 10.1055/s-2008-1071578. Neuropediatrics. 1994. PMID: 8208348

8

Statistical process control (SPC)--a simple objective method for monitoring seizure frequency and evaluating effectiveness of drug interventions in refractory childhood epilepsy.

Pujar S, Calvert S, Cortina-Borja M, Chin RF, Smith RA, Cross JH, Das K, Pitt M, Scott RC. Pujar S, et al. Epilepsy Res. 2010 Oct;91(2-3):205-13. doi: 10.1016/j.eplepsyres.2010.07.013. Epilepsy Res. 2010. PMID: 20810251 Clinical Trial.

9

Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathy.

Chan SH, Foley AR, Phadke R, Mathew AA, Pitt M, Sewry C, Muntoni F. Chan SH, et al. Neuromuscul Disord. 2014 Aug;24(8):677-83. doi: 10.1016/j.nmd.2014.05.008. Epub 2014 Jun 2. Neuromuscul Disord. 2014. PMID: 24957499

10

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies.

Belaya K, Rodríguez Cruz PM, Liu WW, Maxwell S, McGowan S, Farrugia ME, Petty R, Walls TJ, Sedghi M, Basiri K, Yue WW, Sarkozy A, Bertoli M, Pitt M, Kennett R, Schaefer A, Bushby K, Parton M, Lochmüller H, Palace J, Muntoni F, Beeson D. Belaya K, et al. Brain. 2015 Sep;138(Pt 9):2493-504. doi: 10.1093/brain/awv185. Epub 2015 Jun 30. Brain. 2015. PMID: 26133662 Free PMC article.

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