Thomas PK - Search Results

1

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome.

Tyson J, Ellis D, Fairbrother U, King RH, Muntoni F, Jacobs J, Malcolm S, Harding AE, Thomas PK. Tyson J, et al. Among authors: thomas pk. Brain. 1997 Jan;120 ( Pt 1):47-63. doi: 10.1093/brain/120.1.47. Brain. 1997. PMID: 9055797

2

Peripheral neuropathy in the Chediak-Higashi syndrome.

Misra VP, King RH, Harding AE, Muddle JR, Thomas PK. Misra VP, et al. Among authors: thomas pk. Acta Neuropathol. 1991;81(3):354-8. doi: 10.1007/BF00305881. Acta Neuropathol. 1991. PMID: 2058369

3

Focal cranial nerve involvement in chronic inflammatory demyelinating polyneuropathy: clinical and MRI evidence of peripheral and central lesions.

Waddy HM, Misra VP, King RH, Thomas PK, Middleton L, Ormerod IE. Waddy HM, et al. Among authors: thomas pk. J Neurol. 1989 Oct;236(7):400-5. doi: 10.1007/BF00314898. J Neurol. 1989. PMID: 2809641

4

The clinical features of hereditary motor and sensory neuropathy types I and II.

Harding AE, Thomas PK. Harding AE, et al. Among authors: thomas pk. Brain. 1980 Jun;103(2):259-80. doi: 10.1093/brain/103.2.259. Brain. 1980. PMID: 7397478

5

Autosomal recessive hereditary sensory neuropathy with spastic paraplegia.

Thomas PK, Misra VP, King RH, Muddle JR, Wroe S, Bhatia KP, Anderson M, Cabello A, Vilchez J, Wadia NH. Thomas PK, et al. Brain. 1994 Aug;117 ( Pt 4):651-9. doi: 10.1093/brain/117.4.651. Brain. 1994. PMID: 7922454

6

Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.

Gregory R, Thomas PK, King RH, Hallam PL, Malcolm S, Hughes RA, Harding AE. Gregory R, et al. Among authors: thomas pk. Ann Neurol. 1993 Jun;33(6):649-52. doi: 10.1002/ana.410330615. Ann Neurol. 1993. PMID: 8498845

7

Focal upper limb demyelinating neuropathy.

Thomas PK, Claus D, Jaspert A, Workman JM, King RH, Larner AJ, Anderson M, Emerson JA, Ferguson IT. Thomas PK, et al. Brain. 1996 Jun;119 ( Pt 3):765-74. doi: 10.1093/brain/119.3.765. Brain. 1996. PMID: 8673489

8

Deletions of chromosome 17p11.2 in multifocal neuropathies.

Tyson J, Malcolm S, Thomas PK, Harding AE. Tyson J, et al. Among authors: thomas pk. Ann Neurol. 1996 Feb;39(2):180-6. doi: 10.1002/ana.410390207. Ann Neurol. 1996. PMID: 8967749

9

The phenotypic manifestations of chromosome 17p11.2 duplication.

Thomas PK, Marques W Jr, Davis MB, Sweeney MG, King RH, Bradley JL, Muddle JR, Tyson J, Malcolm S, Harding AE. Thomas PK, et al. Brain. 1997 Mar;120 ( Pt 3):465-78. doi: 10.1093/brain/120.3.465. Brain. 1997. PMID: 9126058

10

Epineurial microvasculitis in proximal diabetic neuropathy.

Llewelyn JG, Thomas PK, King RH. Llewelyn JG, et al. Among authors: thomas pk. J Neurol. 1998 Mar;245(3):159-65. doi: 10.1007/s004150050197. J Neurol. 1998. PMID: 9553846

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