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Items: 1 to 20 of 102

1.
2.

Hereditary sensory neuropathy with deafness: a familial multisystem atrophy.

Horoupian DS.

Neurology. 1989 Feb;39(2 Pt 1):244-8.

PMID:
2915797
3.

Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study.

Hojo K, Imamura T, Takanashi M, Ishii K, Sasaki M, Imura S, Ozono R, Takatsuki Y, Takauchi S, Mori E.

Eur J Neurol. 1999 May;6(3):357-61.

PMID:
10210919
4.

Hereditary sensory neuropathy with sensorineural deafness and early-onset dementia.

Wright A, Dyck PJ.

Neurology. 1995 Mar;45(3 Pt 1):560-2.

PMID:
7898717
5.

Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings.

Lindahl AJ, Lhatoo SD, Campbell MJ, Nicholson G, Love S.

Clin Neurol Neurosurg. 2006 Dec;108(8):780-3.

PMID:
16271825
6.

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.

Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD.

Brain. 2005 Dec;128(Pt 12):2797-810.

7.
8.

Aberrant neuronal-glial differentiation in Taylor-type focal cortical dysplasia (type IIA/B).

Englund C, Folkerth RD, Born D, Lacy JM, Hevner RF.

Acta Neuropathol. 2005 May;109(5):519-33.

PMID:
15877232
9.

Association of alpha-synuclein immunoreactivity with inflammatory activity in multiple sclerosis lesions.

Lu JQ, Fan Y, Mitha AP, Bell R, Metz L, Moore GR, Yong VW.

J Neuropathol Exp Neurol. 2009 Feb;68(2):179-89. doi: 10.1097/NEN.0b013e318196e905.

10.

[Clinico-pathological investigation of two patients with dementia with motor neuron disease].

Yamamoto R, Iseki E, Murayama N, Minegishi M, Kimura M, Eto K, Arai H, Ohbu S, Hatanaka D, Hino H, Fujisawa K.

Brain Nerve. 2007 Mar;59(3):263-9. Japanese.

PMID:
17370652
11.

Hereditary sensory neuropathy type I.

Auer-Grumbach M.

Orphanet J Rare Dis. 2008 Mar 18;3:7. doi: 10.1186/1750-1172-3-7. Review.

12.

Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?

Tan CF, Piao YS, Kakita A, Yamada M, Takano H, Tanaka M, Mano A, Makino K, Nishizawa M, Wakabayashi K, Takahashi H.

Acta Neuropathol. 2005 Mar;109(3):329-38.

PMID:
15841415
13.

Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation.

Pontikis CC, Cella CV, Parihar N, Lim MJ, Chakrabarti S, Mitchison HM, Mobley WC, Rezaie P, Pearce DA, Cooper JD.

Brain Res. 2004 Oct 15;1023(2):231-42.

PMID:
15374749
14.

Hereditary sensory neuropathy with macular dystrophy.

Tallman MS, Levy M.

South Med J. 1985 Mar;78(3):345-8.

PMID:
3856327
15.
16.

Cellular pathology in multiple system atrophy.

Wakabayashi K, Takahashi H.

Neuropathology. 2006 Aug;26(4):338-45. Review.

PMID:
16961071
17.

Hereditary sensory neuropathies.

Thomas PK.

Brain Pathol. 1993 Apr;3(2):157-63. Review.

PMID:
8293177
18.

Neuronal and glial apoptosis in human traumatic brain injury.

Dressler J, Hanisch U, Kuhlisch E, Geiger KD.

Int J Legal Med. 2007 Sep;121(5):365-75.

PMID:
17106737
19.

Hereditary motor and sensory neuropathy type 1A associated with sensorineural deafness.

Stone J, Moran G, Walls TJ.

J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):403. No abstract available.

20.

Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics.

Itoh K, Shiga K, Shimizu K, Muranishi M, Nakagawa M, Fushiki S.

Acta Neuropathol. 2006 Jan;111(1):39-45.

PMID:
16328511
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