-
1
-
-
1942503528
-
Review of diagnostic cases
-
Anonymous. Review of diagnostic cases. Surveillance 18(1), 3, 1991
-
(1991)
Surveillance
, vol.18
, Issue.1
, pp. 3
-
-
-
2
-
-
0032517733
-
Conformational changes of the smooth endoplasmic reticulum are facilitated by l-glutamate and its receptors in rat purkinje cells
-
Banno T, Kohno K. Conformational changes of the smooth endoplasmic reticulum are facilitated by L-glutamate and its receptors in rat Purkinje cells. Journal of Comparative Neurology 402, 252–63, 1998
-
(1998)
Journal of Comparative Neurology
, vol.402
, pp. 252-263
-
-
Banno, T.1
Kohno, K.2
-
3
-
-
0036836191
-
Neonatal cerebellar ataxia in coton de tulear dogs
-
Coates JR, O’Brien DP, Kline KL, Storts RW Johnson GC, Shelton GD, Patterson EE, Abbot LC. Neonatal cerebellar ataxia in Coton de Tulear dogs. Journal ofVeterinary Internal Medicine 16, 680–9, 2002
-
(2002)
Journal Ofveterinary Internal Medicine
, vol.16
, pp. 680-689
-
-
Coates, J.R.1
O’Brien, D.P.2
Kline, K.L.3
Storts Rw Johnson, G.C.4
Shelton, G.D.5
Patterson, E.E.6
Abbot, L.C.7
-
4
-
-
85008777917
-
Cerebellar cortical atrophy in lambs (Daft lamb disease)
-
Cox B. Cerebellar cortical atrophy in lambs (daft lamb disease). Surveillance 19(4), 26, 1992
-
(1992)
Surveillance
, vol.19
, Issue.4
, pp. 26
-
-
Cox, B.1
-
5
-
-
77956903147
-
The role of mitochondrial genome mutations in neurodegenerative disease
-
Mattson MP, JAI Press Inc, Stamford, Connecticut, USA
-
Glazner GW The role of mitochondrial genome mutations in neurodegenerative disease. In: Mattson MP (ed). Genetic Aberrancies and Neurodegenerative Disorders. Pp 313–54. JAI Press Inc, Stamford, Connecticut, USA, 1999
-
(1999)
Genetic Aberrancies and Neurodegenerative Disorders
, pp. 313-354
-
-
Glazner, G.W.1
-
6
-
-
0022566697
-
Cerebellar abiotrophy and segmental axonopathy: Two syndromes of progressive ataxia of merino sheep
-
Harper PA, Duncan DW, Plant JW, Smeal MG. Cerebellar abiotrophy and segmental axonopathy: two syndromes of progressive ataxia of merino sheep. Australian Veterinary Journal 63, 18–21, 1986
-
(1986)
Australian Veterinary Journal
, vol.63
, pp. 18-21
-
-
Harper, P.A.1
Duncan, D.W.2
Plant, J.W.3
Smeal, M.G.4
-
7
-
-
0141593554
-
Reversibility of cisternal stack formation during hypoxic hypoxia and subsequent reoxygenation in cerebellar purkinje cells
-
Ikemoto T, Yorifuji H, Satoh T, Vizi ES. Reversibility of cisternal stack formation during hypoxic hypoxia and subsequent reoxygenation in cerebellar Purkinje cells. Neurochemical Research 28, 1535–42, 2003
-
(2003)
Neurochemical Research
, vol.28
, pp. 1535-1542
-
-
Ikemoto, T.1
Yorifuji, H.2
Satoh, T.3
Vizi, E.S.4
-
9
-
-
0036176571
-
Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease)
-
Jolly RD, Brown S, Das AM, Walkley SU. Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease). Neurochemistry International 40, 565–71, 2002
-
(2002)
Neurochemistry International
, vol.40
, pp. 565-571
-
-
Jolly, R.D.1
Brown, S.2
Das, A.M.3
Walkley, S.U.4
-
11
-
-
77956865373
-
Genetic contributions to the pathogenesis of alzheimer’s disease
-
JAI Press Inc, Stamford, Connecticut, USA
-
Mattson MP. Genetic contributions to the pathogenesis of Alzheimer’s disease. Genetic Aberrancies and Neurodegenerative Disorders. Pp 1–31. JAI Press Inc, Stamford, Connecticut, USA, 1999
-
(1999)
Genetic Aberrancies and Neurodegenerative Disorders
, pp. 1-31
-
-
Mattson, M.P.1
-
12
-
-
0037941588
-
When calcium goes wrong: Genetic alterations of a ubiquitous signaling route
-
Rizzuto R, Pozzan T. When calcium goes wrong: genetic alterations of a ubiquitous signaling route. Nature Genetics 34, 135–41, 2003
-
(2003)
Nature Genetics
, vol.34
, pp. 135-141
-
-
Rizzuto, R.1
Pozzan, T.2
-
13
-
-
0004166784
-
-
Mosby, St Louis, USA
-
Summers BA, Cummings JF, deLahunta A. Veterinary Neuropathology, Pp 3017. Mosby, St Louis, USA, 1995
-
(1995)
Veterinary Neuropathology
, pp. 3017
-
-
Summers, B.A.1
Cummings, J.F.2
DeLahunta, A.3
-
14
-
-
1942535364
-
An hereditary defect of newly born lambs
-
White RG, Rowlands WT. An hereditary defect of newly born lambs. Veterinary Record 57, 491–2, 1945
-
(1945)
Veterinary Record
, vol.57
, pp. 491-492
-
-
White, R.G.1
Rowlands, W.T.2
-
15
-
-
0036616280
-
Cytodifferentiation ofbergmann glia and its relationship with purkinje cells
-
Yamada K, Watanabe M. Cytodifferentiation ofBergmann glia and its relationship with Purkinje cells. Anatomical Science International 77, 94–110, 2002
-
(2002)
Anatomical Science International
, vol.77
, pp. 94-110
-
-
Yamada, K.1
Watanabe, M.2
|