-
1
-
-
0028864352
-
Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum
-
Bhatia KP, Brown P, Gregory R, Lennox GG, Manji H, Thompson PD, et al. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain 1995; 118: 1087-93.
-
(1995)
Brain
, vol.118
, pp. 1087-1093
-
-
Bhatia, K.1
Brown, P.2
Gregory, R.3
Lennox, G.G.4
Manji, H.5
Thompson, P.D.6
-
2
-
-
0028036140
-
Evaluation of the gliadin antibody test for diagnosing coeliac disease
-
Bode S, Gudmand-Hoyer E. Evaluation of the gliadin antibody test for diagnosing coeliac disease. Scand J Gastroenterol 1994; 29: 148-52.
-
(1994)
Scand J Gastroenterol
, vol.29
, pp. 148-152
-
-
Bode, S.1
Gudmand-Hoyer, E.2
-
3
-
-
0027489676
-
The diagnostic value of the gliadin antibody test in coeliac disease in children: A prospective study
-
Bodé S, Weile B, Krasilnikoff PA, Gudmand-Hoyer E. The diagnostic value of the gliadin antibody test in coeliac disease in children: a prospective study. J Pediatr Gastroenterol Nutr 1993; 17: 260-4.
-
(1993)
J Pediatr Gastroenterol Nutr
, vol.17
, pp. 260-264
-
-
Bodé, S.1
Weile, B.2
Krasilnikoff, P.A.3
Gudmand-Hoyer, E.4
-
4
-
-
0025814831
-
Antigliadin and antiendomysium antibody determination for coeliac disease
-
Bürgin-Wolff A, Gaze E, Hadziselimovic F, Huber H, Lentze MJ, Nusslé D, et al. Antigliadin and antiendomysium antibody determination for coeliac disease. Arch Dis Child 1991; 66: 941-7.
-
(1991)
Arch Dis Child
, vol.66
, pp. 941-947
-
-
Bürgin-Wolff, A.1
Gaze, E.2
Hadziselimovic, F.3
Huber, H.4
Lentze, M.J.5
Nusslé, D.6
-
5
-
-
0029959667
-
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3
-
Bürk K, Abele M, Fetter M, Dichgans J, Skalej M, Laccone F, et al. Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3. Brain 1996; 119: 1497-505.
-
(1996)
Brain
, vol.119
, pp. 1497-1505
-
-
Bürk, K.1
Abele, M.2
Fetter, M.3
Dichgans, J.4
Skalej, M.5
Laccone, F.6
-
6
-
-
0345435256
-
Cognitive deficits in spinocerebellar ataxia 2
-
Bürk K, Globas C, Bösch S, Gräber S, Abele M, Brice A, et al. Cognitive deficits in spinocerebellar ataxia 2. Brain 1999; 122: 769-77.
-
(1999)
Brain
, vol.122
, pp. 769-777
-
-
Bürk, K.1
Globas, C.2
Bösch, S.3
Gräber, S.4
Abele, M.5
Brice, A.6
-
7
-
-
13344270899
-
Friedreich’s ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, et al. Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 1996; 271: 1423-7.
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
Montermini, L.2
Molto, M.D.3
Pianese, L.4
Cossee, M.5
Cavalcanti, F.6
-
8
-
-
0029134707
-
Memory and skill acquisition in Parkinson’s disease and frontal lobe dysfunction
-
Daum I, Schugens MM, Spieker S, Poser U, Schönle PW, Birbaumer N. Memory and skill acquisition in Parkinson’s disease and frontal lobe dysfunction. Cortex 1995; 31: 413-32.
-
(1995)
Cortex
, vol.31
, pp. 413-432
-
-
Daum, I.1
Schugens, M.M.2
Spieker, S.3
Poser, U.4
Schönle, P.W.5
Birbaumer, N.6
-
9
-
-
16944364511
-
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
-
David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, et al. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet 1997; 17: 65-70.
-
(1997)
Nat Genet
, vol.17
, pp. 65-70
-
-
David, G.1
Abbas, N.2
Stevanin, G.3
Dürr, A.4
Yvert, G.5
Cancel, G.6
-
10
-
-
49749155937
-
Tropical sprue and pernicious anaemia, aetiology and treatment
-
Elders C. Tropical sprue and pernicious anaemia, aetiology and treatment. Lancet 1925; 1: 75-7.
-
(1925)
Lancet
, vol.1
, pp. 75-77
-
-
Elders, C.1
-
11
-
-
0033081705
-
Consensus statement on the diagnosis of multiple system atrophy
-
Gilman S, Low PA, Quinn N, Albanese A, Ben-Shlomo Y, Fowler CJ, et al. Consensus statement on the diagnosis of multiple system atrophy. J Neurol Sci 1999; 163: 94-8.
-
(1999)
J Neurol Sci
, vol.163
, pp. 94-98
-
-
Gilman, S.1
Low, P.A.2
Quinn, N.3
Albanese, A.4
Ben-Shlomo, Y.5
Fowler, C.J.6
-
12
-
-
0000265471
-
-
Gjertson DW and Terasaki PI, editors, HLA 1998. Lenexa: American Society for Histocompatibility
-
Gjerston DW and Lee SH. HLA -A/B and -DRB1/DQB1 allele-level haplotype frequencies. In: Gjertson DW and Terasaki PI, editors, HLA 1998. Lenexa: American Society for Histocompatibility; 1998. p. 365-77.
-
(1998)
HLA -A/B and -DRB1/DQB1 Allele-level Haplotype Frequencies
, pp. 365-377
-
-
Gjerston, D.W.1
Lee, S.H.2
-
13
-
-
0030027634
-
Does cryptic gluten sensitivity play a part in neurological illness?
-
Hadjivassiliou M, Gibson A, Davies-Jones GA, Lobo AJ, Stephenson TJ, Milford-Ward A. Does cryptic gluten sensitivity play a part in neurological illness? Lancet 1996; 347: 369-71.
-
(1996)
Lancet
, vol.347
, pp. 369-371
-
-
Hadjivassiliou, M.1
Gibson, A.2
Davies-Jones, G.A.3
Lobo, A.J.4
Stephenson, T.J.5
Milford-Ward, A.6
-
14
-
-
0032517527
-
Clinical, radiological, neurophysiological, and neuropathological characteristics of gluten ataxia
-
Hadjivassiliou M, Grünewald RA, Chattopadhyay AK, Davies-Jones GA, Gibson A, Jarratt JA, et al. Clinical, radiological, neurophysiological, and neuropathological characteristics of gluten ataxia. Lancet 1998; 352: 1582-5.
-
(1998)
Lancet
, vol.352
, pp. 1582-1585
-
-
Hadjivassiliou, M.1
Grünewald, R.A.2
Chattopadhyay, A.K.3
Davies-Jones, G.A.4
Gibson, A.5
Jarratt, J.A.6
-
16
-
-
0019484086
-
’Idiopathic’ late onset cerebellar ataxia. A clinical and genetic study of 36 cases
-
Harding AE. ’Idiopathic’ late onset cerebellar ataxia. A clinical and genetic study of 36 cases. J Neurol Sci 1981; 51: 259-71.
-
(1981)
J Neurol Sci
, vol.51
, pp. 259-271
-
-
Harding, A.E.1
-
17
-
-
0000817016
-
Neurological and psychiatric complications in coeliac disease
-
Gobbi G, Anderman F, Naccarato S, Banchini G, editors. London: John Libbey
-
Holmes GK. Neurological and psychiatric complications in coeliac disease. In: Gobbi G, Anderman F, Naccarato S, Banchini G, editors. Epilepsy and other neurological disorders in coeliac disease. London: John Libbey; 1997. p. 251-64.
-
(1997)
Epilepsy and Other Neurological Disorders in Coeliac Disease
, pp. 251-264
-
-
Holmes, G.K.1
-
18
-
-
0024514799
-
Malignancy in coeliac disease - Effect of a gluten free diet
-
Holmes GK, Prior P, Lane MR, Pope D, Allan RN. Malignancy in coeliac disease - effect of a gluten free diet. Gut 1989; 30: 333-8.
-
(1989)
Gut
, vol.30
, pp. 333-338
-
-
Holmes, G.K.1
Prior, P.2
Lane, M.R.3
Pope, D.4
Allan, R.N.5
-
19
-
-
0019423594
-
Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: A comparison between ABC and unlabeled antibody (PAP) procedures
-
Hsu SM, Raine L, Fanger H. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem 1981; 29: 577-80.
-
(1981)
J Histochem Cytochem
, vol.29
, pp. 577-580
-
-
Hsu, S.M.1
Raine, L.2
Fanger, H.3
-
20
-
-
0030294345
-
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
-
Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, et al. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nat Genet 1996; 14: 285-91.
-
(1996)
Nat Genet
, vol.14
, pp. 285-291
-
-
Imbert, G.1
Saudou, F.2
Yvert, G.3
Devys, D.4
Trottier, Y.5
Garnier, J.M.6
-
21
-
-
0026515461
-
Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity (’celiac sprue’)
-
Marsh MN. Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity (’celiac sprue’). [Review], Gastroenterology 1992; 102: 330-54.
-
(1992)
Gastroenterology
, vol.102
, pp. 330-354
-
-
Marsh, M.N.1
-
22
-
-
0025893355
-
Cerebellar syndrome in adult celiac disease with vitamin E deficiency
-
Mauro A, Orsi L, Mortara P, Costa P, Schiffer D. Cerebellar syndrome in adult celiac disease with vitamin E deficiency. Acta Neurol Scand 1991; 84: 167-70.
-
(1991)
Acta Neurol Scand
, vol.84
, pp. 167-170
-
-
Mauro, A.1
Orsi, L.2
Mortara, P.3
Costa, P.4
Schiffer, D.5
-
23
-
-
0032992333
-
Idiopathic cerebellar ataxia associated with celiac disease: Lack of distinctive neurological features
-
Pellecchia MT, Scala R, Filla A, De Michele G, Ciacci C, Barone P. Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features. J Neurol Neurosurg Psychiatry 1999; 66: 32-5.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.66
, pp. 32-35
-
-
Pellecchia, M.T.1
Scala, R.2
Filla, A.3
De Michele, G.4
Ciacci, C.5
Barone, P.6
-
24
-
-
0029952691
-
Serological screening for coeliac disease: Methodological standards and quality control
-
Stern M, Teuscher M, Wechmann T. Serological screening for coeliac disease: methodological standards and quality control. Acta Paediatr Suppl 1996; 412: 49-51.
-
(1996)
Acta Paediatr Suppl
, vol.412
, pp. 49-51
-
-
Stern, M.1
Teuscher, M.2
Wechmann, T.3
-
25
-
-
0026423260
-
Celiac sprue
-
Trier JS. Celiac sprue. [Review]. N Engl J Med 1991; 325: 1709-18.
-
(1991)
N Engl J Med
, vol.325
, pp. 1709-1718
-
-
Trier, J.S.1
-
26
-
-
0028270213
-
Changing clinical features of coeliac disease
-
Visakorpi JK, Mäki M. Changing clinical features of coeliac disease. Acta Paediatr Suppl 1994; 395: 10-3.
-
(1994)
Acta Paediatr Suppl
, vol.395
, pp. 10-13
-
-
Visakorpi, J.K.1
Mäki, M.2
-
27
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 1997, 15: 62-9.
-
(1997)
Nat Genet
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
Ashizawa, T.4
Stockton, D.W.5
Amos, C.6
|