-
2
-
-
0034614125
-
Clinical features of and recent advances in therapy for Fabry disease
-
Brady RO, Schiffmann R (2000). Clinical features of and recent advances in therapy for Fabry disease. J Am Med Assoc 284:2771-2775.
-
(2000)
J Am Med Assoc
, vol.284
, pp. 2771-2775
-
-
Brady, R.O.1
Schiffmann, R.2
-
3
-
-
0034502483
-
Fabry disease. Clinical and genetic aspects. Therapeutic perspectives
-
Germain DP (2000). Fabry disease. Clinical and genetic aspects. Therapeutic perspectives. Rev Med Interne 21:1086-1103.
-
(2000)
Rev Med Interne
, vol.21
, pp. 1086-1103
-
-
Germain, D.P.1
-
4
-
-
0027373749
-
Psychiatric disorders in patients with Fabry's diseaes
-
Grewal RP (1993). Psychiatric disorders in patients with Fabry's diseaes. Int J Psychiatry Med 23:307-312.
-
(1993)
Int J Psychiatry Med
, vol.23
, pp. 307-312
-
-
Grewal, R.P.1
-
5
-
-
0035113346
-
Histopathologic findings of cornea verticillata in a woman heterozygous for Fabry's disease
-
Hirano K, Murata K, Miyagawa A, Terasaki H, Saigusa J, Nagasaka T, Kobayashi M (2001). Histopathologic findings of cornea verticillata in a woman heterozygous for Fabry's disease. Cornea 20:233-236.
-
(2001)
Cornea
, vol.20
, pp. 233-236
-
-
Hirano, K.1
Murata, K.2
Miyagawa, A.3
Terasaki, H.4
Saigusa, J.5
Nagasaka, T.6
Kobayashi, M.7
-
6
-
-
0034622451
-
Canadian normative data for the SF-36 health survey
-
Hopman WH, Towheed T, Anastassiades T, Tenenhouse A, Poliquin S, Berger C, et al., and The Canadian Multicentre Osteoporosis Study Research Group (2000). Canadian normative data for the SF-36 health survey. Canadian Medical Association Journal (CMAJ) 163:265-271.
-
(2000)
Canadian Medical Association Journal (CMAJ)
, vol.163
, pp. 265-271
-
-
Hopman, W.H.1
Towheed, T.2
Anastassiades, T.3
Tenenhouse, A.4
Poliquin, S.5
Berger, C.6
-
7
-
-
0025852268
-
Fabry disease in a large Nova Scotia kindred: Carrier detection using leucocyte alpha-galactosidase activity and an Ncol polymorphism detected by an alpha-galactosidase cDNA clone
-
Kirkilionis AJ, Riddell DC, Spence MW, Fenwick RG (1991). Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an Ncol polymorphism detected by an alpha-galactosidase cDNA clone. J Med Genet 28:232-240.
-
(1991)
J Med Genet
, vol.28
, pp. 232-240
-
-
Kirkilionis, A.J.1
Riddell, D.C.2
Spence, M.W.3
Fenwick, R.G.4
-
8
-
-
0034627356
-
Fabry's disease; towards a treatment
-
Linthorst GE, Hollak CE, Bosman DK, Heymans HS, Aerts JM (2000). Fabry's disease; towards a treatment. Ned Tijdschr Geneeskd 144:2391-2395.
-
(2000)
Ned Tijdschr Geneeskd
, vol.144
, pp. 2391-2395
-
-
Linthorst, G.E.1
Hollak, C.E.2
Bosman, D.K.3
Heymans, H.S.4
Aerts, J.M.5
-
9
-
-
0034754467
-
Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 60 obligate carrier females
-
MacDermot KD, Holmes A, Miners AH (2001). Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet 38:769-775.
-
(2001)
J Med Genet
, vol.38
, pp. 769-775
-
-
MacDermot, K.D.1
Holmes, A.2
Miners, A.H.3
-
10
-
-
0025360465
-
The neurological complications of Anderson-Fabry disease (alpha-galactosidase A deficiency) - Investigation of symptomatic and presymptomatic patients
-
Morgan SH, Rudge P, Smith SJ, Bronstein AM, Kendall BE, Holly E, et al. (1990). The neurological complications of Anderson-Fabry disease (alpha-galactosidase A deficiency) - investigation of symptomatic and presymptomatic patients. Q J Med 75:491-507.
-
(1990)
Q J Med
, vol.75
, pp. 491-507
-
-
Morgan, S.H.1
Rudge, P.2
Smith, S.J.3
Bronstein, A.M.4
Kendall, B.E.5
Holly, E.6
-
11
-
-
0035666723
-
Standardizing the Hamilton Depression Rating Scale: Past, present, and future
-
Williams JB (2001). Standardizing the Hamilton Depression Rating Scale: past, present, and future. Eur Arch Psychiatry Clin Neurosci 251 (suppl 2):116-1112.
-
(2001)
Eur Arch Psychiatry Clin Neurosci
, vol.251
, Issue.SUPPL. 2
, pp. 116-1112
-
-
Williams, J.B.1
-
12
-
-
0035178136
-
Molecular genetic, biochemical, and clinical studies in three families with cardiac Fabry's disease
-
Yoshitama T, Nakao S, Takenaka T, Teraguchi H, Sasaki T, Kodama C, et al. (2001). Molecular genetic, biochemical, and clinical studies in three families with cardiac Fabry's disease. Am J Cardiol 87:71-75.
-
(2001)
Am J Cardiol
, vol.87
, pp. 71-75
-
-
Yoshitama, T.1
Nakao, S.2
Takenaka, T.3
Teraguchi, H.4
Sasaki, T.5
Kodama, C.6
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