-
2
-
-
0028031125
-
Guidelines for the molecular genetics predictive test in Huntington's disease
-
Broholm J, Cassiman JJ, Craufurd D et al. (1994), Guidelines for the molecular genetics predictive test in Huntington's disease. Neurology 44:1533-1536
-
(1994)
Neurology
, vol.44
, pp. 1533-1536
-
-
Broholm, J.1
Cassiman, J.J.2
Craufurd, D.3
-
3
-
-
0033981585
-
Genetics of childhood disorders: X. Huntington disease
-
DiFiglia M (2000), Genetics of childhood disorders: X. Huntington disease. J Am Acad Child Adolesc Psychiatry 39:120-122
-
(2000)
J Am Acad Child Adolesc Psychiatry
, vol.39
, pp. 120-122
-
-
DiFiglia, M.1
-
4
-
-
0036080240
-
Chorea Huntington: A rare case of childhood onset
-
Gencik M, Hammans C, Strehl H, Wagner N, Epplen JT (2002), Chorea Huntington: a rare case of childhood onset. Neuropediatrics 33:90-92
-
(2002)
Neuropediatrics
, vol.33
, pp. 90-92
-
-
Gencik, M.1
Hammans, C.2
Strehl, H.3
Wagner, N.4
Epplen, J.T.5
-
5
-
-
0021028244
-
A polymorphic DNA marker genetically linked to Huntington's disease
-
Gusella JF, Wexler NS, Conneally PM (1983), A polymorphic DNA marker genetically linked to Huntington's disease. Nature 306:234-238
-
(1983)
Nature
, vol.306
, pp. 234-238
-
-
Gusella, J.F.1
Wexler, N.S.2
Conneally, P.M.3
-
7
-
-
0027340292
-
Neuropsychological and neuroradiological study of a case of early-onset Huntington's chorea
-
Lenti C, Bianchini E (1993), Neuropsychological and neuroradiological study of a case of early-onset Huntington's chorea. Dev Med Child Neurol 35:1007-1014
-
(1993)
Dev Med Child Neurol
, vol.35
, pp. 1007-1014
-
-
Lenti, C.1
Bianchini, E.2
-
8
-
-
0028168638
-
The aetiology and pathogenesis of Huntington's disease: Recent advances
-
Meierkord H, Pfeiffer L, Ludolph A (1994), The aetiology and pathogenesis of Huntington's disease: recent advances. Nervenarzt 65:519-526
-
(1994)
Nervenarzt
, vol.65
, pp. 519-526
-
-
Meierkord, H.1
Pfeiffer, L.2
Ludolph, A.3
-
9
-
-
0034847765
-
Juvenile onset Huntington's disease: Clinical and research perspectives
-
Nance MA, Myers RH (2001), Juvenile onset Huntington's disease: clinical and research perspectives. Ment Retard Disabil Res Rev 7:153-157
-
(2001)
Ment Retard Disabil Res Rev
, vol.7
, pp. 153-157
-
-
Nance, M.A.1
Myers, R.H.2
-
10
-
-
0032946333
-
The genetic self. The human genome project, genetic counselling and family therapy
-
Peters J, Djurdjinovic L, Baker D (1999), The genetic self. The human genome project, genetic counselling and family therapy. Fam Syst Health 17:5-25
-
(1999)
Fam Syst Health
, vol.17
, pp. 5-25
-
-
Peters, J.1
Djurdjinovic, L.2
Baker, D.3
-
11
-
-
0029007707
-
Exploration of the effects of predictive testing for Huntington disease on intimate relationships
-
Quaid K, Wesson M (1995), Exploration of the effects of predictive testing for Huntington disease on intimate relationships. Am J Med Genet 57:46-51
-
(1995)
Am J Med Genet
, vol.57
, pp. 46-51
-
-
Quaid, K.1
Wesson, M.2
-
12
-
-
0033771298
-
Huntington disease in children: Genotype-phenotype correlation
-
Rasmussen A, Macias R, Yescas P, Ochoa A, Davila G, Alonso E (2000), Huntington disease in children: genotype-phenotype correlation. Neuropediatrics 31:190-194
-
(2000)
Neuropediatrics
, vol.31
, pp. 190-194
-
-
Rasmussen, A.1
Macias, R.2
Yescas, P.3
Ochoa, A.4
Davila, G.5
Alonso, E.6
-
13
-
-
0025482960
-
Anticipatory loss: A family systems developmental framework
-
Rolland J (1990), Anticipatory loss: a family systems developmental framework. Fam Process 29:229-244
-
(1990)
Fam Process
, vol.29
, pp. 229-244
-
-
Rolland, J.1
-
14
-
-
0025059035
-
Ethical issues policy statement on Huntington's disease molecular genetics predictive test
-
Went L (1990), Ethical issues policy statement on Huntington's disease molecular genetics predictive test. J Med Genet 27:34-38
-
(1990)
J Med Genet
, vol.27
, pp. 34-38
-
-
Went, L.1
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