-
1
-
-
0009628056
-
Dystrophia myotonic and allied diseases
-
ed. Penrose, L.S., Cambridge University Press, Cambridge
-
BELL, J. (1947) Dystrophia myotonic and allied diseases, in Treasury of Human Inheritance 4, Part V, ed. Penrose, L.S., Cambridge University Press, Cambridge.
-
(1947)
Treasury of Human Inheritance
, vol.4
, Issue.PART V
-
-
Bell, J.1
-
2
-
-
0024023153
-
Spreading of the gene for myotonic dystrophy in saguenay (Quebec)
-
BOUCHARD, G., ROY, R., DECLOS, M., KOULADJIAN, K. and MATHIEU, J. (1988) Spreading of the gene for myotonic dystrophy in Saguenay (Quebec). Journal de Génétique Humaine 36, 221-237.
-
(1988)
Journal de Génétique Humaine
, vol.36
, pp. 221-237
-
-
Bouchard, G.1
Roy, R.2
Declos, M.3
Kouladjian, K.4
Mathieu, J.5
-
4
-
-
37349026285
-
A correction for ascertainment bias in estimating rates of onset of highly penetrant genetic disorders
-
ESPINOSA, C. and MACDONALD, A.S. (2007) A correction for ascertainment bias in estimating rates of onset of highly penetrant genetic disorders. ASTIN Bulletin, 37, 429-452.
-
(2007)
ASTIN Bulletin
, vol.37
, pp. 429-452
-
-
Espinosa, C.1
Macdonald, A.S.2
-
5
-
-
33748857886
-
Myotonic dystrophy in Otago, New Zealand
-
FORD, C., KIDD, A. and HAMMOND-TOOKE, G. (2006) Myotonic dystrophy in Otago, New Zealand. New Zealand Medical Journal, 119, U2145
-
(2006)
New Zealand Medical Journal
, vol.119
-
-
Ford, C.1
Kidd, A.2
Hammond-Tooke, G.3
-
6
-
-
84855178531
-
The CTG expansion mutation in myotonic dystrophy: Genotype-phenotype comparisons and the relevance to insurance
-
Unpublished dissertation, University of Nottingham
-
FROHOCK, A.M. (2003) The CTG expansion mutation in myotonic dystrophy: Genotype-phenotype comparisons and the relevance to insurance. Final Year Honours Project. Unpublished dissertation, University of Nottingham.
-
(2003)
Final Year Honours Project
-
-
Frohock, A.M.1
-
7
-
-
84855178534
-
-
Ph.D. Thesis. University of Göttingen
-
GRIMM, T. (1975) Myotonic dystrophy. Ph.D. Thesis. University of Göttingen.
-
(1975)
Myotonic Dystrophy
-
-
Grimm, T.1
-
9
-
-
84855180275
-
A nelson-aalen estimate of the incidence rates of early-onset alzheimer's disease associated with the presenilin-1 gene
-
GUI, E.H. and MACDONALD, A.S. (2002) A Nelson-Aalen estimate of the incidence rates of early-onset Alzheimer's disease associated with the Presenilin-1 gene. ASTIN Bulletin, 32, 1-42.
-
(2002)
ASTIN Bulletin
, vol.32
, pp. 1-42
-
-
Gui, E.H.1
Macdonald, A.S.2
-
10
-
-
84858605753
-
The genetics of breast and ovarian cancer III: A new model of family history with insurance applications
-
GUI, E.H., LU, B., MACDONALD, A.S., WATERS, H.R. and WEKWETE, C. (2006) The genetics of breast and ovarian cancer III: A new model of family history with insurance applications. Scandinavian Actuarial Journal, 2006, 338-367.
-
(2006)
Scandinavian Actuarial Journal
, vol.2006
, pp. 338-367
-
-
Gui, E.H.1
Lu, B.2
Macdonald, A.S.3
Waters, H.R.4
Wekwete, C.5
-
11
-
-
85011195935
-
Adult polycystic kidney disease and critical illness insurance
-
GUTIÉRREZ, C. and MACDONALD, A.S. (2003) Adult polycystic kidney disease and critical illness insurance. North American Actuarial Journal, 7, 93-115.
-
(2003)
North American Actuarial Journal
, vol.7
, pp. 93-115
-
-
Gutiérrez, C.1
Macdonald, A.S.2
-
12
-
-
29144529387
-
Huntington's disease, critical illness insurance and life insurance
-
GUTIÉRREZ, C. and MACDONALD, A.S. (2004) Huntington's disease, critical illness insurance and life insurance. Scandinavian Actuarial Journal, 2004, 279-313.
-
(2004)
Scandinavian Actuarial Journal
, vol.2004
, pp. 279-313
-
-
Gutiérrez, C.1
Macdonald, A.S.2
-
13
-
-
38649101987
-
Adult polycystic kidney disease and insurance: A case study in genetic heterogeneity
-
GUTIÉRREZ, C. and MACDONALD, A.S. (2007) Adult polycystic kidney disease and insurance: A case study in genetic heterogeneity. North American Actuarial Journal, 11, 90-118.
-
(2007)
North American Actuarial Journal
, vol.11
, pp. 90-118
-
-
Gutiérrez, C.1
Macdonald, A.S.2
-
14
-
-
0015878384
-
Pre-symptomatic detection and genetic counselling in myotonic dystrophy
-
HARPER, P.S. (1973) Pre-symptomatic detection and genetic counselling in myotonic dystrophy. Clinical Genetics, 4, 134-140.
-
(1973)
Clinical Genetics
, vol.4
, pp. 134-140
-
-
Harper, P.S.1
-
18
-
-
84855178538
-
Whose hands on your genes?
-
HGC London
-
HGC (2000) Whose hands on your genes? Human Genetics Commission, London.
-
(2000)
Human Genetics Commission
-
-
-
19
-
-
1642264639
-
-
eds. Elston, R., Olson, J. & Palmer, L. John Wiley
-
HODGE, S.E. (2002) Ascertainment, in Biostatistical genetics and genetic epidemiology, eds. Elston, R., Olson, J. & Palmer, L. John Wiley.
-
(2002)
Ascertainment, in Biostatistical Genetics and Genetic Epidemiology
-
-
Hodge, S.E.1
-
21
-
-
0043163661
-
Epidemiological and genetic studies of myotonic dystrophy type 1 in Taiwan
-
DOI 10.1159/000071191
-
HSIAO, K.M., CHEN, S.S., LI, S.Y., CHIANG, S.Y., LIN, H.M., PAN, H., HUANG, C.C., KUO, H.C., JOU, S.B., SU, C.C., RO, L.S., LIU, C.S., LO, M.C., CHEN, C.M. and LIN, C.C. (2003) Epidemiological and genetic studies of myotonic dystrophy type 1 in Taiwan. Neuroepidemiology, 22, 283-289. (Pubitemid 36993909)
-
(2003)
Neuroepidemiology
, vol.22
, Issue.5
, pp. 283-289
-
-
Hsiao, K.M.1
Chen, S.S.2
Li, S.Y.3
Chiang, S.Y.4
Lin, H.M.5
Pan, H.6
Huang, C.C.7
Kuo, H.C.8
Jou, S.B.9
Su, C.C.10
Ro, L.S.11
Liu, C.S.12
Lo, M.C.13
Chen, C.M.14
Lin, C.C.15
-
22
-
-
0343137643
-
La dystrophie myotonique (Steinert) et la myotonie congénitale (Thomsen) en suisse: Étude clinique, génétique et démographique
-
KLEIN, D. (1958) La dystrophie myotonique (Steinert) et la myotonie congénitale (Thomsen) en Suisse: étude clinique, génétique et démographique. Journal de Géné tique Humaine, 7 SUPPL, 1-328.
-
(1958)
Journal de Génétique Humaine
, vol.7
, Issue.SUPPL.
, pp. 1-328
-
-
Klein, D.1
-
23
-
-
0027304415
-
Prevalence of myotonic dystrophy in guipúzcoa (Basque country, Spain)
-
LÓPEZ DE MUNAIN, A., EMPARANZA, J.I., POZA, J.J., MARTÍ MASSÓ, J.F., COBO, A., MARTORELL, L., BAIGET, M. and MARTÍNEZ LAGE, J.M. (1993) Prevalence of myotonic dystrophy in Guipúzcoa (Basque Country, Spain). Neurology, 43, 1573-1576.
-
(1993)
Neurology
, vol.43
, pp. 1573-1576
-
-
López De Munain, A.1
Emparanza, J.I.2
Poza, J.J.3
Martí Massó, J.F.4
Cobo, A.5
Martorell, L.6
Baiget, M.7
Martínez Lage, J.M.8
-
24
-
-
84855179661
-
A dynamic family history model of hereditary nonpolyposis colorectal cancer and critical illness insurance
-
LU, L., MACDONALD, A.S., WATERS, H.R. and YU, F. (2007) A dynamic family history model of hereditary nonpolyposis colorectal cancer and critical illness insurance. Annals of Actuarial Science, 2, 289-325.
-
(2007)
Annals of Actuarial Science
, vol.2
, pp. 289-325
-
-
Lu, L.1
Macdonald, A.S.2
Waters, H.R.3
Yu, F.4
-
26
-
-
0040226082
-
How will improved forecasts of individual lifetimes affect underwriting?
-
MACDONALD, A.S. (1997) How will improved forecasts of individual lifetimes affect underwriting? British Actuarial Journal, 3, 1044-1058.
-
(1997)
British Actuarial Journal
, vol.3
, pp. 1044-1058
-
-
Macdonald, A.S.1
-
27
-
-
85011186795
-
Modelling the impact of genetics on insurance
-
MACDONALD, A.S. (1999) Modelling the impact of genetics on insurance. North American Actuarial Journal, 3, 83-101.
-
(1999)
North American Actuarial Journal
, vol.3
, pp. 83-101
-
-
Macdonald, A.S.1
-
28
-
-
34548225357
-
Genetics and insurance: What we have learned so far?
-
MACDONALD, A.S. (2003a) Genetics and insurance: What we have learned so far? Scandinavian Actuarial Journal, 2003, 324-328.
-
(2003)
Scandinavian Actuarial Journal
, vol.2003
, pp. 324-328
-
-
Macdonald, A.S.1
-
29
-
-
17444418746
-
Moratoria on the use of genetic tests and family history for mortgagerelated life insurance
-
MACDONALD, A.S. (2003b) Moratoria on the use of genetic tests and family history for mortgagerelated life insurance. British Actuarial Journal, 9, 279-311.
-
(2003)
British Actuarial Journal
, vol.9
, pp. 279-311
-
-
Macdonald, A.S.1
-
30
-
-
37349035563
-
The genetics of breast and ovarian cancer I: A model of family history
-
MACDONALD, A.S., WATERS, H.R. and WEKWETE, C.T. (2003a) The genetics of breast and ovarian cancer I: A model of family history. Scandinavian Actuarial Journal, 2003, 1-27.
-
(2003)
Scandinavian Actuarial Journal
, vol.2003
, pp. 1-27
-
-
Macdonald, A.S.1
Waters, H.R.2
Wekwete, C.T.3
-
31
-
-
33847743999
-
The genetics of breast and ovarian cancer II: A model of critical insurance
-
MACDONALD, A.S., WATERS, H.R. and WEKWETE, C.T. (2003b) The genetics of breast and ovarian cancer II: A model of critical insurance. Scandinavian Actuarial Journal, 2003, 28-50.
-
(2003)
Scandinavian Actuarial Journal
, vol.2003
, pp. 28-50
-
-
Macdonald, A.S.1
Waters, H.R.2
Wekwete, C.T.3
-
32
-
-
77949296032
-
Multifactorial genetic disorders and adverse selection: Epidemiology meets economics
-
MACDONALD, A.S. and TAPADAR, P. (2010) Multifactorial genetic disorders and adverse selection: Epidemiology meets economics. Journal of Risk and Insurance, 77(1), 155-182.
-
(2010)
Journal of Risk and Insurance
, vol.77
, Issue.1
, pp. 155-182
-
-
Macdonald, A.S.1
Tapadar, P.2
-
34
-
-
0026005970
-
Single-gene neurological disorders in south wales: An epidemiological study
-
MACMILLAN, J.C., and HARPER, P.S. (1991) Single-gene neurological disorders in South Wales: an epidemiological study. Annals of Neurology, 30, 411-414.
-
(1991)
Annals of Neurology
, vol.30
, pp. 411-414
-
-
Macmillan, J.C.1
Harper, P.S.2
-
35
-
-
0033499746
-
The epidemiology of myotonic dystrophy in Northern Ireland
-
MAGEE, A. and NEVIN, N.C. (1999) The epidemiology of myotonic dystrophy in Northern Ireland. Community Genetics, 2, 179-183. (Pubitemid 30415623)
-
(1999)
Community Genetics
, vol.2
, Issue.4
, pp. 179-183
-
-
Magee, A.1
Nevin, N.C.2
-
36
-
-
0025266778
-
Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)
-
MATHIEU, J., BRAEKELEER, M. and PRÉVOST, C. (1990) Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada). Neurology, 40, 839-842. (Pubitemid 20159628)
-
(1990)
Neurology
, vol.40
, Issue.5
, pp. 839-842
-
-
Mathieu, J.1
De Braekeleer, M.2
Prevost, C.3
-
37
-
-
0030996220
-
Genetic epidemiology of myotonic dystrophy in Istria, Croatia
-
MEDICA, I., MARKOVIC, D., and PETERLIN, B. (1997) Genetic epidemiology of myotonic dystrophy in Istria, Croatia. Acta Neurologica Scandinavica, 95(3), 164-166. (Pubitemid 27149405)
-
(1997)
Acta Neurologica Scandinavica
, vol.95
, Issue.3
, pp. 164-166
-
-
Medica, I.1
Markovic, D.2
Peterlin, B.3
-
38
-
-
27344436504
-
Epidemiology of myotonic dystrophy type 1 in the population of central Serbia
-
MLADENOVIC, J., PEKMEZOVIC, T., TODOROVIC, S., RAKOCEVIC-STOJANOVIC, V., ROMAC, S. and APOSTOLSKI, S. (2005) Epidemiology of myotonic dystrophy type 1 in the population of central Serbia. Vojnosanitetski pregled, 62, 377-382.
-
(2005)
Vojnosanitetski Pregled
, vol.62
, pp. 377-382
-
-
Mladenovic, J.1
Pekmezovic, T.2
Todorovic, S.3
Rakocevic-Stojanovic, V.4
Romac, S.5
Apostolski, S.6
-
39
-
-
33744750564
-
Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade
-
DOI 10.1111/j.1468-1331.2006.01261.x
-
MLADENOVIC, J., PEKMEZOVIC, T., TODOROVIC, S., RAKOCEVIC-STOJANOVIC, V., SAVIC, D., ROMAC, S., and APOSTOLSKI, S. (2006) Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade. European Journal of Neurology, 13, 451-454. (Pubitemid 43823357)
-
(2006)
European Journal of Neurology
, vol.13
, Issue.5
, pp. 451-454
-
-
Mladenovic, J.1
Pekmezovic, T.2
Todorovic, S.3
Rakocevic-Stojanovic, V.4
Savic, D.5
Romac, S.6
Apostolski, S.7
-
40
-
-
0031105931
-
The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats
-
MOR-COHEN, R., MAGAL, N., GADOTH, N., ACHIRON, A., SHOHAT, T. and SHOHAT, M. (1997) The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats. Israeli Journal of Medical Science, 33, 190-193. (Pubitemid 27410090)
-
(1997)
Israel Journal of Medical Sciences
, vol.33
, Issue.3
, pp. 190-193
-
-
Mor-Cohen, R.1
Magal, N.2
Gadoth, N.3
Achiron, A.4
Shohat, T.5
Shohat, M.6
-
41
-
-
0023261759
-
Genetic epidemiology of myotonic dystrophy
-
MOSTACCIULOL, M.L., BARBUJANI, G., ARMANI, M., DANIELI, G.A. and ANGELINI, C. (1987) Genetic epidemiology of myotonic dystrophy. Genetic Epidemiology, 4, 289-298. (Pubitemid 17142430)
-
(1987)
Genetic Epidemiology
, vol.4
, Issue.4
, pp. 289-298
-
-
Mostacciuolo, M.L.1
Barbujani, G.2
Armani, M.3
Danieli, G.A.4
Angelini, C.5
-
42
-
-
0020983310
-
Myotonic dystrophy
-
NESTEROV, L.N., SUSHCHEVA, G.P., VIATKINA, S., and NESTEROVA, I. (1983) Myotonic Dystrophy. Zh Nevropatol Psikhiatr Im S S Korsakova, 83, 1634-1641.
-
(1983)
Zh Nevropatol Psikhiatr im S S Korsakova
, vol.83
, pp. 1634-1641
-
-
Nesterov, L.N.1
Sushcheva, G.P.2
Viatkina, S.3
Nesterova, I.4
-
43
-
-
0021063874
-
Genetic epidemiology of myotonic dystrophy in Kagoshima and Okinawa districts in Japan
-
OSAME, M. and FURUSHO, T. (1983) Genetic epidemiology of myotonic dystrophy in Kagoshima and Okinawa districts in Japan. Rinsho Shinkeigaku, 23, 1067-1071. (Pubitemid 14167427)
-
(1983)
Clinical Neurology
, vol.23
, Issue.12
, pp. 1067-1071
-
-
Osame, M.1
Furusho, T.2
-
46
-
-
0035002073
-
Epidemiology of myotonic dystrophy in Italy: Re-apprisal after genetic diagnosis
-
DOI 10.1034/j.1399-0004.2001.590508.x
-
SICILIANO, G., MANCA, M., GENNARELLI, M., ANGELINI, C., ROCCHI, A., IUDICE, A., MIORIN, M. and MOSTACCIULOL, M. (2001) Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis. Clinical Genetics, 59, 344-349. (Pubitemid 32451973)
-
(2001)
Clinical Genetics
, vol.59
, Issue.5
, pp. 344-349
-
-
Siciliano, G.1
Manca, M.L.2
Gennarelli, M.3
Angelini, C.4
Rocchi, A.5
Iudice, A.6
Miorin, M.7
Mostacciuolo, M.L.8
-
47
-
-
0004207391
-
-
Universitetsforlaget
-
THOMASEN, E. (1948) Myotonia. Universitetsforlaget.
-
(1948)
Myotonia
-
-
Thomasen, E.1
-
48
-
-
84855183292
-
Report by the independent actuary on the application by the association of British insurers to the genetics and insurance committee for approval to use genetic test results for insurance risk assessment - Use of huntington's disease test in life insurance
-
Department of Health, London
-
WILKIE, A.D. (2000) Report by the independent actuary on the application by the Association of British Insurers to the Genetics and Insurance Committee for approval to use genetic test results for insurance risk assessment - use of Huntington's disease test in life insurance. Genetics and Insurance Committee, Department of Health, London.
-
(2000)
Genetics and Insurance Committee
-
-
Wilkie, A.D.1
|