-
1
-
-
0024297398
-
Vincent van Gogh and the thujone connection
-
Arnold WN. 1988. Vincent van Gogh and the thujone connection. JAMA 260:3042-3044.
-
(1988)
JAMA
, vol.260
, pp. 3042-3044
-
-
Arnold, W.N.1
-
3
-
-
33646206120
-
-
New York: Alfred A. Knopf
-
Ayling S. 1972. George the Third. New York: Alfred A. Knopf. p 15-461.
-
(1972)
George the Third
, pp. 15-461
-
-
Ayling, S.1
-
4
-
-
0032574641
-
Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997
-
Beighton P, De Paepe A, Steinmann B, Tsipouras P, Wenstrup RJ. 1998. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Am J Med Genet 77:31-37.
-
(1998)
Am J Med Genet
, vol.77
, pp. 31-37
-
-
Beighton, P.1
De Paepe, A.2
Steinmann, B.3
Tsipouras, P.4
Wenstrup, R.J.5
-
6
-
-
84944967356
-
-
Westport, CT: Greenwood Press
-
De Saussune R. 1970. Paganini. Westport, CT: Greenwood Press.
-
(1970)
Paganini
-
-
De Saussune, R.1
-
8
-
-
0028831359
-
Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype
-
Eldadah ZA, Brenn T, Furthmayr H, Dietz HC. 1995. Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype. J Clin Invest 95:874-880.
-
(1995)
J Clin Invest
, vol.95
, pp. 874-880
-
-
Eldadah, Z.A.1
Brenn, T.2
Furthmayr, H.3
Dietz, H.C.4
-
11
-
-
0029317231
-
What dwarfed Toulouse-Lautrec?
-
Frey JB. 1995a. What dwarfed Toulouse-Lautrec? Nat Genet 10:128-130.
-
(1995)
Nat Genet
, vol.10
, pp. 128-130
-
-
Frey, J.B.1
-
12
-
-
84966171004
-
In reply: Toulouse-Lautrec's diagnosis
-
Frey JB. 1995b. In reply: Toulouse-Lautrec's diagnosis. Nat Genet 11:363.
-
(1995)
Nat Genet
, vol.11
, pp. 363
-
-
Frey, J.B.1
-
14
-
-
0029809357
-
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency
-
Gelb B, Shi G-P, Chapman H, Desnick R. 1996. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science 273:1236-1238.
-
(1996)
Science
, vol.273
, pp. 1236-1238
-
-
Gelb, B.1
Shi, G.-P.2
Chapman, H.3
Desnick, R.4
-
15
-
-
0025030265
-
Genetic mapping of common diseases: The challenges of manic-depressive illness and schizophrenia
-
Gershon ES, Martinez N, Goldin LR, Gejman PV. 1990. Genetic mapping of common diseases: the challenges of manic-depressive illness and schizophrenia. Trends Genet 6:282-287.
-
(1990)
Trends Genet
, vol.6
, pp. 282-287
-
-
Gershon, E.S.1
Martinez, N.2
Goldin, L.R.3
Gejman, P.V.4
-
16
-
-
0043132844
-
Abraham Lincoln: Medical appraisal
-
Gordon AM. 1962. Abraham Lincoln: medical appraisal. J Kentucky Med Assoc 60:249-253.
-
(1962)
J Kentucky Med Assoc
, vol.60
, pp. 249-253
-
-
Gordon, A.M.1
-
18
-
-
33646213429
-
-
Lexington: University Press of Kentucky
-
Harrison LH. 2000. Lincoln of Kentucky. Lexington: University Press of Kentucky. p 36.
-
(2000)
Lincoln of Kentucky
, pp. 36
-
-
Harrison, L.H.1
-
20
-
-
0005876390
-
The illness of Vincent Van Gogh
-
Hemphill RE. 1961. The illness of Vincent van Gogh. Proc R Soc Med 54:1083-1088.
-
(1961)
Proc R Soc Med
, vol.54
, pp. 1083-1088
-
-
Hemphill, R.E.1
-
21
-
-
33646226864
-
-
Springfield, IL: Herndon's Lincoln Publishing
-
Herndon WH, Weik JW. 1921. Herndon's Lincoln, vol. 2. Springfield, IL: Herndon's Lincoln Publishing. p 408.
-
(1921)
Herndon's Lincoln
, vol.2
, pp. 408
-
-
Herndon, W.H.1
Weik, J.W.2
-
23
-
-
0032880960
-
Mutations of CTSK result in pycnodysostosis via a reduction of cathepsin K protein
-
Ho N, Punturieri A, Wilkin D, Szabo J, Johnson M, Whaley J, Davis J, Clark A, Weiss S, Francomano C. 1999. Mutations of CTSK result in pycnodysostosis via a reduction of cathepsin K protein. J Bone Miner Res 14:1649-1653.
-
(1999)
J Bone Miner Res
, vol.14
, pp. 1649-1653
-
-
Ho, N.1
Punturieri, A.2
Wilkin, D.3
Szabo, J.4
Johnson, M.5
Whaley, J.6
Davis, J.7
Clark, A.8
Weiss, S.9
Francomano, C.10
-
24
-
-
33646224513
-
-
New York: St. Martin's Press
-
Hough R. 1996. Victoria and Albert. New York: St. Martin's Press. p 1-210.
-
(1996)
Victoria and Albert
, pp. 1-210
-
-
Hough, R.1
-
26
-
-
0029800843
-
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis
-
Johnson M, Polymeropoulos M, Vos H, de Ortiz Luna R, Francomano C. 1996. A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis. Genome Res 6:1050-1055.
-
(1996)
Genome Res
, vol.6
, pp. 1050-1055
-
-
Johnson, M.1
Polymeropoulos, M.2
Vos, H.3
De Ortiz Luna, R.4
Francomano, C.5
-
27
-
-
0010976492
-
Abraham Lincoln's organic and emotional neurosis
-
Kempf EJ. 1952. Abraham Lincoln's organic and emotional neurosis. AMA Arch Neurol Psychiatry 67:419-433.
-
(1952)
AMA Arch Neurol Psychiatry
, vol.67
, pp. 419-433
-
-
Kempf, E.J.1
-
29
-
-
0026349315
-
Vincent can Gogh's illness: Acute intermittent porphyria?
-
Loftus LS, Arnold WN. 1991. Vincent can Gogh's illness: acute intermittent porphyria? Br Med J 303:1589-1591.
-
(1991)
Br Med J
, vol.303
, pp. 1589-1591
-
-
Loftus, L.S.1
Arnold, W.N.2
-
31
-
-
0014404385
-
Porphyria in the royal houses of Stuart, Hanover, and Prussia: A follow-up study of George III's illness
-
Macalpine I, Hunter R, Rimington C. 1968. Porphyria in the royal houses of Stuart, Hanover, and Prussia: a follow-up study of George III's illness. Br Med J 1:7-18.
-
(1968)
Br Med J
, vol.1
, pp. 7-18
-
-
Macalpine, I.1
Hunter, R.2
Rimington, C.3
-
32
-
-
0035822038
-
The hemophilias - From royal genes to gene therapy
-
Mannucci PM, Tuddenham EGD. 2001. The hemophilias - from royal genes to gene therapy. N Engl J Med 344:1773-1779.
-
(2001)
N Engl J Med
, vol.344
, pp. 1773-1779
-
-
Mannucci, P.M.1
Tuddenham, E.G.D.2
-
33
-
-
84966157547
-
Toulouse-Lautrec's diagnosis
-
Maroteaux P. 1995. Toulouse-Lautrec's diagnosis. Nat Genet 11:362.
-
(1995)
Nat Genet
, vol.11
, pp. 362
-
-
Maroteaux, P.1
-
34
-
-
73649185887
-
La pyknodysostose
-
Maroteaux P, Lamy M. 1962. La pyknodysostose. Presse Med 38:999-1002.
-
(1962)
Presse Med
, vol.38
, pp. 999-1002
-
-
Maroteaux, P.1
Lamy, M.2
-
35
-
-
0001824376
-
The royal hemophilia
-
McKusick VA. 1965. The royal hemophilia. Sci Am 213:88-95.
-
(1965)
Sci Am
, vol.213
, pp. 88-95
-
-
McKusick, V.A.1
-
36
-
-
0025912424
-
The defect in Marfan syndrome
-
McKusick VA. 1991. The defect in Marfan syndrome. Nature 352:279-281.
-
(1991)
Nature
, vol.352
, pp. 279-281
-
-
McKusick, V.A.1
-
37
-
-
36849145505
-
Abraham Lincoln and Marfan syndrome
-
McKusick VA. 1991. Abraham Lincoln and Marfan syndrome. Nature 352:280.
-
(1991)
Nature
, vol.352
, pp. 280
-
-
McKusick, V.A.1
-
38
-
-
0030140415
-
A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria
-
Meissner PN, Dailey TA, Hift RJ, Ziman M, Corrigall AV, Roberts AG, Meissner DM, Kirsch RE, Dailey HA. 1996. A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria. Nat Genet 13:95-97.
-
(1996)
Nat Genet
, vol.13
, pp. 95-97
-
-
Meissner, P.N.1
Dailey, T.A.2
Hift, R.J.3
Ziman, M.4
Corrigall, A.V.5
Roberts, A.G.6
Meissner, D.M.7
Kirsch, R.E.8
Dailey, H.A.9
-
39
-
-
0017889675
-
Variegate porphyria
-
Mustajoki P. 1978. Variegate porphyria. Ann Intern Med 89:238-244.
-
(1978)
Ann Intern Med
, vol.89
, pp. 238-244
-
-
Mustajoki, P.1
-
41
-
-
0043132846
-
-
Boston: Little, Brown
-
Randall PR. 1955. Lincoln's sons. Boston: Little, Brown. p 7,307,308.
-
(1955)
Lincoln's Sons
, pp. 7
-
-
Randall, P.R.1
-
42
-
-
33646216293
-
-
New York: Abradale Press
-
Schapiro M. 1993. Vincent van Gogh. New York: Abradale Press. p 1-10.
-
(1993)
Vincent Van Gogh
, pp. 1-10
-
-
Schapiro, M.1
-
43
-
-
0017837987
-
Nicolo Paganini: Musical magician and Marfan mutant?
-
Schonfeld M. 1978. Nicolo Paganini: musical magician and Marfan mutant? JAMA 239:40-42.
-
(1978)
JAMA
, vol.239
, pp. 40-42
-
-
Schonfeld, M.1
-
44
-
-
33646208966
-
Abraham Lincoln and the Marfan syndrome
-
Schwartz H. 1964. Abraham Lincoln and the Marfan syndrome. JAMA 187:473-479.
-
(1964)
JAMA
, vol.187
, pp. 473-479
-
-
Schwartz, H.1
-
47
-
-
0033109018
-
The history of haemophilia in the royal families of Europe
-
Stevens RF. 1999. The history of haemophilia in the royal families of Europe. Br J Haemat 105:25-32.
-
(1999)
Br J Haemat
, vol.105
, pp. 25-32
-
-
Stevens, R.F.1
-
53
-
-
0029039191
-
Fatal hemoptysis in Ehlers-Danlas syndrome. Old malady with a neu-curse
-
Yost BA, Vogelsang JP, Lie JT. 1995. Fatal hemoptysis in Ehlers-Danlas syndrome. Old malady with a neu-curse. Chest 107:1465-1467.
-
(1995)
Chest
, vol.107
, pp. 1465-1467
-
-
Yost, B.A.1
Vogelsang, J.P.2
Lie, J.T.3
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