-
3
-
-
0000043603
-
Over cen zeer merkwaardige, gecombineerde familiaire polyposis van de slijmvliezen van den tractus intestinalis met die van de neuskeelholte en gepaard met eigenaardige pigmentaties van huid en slijmvliezen
-
Peutz JLA. Over cen zeer merkwaardige, gecombineerde familiaire polyposis van de slijmvliezen van den tractus intestinalis met die van de neuskeelholte en gepaard met eigenaardige pigmentaties van huid en slijmvliezen. Ned Maandschr Geneeskd 1921;10:134-46.
-
(1921)
Ned Maandschr Geneeskd
, vol.10
, pp. 134-146
-
-
Peutz, J.L.A.1
-
4
-
-
0000152018
-
Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits
-
Jeghers H, McKusick VA, Katz KH. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits. N Engl J Med 1949;241:992-1005, 1031-6.
-
(1949)
N Engl J Med
, vol.241
, pp. 992-1005
-
-
Jeghers, H.1
McKusick, V.A.2
Katz, K.H.3
-
5
-
-
0024400328
-
Gastrointestinal polyposis syndromes
-
Finan MC, Ray MK. Gastrointestinal polyposis syndromes. Dermatol Clin 1989;7:419-34.
-
(1989)
Dermatol Clin
, vol.7
, pp. 419-434
-
-
Finan, M.C.1
Ray, M.K.2
-
7
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 1998;391:184-7.
-
(1998)
Nature
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
-
8
-
-
17344367301
-
Peutz-Jeghers disease: Most, but not all, families are compatible with linkage to 19p13.3
-
Olschwang S, Markie D, Seal S, Neale K, Phillips R, Cottrell S. et al. Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. J Med Genet 1998;35:42-4.
-
(1998)
J Med Genet
, vol.35
, pp. 42-44
-
-
Olschwang, S.1
Markie, D.2
Seal, S.3
Neale, K.4
Phillips, R.5
Cottrell, S.6
-
9
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, et al. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 1998;18:38-43.
-
(1998)
Nat Genet
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, H.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
-
10
-
-
0033012429
-
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families
-
Westerman AM, Entius MM, Boor PPC, Koole R, Baar E de, Offerhaus GJA, et al. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. Hum Mutat 1999;13:476-81.
-
(1999)
Hum Mutat
, vol.13
, pp. 476-481
-
-
Westerman, A.M.1
Entius, M.M.2
Boor, P.P.C.3
Koole, R.4
De Baar, E.5
Offerhaus, G.J.A.6
-
11
-
-
17344365130
-
Peutz-Jeghers syndrome: Confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4
-
Mehenni H, Blouin JL, Radhakrishna U, Bhardwaj SS, Bhardwaj K, Dixit VB. et al. Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4. Am J Hum Genet 1997;61:1327-34.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1327-1334
-
-
Mehenni, H.1
Blouin, J.L.2
Radhakrishna, U.3
Bhardwaj, S.S.4
Bhardwaj, K.5
Dixit, V.B.6
-
12
-
-
0031662147
-
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome
-
Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, et al. Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome. Hum Genet 1998;103:168-72.
-
(1998)
Hum Genet
, vol.103
, pp. 168-172
-
-
Nakagawa, H.1
Koyama, K.2
Miyoshi, Y.3
Ando, H.4
Baba, S.5
Watatani, M.6
-
13
-
-
0032471851
-
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity
-
Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, et al. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity. Am J Hum Genet 1998; 63:1641-50.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1641-1650
-
-
Mehenni, H.1
Gehrig, C.2
Nezu, J.3
Oku, A.4
Shimane, M.5
Rossier, C.6
-
14
-
-
0019403076
-
Does Peutz-Jeghers syndrome predispose to gastrointestinal malignancy? A later look
-
Linos DA, Dozois RR, Dahlin DC, Bartholomew LG. Does Peutz-Jeghers syndrome predispose to gastrointestinal malignancy? A later look. Arch Surg 1981;116:1182-4.
-
(1981)
Arch Surg
, vol.116
, pp. 1182-1184
-
-
Linos, D.A.1
Dozois, R.R.2
Dahlin, D.C.3
Bartholomew, L.G.4
-
15
-
-
0023192463
-
Increased risk of cancer in the Peutz-Jeghers syndrome
-
Giardiello FM, Welsh SB, Hamilton SR, Offerhaus GJA, Gittelsohn AM, Booker SV, et al. Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Mod 1987;316:1511-4.
-
(1987)
N Engl J Mod
, vol.316
, pp. 1511-1514
-
-
Giardiello, F.M.1
Welsh, S.B.2
Hamilton, S.R.3
Offerhaus, G.J.A.4
Gittelsohn, A.M.5
Booker, S.V.6
-
16
-
-
0024238366
-
Peutz-Jeghers syndrome: A clinicopathologic survey of the 'Harrishurg family' with a 49-year follow-up
-
Foley TR, McGarrity TJ, Abt AB. Peutz-Jeghers syndrome: a clinicopathologic survey of the 'Harrishurg family' with a 49-year follow-up. Gastroenterology 1988;95:1535-40.
-
(1988)
Gastroenterology
, vol.95
, pp. 1535-1540
-
-
Foley, T.R.1
McGarrity, T.J.2
Abt, A.B.3
-
18
-
-
15444350943
-
Increased risk for cancer in patients with the Peutz-Jeghers syndrome
-
Boardman LA, Thibodeau SN, Schaid DJ, Lindor NM, McDonnell SK, Burgart LJ, et al. Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 1998;128:896-9.
-
(1998)
Ann Intern Med
, vol.128
, pp. 896-899
-
-
Boardman, L.A.1
Thibodeau, S.N.2
Schaid, D.J.3
Lindor, N.M.4
McDonnell, S.K.5
Burgart, L.J.6
-
19
-
-
0033541557
-
Peutz-Jeghers syndrome: 78-year follow-up of the original family
-
Westerman AM, Entius MM, Baar E de, Boor PPC, Koole R, Velthuysen MLF van, et al. Peutz-Jeghers syndrome: 78-year follow-up of the original family. Lancet 1999;353:1211-5.
-
(1999)
Lancet
, vol.353
, pp. 1211-1215
-
-
Westerman, A.M.1
Entius, M.M.2
De Baar, E.3
Boor, P.P.C.4
Koole, R.5
Van Velthuysen, M.L.F.6
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