-
1
-
-
18844425185
-
Genetic testing for inherited colon cancer
-
Burt R, Neklason DW Genetic testing for inherited colon cancer. Gastroenterology 2005, 128(6):1696-1716.
-
(2005)
Gastroenterology
, vol.128
, Issue.6
, pp. 1696-1716
-
-
Burt, R.1
Neklason, D.W.2
-
2
-
-
4944240144
-
Genetic predisposition to colorectal cancer
-
de la Chapelle A Genetic predisposition to colorectal cancer. Nat Rev Cancer 2004, 4(10):769-780.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.10
, pp. 769-780
-
-
de la Chapelle, A.1
-
4
-
-
0036091661
-
When is molecular genetic testing for colorectal cancer indicated?
-
Leggett B When is molecular genetic testing for colorectal cancer indicated?. J Gastroenterol Hepatol 2002, 17(4):389-393.
-
(2002)
J Gastroenterol Hepatol
, vol.17
, Issue.4
, pp. 389-393
-
-
Leggett, B.1
-
5
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer
-
Barnetson RA, Tenesa A, Farrington SM, et al. Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med 2006, 354(26):2751-2763.
-
(2006)
N Engl J Med
, vol.354
, Issue.26
, pp. 2751-2763
-
-
Barnetson, R.A.1
Tenesa, A.2
Farrington, S.M.3
-
6
-
-
27744512989
-
Testing for defective DNA mismatch repair in colorectal carcinoma: A practical guide
-
Burgart LJ Testing for defective DNA mismatch repair in colorectal carcinoma: A practical guide. Arch Pathol Lab Med 2005, 129(11):1385-1389.
-
(2005)
Arch Pathol Lab Med
, vol.129
, Issue.11
, pp. 1385-1389
-
-
Burgart, L.J.1
-
7
-
-
0034642605
-
Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer
-
Gryfe R, Kim H, Hsieh ET, et al. Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer. N Engl J Med 2000, 342(2):69-77.
-
(2000)
N Engl J Med
, vol.342
, Issue.2
, pp. 69-77
-
-
Gryfe, R.1
Kim, H.2
Hsieh, E.T.3
-
8
-
-
0033941821
-
Pathology of hereditary nonpolyposis colorectal cancer
-
discussion 73-74
-
Jass JR Pathology of hereditary nonpolyposis colorectal cancer. Ann NY Acad Sci 2000, 910:62-73. discussion 73-74.
-
(2000)
Ann NY Acad Sci
, vol.910
, pp. 62-73
-
-
Jass, J.R.1
-
9
-
-
12844251981
-
Role of the pathologist in the diagnosis of hereditary nonpolyposis colorectal cancer
-
Jass JR Role of the pathologist in the diagnosis of hereditary nonpolyposis colorectal cancer. Dis Markers 2004, 20(4-5):215-224.
-
(2004)
Dis Markers
, vol.20
, Issue.4-5
, pp. 215-224
-
-
Jass, J.R.1
-
10
-
-
33947546541
-
Prognostic and predictive roles of high-degree microsatellite instability in colon cancer: A National Cancer Institute-National Surgical Adjuvant Breast and Bowel Project Collaborative Study
-
Kim GP, Colangelo LH, Wieand HS, et al. Prognostic and predictive roles of high-degree microsatellite instability in colon cancer: A National Cancer Institute-National Surgical Adjuvant Breast and Bowel Project Collaborative Study. J Clin Oncol 2007, 25(7):767-772.
-
(2007)
J Clin Oncol
, vol.25
, Issue.7
, pp. 767-772
-
-
Kim, G.P.1
Colangelo, L.H.2
Wieand, H.S.3
-
11
-
-
33847794097
-
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics
-
Lagerstedt Robinson K, Liu T, Vandrocova J, et al. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. J Natl Cancer Inst 2007, 99(4):291-299.
-
(2007)
J Natl Cancer Inst
, vol.99
, Issue.4
, pp. 291-299
-
-
Lagerstedt Robinson, K.1
Liu, T.2
Vandrocova, J.3
-
12
-
-
12844275378
-
Lynch syndrome: History and current status
-
Lynch HT, Lynch JF Lynch syndrome: History and current status. Dis Markers 2004, 20(4-5):181-198.
-
(2004)
Dis Markers
, vol.20
, Issue.4-5
, pp. 181-198
-
-
Lynch, H.T.1
Lynch, J.F.2
-
13
-
-
12944274799
-
Colorectal carcinogenesis: MSI-H versus MSI-L
-
Pawlik TM, Raut CP, Rodriguez-Bigas MA, et al. Colorectal carcinogenesis: MSI-H versus MSI-L. Dis Markers 2004, 20(4-5):199-206.
-
(2004)
Dis Markers
, vol.20
, Issue.4-5
, pp. 199-206
-
-
Pawlik, T.M.1
Raut, C.P.2
Rodriguez-Bigas, M.A.3
-
14
-
-
4544310802
-
Mutations associated with HNPCC predisposition: Update of ICG-HNPCC/INSiGHT mutation database
-
Peltomaki P, Vasen H Mutations associated with HNPCC predisposition: Update of ICG-HNPCC/INSiGHT mutation database. Dis Markers 2004, 20(4-5):269-276.
-
(2004)
Dis Markers
, vol.20
, Issue.4-5
, pp. 269-276
-
-
Peltomaki, P.1
Vasen, H.2
-
15
-
-
0038002279
-
Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer
-
Ribic CM, Sargent DJ, Moore MJ, et al. Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer. N Engl J Med 2003, 349(3):247-257.
-
(2003)
N Engl J Med
, vol.349
, Issue.3
, pp. 247-257
-
-
Ribic, C.M.1
Sargent, D.J.2
Moore, M.J.3
-
16
-
-
33645672858
-
Microsatellite instability in colorectal cancer
-
Soreide K, Janssen EA, Söiland H, et al. Microsatellite instability in colorectal cancer. Br J Surg 2006, 93(4):395-406.
-
(2006)
Br J Surg
, vol.93
, Issue.4
, pp. 395-406
-
-
Soreide, K.1
Janssen, E.A.2
Söiland, H.3
-
17
-
-
0036893598
-
Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR
-
Suraweera N, Duval A, Reperant M, et al. Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR. Gastroenterology 2002, 123(6):1804-1811.
-
(2002)
Gastroenterology
, vol.123
, Issue.6
, pp. 1804-1811
-
-
Suraweera, N.1
Duval, A.2
Reperant, M.3
-
18
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004, 96(4):261-268.
-
(2004)
J Natl Cancer Inst
, vol.96
, Issue.4
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
-
19
-
-
1042290354
-
Testing guidelines for hereditary nonpolyposis colorectal cancer
-
Umar A, Risinger JI, Hawk ET, Barrett JC Testing guidelines for hereditary nonpolyposis colorectal cancer. Nat Rev Cancer 2004, 4(2):153-158.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.2
, pp. 153-158
-
-
Umar, A.1
Risinger, J.I.2
Hawk, E.T.3
Barrett, J.C.4
-
20
-
-
12844266901
-
Identification of HNPCC by molecular analysis of colorectal and endometrial tumors
-
Vasen HF, Hendriks Y, de Jong AE, et al. Identification of HNPCC by molecular analysis of colorectal and endometrial tumors. Dis Markers 2004, 20(4-5):207-213.
-
(2004)
Dis Markers
, vol.20
, Issue.4-5
, pp. 207-213
-
-
Vasen, H.F.1
Hendriks, Y.2
de Jong, A.E.3
-
22
-
-
33846074011
-
Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): A review of the literature
-
Nieuwenhuis MH, Vasen HF Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): A review of the literature. Crit Rev Oncol Hematol 2007, 61(2):153-161.
-
(2007)
Crit Rev Oncol Hematol
, vol.61
, Issue.2
, pp. 153-161
-
-
Nieuwenhuis, M.H.1
Vasen, H.F.2
-
23
-
-
0141576687
-
The significance of unstable chromosomes in colorectal cancer
-
Rajagopalan H, Nowak MA, Vogelstein B, Lengauer C The significance of unstable chromosomes in colorectal cancer. Nat Rev Cancer 2003, 3(9):695-701.
-
(2003)
Nat Rev Cancer
, vol.3
, Issue.9
, pp. 695-701
-
-
Rajagopalan, H.1
Nowak, M.A.2
Vogelstein, B.3
Lengauer, C.4
-
24
-
-
33749006194
-
Familial adenomatous polyposis: The practical applications of clinical and molecular screening
-
Rozen P, Macrae F Familial adenomatous polyposis: The practical applications of clinical and molecular screening. Fam Cancer 2006, 5(3):227-235.
-
(2006)
Fam Cancer
, vol.5
, Issue.3
, pp. 227-235
-
-
Rozen, P.1
Macrae, F.2
-
26
-
-
0037468517
-
Multiple colorectal adenomas, classic adenomatous polyposis, and germline mutations in MYH.
-
Sieber OM, Lipton L, Crabtree M, et al. Multiple colorectal adenomas, classic adenomatous polyposis, and germline mutations in MYH. N Engl J Med 2003, 348(9):791-799.
-
(2003)
N Engl J Med
, vol.348
, Issue.9
, pp. 791-799
-
-
Sieber, O.M.1
Lipton, L.2
Crabtree, M.3
-
27
-
-
33749185580
-
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation
-
Sieber OM, Segditsas S, Knudsen AL, et al. Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation. Gut 2006, 55(10):1440-1448.
-
(2006)
Gut
, vol.55
, Issue.10
, pp. 1440-1448
-
-
Sieber, O.M.1
Segditsas, S.2
Knudsen, A.L.3
-
28
-
-
2942538325
-
High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis
-
Venesio T, Molatore S, Cattaneo F, et al. High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis. Gastroenterology 2004, 126(7):1681-1685.
-
(2004)
Gastroenterology
, vol.126
, Issue.7
, pp. 1681-1685
-
-
Venesio, T.1
Molatore, S.2
Cattaneo, F.3
-
29
-
-
34347221599
-
Risk of colorectal cancer in juvenile polyposis
-
Brosens LA, van Hattem A, Hylind LM, et al. Risk of colorectal cancer in juvenile polyposis. Gut 2007, 57(5):965-967.
-
(2007)
Gut
, vol.57
, Issue.5
, pp. 965-967
-
-
Brosens, L.A.1
van Hattem, A.2
Hylind, L.M.3
-
30
-
-
33644792947
-
A review of juvenile polyposis syndrome
-
Chow E, Macrae F A review of juvenile polyposis syndrome. J Gastroenterol Hepatol 2005, 20(11):1634-1640.
-
(2005)
J Gastroenterol Hepatol
, vol.20
, Issue.11
, pp. 1634-1640
-
-
Chow, E.1
Macrae, F.2
-
31
-
-
33645838599
-
Peutz-Jeghers syndrome and management recommendations
-
Giardiello FM, Trimbath JD Peutz-Jeghers syndrome and management recommendations. Clin Gastroenterol Hepatol 2006, 4(4):408-415.
-
(2006)
Clin Gastroenterol Hepatol
, vol.4
, Issue.4
, pp. 408-415
-
-
Giardiello, F.M.1
Trimbath, J.D.2
-
32
-
-
33749070180
-
Peutz-Jeghers syndrome: Clinicopathology and molecular alterations
-
McGarrity TJ, Amos C Peutz-Jeghers syndrome: Clinicopathology and molecular alterations. Cell Mol Life Sci 2006, 63(18):2135-2144.
-
(2006)
Cell Mol Life Sci
, vol.63
, Issue.18
, pp. 2135-2144
-
-
McGarrity, T.J.1
Amos, C.2
-
33
-
-
3342929410
-
Genetic conditions associated with intestinal juvenile polyps
-
Merg A, Howe JR Genetic conditions associated with intestinal juvenile polyps. Am J Med Genet C: Semin Med Genet 2004, 129(1):44-55.
-
(2004)
Am J Med Genet C: Semin Med Genet
, vol.129
, Issue.1
, pp. 44-55
-
-
Merg, A.1
Howe, J.R.2
-
34
-
-
10344260184
-
CpG-island methylator phenotype in cancer
-
Issa JP CpG-island methylator phenotype in cancer. Nat Rev Cancer 2004, 4(12):988-993.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.12
, pp. 988-993
-
-
Issa, J.P.1
-
35
-
-
33845608798
-
Classification of colorectal cancer based on correlation of clinical, morphological and molecular features
-
Jass JR Classification of colorectal cancer based on correlation of clinical, morphological and molecular features. Histopathology 2007, 50(1):113-130.
-
(2007)
Histopathology
, vol.50
, Issue.1
, pp. 113-130
-
-
Jass, J.R.1
-
36
-
-
34247638013
-
CpG-island methylation, response to combination chemotherapy, and patient survival in advanced microsatellite stable colorectal carcinoma
-
Ogino S, Meyerhardt JA, Kawasaki T, et al. CpG-island methylation, response to combination chemotherapy, and patient survival in advanced microsatellite stable colorectal carcinoma. Virchows Arch 2007, 450(5):529-537.
-
(2007)
Virchows Arch
, vol.450
, Issue.5
, pp. 529-537
-
-
Ogino, S.1
Meyerhardt, J.A.2
Kawasaki, T.3
-
37
-
-
34247570795
-
Evaluation of markers for CpG-island methylator phenotype (CIMP) in colorectal cancer by a large population-based sample
-
Ogino S, Kawasaki T, Kirkner GJ, et al. Evaluation of markers for CpG-island methylator phenotype (CIMP) in colorectal cancer by a large population-based sample. J Mol Diagn 2007, 9(3):305-314.
-
(2007)
J Mol Diagn
, vol.9
, Issue.3
, pp. 305-314
-
-
Ogino, S.1
Kawasaki, T.2
Kirkner, G.J.3
-
38
-
-
0041524111
-
CpG-island methylator phenotype is an independent predictor of survival benefit from 5-fluorouracil in stage III colorectal cancer
-
Van Rijnsoever M, Elsaleh H, Joseph D, et al. CpG-island methylator phenotype is an independent predictor of survival benefit from 5-fluorouracil in stage III colorectal cancer. Clin Cancer Res 2003, 9(8):2898-2903.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.8
, pp. 2898-2903
-
-
Van Rijnsoever, M.1
Elsaleh, H.2
Joseph, D.3
-
39
-
-
4043181214
-
Cancer genes and the pathways they control
-
Vogelstein B, Kinzler KW Cancer genes and the pathways they control. Nat Med 2004, 10(8):789-799.
-
(2004)
Nat Med
, vol.10
, Issue.8
, pp. 789-799
-
-
Vogelstein, B.1
Kinzler, K.W.2
-
40
-
-
33745541234
-
CpG-island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer
-
Weisenberger DJ, Siegmund KD, Campan M, et al. CpG-island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet 2006, 38(7):787-793.
-
(2006)
Nat Genet
, vol.38
, Issue.7
, pp. 787-793
-
-
Weisenberger, D.J.1
Siegmund, K.D.2
Campan, M.3
-
41
-
-
33846008439
-
Colorectal cancer: A model for epigenetic tumorigenesis
-
Wong JJ, Hawkins NJ, Ward RL Colorectal cancer: A model for epigenetic tumorigenesis. Gut 2007, 56(1):140-148.
-
(2007)
Gut
, vol.56
, Issue.1
, pp. 140-148
-
-
Wong, J.J.1
Hawkins, N.J.2
Ward, R.L.3
-
42
-
-
0037331882
-
DNA fingerprinting abnormalities can distinguish ulcerative colitis patients with dysplasia and cancer from those who are dysplasia/cancer free
-
Chen R, Rabinovitch PS, Crispin DA, et al. DNA fingerprinting abnormalities can distinguish ulcerative colitis patients with dysplasia and cancer from those who are dysplasia/cancer free. Am J Pathol 2003, 162(2):665-672.
-
(2003)
Am J Pathol
, vol.162
, Issue.2
, pp. 665-672
-
-
Chen, R.1
Rabinovitch, P.S.2
Crispin, D.A.3
-
43
-
-
26444514901
-
Characterization of genomic instability in ulcerative colitis neoplasia leads to discovery of putative tumor suppressor regions
-
Chen R, Bronner MP, Crispin DA, et al. Characterization of genomic instability in ulcerative colitis neoplasia leads to discovery of putative tumor suppressor regions. Cancer Genet Cytogenet 2005, 162:99-106.
-
(2005)
Cancer Genet Cytogenet
, vol.162
, pp. 99-106
-
-
Chen, R.1
Bronner, M.P.2
Crispin, D.A.3
-
44
-
-
4043088499
-
IKKβ links inflammation and tumorigenesis in a mouse model of colitis-associated cancer
-
Greten FR, Eckmann L, Greten TF, et al. IKKβ links inflammation and tumorigenesis in a mouse model of colitis-associated cancer. Cell 2004, 118(3):285-296.
-
(2004)
Cell
, vol.118
, Issue.3
, pp. 285-296
-
-
Greten, F.R.1
Eckmann, L.2
Greten, T.F.3
-
45
-
-
33748096092
-
Molecular biology of dysplasia and cancer in inflammatory bowel disease
-
Itkowitz SH Molecular biology of dysplasia and cancer in inflammatory bowel disease. Gastroenterol Clin N Am 2006, 35:553-571.
-
(2006)
Gastroenterol Clin N Am
, vol.35
, pp. 553-571
-
-
Itkowitz, S.H.1
-
46
-
-
33748114138
-
Epidemiology and risk factors for colorectal dysplasia and cancer in ulcerative colitis
-
Loftus EV Epidemiology and risk factors for colorectal dysplasia and cancer in ulcerative colitis. Gastroenterol Clin N Am 2006, 35:517-531.
-
(2006)
Gastroenterol Clin N Am
, vol.35
, pp. 517-531
-
-
Loftus, E.V.1
-
47
-
-
33748099518
-
Pathology of dysplasia and cancer in inflammatory bowel disease
-
Odze RD Pathology of dysplasia and cancer in inflammatory bowel disease. Gastroenterol Clin N Am 2006, 35:533-552.
-
(2006)
Gastroenterol Clin N Am
, vol.35
, pp. 533-552
-
-
Odze, R.D.1
-
48
-
-
18644370262
-
Chromosomal instability in ulcerative colitis is related to telomere shortening
-
O'Sullivan JN, Bronner MP, Brentnall TA, et al. Chromosomal instability in ulcerative colitis is related to telomere shortening. Nat Genet 2002, 32:280-284.
-
(2002)
Nat Genet
, vol.32
, pp. 280-284
-
-
O'Sullivan, J.N.1
Bronner, M.P.2
Brentnall, T.A.3
-
49
-
-
33746260282
-
Cancer surveillance in inflammatory bowel disease: New molecular approaches
-
Risques R, Rabinovitch PS, Brentnall TA Cancer surveillance in inflammatory bowel disease: New molecular approaches. Curr Opin Gastroenterol 2006, 22(4):382-390.
-
(2006)
Curr Opin Gastroenterol
, vol.22
, Issue.4
, pp. 382-390
-
-
Risques, R.1
Rabinovitch, P.S.2
Brentnall, T.A.3
-
51
-
-
23944476156
-
PDGFRα mutations in gastrointestinal stromal tumors: Frequency, spectrum and in vitro sensitivity to imatinib
-
Corless CL, Schroeder A, Griffith D, et al. PDGFRα mutations in gastrointestinal stromal tumors: Frequency, spectrum and in vitro sensitivity to imatinib. J Clin Oncol 2005, 23(23):5357-5364.
-
(2005)
J Clin Oncol
, vol.23
, Issue.23
, pp. 5357-5364
-
-
Corless, C.L.1
Schroeder, A.2
Griffith, D.3
-
53
-
-
33846243226
-
Diagnostic morphological features of PDGFRα-mutated gastrointestinal stromal tumors: Molecular genetic and histologic analysis of 60 cases of gastric gastrointestinal stromal tumors
-
Daum O, Grossmann P, Vanecek T, et al. Diagnostic morphological features of PDGFRα-mutated gastrointestinal stromal tumors: Molecular genetic and histologic analysis of 60 cases of gastric gastrointestinal stromal tumors. Ann Diagn Pathol 2007, 11(1):27-33.
-
(2007)
Ann Diagn Pathol
, vol.11
, Issue.1
, pp. 27-33
-
-
Daum, O.1
Grossmann, P.2
Vanecek, T.3
-
54
-
-
0029947186
-
Effects of a selective inhibitor of the ABL tyrosine kinase on the growth of BCR/ABL positive cells
-
Druker BJ, Tamura S, Buchdunger E, et al. Effects of a selective inhibitor of the ABL tyrosine kinase on the growth of BCR/ABL positive cells. Nat Med 1996, 2(5):561-566.
-
(1996)
Nat Med
, vol.2
, Issue.5
, pp. 561-566
-
-
Druker, B.J.1
Tamura, S.2
Buchdunger, E.3
-
55
-
-
0032955439
-
Prognosis of gastrointestinal smooth-muscle (stromal) tumors: Dependence on anatomic site
-
Emory TS, Sobin LH, Lukes L, et al. Prognosis of gastrointestinal smooth-muscle (stromal) tumors: Dependence on anatomic site. Am J Surg Pathol 1999, 23(1):82-87.
-
(1999)
Am J Surg Pathol
, vol.23
, Issue.1
, pp. 82-87
-
-
Emory, T.S.1
Sobin, L.H.2
Lukes, L.3
-
56
-
-
0036081738
-
Diagnosis of gastrointestinal stromal tumors: A consensus approach
-
Fletcher CD, Berman JJ, Corless C, et al. Diagnosis of gastrointestinal stromal tumors: A consensus approach. Int J Surg Pathol 2002, 10(2):81-89.
-
(2002)
Int J Surg Pathol
, vol.10
, Issue.2
, pp. 81-89
-
-
Fletcher, C.D.1
Berman, J.J.2
Corless, C.3
-
57
-
-
0242670019
-
PDGFR-activating mutations in gastrointestinal stromal tumors
-
Heinrich MC, Corless CL, Duensing A, et al. PDGFR-activating mutations in gastrointestinal stromal tumors. Science 2003, 299(5607):708-710.
-
(2003)
Science
, vol.299
, Issue.5607
, pp. 708-710
-
-
Heinrich, M.C.1
Corless, C.L.2
Duensing, A.3
-
58
-
-
15644363454
-
Gain-of-function mutations of c-Kit in human gastrointestinal stromal tumors
-
Hirota S, Isozaki K, Moriyama Y, et al. Gain-of-function mutations of c-Kit in human gastrointestinal stromal tumors. Science 1998, 279(5350):577-580.
-
(1998)
Science
, vol.279
, Issue.5350
, pp. 577-580
-
-
Hirota, S.1
Isozaki, K.2
Moriyama, Y.3
-
59
-
-
0031947592
-
Gastrointestinal pacemaker cell tumor (GIPACT): Gastrointestinal stromal tumors show phenotypic characteristics of the interstitial cells of Cajal
-
Kindblom LG, Remotti HE, Aldenborg F, Meis-Kindblom JM Gastrointestinal pacemaker cell tumor (GIPACT): Gastrointestinal stromal tumors show phenotypic characteristics of the interstitial cells of Cajal. Am J Pathol 1998, 152(5):1259-1269.
-
(1998)
Am J Pathol
, vol.152
, Issue.5
, pp. 1259-1269
-
-
Kindblom, L.G.1
Remotti, H.E.2
Aldenborg, F.3
Meis-Kindblom, J.M.4
-
60
-
-
0026703726
-
Family history and the risk of stomach and colorectal cancer
-
La Vecchia C, Negri E, Franceschi S, Gentile A Family history and the risk of stomach and colorectal cancer. Cancer 1992, 70(1):50-55.
-
(1992)
Cancer
, vol.70
, Issue.1
, pp. 50-55
-
-
La Vecchia, C.1
Negri, E.2
Franceschi, S.3
Gentile, A.4
-
61
-
-
70449550205
-
Intramural myoid tumors of the stomach: Microscopic considerations on 6 cases
-
Martin JF, Bazin P, Feroldi J, Cabanne F Intramural myoid tumors of the stomach: Microscopic considerations on 6 cases. Ann Anat Pathol (Paris) 1960, 5:484-497.
-
(1960)
Ann Anat Pathol (Paris)
, vol.5
, pp. 484-497
-
-
Martin, J.F.1
Bazin, P.2
Feroldi, J.3
Cabanne, F.4
-
62
-
-
0020514752
-
Gastric stromal tumors: Reappraisal of histogenesis
-
Mazur MT, Clark HB Gastric stromal tumors: Reappraisal of histogenesis. Am J Surg Pathol 1983, 7(6):507-519.
-
(1983)
Am J Surg Pathol
, vol.7
, Issue.6
, pp. 507-519
-
-
Mazur, M.T.1
Clark, H.B.2
-
63
-
-
0032862462
-
Gastrointestinal stromal tumors/smooth muscle tumors (GISTs) primary in the omentum and mesentery: Clinicopathologic and immunohistochemical study of 26 cases
-
Miettinen M, Monihan JM, Sarlomo-Rikala M, et al. Gastrointestinal stromal tumors/smooth muscle tumors (GISTs) primary in the omentum and mesentery: Clinicopathologic and immunohistochemical study of 26 cases. Am J Surg Pathol 1999, 23(9):1109-1118.
-
(1999)
Am J Surg Pathol
, vol.23
, Issue.9
, pp. 1109-1118
-
-
Miettinen, M.1
Monihan, J.M.2
Sarlomo-Rikala, M.3
-
64
-
-
14344256167
-
PDGFRα- and c-Kit-mutated gastrointestinal stromal tumours (GISTs) are characterized by distinctive histological and immunohistochemical features
-
Pauls K, Merkelbach-Bruse S, Thal D, et al. PDGFRα- and c-Kit-mutated gastrointestinal stromal tumours (GISTs) are characterized by distinctive histological and immunohistochemical features. Histopathology 2005, 46(2):166-175.
-
(2005)
Histopathology
, vol.46
, Issue.2
, pp. 166-175
-
-
Pauls, K.1
Merkelbach-Bruse, S.2
Thal, D.3
-
65
-
-
5444222014
-
Myxoid epithelioid gastrointestinal stromal tumor (GIST) with mast cell infiltrations: A subtype of GIST with mutations of platelet-derived growth factor receptorα gene
-
Sakurai S, Hasegawa T, Sakuma Y, et al. Myxoid epithelioid gastrointestinal stromal tumor (GIST) with mast cell infiltrations: A subtype of GIST with mutations of platelet-derived growth factor receptorα gene. Hum Pathol 2004, 35(10):1223-1230.
-
(2004)
Hum Pathol
, vol.35
, Issue.10
, pp. 1223-1230
-
-
Sakurai, S.1
Hasegawa, T.2
Sakuma, Y.3
-
66
-
-
0032935024
-
Interstitial cells of Cajal as precursors of gastrointestinal stromal tumors
-
Sircar K, Hewlett BR, Huizinga JD, et al. Interstitial cells of Cajal as precursors of gastrointestinal stromal tumors. Am J Surg Pathol 1999, 23(4):377-389.
-
(1999)
Am J Surg Pathol
, vol.23
, Issue.4
, pp. 377-389
-
-
Sircar, K.1
Hewlett, B.R.2
Huizinga, J.D.3
-
67
-
-
84965085738
-
Bizarre smooth muscle tumors of the stomach
-
Stout AP Bizarre smooth muscle tumors of the stomach. Cancer 1962, 15:400-409.
-
(1962)
Cancer
, vol.15
, pp. 400-409
-
-
Stout, A.P.1
-
68
-
-
0031686121
-
Mutations of the human E-cadherin (CDH1) gene
-
Berx G, Becker KF, Höfler H, van Roy F Mutations of the human E-cadherin (CDH1) gene. Hum Mutat 1998, 12(4):226-237.
-
(1998)
Hum Mutat
, vol.12
, Issue.4
, pp. 226-237
-
-
Berx, G.1
Becker, K.F.2
Höfler, H.3
van Roy, F.4
-
69
-
-
3142695439
-
Germline E-cadherin mutations in hereditary diffuse gastric cancer: Assessment of 42 new families and review of genetic screening criteria
-
Brooks-Wilson AR, Kaurah P, Suriano G, et al. Germline E-cadherin mutations in hereditary diffuse gastric cancer: Assessment of 42 new families and review of genetic screening criteria. J Med Genet 2004, 41(7):508-517.
-
(2004)
J Med Genet
, vol.41
, Issue.7
, pp. 508-517
-
-
Brooks-Wilson, A.R.1
Kaurah, P.2
Suriano, G.3
-
70
-
-
0033432725
-
Familial gastric cancer: Overview and guidelines for management
-
Caldas C, Carneiro F, Lynch HT, et al. Familial gastric cancer: Overview and guidelines for management. J Med Genet 1999, 36(12):873-880.
-
(1999)
J Med Genet
, vol.36
, Issue.12
, pp. 873-880
-
-
Caldas, C.1
Carneiro, F.2
Lynch, H.T.3
-
71
-
-
0348229127
-
The role of the E-cadherin gene (CDH1) in diffuse gastric cancer susceptibility: From the laboratory to clinical practice
-
Graziano F, Humar B, Guilford P, et al. The role of the E-cadherin gene (CDH1) in diffuse gastric cancer susceptibility: From the laboratory to clinical practice. Ann Oncol 2003, 14(12):1705-1713.
-
(2003)
Ann Oncol
, vol.14
, Issue.12
, pp. 1705-1713
-
-
Graziano, F.1
Humar, B.2
Guilford, P.3
-
72
-
-
34249989159
-
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer
-
Kaurah P, MacMillan A, Boyd N, et al. Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. JAMA 2007, 297(21):2360-2372.
-
(2007)
JAMA
, vol.297
, Issue.21
, pp. 2360-2372
-
-
Kaurah, P.1
MacMillan, A.2
Boyd, N.3
-
73
-
-
18344384564
-
Screening E-cadherin in gastric cancer families reveals germline mutations only in hereditary diffuse gastric cancer kindred
-
Oliveira C, Bordin MC, Grehan N, et al. Screening E-cadherin in gastric cancer families reveals germline mutations only in hereditary diffuse gastric cancer kindred. Hum Mutat 2002, 19(5):510-517.
-
(2002)
Hum Mutat
, vol.19
, Issue.5
, pp. 510-517
-
-
Oliveira, C.1
Bordin, M.C.2
Grehan, N.3
-
74
-
-
0035211026
-
Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families
-
Pharoah PD, Guilford P, Caldas C, International Gastric Cancer Linkage Consortium Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. Gastroenterology 2001, 121(6):1348-1353.
-
(2001)
Gastroenterology
, vol.121
, Issue.6
, pp. 1348-1353
-
-
Pharoah, P.D.1
Guilford, P.2
Caldas, C.3
International Gastric Cancer Linkage Consortium4
-
75
-
-
23044486914
-
Characterization of a recurrent germline mutation of the E-cadherin gene: Implications for genetic testing and clinical management
-
Suriano G, Yew S, Ferreira P, et al. Characterization of a recurrent germline mutation of the E-cadherin gene: Implications for genetic testing and clinical management. Clin Cancer Res 2005, 11(15):5401-5409.
-
(2005)
Clin Cancer Res
, vol.11
, Issue.15
, pp. 5401-5409
-
-
Suriano, G.1
Yew, S.2
Ferreira, P.3
-
76
-
-
33744521128
-
The development of a fluorescence in situ hybridization assay for the detection of dysplasia and adenocarcinoma in Barrett's esophagus
-
Brankley SM, Wang KK, Harwood AR, et al. The development of a fluorescence in situ hybridization assay for the detection of dysplasia and adenocarcinoma in Barrett's esophagus. J Med Diagn 2006, 8(2):260-267.
-
(2006)
J Med Diagn
, vol.8
, Issue.2
, pp. 260-267
-
-
Brankley, S.M.1
Wang, K.K.2
Harwood, A.R.3
-
77
-
-
33845660390
-
Barrett's oesophagus: A pathologist's view
-
Flejou J-F, Svrcek M Barrett's oesophagus: A pathologist's view. Histopathology 2007, 50:3-14.
-
(2007)
Histopathology
, vol.50
, pp. 3-14
-
-
Flejou, J.-F.1
Svrcek, M.2
-
78
-
-
33746441430
-
Clinical use of p53 in Barrett's esophagus
-
Keswani RN, Noffsinger A, Waxman I, Bissonnette M Clinical use of p53 in Barrett's esophagus. Cancer Epidemiol Biomarkers Prev 2006, 15(7):1243-1249.
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, Issue.7
, pp. 1243-1249
-
-
Keswani, R.N.1
Noffsinger, A.2
Waxman, I.3
Bissonnette, M.4
-
80
-
-
0036198076
-
R Quantitative detection of Tropheryma whipplei DNA by real-time PCR
-
Fenollar F, Fournier PE, Raoult D, et al. R Quantitative detection of Tropheryma whipplei DNA by real-time PCR. J Clin Microbiol 2002, 40(3):1119-1120.
-
(2002)
J Clin Microbiol
, vol.40
, Issue.3
, pp. 1119-1120
-
-
Fenollar, F.1
Fournier, P.E.2
Raoult, D.3
-
81
-
-
0347093249
-
Use of genome selected repeated sequences increases the sensitivity of PCR detection of Tropheryma whipplei.
-
Fenollar F, Fournier PE, Robert C, Raoult D Use of genome selected repeated sequences increases the sensitivity of PCR detection of Tropheryma whipplei. J Clin Microbiol 2004, 42(1):401-403.
-
(2004)
J Clin Microbiol
, vol.42
, Issue.1
, pp. 401-403
-
-
Fenollar, F.1
Fournier, P.E.2
Robert, C.3
Raoult, D.4
-
82
-
-
33846003174
-
Whipple's disease
-
Fenollar F, Puechal X, Raoult D, et al. Whipple's disease. N Engl J Med 2007, 356(1):55-66.
-
(2007)
N Engl J Med
, vol.356
, Issue.1
, pp. 55-66
-
-
Fenollar, F.1
Puechal, X.2
Raoult, D.3
-
83
-
-
0038207065
-
Whipple's disease: Immunospecific and quantitative immunohistochemical study of intestinal biopsy specimens
-
Lepidi H, Fenollar F, Gerolami R, et al. Whipple's disease: Immunospecific and quantitative immunohistochemical study of intestinal biopsy specimens. Hum Pathol 2003, 34(6):589-596.
-
(2003)
Hum Pathol
, vol.34
, Issue.6
, pp. 589-596
-
-
Lepidi, H.1
Fenollar, F.2
Gerolami, R.3
-
84
-
-
33749452587
-
Culture of T. whipplei from the stool of a patient with Whipple's disease
-
Raoult D, Fenollar F, Birg ML, et al. Culture of T. whipplei from the stool of a patient with Whipple's disease. N Engl J Med 2006, 355(14):1503-1505.
-
(2006)
N Engl J Med
, vol.355
, Issue.14
, pp. 1503-1505
-
-
Raoult, D.1
Fenollar, F.2
Birg, M.L.3
-
85
-
-
34250161774
-
False-positive PCR detection of Tropheryma whipplei in the saliva of healthy people
-
Rolain JM, Fenollar F, Raoult D, et al. False-positive PCR detection of Tropheryma whipplei in the saliva of healthy people. BMC Microbiol 2007, 7:48.
-
(2007)
BMC Microbiol
, vol.7
, pp. 48
-
-
Rolain, J.M.1
Fenollar, F.2
Raoult, D.3
-
86
-
-
0141724605
-
The genetics of pancreatic cancer
-
Cowgill SM, Muscarella P The genetics of pancreatic cancer. Am J Surg 2003, 186(3):279-286.
-
(2003)
Am J Surg
, vol.186
, Issue.3
, pp. 279-286
-
-
Cowgill, S.M.1
Muscarella, P.2
-
88
-
-
0031015729
-
Telomerase activity is detected in pancreatic cancer but not in benign tumors
-
Hiyama E, Kodama T, Shinbara K, et al. Telomerase activity is detected in pancreatic cancer but not in benign tumors. Cancer Res 1997, 57(2):326-331.
-
(1997)
Cancer Res
, vol.57
, Issue.2
, pp. 326-331
-
-
Hiyama, E.1
Kodama, T.2
Shinbara, K.3
-
89
-
-
9344237719
-
Use of microsatellite marker loss of heterozygosity in accurate diagnosis of pancreaticobiliary malignancy from brush cytology samples
-
Khalid A, Pal R, Sasatomi E, et al. Use of microsatellite marker loss of heterozygosity in accurate diagnosis of pancreaticobiliary malignancy from brush cytology samples. Gut 2004, 53(12):1860-1865.
-
(2004)
Gut
, vol.53
, Issue.12
, pp. 1860-1865
-
-
Khalid, A.1
Pal, R.2
Sasatomi, E.3
-
90
-
-
14644405525
-
Molecular diagnosis of solid and cystic lesions of the pancreas
-
Khalid A, Finkelstein S, McGrath K, et al. Molecular diagnosis of solid and cystic lesions of the pancreas. Clin Lab Med 2005, 25(1):101-116.
-
(2005)
Clin Lab Med
, vol.25
, Issue.1
, pp. 101-116
-
-
Khalid, A.1
Finkelstein, S.2
McGrath, K.3
-
91
-
-
4544351296
-
A comparison of routine cytology and fluorescence in situ hybridization for the detection of malignant bile duct structures
-
Kipp BR, Stadheim L, Halling SA, et al. A comparison of routine cytology and fluorescence in situ hybridization for the detection of malignant bile duct structures. Am J Gastroenterol 2004, 99:1675-1681.
-
(2004)
Am J Gastroenterol
, vol.99
, pp. 1675-1681
-
-
Kipp, B.R.1
Stadheim, L.2
Halling, S.A.3
-
92
-
-
33645241968
-
Determination of qualitative telomerase activity as an adjunct to the diagnosis of pancreatic adenocarcinoma by EUS-guided fine-needle aspiration
-
Mishra G, Zhao Y, Sweeney J, et al. Determination of qualitative telomerase activity as an adjunct to the diagnosis of pancreatic adenocarcinoma by EUS-guided fine-needle aspiration. Gastrointest Endosc 2006, 63(4):648-654.
-
(2006)
Gastrointest Endosc
, vol.63
, Issue.4
, pp. 648-654
-
-
Mishra, G.1
Zhao, Y.2
Sweeney, J.3
-
93
-
-
2342504277
-
Genetic abnormalities in pancreatic cancer
-
Moore PS, Beghelli S, Zamboni G, Scarpa A Genetic abnormalities in pancreatic cancer. Mol Cancer 2003, 2:7.
-
(2003)
Mol Cancer
, vol.2
, pp. 7
-
-
Moore, P.S.1
Beghelli, S.2
Zamboni, G.3
Scarpa, A.4
-
94
-
-
33749336094
-
Advanced cytologic techniques for the detection of malignant pancreatobiliary strictures
-
Moreno Luna LE, Kipp B, Halling KC, et al. Advanced cytologic techniques for the detection of malignant pancreatobiliary strictures. Gastroenterology 2006, 131:1064-1072.
-
(2006)
Gastroenterology
, vol.131
, pp. 1064-1072
-
-
Moreno Luna, L.E.1
Kipp, B.2
Halling, K.C.3
-
95
-
-
0038408793
-
Chromosomal instability in pancreatic ductal cells from patients with chronic pancreatitis and pancreatic adenocarcinoma
-
Moskovitz AH, Linford N, Brentnall TA, et al. Chromosomal instability in pancreatic ductal cells from patients with chronic pancreatitis and pancreatic adenocarcinoma. Genes Chromosomes Cancer 2003, 37:201-206.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 201-206
-
-
Moskovitz, A.H.1
Linford, N.2
Brentnall, T.A.3
-
96
-
-
0036895026
-
Prognostic implications of routine, immunohistochemical, and molecular staging in resectable pancreatic adenocarcinoma
-
Niedergethmann M, Rexin M, Hildenbrand R, et al. Prognostic implications of routine, immunohistochemical, and molecular staging in resectable pancreatic adenocarcinoma. Am J Surg Pathol 2002, 26(12):1578-1587.
-
(2002)
Am J Surg Pathol
, vol.26
, Issue.12
, pp. 1578-1587
-
-
Niedergethmann, M.1
Rexin, M.2
Hildenbrand, R.3
-
97
-
-
33845885517
-
Palladin mutation causes familial pancreatic cancer and suggests a new cancer mechanism
-
Pogue-Geile KL, Chen R, Bronner MP, et al. Palladin mutation causes familial pancreatic cancer and suggests a new cancer mechanism. PLoS Med 2006, 3(12):2216-2228.
-
(2006)
PLoS Med
, vol.3
, Issue.12
, pp. 2216-2228
-
-
Pogue-Geile, K.L.1
Chen, R.2
Bronner, M.P.3
-
98
-
-
0036305839
-
Aberrant methylation of CpG islands in intraductal papillary mucinous neoplasms of the pancreas
-
Sato N, Ueki T, Fukushima N, et al. Aberrant methylation of CpG islands in intraductal papillary mucinous neoplasms of the pancreas. Gastroenterology 2002, 123(1):365-372.
-
(2002)
Gastroenterology
, vol.123
, Issue.1
, pp. 365-372
-
-
Sato, N.1
Ueki, T.2
Fukushima, N.3
-
99
-
-
33749188496
-
Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
-
Aretz S, Koch A, Uhlhaas S, et al. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?. Pediatr Blood Cancer 2006, 47(6):811-818.
-
(2006)
Pediatr Blood Cancer
, vol.47
, Issue.6
, pp. 811-818
-
-
Aretz, S.1
Koch, A.2
Uhlhaas, S.3
-
101
-
-
33750613935
-
Transcriptomic and genomic analysis of human hepatocellular carcinomas and hepatoblastomas
-
Luo JH, Ren B, Keryanov S, et al. Transcriptomic and genomic analysis of human hepatocellular carcinomas and hepatoblastomas. Hepatology 2006, 44(4):1012-1024.
-
(2006)
Hepatology
, vol.44
, Issue.4
, pp. 1012-1024
-
-
Luo, J.H.1
Ren, B.2
Keryanov, S.3
-
102
-
-
33645112972
-
Molecular insights into the pathogenesis of hereditary haemochromatosis
-
Pietrangelo A Molecular insights into the pathogenesis of hereditary haemochromatosis. Gut 2006, 55(4):564-568.
-
(2006)
Gut
, vol.55
, Issue.4
, pp. 564-568
-
-
Pietrangelo, A.1
-
103
-
-
33646899011
-
Hereditary hemochromatosis: Genetic complexity and new diagnostic approaches
-
Swinkels DW, Janssen MC, Bergmans J, Marx JJ Hereditary hemochromatosis: Genetic complexity and new diagnostic approaches. Clin Chem 2006, 52(6):950-968.
-
(2006)
Clin Chem
, vol.52
, Issue.6
, pp. 950-968
-
-
Swinkels, D.W.1
Janssen, M.C.2
Bergmans, J.3
Marx, J.J.4
-
104
-
-
13444253875
-
The current management of hepatoblastoma: A combination of chemotherapy, conventional resection, and liver transplantation
-
Tiao GM, Bobey N, Allen S, et al. The current management of hepatoblastoma: A combination of chemotherapy, conventional resection, and liver transplantation. J Pediatr 2005, 146(2):204-211.
-
(2005)
J Pediatr
, vol.146
, Issue.2
, pp. 204-211
-
-
Tiao, G.M.1
Bobey, N.2
Allen, S.3
-
105
-
-
33847069207
-
Genomics and signaling pathways in hepatocellular carcinoma
-
Villanueva A, Newell P, Chiang DY, et al. Genomics and signaling pathways in hepatocellular carcinoma. Semin Liver Dis 2007, 27(1):55-76.
-
(2007)
Semin Liver Dis
, vol.27
, Issue.1
, pp. 55-76
-
-
Villanueva, A.1
Newell, P.2
Chiang, D.Y.3
-
106
-
-
33646153508
-
Revisiting hereditary hemochromatosis: Current concepts and progress
-
Yen AW, Fancher TL, Bowlus CL Revisiting hereditary hemochromatosis: Current concepts and progress. Am J Med 2006, 119(5):391-399.
-
(2006)
Am J Med
, vol.119
, Issue.5
, pp. 391-399
-
-
Yen, A.W.1
Fancher, T.L.2
Bowlus, C.L.3
-
107
-
-
33645223878
-
Genotype-phenotype correlation in hepatocellular adenoma: New classification and relationship with HCC
-
Zucman-Rossi J, Jeannot E, Nhieu JT, et al. Genotype-phenotype correlation in hepatocellular adenoma: New classification and relationship with HCC. Hepatology 2006, 43(3):515-524.
-
(2006)
Hepatology
, vol.43
, Issue.3
, pp. 515-524
-
-
Zucman-Rossi, J.1
Jeannot, E.2
Nhieu, J.T.3
-
108
-
-
0036086034
-
Type I glycogen storage diseases: Disorders of the glucose-6-phosphatase complex
-
Chou JY, Matern D, Mansfield BC, Chen YT, et al. Type I glycogen storage diseases: Disorders of the glucose-6-phosphatase complex. Curr Mol Med 2002, 2(2):121-143.
-
(2002)
Curr Mol Med
, vol.2
, Issue.2
, pp. 121-143
-
-
Chou, J.Y.1
Matern, D.2
Mansfield, B.C.3
Chen, Y.T.4
-
109
-
-
0027057809
-
Glycogen debranching enzyme deficiency: Long-term study of serum enzyme activities and clinical features
-
Coleman RA, Winter HS, Wolf B, et al. Glycogen debranching enzyme deficiency: Long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis 1992, 15(6):869-881.
-
(1992)
J Inherit Metab Dis
, vol.15
, Issue.6
, pp. 869-881
-
-
Coleman, R.A.1
Winter, H.S.2
Wolf, B.3
-
110
-
-
33846617279
-
Glycogen storage disease type III: Hepatocellular carcinoma a long-term complication?
-
Demo E, Frush D, Gottfried M, et al. Glycogen storage disease type III: Hepatocellular carcinoma a long-term complication?. J Hepatol 2007, 46(3):492-498.
-
(2007)
J Hepatol
, vol.46
, Issue.3
, pp. 492-498
-
-
Demo, E.1
Frush, D.2
Gottfried, M.3
-
111
-
-
0025070103
-
Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III
-
Ding JH, de Barsy T, Brown BI, et al. Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III. J Pediatr 1990, 116(1):95-100.
-
(1990)
J Pediatr
, vol.116
, Issue.1
, pp. 95-100
-
-
Ding, J.H.1
de Barsy, T.2
Brown, B.I.3
-
112
-
-
0036293277
-
Histologic features of the liver in type Ia glycogen storage disease: Comparative study between different age groups and consecutive biopsies
-
Gogus S, Kocak N, et al. Histologic features of the liver in type Ia glycogen storage disease: Comparative study between different age groups and consecutive biopsies. Pediatr Dev Pathol 2002, 5(3):299-304.
-
(2002)
Pediatr Dev Pathol
, vol.5
, Issue.3
, pp. 299-304
-
-
Gogus, S.1
Kocak, N.2
-
113
-
-
0016244439
-
Glycogen storage disease, types I to X: Criteria for morphologic diagnosis
-
McAdams AJ, Hug G, Bove KE Glycogen storage disease, types I to X: Criteria for morphologic diagnosis. Hum Pathol 1974, 5(4):463-487.
-
(1974)
Hum Pathol
, vol.5
, Issue.4
, pp. 463-487
-
-
McAdams, A.J.1
Hug, G.2
Bove, K.E.3
-
114
-
-
0036082990
-
The variable presentations of glycogen storage disease type IV: A review of clinical, enzymatic and molecular studies
-
Moses SW, Parvari R The variable presentations of glycogen storage disease type IV: A review of clinical, enzymatic and molecular studies. Curr Mol Med 2002, 2(2):177-188.
-
(2002)
Curr Mol Med
, vol.2
, Issue.2
, pp. 177-188
-
-
Moses, S.W.1
Parvari, R.2
-
115
-
-
0034091934
-
Glycogen storage disease type Ia: Recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart
-
Rake JP, ten Berge AM, Visser G, et al. Glycogen storage disease type Ia: Recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart. Eur J Pediatr 2000, 159(5):322-330.
-
(2000)
Eur J Pediatr
, vol.159
, Issue.5
, pp. 322-330
-
-
Rake, J.P.1
ten Berge, A.M.2
Visser, G.3
-
116
-
-
0036387417
-
Glycogen storage disease type I: Diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I)
-
SUPPL.1
-
Rake JP, Visser G, Labrune P, et al. Glycogen storage disease type I: Diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I). Eur J Pediatr 2002, 161(Suppl 1):S20-S34.
-
(2002)
Eur J Pediatr
, vol.161
-
-
Rake, J.P.1
Visser, G.2
Labrune, P.3
-
117
-
-
0036079985
-
Molecular characterization of glycogen storage disease type III
-
Shen JJ, Chen YT Molecular characterization of glycogen storage disease type III. Curr Mol Med 2002, 2(2):167-175.
-
(2002)
Curr Mol Med
, vol.2
, Issue.2
, pp. 167-175
-
-
Shen, J.J.1
Chen, Y.T.2
-
118
-
-
33749250737
-
Glycogen storage disease: Clinical, biochemical, and molecular heterogeneity
-
Shin YS Glycogen storage disease: Clinical, biochemical, and molecular heterogeneity. Semin Pediatr Neurol 2006, 13(2):115-120.
-
(2006)
Semin Pediatr Neurol
, vol.13
, Issue.2
, pp. 115-120
-
-
Shin, Y.S.1
-
119
-
-
0028147648
-
Glycogen storage disease in adults
-
Talente GM, Coleman RA, Alter C, et al. Glycogen storage disease in adults. Ann Intern Med 1994, 120(3):218-226.
-
(1994)
Ann Intern Med
, vol.120
, Issue.3
, pp. 218-226
-
-
Talente, G.M.1
Coleman, R.A.2
Alter, C.3
|