LE WE PMID CA
Neoplasia (Inherited)3432Neubildung (Hereditaer)

Anemia (Fanconi s anemia)

Bannayan Riley Ruvalcaba syndrome

Basal cell carcinoma

Basaloid follicular hamartoma

Bazex acrokeratosis paraneoplastica

Birt Hogg Dube syndrome

Brooke Spiegler syndrome

Carney s complex

Cdh1

Chemoprevention

Colon and rectum (Neoplasia)

Cowden s syndrome

Cronkhite Canada syndrome

CYLD Cylindromatosis

Data base (Medicine Biology Pharmacology)

DNA (Repair and Toxicology)

Endometrium (Neoplasia)

Familial adenomatous polyposis

Familial cylindromatosis

Fibrofolliculoma

FLCN Folliculin

Fumarate hydratase

Gastrointestinal stromal cell tumor GIST

Generalised basaloid follicular hamartoma syndrome

Genetics (Microsatellite)

Gorlin Goltz phacomatosis Gorlin s syndrome Naevoid basal cell carcinoma

Hamartomatous polyposis syndromes

Intestines (Neoplasia)

Keratoacanthoma

Kidney (Neoplasm)

Leukemia (chronic lymphatic)

Leukemia and lymphoma (BASKET)

Lynch syndrome

Mammary gland (Neoplasia)

Medical ethics

MLH1

Mltiple familial trichoepitheliomas

MSH2

MSH6

Muir Torre s syndrome

Multiple hereditary infundibulocystic basal cell carcinoma

Neoplasia (Inherited)

Nervous system (Neoplasia Paraganglioma)

Neuroendocrine system (Neoplasia)

Ovary (Neoplasia)

Pancreas (Neoplasia)

Peutz Jeghers syndrome

PHOX2B

PMS2

Preventive surgery

PTCH

PTEN MMAC1 TEP1

Runx1 AML1

Seabceous epithelioma

Sebaceous adenoma

Sebaceous carcinoma

Skin (Neoplasia)

Sleep apnea (central)

Spiradenoma

Stomach (Neoplasia)

Thyroid (Neoplasia)

Trichilemmoma

Trichodiscoma

Trichoepithelioma

Von Hippel Lindau syndrome

2006  
1
Mucocutaneous neuromas: an underrecognized manifestation of PTEN hamartoma-tumor syndrome.
[16702501] Arch Dermatol 142(5): 625-32 (2006)
1999  
2
Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome.
[10522671] Arch Dermatol 135(10): 1227-35 (1999)
2002  
3
Cowden disease or multiple hamartoma syndrome--cutaneous clue to internal malignancy.
[12370126] Eur J Dermatol 12(5): 411-21 (2002)
2008  
4
Extracolonic manifestations of hereditary colorectal cancer syndromes.
[20011437] Clin Colon Rectal Surg 21(4): 263-72 (2008)
2008  
5
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency.
[18366737] BMC Med Genet 9(-): 20 (2008)
2008  
6
BRCA1/2 associated hereditary breast cancer.
[18257128] J Zhejiang Univ Sci B 9(2): 85-9 (2008)
1982  
7
Multiple primary carcinomas of the colon and associated extracolonic primary malignant tumors.
[7065754] Ann Surg 195(4): 501-7 (1982)
2007  
8
Selected aspects of inherited susceptibility to prostate cancer and tumours of different site of origin.
[19725994] Hered Cancer Clin Pract 5(3): 164-79 (2007)
1998  
9
Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee.
[9818066] Ann Oncol 9(9): 939-50 (1998)
1979  
10
Hereditary cancer: ascertainment and management.
[36967] CA Cancer J Clin 29(4): 216-32 (1979)
2008  
11
Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management, and controversies.
[18798544] Cancer 113(7 Suppl): 1807-43 (2008)
2008  
12
Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy.
[18442100] Cancer 112(12): 2655-63 (2008)
1999  
13
Chemoprevention in hereditary colorectal cancer syndromes.
[10630181] Cancer 86(11 Suppl): 2551-63 (1999)
1999  
14
Genetic testing and counseling for hereditary forms of colorectal cancer.
[10630180] Cancer 86(11 Suppl): 2540-50 (1999)
1999  
15
Clinical challenges in management of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.
[10630179] Cancer 86(11 Suppl): 2533-9 (1999)
1999  
16
Managing hereditary ovarian cancer risk.
[10630177] Cancer 86(11 Suppl): 2517-24 (1999)
1999  
17
Prophylactic mastectomy and inherited predisposition to breast carcinoma.
[10630176] Cancer 86(11 Suppl): 2502-16 (1999)
1999  
18
Inherited genetic predisposition in breast cancer. A population-based perspective.
[10630175] Cancer 86(11 Suppl): 2493-501 (1999)
1999  
19
Genetic cancer risk assessment. Putting it all together.
[10630174] Cancer 86(11 Suppl): 2483-92 (1999)
1999  
20
Von Hippel-Lindau syndrome. A pleomorphic condition.
[10630173] Cancer 86(11 Suppl): 2478-82 (1999)
1999  
21
The genetics of hereditary melanoma and nevi. 1998 update.
[10630172] Cancer 86(11 Suppl): 2464-77 (1999)
2007  
22
New issues in genetic counseling of hereditary colon cancer.
[18006790] Clin Cancer Res 13(22 Pt 2): 6857s-61s (2007)
2004  
23
Recognition and management of hereditary breast cancer syndromes.
[14755011] Oncologist 9(1): 13-24 (2004)
1987  
24
Genetics of cancer predisposition.
[2889524] Cancer Res 47(21): 5518-27 (1987)
2002  
25
Why have we failed to find the low penetrance genetic constituents of common cancers?
[12496041] Cancer Epidemiol Biomarkers Prev 11(12): 1544-9 (2002)
2009  
26
Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model.
[19654196] CMAJ 181(5): 273-80 (2009)
2008  
27
Cancer surveillance based on imaging techniques in carriers of BRCA1/2 gene mutations: a systematic review.
[18208856] Br J Radiol 81(963): 172-9 (2008)
2004  
28
Hereditary cancer: guidelines in clinical practice--general overview.
[15477294] Ann Oncol 15 Suppl 4(-): iv121-5 (2004)
2004  
29
Hereditary cancer: guidelines in clinical practice. Colorectal cancer genetics.
[15477295] Ann Oncol 15 Suppl 4(-): iv127-31 (2004)
2004  
30
Hereditary cancer: guidelines in clinical practice. Breast and ovarian cancer genetics.
[15477297] Ann Oncol 15 Suppl 4(-): iv133-8 (2004)
2010  
31
Genetic counselling for hereditary predisposition to ovarian and breast cancer.
[20943638] Ann Oncol 21 Suppl 7(-): vii334-8 (2010)
2009  
32
Familial colorectal cancer risk: ESMO clinical recommendations.
[19454462] Ann Oncol 20 Suppl 4(-): 51-3 (2009)
2009  
33
Carney triad: a syndrome featuring paraganglionic, adrenocortical, and possibly other endocrine tumors.
[19723753] J Clin Endocrinol Metab 94(10): 3656-62 (2009)
2011  
34
Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency.
[21880633] Haematologica 96(12): 1892-4 (2011)
2010  
35
Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation.
[20015892] Haematologica 95(5): 841-4 (2010)
2010  
36
Constitutional mismatch repair-deficiency syndrome.
[20442441] Haematologica 95(5): 699-701 (2010)
2010  
37
Hereditary myeloproliferative disorders.
[20065077] Haematologica 95(1): 6-8 (2010)
2007  
38
Genetic susceptibility to lymphoma.
[17606447] Haematologica 92(7): 960-9 (2007)
2011  
39
BRCA and beyond: A genome-first approach to familial breast cancer risk assessment.
[22127114] Discov Med 12(66): 433-43 (2011)
2010  
40
The inherited genetics of ovarian and endometrial cancer.
[20456938] Curr Opin Genet Dev 20(3): 231-8 (2010)
2010  
41
Candidate gene association studies: successes and failures.
[20417090] Curr Opin Genet Dev 20(3): 257-61 (2010)
2010  
42
Advances in the genetics of familial renal cancer.
[20484339] Oncologist 15(6): 532-8 (2010)
2009  
43
Genetic aspects of familial thyroid cancer.
[19465682] Oncologist 14(6): 571-7 (2009)
2009  
44
Hereditary kidney cancer: unique opportunity for disease-based therapy.
[19402075] Cancer 115(10 Suppl): 2252-61 (2009)
2010  
45
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.
[20208042] Am J Respir Crit Care Med 181(6): 626-44 (2010)
2010  
46
Susceptibility pathways in Fanconi's anemia and breast cancer.
[20484397] N Engl J Med 362(20): 1909-19 (2010)
2003  
47
2011  
48
Hereditary breast and ovarian cancer: new genes, new treatments, new concepts.
[21637635] Dtsch Arztebl Int 108(19): 323-30 (2011)
2004  
49
Inherited forms of renal cell carcinoma.
[15285561] Scand J Surg 93(2): 103-11 (2004)
2009  
50
Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information.
[19319160] Eur J Hum Genet 17(7): 872-80 (2009)
2010  
51
Hereditary and familial colon cancer.
[20420945] Gastroenterology 138(6): 2044-58 (2010)
2010  
52
2010  
53
2010  
54
Cancer genetics: risks and mechanisms of cancer in women with inherited susceptibility to epithelial ovarian cancer.
[20811826] Cancer Treat Res 156(-): 69-85 (2010)
2010  
55
Familial chronic lymphocytic leukemia.
[20389242] Curr Opin Hematol 17(4): 350-5 (2010)
2004  
56
Identifying and testing for hereditary susceptibility to common cancers.
[15537575] CA Cancer J Clin 54(6): 309-26 (2004)
2011  
57
Educational paper: screening in cancer predisposition syndromes: guidelines for the general pediatrician.
[21210147] Eur J Pediatr 170(3): 285-94 (2011)
2007  
58
Lessons learned from DNA repair defective syndromes.
[17518994] Exp Dermatol 16(6): 532-44 (2007)
2008  
59
Hereditary diffuse gastric cancer: prophylactic surgical oncology implications.
[18672140] Surg Clin North Am 88(4): 759-78, vi-vii (2008)
2008  
60
2009  
61
2009  
62
Family cancer syndromes: inherited deficiencies in systems for the maintenance of genomic integrity.
[19056039] Surg Oncol Clin N Am 18(1): 1-17, vii (2009)
2011  
63
Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany.
[22109790] J Community Genet 2(2): 53-69 (2011)
2010  
64
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
[20587412] J Med Genet 47(9): 579-85 (2010)
2005  
65
Genetics of skin appendage neoplasms and related syndromes.
[16272260] J Med Genet 42(11): 811-9 (2005)
2008  
66
Mechanisms of inherited cancer susceptibility.
[18196605] J Zhejiang Univ Sci B 9(1): 1-4 (2008)
2009  
67
Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives.
[19125126] Genet Med 11(1): 35-41 (2009)
2009  
68
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
[19125127] Genet Med 11(1): 42-65 (2009)
2010  
69
Mendelian genetics of rare--and not so rare--cancers.
[20946573] Ann N Y Acad Sci 1214(): 70-82 (2010)
2010  
70
Mouse models of inherited cancer syndromes.
[21075289] Hematol Oncol Clin North Am 24(6): 1205-28 (2010)
2010  
71
Rare and unusual endocrine cancer syndromes with mutated genes.
[21167385] Semin Oncol 37(6): 680-90 (2010)

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  • Neubildung (Hereditaer)

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