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Longer titles found: Hereditary breast–ovarian cancer syndrome (view), Mismatch repair cancer syndrome (view), Hereditary leiomyomatosis and renal cell cancer syndrome (view)

searching for Cancer syndrome 34 found (69 total)

alternate case: cancer syndrome

Multiple cutaneous leiomyoma (128 words) [view diff] exact match in snippet view article find links to article

be a manifestation of the hereditary leiomyomatosis and renal cell cancer syndrome. List of cutaneous conditions "Hereditary leiomyomatosis and renal
Polymerase proofreading-associated polyposis (153 words) [view diff] exact match in snippet view article find links to article
proofreading-associated polyposis (PPAP) is an autosomal dominant hereditary cancer syndrome, which is characterized by numerous polyps in the colon and an increased
Cowden syndrome (1,932 words) [view diff] exact match in snippet view article find links to article
Cowden's patients as compared to individuals without a hereditary cancer syndrome. Central Nervous System Macrocephaly is observed in 84% of patients
Hereditary lobular breast cancer (605 words) [view diff] exact match in snippet view article find links to article
and without apparent correlation with the hereditary diffuse gastric cancer syndrome. Research studies identified novel CDH1 germline variants in women
Edward Baker Lincoln (752 words) [view diff] exact match in snippet view article find links to article
two of his brothers had several features compatible with the genetic cancer syndrome multiple endocrine neoplasia type 2b (MEN2B), (d) Eddie's thick, asymmetric
Hereditary diffuse gastric cancer (1,263 words) [view diff] exact match in snippet view article find links to article
with hereditary cancer syndromes. HDGC is the most common hereditary cancer syndrome of the stomach. HDGC was originally discovered through studies of Maori
DPF2 (610 words) [view diff] exact match in snippet view article find links to article
candidate gene for multiple endocrine neoplasia type I, an inherited cancer syndrome involving multiple parathyroid, enteropancreatic, and pituitary tumors
Colorectal polyp (2,833 words) [view diff] exact match in snippet view article find links to article
RPS20. Familial adenomatous polyposis (FAP) is a form of hereditary cancer syndrome involving the APC gene located on chromosome q521. The syndrome was
RPS6KA5 (1,133 words) [view diff] exact match in snippet view article find links to article
(2001). "Phosphorylation of the protein kinase mutated in Peutz-Jeghers cancer syndrome, LKB1/STK11, at Ser431 by p90(RSK) and cAMP-dependent protein kinase
Chromosome 3 (1,743 words) [view diff] exact match in snippet view article find links to article
syndrome Moyamoya disease Mucopolysaccharidosis Muir–Torre family cancer syndrome Myotonic dystrophy Neuropathy, hereditary motor and sensory, Okinawa
Ataxia telangiectasia and Rad3 related (3,418 words) [view diff] exact match in snippet view article find links to article
mutation. ATR is also linked to familial cutaneous telangiectasia and cancer syndrome. ATR/ChK1 inhibitors can potentiate the effect of DNA cross-linking
Amsterdam criteria (705 words) [view diff] exact match in snippet view article find links to article
colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome". Surg. Oncol. Clin. N. Am. 18 (4): 637–45. doi:10.1016/j.soc.2009
Sebaceous gland (3,324 words) [view diff] exact match in snippet view article find links to article
slow-growing tumour—which may, however, in rare cases be a precursor to a cancer syndrome known as Muir–Torre syndrome. Sebaceous carcinoma, an uncommon and
Multiple endocrine neoplasia (2,138 words) [view diff] exact match in snippet view article find links to article
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary endocrine cancer syndrome characterized primarily by tumors of the parathyroid glands (95% of
STK11 (2,391 words) [view diff] exact match in snippet view article find links to article
2001). "Phosphorylation of the protein kinase mutated in Peutz-Jeghers cancer syndrome, LKB1/STK11, at Ser431 by p90(RSK) and cAMP-dependent protein kinase
RET proto-oncogene (2,252 words) [view diff] exact match in snippet view article find links to article
Activating point mutations in RET can give rise to the hereditary cancer syndrome known as multiple endocrine neoplasia type 2 (MEN 2). There are three
Genetic testing (5,178 words) [view diff] exact match in snippet view article find links to article
risk of breast cancer. Hereditary breast cancer along with ovarian cancer syndrome are caused by gene alterations in the genes BRCA1 and BRCA2. Major
First family of the United States (234 words) [view diff] exact match in snippet view article find links to article
wasting disease called medullary thyroid cancer as part of the genetic cancer syndrome – multiple endocrine neoplasia, type 2B – that his father and two of
Phakomatosis (1,973 words) [view diff] exact match in snippet view article find links to article
inherited or de novo germline mutation, with the inherited familial cancer syndrome predisposing individuals for genetic mutations in the VHL gene. In
RHBDF2 (818 words) [view diff] exact match in snippet view article find links to article
"RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome". American Journal of Human Genetics. 90 (2): 340–6. doi:10.1016/j
Papillary thyroid cancer (3,828 words) [view diff] exact match in snippet view article find links to article
20 years after the exposure to radiation. Family history of thyroid cancer syndrome such as familial adenomatous polyposis, Carney complex, Multiple endocrine
Colorectal cancer (13,001 words) [view diff] exact match in snippet view article find links to article
familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome". Langenbecks Arch. Surg. 388 (1): 9–16. doi:10.1007/s00423-003-0364-8
Exonuclease 1 (1,528 words) [view diff] exact match in snippet view article find links to article
mutants identified in atypical hereditary nonpolyposis colorectal cancer syndrome". Cancer Res. 62 (21): 6026–30. PMID 12414623. Strausberg RL, Feingold
Hysterectomy (7,614 words) [view diff] exact match in snippet view article find links to article
manifestation of an undiagnosed hereditary leiomyomatosis and renal cell cancer syndrome. Removal of the uterus without removing the ovaries can produce a situation
Sebaceous carcinoma (3,242 words) [view diff] exact match in snippet view article find links to article
reported of SGc arising from nevus sebaceus. MTS is an autosomal dominant cancer syndrome characterized by multiple sebaceous and visceral neoplasms, the most
Uterine fibroid (6,569 words) [view diff] exact match in snippet view article find links to article
part or early symptom of the hereditary leiomyomatosis and renal cell cancer syndrome. Most fibroids do not require treatment unless they are causing symptoms
NTHL1 (1,338 words) [view diff] exact match in snippet view article find links to article
PMID 22331172. Kuiper RP, Hoogerbrugge N (2015). "NTHL1 defines novel cancer syndrome". Oncotarget. 6 (33): 34069–70. doi:10.18632/oncotarget.5864. PMC 4741436
Roxana Moslehi (1,221 words) [view diff] exact match in snippet view article find links to article
mutations in an Iranian family with hereditary breast and ovarian cancer syndrome". American Journal of Medical Genetics. 117A (3): 304–305. doi:10.1002/ajmg
MSH2 (4,089 words) [view diff] exact match in snippet view article find links to article
(2002). "Mismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC)". Cancer Invest. 20 (1): 102–9. doi:10.1081/cnv-120000371.
Computed tomography of the thyroid (5,700 words) [view diff] exact match in snippet view article find links to article
body radiation exposure, and familial thyroid carcinoma or thyroid cancer syndrome. Syndromes associated with thyroid cancer include multiple endocrine
Renal cell carcinoma (10,773 words) [view diff] exact match in snippet view article find links to article
sporadically Only 2 – 4% of the cases presenting as part of an inherited cancer syndrome Papillary Renal Cell Carcinoma (PRCC) Type 1 PRCC consist of papillae
DNA repair-deficiency disorder (3,785 words) [view diff] exact match in snippet view article find links to article
PMID 23545420. Kuiper RP, Hoogerbrugge N (2015). "NTHL1 defines novel cancer syndrome". Oncotarget. 6 (33): 34069–70. doi:10.18632/oncotarget.5864. PMC 4741436
J. William Harbour (2,045 words) [view diff] exact match in snippet view article find links to article
Discovered the first germline BAP1 mutation and the BAP1 familial cancer syndrome. Discovered that histone deacetylase inhibitors reverse the biochemical
Breast cancer classification (9,206 words) [view diff] exact match in snippet view article find links to article
that arise in familial clusters, such as Hereditary breast—ovarian cancer syndrome, may have a dissimilar prognosis. Also potentially dissimilar treatment