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1. Full Text Lifetime cancer risks in individuals with germline PTEN mutations
by Tan, Min-Han and Mester, Jessica L and Ngeow, Joanne and Rybicki, Lisa A and Orloff, Mohammed S and Eng, Charis
Clinical Cancer Research, ISSN 1078-0432, 01/2012, Volume 18, Issue 2, pp. 400 - 407
Purpose: Age-adjusted cancer incidence and age-related penetrance studies have helped guide cancer risk assessment and management. PTEN hamartoma tumor... 
COWDEN-SYNDROME | MELANOMA | AUTISM | ONCOLOGY | HAMARTOMA-TUMOR-SYNDROME | DISEASE | WILL | BRCA1 | SPECTRUM | CARRIERS | SYNDROME PLEASE STAND | Colorectal Neoplasms - epidemiology | PTEN Phosphohydrolase - genetics | Kidney Neoplasms - genetics | Hamartoma Syndrome, Multiple - genetics | Kidney Neoplasms - epidemiology | Prospective Studies | Genetic Association Studies | Colorectal Neoplasms - genetics | Humans | Risk Factors | Thyroid Neoplasms - epidemiology | Penetrance | Codon, Nonsense | Endometrial Neoplasms - epidemiology | Mutation, Missense | Hamartoma Syndrome, Multiple - epidemiology | Incidence | Thyroid Neoplasms - genetics | Breast Neoplasms - genetics | Endometrial Neoplasms - genetics | Germ-Line Mutation | Female | Breast Neoplasms - epidemiology | Cowden syndrome | cancer risk assessment and genetic counseling | PTEN | lifetime cancer risk
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2. Full Text PTEN, DICER1, FH, and their associated tumor susceptibility syndromes: Clinical features, genetics, and surveillance recommendations in childhood
by Schultz, Kris Ann P and Rednam, Surya P and Kamihara, Junne and Doros, Leslie and Achatz, Maria Isabel and Wasserman, Jonathan D and Diller, Lisa R and Brugières, Laurence and Druker, Harriet and Schneider, Katherine A and McGee, Rose B and Foulkes, William D
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e76 - e82
PTEN hamartoma tumor syndrome (PHTS), DICER1 syndrome, and hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome are pleiotropic tumor... 
PLEUROPULMONARY BLASTOMA REGISTRY | GENOTYPE-PHENOTYPE CORRELATIONS | HLRCC | ONCOLOGY | GERMLINE MUTATIONS | HEREDITARY LEIOMYOMATOSIS | FUMARATE-HYDRATASE | THYROID-NODULES | RISK-ASSESSMENT | RENAL-CELL CANCER | CHILDREN | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Leiomyomatosis - epidemiology | PTEN Phosphohydrolase - genetics | Neoplastic Syndromes, Hereditary - pathology | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Ribonuclease III - genetics | Early Detection of Cancer | Uterine Neoplasms - pathology | Humans | Risk Factors | Uterine Neoplasms - epidemiology | Fumarate Hydratase - genetics | Skin Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | DEAD-box RNA Helicases - genetics | Neoplastic Syndromes, Hereditary - epidemiology | Skin Neoplasms - genetics | Leiomyomatosis - pathology | Neoplastic Syndromes, Hereditary - genetics | Leiomyomatosis - genetics | Child | Brain | Brain tumors | Pineal gland | Melanoma | Disorders | Health risks | Risk | Neoplasms | Thyroid carcinoma | Thyroid cancer | Uterus | Goiter | Pituitary | Genetics | Adults | Children | Health risk assessment | Neoplasia | Endometrium | PTEN protein | Clear cell-type renal cell carcinoma | Cancer | Thyroid | Tumors
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3. Full Text Frequent Gastrointestinal Polyps and Colorectal Adenocarcinomas in a Prospective Series of PTEN Mutation Carriers
by Heald, Brandie and Mester, Jessica and Rybicki, Lisa and Orloff, Mohammed S and Burke, Carol A and Eng, Charis
Gastroenterology, ISSN 0016-5085, 2010, Volume 139, Issue 6, pp. 1927 - 1933
Background & Aims Germline phosphatase and tensin homolog ( PTEN ) mutations cause Cowden syndrome (CS), associated with breast and thyroid cancers. Case... 
Gastroenterology and Hepatology | Colorectal Cancer | PTEN | Cowden Syndrome | Hamartomatous Polyposis | DISEASE MULTIPLE HAMARTOMA | CARCINOMAS | COWDENS-DISEASE | GASTROENTEROLOGY & HEPATOLOGY | Adenocarcinoma - pathology | Colorectal Neoplasms - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Young Adult | Intestinal Polyps - genetics | Gene Deletion | Adult | Female | Adenocarcinoma - genetics | Child | Colorectal Neoplasms - epidemiology | Intestinal Polyps - epidemiology | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Risk Factors | Endoscopy, Gastrointestinal | Hamartoma Syndrome, Multiple - epidemiology | Point Mutation | Phenotype | Adolescent | Intestinal Polyps - pathology | Aged | Adenocarcinoma - epidemiology | Colorectal Neoplasms - pathology | Genetic research | Medical colleges | Genetic aspects | Thyroid cancer | Phosphatases | Gastrointestinal diseases | Sects | Cowden syndrome | colorectal cancer | hamartomatous polyposis
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4. Full Text Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood
by Achatz, M.I and Porter, C.C and Brugieres, L and ker, H and Frebourg, T and Foulkes, W.D and Kratz, C.P and Kuiper, R.P and Hansford, J.R and Hernandez, H.S and Nathanson, K.L and Kohlmann, W.K and Doros, L and Onel, K and Schneider, K.W and Scollon, S.R and Tabori, U and Tomlinson, G.E and Evans, D.G and Plon, S.E
Clinical Cancer Research, ISSN 1078-0432, 2017, Volume 23, Issue 13, pp. e107 - e114
Hereditary gastrointestinal cancer predisposition syndromes have been well characterized, but management strategies and surveillance remain a major challenge,... 
ONCOLOGY | SURVEILLANCE RECOMMENDATIONS | PEUTZ-JEGHERS-SYNDROME | COLORECTAL-CANCER | GERMLINE MUTATIONS | RISK | FAMILIAL ADENOMATOUS POLYPOSIS | SPECTRUM | MUTYH-ASSOCIATED POLYPOSIS | NATURAL-HISTORY | DESMOID TUMORS | Pediatrics | Genetic Predisposition to Disease | Gastrointestinal Neoplasms - genetics | Genetic Testing | Hamartoma Syndrome, Multiple - genetics | Early Detection of Cancer | Humans | Adenomatous Polyposis Coli - epidemiology | Gastrointestinal Neoplasms - diagnosis | Peutz-Jeghers Syndrome - epidemiology | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - epidemiology | Gastrointestinal Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - diagnosis | Peutz-Jeghers Syndrome - diagnosis | Adenomatous Polyposis Coli - genetics | Child | Adenomatous Polyposis Coli - diagnosis | Disorders | Health risks | Management | Polyposis coli | Medical screening | Smad4 protein | Genetic screening | Neoplasms | Adenomatous polyposis coli | Literature reviews | LKB1 protein | Surveillance | Mismatch repair | Children | Repair | Neoplasia | Risk management | PTEN protein | Cancer
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5. Full Text Incidence and Clinical Characteristics of Thyroid Cancer in Prospective Series of Individuals with Cowden and Cowden-Like Syndrome Characterized by Germline PTEN, SDH, or KLLN Alterations
by Ngeow, Joanne and Mester, Jessica and Rybicki, Lisa A and Ni, Ying and Milas, Mira and Eng, Charis
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 12/2011, Volume 96, Issue 12, pp. E2063 - E2071
Context: Thyroid cancer is believed to be an important component of Cowden syndrome (CS). Germline PTEN and SDHx mutations and KLLN epimutation cause CS and... 
GENE-MUTATIONS | PROTEIN | BANNAYAN-ZONANA-SYNDROME | DISEASE | ENDOCRINOLOGY & METABOLISM | PROMOTER MUTATIONS | HEREDITARY PARAGANGLIOMA | RILEY-RUVALCABA-SYNDROME | SPECTRUM | EXPRESSION | DELETIONS | Adenocarcinoma - pathology | Prospective Studies | Humans | Middle Aged | Thyroid Neoplasms - epidemiology | Male | Incidence | DNA Mutational Analysis | Tumor Suppressor Proteins - genetics | Aged, 80 and over | Adult | Female | Adenocarcinoma - genetics | Child | PTEN Phosphohydrolase - genetics | Promoter Regions, Genetic | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Hamartoma Syndrome, Multiple - epidemiology | Polymorphism, Genetic | Thyroid Neoplasms - genetics | Succinate Dehydrogenase - genetics | Adolescent | Aged | Adenocarcinoma - epidemiology | Thyroid Neoplasms - pathology | Advances in Genetics | JCEM Online
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6. Genetic skin diseases predisposing to basal cell carcinoma
by Castori, Marco and Morrone, Aldo and Kanitakis, Jean and Grammatico, Paola
European Journal of Dermatology, ISSN 1167-1122, 05/2012, Volume 22, Issue 3, pp. 299 - 309
Basal cell carcinoma (BCC) is the commonest cancer in humans. Predisposing factors reflect common genetic variations and environmental influences in most... 
Xeroderma pigmentosum | Folliculo-sebaceus unit | Basal cell carcinoma | Gorlin syndrome | Bazex-Dupré-Christol syndrome | Epidermal nevus syndrome | epidermal nevus syndrome | EPIDERMODYSPLASIA-VERRUCIFORMIS | CARTILAGE-HAIR HYPOPLASIA | xeroderma pigmentosum | DUPRE-CHRISTOL-SYNDROME | COARSE SPARSE HAIR | Bazex-Dupre-Christol syndrome | folliculo-sebaceus unit | SCHULZ-PASSARGE SYNDROME | DERMATOLOGY | FOLLICULAR HAMARTOMA SYNDROME | XERODERMA-PIGMENTOSUM | NEVUS SEBACEUS | basal cell carcinoma | ROTHMUND-THOMSON-SYNDROME | PHAKOMATOSIS-PIGMENTOKERATOTICA | Genetic Testing | Carcinoma, Basal Cell - genetics | Xeroderma Pigmentosum - genetics | Humans | Hypotrichosis - genetics | Rothmund-Thomson Syndrome - epidemiology | Carcinoma, Basal Cell - epidemiology | Carcinoma, Skin Appendage - genetics | Skin Diseases, Genetic - genetics | Nevus, Sebaceous of Jadassohn - epidemiology | Skin Diseases, Genetic - epidemiology | Werner Syndrome - genetics | Histiocytoma, Benign Fibrous - epidemiology | Facial Dermatoses - epidemiology | Histiocytoma, Benign Fibrous - genetics | Hamartoma Syndrome, Multiple - genetics | Facial Dermatoses - genetics | Hypotrichosis - epidemiology | Comorbidity | Cyanosis - epidemiology | Cyanosis - genetics | Basal Cell Nevus Syndrome - epidemiology | Xeroderma Pigmentosum - epidemiology | DNA Replication | Skin Neoplasms - epidemiology | Werner Syndrome - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | Rothmund-Thomson Syndrome - genetics | Skin Neoplasms - genetics | Carcinoma, Skin Appendage - epidemiology | Nevus, Sebaceous of Jadassohn - genetics | Basal Cell Nevus Syndrome - genetics | Mutation
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7. Full Text Correlates of multiple basal cell carcinoma in a retrospective cohort study: Sex, histologic subtypes, and anatomic distribution
by Kuo, Karen Y., MD and Batra, Prag, BS and Cho, Hyunje G., BA and Li, Shufeng, MS and Chahal, Harvind S., BA and Rieger, Kerri E., MD, PhD and Tang, Jean Y., MD, PhD and Sarin, Kavita Y., MD, PhD
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2017, Volume 77, Issue 2, pp. 233 - 234.e2
Dermatology | DERMATOLOGY | Immunohistochemistry | Skin Neoplasms - pathology | Age Distribution | Carcinoma, Basal Cell - therapy | Hamartoma Syndrome, Multiple - pathology | Prognosis | Skin Neoplasms - therapy | Humans | Middle Aged | Male | Carcinoma, Basal Cell - epidemiology | Carcinoma, Basal Cell - pathology | Skin Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | Incidence | Hamartoma Syndrome, Multiple - therapy | Neoplasm Invasiveness - pathology | Aged, 80 and over | Sex Distribution | Female | Aged | Retrospective Studies | Neoplasm Staging | Cohort Studies | Analysis | Skin cancer
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8. Full Text Papillary Renal Cell Carcinoma Is Associated With PTEN Hamartoma Tumor Syndrome
by Mester, Jessica L and Zhou, Ming and Prescott, Nichole and Eng, Charis
Urology, ISSN 0090-4295, 2012, Volume 79, Issue 5, pp. 1187.e1 - 1187.e7
Objective To formally study the prevalence and histologic classification of renal cell carcinoma (RCC) in a series of patients with PTEN hamartoma tumor... 
Urology | COWDEN-SYNDROME | UROLOGY & NEPHROLOGY | SUPPRESSOR | MUTATIONS | CANCER | EXPRESSION | Immunohistochemistry | PTEN Phosphohydrolase - genetics | Kidney Neoplasms - genetics | Hamartoma Syndrome, Multiple - genetics | Kidney Neoplasms - epidemiology | Prevalence | Carcinoma, Renal Cell - pathology | Humans | Middle Aged | Carcinoma, Renal Cell - genetics | Male | Hamartoma Syndrome, Multiple - epidemiology | Carcinoma, Renal Cell - epidemiology | Sex Factors | Adult | Female | Kidney Neoplasms - pathology | Mutation | Child | Carcinoma | Oncology, Experimental | Research | Carcinoma, Renal cell | Cancer | Hamartoma | Tumors | Cowden syndrome | Bannayan-Riley-Ruvalcaba syndrome | PTEN germline mutations | Carcinoma, Kidney
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9. Full Text Germline Alterations in RASAL1 in Cowden Syndrome Patients Presenting with Follicular Thyroid Cancer and in Individuals with Apparently Sporadic Epithelial Thyroid Cancer
by Ngeow, Joanne and Ni, Ying and Tohme, Rita and Song Chen, Fu and Bebek, Gurkan and Eng, Charis
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 07/2014, Volume 99, Issue 7, pp. E1316 - E1321
Context: RASAL1 has recently been identified as an important tumor suppressor for sporadic thyroid tumorigenesis, particularly for follicular thyroid cancer... 
PATHWAYS | RISKS | GENE | VARIANTS | PIK3CA | ENDOCRINOLOGY & METABOLISM | PTEN | MUTATIONS | BREAST | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Adenocarcinoma, Follicular - epidemiology | Gene Frequency | Humans | Middle Aged | Thyroid Neoplasms - epidemiology | Thyroid Carcinoma, Anaplastic | Adenocarcinoma, Follicular - genetics | Male | Hamartoma Syndrome, Multiple - epidemiology | Thyroid Neoplasms - genetics | Carcinoma, Papillary | Carcinoma - epidemiology | Germ-Line Mutation | Adult | Carcinoma - genetics | Female | Retrospective Studies | GTPase-Activating Proteins - genetics | JCEM Online | Brief Reports
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10. Full Text Characteristics of multiple basal cell carcinomas: The first study on Japanese patients
by Adachi, Koji and Yoshida, Yuichi and Noma, Hisashi and Goto, Hiroyuki and Yamamoto, Osamu
The Journal of Dermatology, ISSN 0385-2407, 10/2018, Volume 45, Issue 10, pp. 1187 - 1190
Basal cell carcinoma (BCC), the most frequent skin cancer, has been increasing in incidence. However, the characteristics of multiple BCC have not been... 
basal cell carcinoma | characteristics | multiple basal cell carcinomas | Japanese | retrospective study | RISK | DERMATOLOGY | Skin Neoplasms - pathology | Torso | Japan - epidemiology | Head | Hamartoma Syndrome, Multiple - pathology | Age Factors | Humans | Middle Aged | Male | Carcinoma, Basal Cell - epidemiology | Carcinoma, Basal Cell - pathology | Skin Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | Incidence | Aged, 80 and over | Adult | Female | Aged | Retrospective Studies | Neck | Skin - pathology | Medicine, Experimental | Medical research | Skin cancer | Head and neck | Population studies | Carcinoma | Public health
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11. Full Text Cumulative risks and rates of subsequent basal cell carcinomas in the Netherlands
by Flohil, S.C and Koljenović, S and de Haas, E.R.M and Overbeek, L.I.H and de Vries, E and Nijsten, T
British Journal of Dermatology, ISSN 0007-0963, 10/2011, Volume 165, Issue 4, pp. 874 - 881
Summary Background  The incidence of multiple basal cell carcinomas (BCCs) is not well documented. Objectives  To calculate the cumulative risks, rates and... 
SURVIVAL | NONMELANOMA SKIN-CANCER | NATIONWIDE | GUIDELINES | FOLLOW-UP | PREVALENCE | TRENDS | DERMATOLOGY | Follow-Up Studies | Humans | Middle Aged | Netherlands - epidemiology | Risk Factors | Male | Carcinoma, Basal Cell - epidemiology | Skin Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - epidemiology | Incidence | Neoplasms, Second Primary - epidemiology | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Risk factors | Histochemistry | Public health | Skin cancer | Cytopathology | Carcinoma | Diagnosis | Health risk assessment | Tumors
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12. Full Text Cowden syndrome: what oncology nurses need to know about increased risk of developing certain cancers
by Beamer, Laura Curr and Beamer, Laura C.urr
Oncology nursing forum, ISSN 0190-535X, 09/2014, Volume 41, Issue 5, pp. 555 - 557
Cowden syndrome (CS) is a genetic disorder characterized by multiple benign tissue growths (i.e., hamartomas) and an increased risk of developing specific... 
Cowden syndrome | risk management | breast cancer | cancer prevention | genetic cancer syndromes | ONCOLOGY | NURSING | GERMLINE PTEN MUTATIONS | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Early Detection of Cancer | Humans | Symptom Assessment | Male | Risk | Neoplasms - diagnosis | Hamartoma Syndrome, Multiple - nursing | Genetic Heterogeneity | Hamartoma Syndrome, Multiple - epidemiology | Succinate Dehydrogenase - genetics | Genes, Dominant | Neoplasms - genetics | Hamartoma Syndrome, Multiple - diagnosis | Tumor Suppressor Proteins - genetics | Oncology Nursing - education | Female | Genes, Tumor Suppressor | Neoplasms - epidemiology | Practice Guidelines as Topic | Care and treatment | Nurses | Oncologic nursing | Practice | Multiple hamartoma syndrome | Methods | Risk factors | Cancer
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13. Full Text StatBite. Lifetime risk of selected cancers for people with Cowden syndrome
Journal of the National Cancer Institute, ISSN 0027-8874, 03/2011, Volume 103, Issue 5, pp. 363 - 363
United States - epidemiology | Neoplasms - genetics | Humans | Thyroid Neoplasms - epidemiology | Female | Risk | Endometrial Neoplasms - epidemiology | Hamartoma Syndrome, Multiple - complications | Hamartoma Syndrome, Multiple - epidemiology | Neoplasms - epidemiology | Breast Neoplasms - epidemiology
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14. Full Text Trichilemmoma in Childhood
by Ng, Doreen W., RN, CPNP
Journal of Pediatric Health Care, ISSN 0891-5245, 2016, Volume 30, Issue 5, pp. 491 - 494
Pediatrics | Advanced Practice Nursing | Cowden syndrome | neck lesion | Benign tumor | pediatric | COWDEN-SYNDROME | NEOPLASMS | NURSING | PEDIATRICS | HEALTH POLICY & SERVICES | Hair Diseases - pathology | Hair Diseases - epidemiology | Hamartoma Syndrome, Multiple - pathology | Humans | Skin Diseases - epidemiology | Skin Diseases - pathology | Child | Hamartoma Syndrome, Multiple - epidemiology | Hair Follicle - pathology
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15. Hamartomatous polyposis
by Sakamoto, Hirotsugu and Yano, Tomonori and Sunada, Keijiro
Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology, ISSN 0446-6586, 2017, Volume 114, Issue 3, p. 422
Adenomatous Polyposis Coli - complications | Age Distribution | Hamartoma Syndrome, Multiple - genetics | Neoplasms - etiology | Humans | Chromosomes, Human | Adenomatous Polyposis Coli - genetics | Hamartoma Syndrome, Multiple - complications | Hamartoma Syndrome, Multiple - epidemiology
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16. Full Text Pulmonary Arterial Hypertension in a Patient With Cowden Syndrome and Anorexigen Exposure
by Natali, Delphine and Girerd, Barbara, PhD and Montani, David, MD, PhD and Soubrier, Florent, MD, PhD and Simonneau, Gérald, MD and Humbert, Marc, MD, PhD and Sitbon, Olivier, MD, PhD
Chest, ISSN 0012-3692, 2011, Volume 140, Issue 4, pp. 1066 - 1068
We report a case of pulmonary arterial hypertension (PAH) occurring in a patient with Cowden syndrome with a mutation in the phosphatase and tensin ( PTEN )... 
Pulmonary/Respiratory | PTEN | RESPIRATORY SYSTEM | CRITICAL CARE MEDICINE | PTEN Phosphohydrolase - genetics | Appetite Depressants - adverse effects | Hamartoma Syndrome, Multiple - genetics | Comorbidity | Humans | Middle Aged | Risk Factors | Dexfenfluramine - adverse effects | Familial Primary Pulmonary Hypertension | Hypertension, Pulmonary - genetics | Hypertension, Pulmonary - epidemiology | Mutation - genetics | Hamartoma Syndrome, Multiple - epidemiology | Pedigree | Female | Case studies | Analysis | Development and progression | Tumor suppressor genes | Genetic aspects | Dexfenfluramine | Multiple hamartoma syndrome | Health aspects | Pulmonary hypertension
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17. Genetics of Cowden syndrome: Through the looking glass of oncology (Review)
by Eng, Charis
International Journal of Oncology, ISSN 1019-6439, 03/1998, Volume 12, Issue 3, pp. 701 - 710
Cowden syndrome (CS) is an autosomal dominant inherited syndrome characterised by hamartoma development in multiple organs and a risk of breast, thyroid and... 
PTEN | Bannayan-Ruvalcaba-Riley | Breast cancer | Cowden | Thyroid cancer | LOCALIZATION | ACTIN | ONCOLOGY | MULTIPLE HAMARTOMA SYNDROME | breast cancer | thyroid cancer | LHERMITTE-DUCLOS DISEASE | RILEY-RUVALCABA-SYNDROME | FAMILY | Predictive Value of Tests | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Humans | Chromosome Mapping | Genetic Counseling | Hamartoma Syndrome, Multiple - epidemiology | Incidence | Phosphoric Monoester Hydrolases | Protein Tyrosine Phosphatases - genetics | PTEN Phosphohydrolase | Mutation | Chromosomes, Human, Pair 10 | Genes, Tumor Suppressor | Tumor Suppressor Proteins
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18. Full Text Breast cancer in cowden syndrome: Manifestation of a familial cancer syndrome
by Erickson, Janetlynne and Lyon, Debra E
Clinical Journal of Oncology Nursing, ISSN 1092-1095, 02/2010, Volume 14, Issue 1, pp. 33 - 35
Cowden syndrome is a familial cancer predisposition syndrome associated with an increased risk for breast, thyroid, and endometrial cancers and benign... 
PTEN | WILL | ONCOLOGY | NURSING | SYNDROME PLEASE STAND | Medical History Taking | United States - epidemiology | Genetic Predisposition to Disease | Breast Neoplasms - genetics | Hamartoma Syndrome, Multiple - genetics | Humans | Adult | Female | Hamartoma Syndrome, Multiple - epidemiology | Breast Neoplasms - epidemiology | Prevention | Complications and side effects | Care and treatment | Prognosis | Gene mutations | Physiological aspects | Breast cancer | Genetic aspects | Risk factors | Hamartoma
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19. Full Text Association of Lhermitte-Duclos and Cowden disease: report of a new case and review of the literature
by Vinchon, M and Blond, S and Lejeune, J P and Krivosik, I and Fossati, P and Assaker, R and Christiaens, J L
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 06/1994, Volume 57, Issue 6, pp. 699 - 704
Lhermitte-Duclos disease is a rare entity, and its pathological features are unique. Pathological findings are characteristic of the disease, with global... 
SURGERY | MRI | PSYCHIATRY | CEREBELLUM | TUBEROUS SCLEROSIS | PREOPERATIVE DIAGNOSIS | DYSPLASTIC GANGLIOCYTOMA | CLINICAL NEUROLOGY | GRANULOMOLECULAR HYPERTROPHY
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20. Full Text A novel PTEN mutation in a Japanese patient with Cowden disease
by Kubo, Y and Urano, Y and Hida, Y and Ikeuchi, T and Nomoto, M and Kunitomo, K and Arase, S
British Journal of Dermatology, ISSN 0007-0963, 06/2000, Volume 142, Issue 6, pp. 1100 - 1105
Cowden disease (CD) is an autosomal dominant syndrome characterized by multiple hamartomatous lesions and an increased risk for malignancies. Recent evidence... 
Cowden disease | genodermatosis | PTEN mutation | Genodermatosis | HUMAN SKIN | PHOSPHATASE | TUMOR-SUPPRESSOR GENE | PTEN/MMAC1 GENE | LOCUS | MMAC1 | BREAST-CANCER | MULTIPLE HAMARTOMA | DERMATOLOGY & VENEREAL DISEASES | GERMLINE MUTATIONS | SQUAMOUS-CELL CARCINOMAS | Japan - epidemiology | Phosphoric Monoester Hydrolases - genetics | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Humans | Middle Aged | Hamartoma Syndrome, Multiple - epidemiology | Polymorphism, Single-Stranded Conformational | PTEN Phosphohydrolase | DNA Mutational Analysis | Polymerase Chain Reaction | Germ-Line Mutation | Adult | Female | Tumor Suppressor Proteins
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