Disease: Cowden syndrome
- A Case of Cowden Syndrome Presenting with Diverse Cutaneous Manifestations
- A New Frameshift Mutation of <em>PTEN</em> Gene Associated with Cowden Syndrome-Case Report and Brief Review of the Literature
- A New Frameshift Mutation of PTEN Gene Associated with Cowden Syndrome-Case Report and Brief Review of the Literature
- A rare case of oral squamous cell carcinoma in a patient with Cowden syndrome: Association or coincidence?
- A young female of Cowden syndrome presenting with Lhermitte-Duclos disease: An illustrative case
- Analysis of clinical features and genetic variant in a child with Cowden syndrome 1
- Anesthetic Considerations for an Adult With Bannayan-Riley-Ruvalcaba Syndrome: A Case Report
- Anesthetic Management for a Patient with Rosai-Dorfman Disease, Cowden Syndrome, and Lhermitte-Duclos Disease: An Extremely Rare Disease Combination
- Arteriovenous malformations as a presenting sign of PTEN hamartoma tumor syndrome: A case series
- Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
- Basaloid follicular hamartoma syndrome: acquired sporadic variant with hypothyroidism, hypohidrosis and alopecia, a rare case
- Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study
- Brain and/or Spinal Cord Tumors Accompanied with Other Diseases or Syndromes
- Case Report - Multinodular goiter in a patient with Congenital Hypothyroidism and Bannayan-Riley-Ruvalcaba syndrome: the possible synergic role of TPO and PTEN mutation
- Case report: Association between PTEN-gene variant and an aggressive case of multiple dAVFs
- Case report: Rare oral manifestations in Cowden syndrome with PTEN mutation
- Cell-free DNA fragmentomics and second malignant neoplasm risk in patients with PTEN hamartoma tumor syndrome
- Cerebellar phenotypes in germline PTEN mutation carriers
- Cerebral dural arteriovenous fistulas in patients with PTEN-related hamartoma tumor syndrome
- Cerebriform Plaques in Proteus Syndrome
- Children and young women in eastern and southern Africa are key to meeting 2030 HIV targets: time to accelerate action
- Clinical and molecular heterogeneity of syndromic hypothalamic hamartoma
- Clinical description of two cases of Cowden syndrome and the implication regarding thyroid cancer
- Clinical Guidelines for Diagnosis and Management of Cowden Syndrome/PTEN Hamartoma Tumor Syndrome in Children and Adults-Secondary Publication
- Colorectal Ganglioneuromas Associated with Cowden Syndrome
- Comparing synaptic proteomes across five mouse models for autism reveals converging molecular similarities including deficits in oxidative phosphorylation and Rho GTPase signaling
- Complications, treatment, and follow-up of peutz-jeghers syndrome: About 2 case reports
- Concurrent PTEN and PDGFRB Alterations Characterize Storiform Collagenoma
- Congenital Retinal Macrovessel and Cavernous Hemangioma in Cowden Syndrome - A Case Report and Review of Literature
- Counselling and management of women with genetic predisposition to gynaecological cancers
- Cowden Disease
- Cowden Syndrome Complicated with Thyroid Lesion: A Pediatric Case Report
- Cowden Syndrome With Gall Bladder Polyps and Incidental Gall Bladder Carcinoma
- Decreased Self-reported Physical Fitness Following SARS-CoV-2 Infection and the Impact of Vaccine Boosters in a Cohort Study
- Detection and yield of thyroid cancer surveillance in adults with PTEN hamartoma tumour syndrome
- Development of informant-report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes
- Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature
- Differential cell cycle checkpoint evasion by PTEN germline mutations associated with dichotomous phenotypes of cancer versus autism spectrum disorder
- Discovering Deleterious Single Nucleotide Polymorphisms of Human AKT1 Oncogene: An In Silico Study
- Early is Better: Report of a Cowden Syndrome
- Esophageal Manifestations of Dermatological Diseases, Diagnosis and Management
- Familial intestinal polyposis and device assisted enteroscopy: where do we stand?
- Familial nonmedullary thyroid cancer: a case series in Iranian patients with a meta-review of case series
- Giant cell collagenoma in a patient with Cowden syndrome: A rare case report and literature review with a focus on the spectrum of sclerotic fibroma and giant cell collagenoma
- Giant cell collagenomas associated with Cowden syndrome: A case report
- Gorlin Syndrome and Cowden Syndrome
- Hamartomatous polyps: Diagnosis, surveillance, and management
- Humoral immune responses associated with control of SARS-CoV-2 breakthrough infections in a vaccinated US military population
- Identification of a novel pathogenic deep intronic variant in PTEN resulting in pseudoexon inclusion in a patient with juvenile polyps
- Identification of c.104T > G, p.Met35Arg (NM_00314.8) variant in heterozygosity in exon 2 of the PTEN gene as the Causative Factor for Cowden Syndrome: A Medical Case Study
- Identification of c.104T>G, p.Met35Arg (NM_00314.8) heterozygous variant in exon 2 of PTEN as the causative factor for Cowden syndrome: a medical case study
- Identification of c.104T>G, p.Met35Arg (NM_00314.8) heterozygous variant in exon 2 of PTEN as the causative factor for Cowden syndrome: a medical case study
- Kidney cancer: Links between hereditary syndromes and sporadic tumorigenesis
- Knowledge Mapping of Cowden Syndrome: a Bibliometric Analysis
- Lhermitte-Duclos disease in a 51-year old patient
- Lhermitte-Duclos disease with concomitant KCNT2 gene mutation: report of an extremely rare combination
- Lhermitte-Duclos disease with excessive calcification in a septuagenarian: A case report
- Lhermitte-Duclos Disease: A Case Series
- Lhermitte-Duclos Disease: A Rare Entity With Typical Histology but Ambiguous Histogenesis
- Lhermitte-Duclos disease: A series of six cases
- Lhermitte-Duclos disease: A systematic review
- Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS)
- Lipomas: genetic basis of common skin lesions and their occurrence in rare diseases
- Longitudinal Analysis of Cancer Risk in Children and Adults With Germline PTEN Variants
- Meningioma getting a common presentation in uncommon Cowden syndrome: A case report
- Morphea after Silicone Implants
- Multiple bronchial carcinoids associated with Cowden syndrome
- Multiple fibrofolliculomas within a fibrous cephalic plaque in a patient with tuberous sclerosis
- Multiple rhabdomyomatous mesenchymal hamartomas in a patient with mosaic Barber-Say syndrome
- Narrow-band imaging with magnification for the diagnosis of colorectal adenoma in a patient with Cronkhite-Canada syndrome
- Neurofibromatosis Type 1
- Non-Odontogenic Tumors of the Jaws
- Novel anti-PTEN C2 domain monoclonal antibodies to analyse the expression and function of PTEN isoform variants
- Novel dermatological and skeletal features associated with PTEN variant in PTEN hamartoma tumor syndrome
- Ophthalmic manifestations and treatments of proteus syndrome: a case report and systematic review
- Optic nerve compression: a rare ocular manifestation of Proteus syndrome
- Orofacial Manifestations in a Middle-Aged Woman with Cowden Syndrome: A Case Image
- Pathologically confirmed pancreatic hamartoma after surgical resection with an aldosterone-producing adrenal tumor: a case report
- Peutz-Jeghers syndrome without <em>STK11</em> mutation may correlate with less severe clinical manifestations in Chinese patients
- Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients
- PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
- PTEN hamartoma tumour syndrome: case report based on data from the Iranian hereditary colorectal cancer registry and literature review
- Quantification of Proteus syndrome-associated lung disease
- Recovery From Psychotic Disorder: A Surgical Case With Lhermitte-Duclos Disease
- Refractory Choroidal Neovascularization in a Patient With Pseudoxanthoma Elasticum and Cowden Syndrome
- Renal Neoplasia Occurring in Patients With PTEN Hamartoma Tumor Syndrome : Clinicopathologic Study of 12 Renal Cell Carcinomas From 9 Patients and Association With Intrarenal "Lipomas"
- Renal Neoplasia Occurring in Patients With PTEN Hamartoma Tumor Syndrome: Clinicopathologic Study of 12 Renal Cell Carcinomas From 9 Patients and Association With Intrarenal "Lipomas"
- Sinonasal Neuroendocrine Carcinoma in Adult Proteus Syndrome
- Squamous Papilloma on the Hard Palate: A Rare Clinical Entity
- Synchronous and metachronous thyroid cancer, breast cancer, and melanoma in a premenopausal patient with Cowden syndrome
- The mitochondrial genome as a modifier of autism versus cancer phenotypes in <em>PTEN</em> hamartoma tumor syndrome
- The mitochondrial genome as a modifier of autism versus cancer phenotypes in PTEN hamartoma tumor syndrome
- Thyroid Nodules and Follicular Cell-Derived Thyroid Carcinomas in Children
- Thyroid pathology, a clue to PTEN hamartoma tumor syndrome
- Total pancreatoduodenectomy for multiple pancreatic cysts in von Hippel-Lindau disease presenting as obstructive jaundice: A case report
- Toward a better understanding of PHTS heterogeneity: commentary on 'Cell-type specific deficits in PTEN-mutant cortical organoids converge on abnormal circuit activity'
- Utilizing PTEN immunohistochemistry as a screening test for Cowden syndrome
- Visceral adiposity in patients with lipomatous hypertrophy of the interatrial septum
- What is in a name-Perifollicular fibroma or fibrofolliculoma?
- Yield of annual endometrial cancer surveillance in women with PTEN Hamartoma Tumor Syndrome