• 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 New Variant of the PTEN Gene in Relation to Cowden Syndrome Type 1
• 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
• Acute acquired comitant esotropia associated with Lhermitte-Duclos disease: a case report
• Analysis of clinical features and genetic variant in a child with Cowden syndrome 1
• Analysis of the loss of phosphatase and tensin homolog expression in thyroid tissue for the diagnosis of Cowden syndrome
• 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
• Autopsy case of linear nevus sebaceous syndrome with KRAS (G12D) mutation
• Basaloid follicular hamartoma syndrome: acquired sporadic variant with hypothyroidism, hypohidrosis and alopecia, a rare case
• Brain and/or Spinal Cord Tumors Accompanied with Other Diseases or Syndromes
• Can thyroid histomorphology identify patients with PTEN hamartoma tumour syndrome?
• 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
• Clinical and molecular heterogeneity of syndromic hypothalamic hamartoma
• Clinical Case of Mild Tatton-Brown-Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene
• 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
• 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 in a male patient with metachronous triple cancers and various clinical features:a case report
• Cowden Syndrome-Oral Finding
• Cowden Syndrome: A Rare Cause of Intestinal Polyposis
• 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
• Developmental and behavioral phenotypes of pediatric patients with PTEN hamartoma tumor syndrome
• 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
• Experience in a PHTS Expertise Centre: Yield of Thyroid Ultrasound Surveillance in Children with PTEN Hamartoma Tumor Syndrome
• Exploring the neurological features of individuals with germline PTEN variants: A multicenter study
• Exploring the Prevalence of Oral Features for Early Detection of PTEN Hamartoma Tumour Syndrome
• Facial Features of Hereditary Cancer Predisposition
• 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
• Genetic analysis of a Chinese pedigree affected with Cowden syndrome due to variant of PTEN gene
• 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
• Good's syndrome associated with multiple basal cell carcinomas
• Good's syndrome associated with multiple basal cell carcinomas
• Gorlin Syndrome and Cowden Syndrome
• Gyratory Seizures in Hypothalamic Hamartoma
• Histopathological phenotyping of cancers in PTEN Hamartoma Tumor Syndrome for improved recognition: A single-center study
• Humoral immune responses associated with control of SARS-CoV-2 breakthrough infections in a vaccinated US military population
• Identification of c.104T &gt; 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&gt;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
• Imaging findings of children with PTEN-related hamartoma tumor syndrome: a 20-year multicentric pediatric cohort
• Increased frequency of infections and autoimmune disease in adults with PTEN Hamartoma Tumour Syndrome
• Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review
• 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 in an Eight-Year-Old Boy: A Case Report
• 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 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
• Lipomatoses
• Meningioma getting a common presentation in uncommon Cowden syndrome: A case report
• Minimally Invasive Plasma Device Management of Multiple Benign Skin Cancers Associated with Rare Genodermatoses-Case Series and Review of the Therapeutic Methods
• Morphea after Silicone Implants
• Multiple bronchial carcinoids associated with Cowden syndrome
• Multiple rhabdomyomatous mesenchymal hamartomas in a patient with mosaic Barber-Say syndrome
• Neurofibromatosis Type 1
• Neuropsychological functioning of adults with PTEN hamartoma tumor syndrome
• Non-Odontogenic Tumors of the Jaws
• Novel anti-PTEN C2 domain monoclonal antibodies to analyse the expression and function of PTEN isoform variants
• 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
• Pediatric Challenges With Cowden Syndrome and Graves' Disease: A Case Report
• Proteus syndrome: a dermatologist's perspective -case report
• PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
• Quantification of Proteus syndrome-associated lung disease
• Sinonasal Neuroendocrine Carcinoma in Adult Proteus Syndrome
• Spinal Dural Arteriovenous Fistulas in a Patient with Cowden Syndrome and a Phosphatase and Tensin Homolog Mutation
• The Burden of Multiple Basal Cell Carcinomas: A Population-wide Study
• The Lhermitte-Duclos disease: A case report
• 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'
• Treatment and Diagnostic Approach for Lhermitte-Duclos Disease and Suspected Cowden Syndrome
• Trichilemmoma
• 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?