Hamartoma Syndrome, Multiple

Multiple Hamartoma Syndrome, also known as Cowden disease, is a hereditary autosomal dominant condition associated with mutations in tumor suppressor PTEN. Here is the latest research.

August 18, 2020

RAGE and TLR4 differentially regulate airway hyperresponsiveness: implications for COPD

Allergy
Venkata Sita Rama Raju AllamMaria B Sukkar
September 10, 2020
Case Report
Open Access

Cutaneous Lesions as the Sole Presentation of Tuberous Sclerosis

Curēus
Mohanad AhmedMohamed Elfatih Mustafa
August 19, 2020
Open Access

Incidental Hamartoma in an elderly patient: a case report

BMC Ophthalmology
Tae-Sung JooJae-Ho Shin
August 18, 2020

Smooth Muscle Hamartoma and Striated Muscle Hamartoma: clinicopathologic characterization of two rare entities and literature review

Journal of Cutaneous Pathology
Iván A González, Louis P Dehner
August 31, 2020
Case Report
Open Access

A Male Patient With Breast Hamartoma: An Uncommon Finding

Curēus
Vincent T PhanQuan D Nguyen
August 25, 2020
Open Access

An extremely rare case of neuromuscular and vascular hamartoma of the appendix

Surgical Case Reports
Takahiro SasakiTakehito Otsubo
September 3, 2020
Case Report
Open Access

Brunner's glands hamartoma with pylorus obstruction: a case report and review of literature

Journal of Surgical Case Reports
Mohammed A BakirKhaled O Alsaad
September 13, 2020
Open Access

A novel TSC2 c.4511 T > C missense variant associated with tuberous sclerosis complex

BMC Medical Genetics
Shunzhi HeJing Li
August 28, 2020

Cryodebulking of endobronchial hamartoma via fibreoptic bronchoscopy and literature review

BMJ Case Reports
Boon Hau NgMohamed Faisal
September 11, 2020
Case Report
Open Access

Hints from a Female Patient with Breast Cancer Who Later Presented with Cowden Syndrome

Journal of breast cancer
Wen-Chung WangYen-Chein Lai
September 11, 2020

Comparative Enhancement of Motor Function and BDNF Expression Following Different Brain Stimulation Approaches in an Animal Model of Ischemic Stroke

Neurorehabilitation and Neural Repair
Serena-Kaye Kinley-Cooper SimsDeAnna L Adkins
August 17, 2020

The Role of Neuro-Ophthalmologists in the Care of Patients With Neurofibromatosis Type 2

Journal of Neuro-ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
Klara Landau
August 19, 2020
Open Access

Cowden syndrome is a risk factor for multiple neoplasm: a case report

World Journal of Surgical Oncology
Sofia MigueloteJ P Araújo Teixeira
September 3, 2020
Case Report
Open Access

Foveal Congenital Simple Hamartoma of Retinal Pigment Epithelium: A Report of Two Cases

Middle East African Journal of Ophthalmology
Abdulrahman H BadawiYahya A Alzahrani
September 10, 2020
Case Report
Open Access

Fetal axillary lymphangioma diagnosed on a 2D/4D ultrasound second trimester scan - a case report and short literature review

Medical Ultrasonography
Bogdan Ioan StefanescuBianca Georgiana Constantin
September 4, 2020
Open Access

Integrative Analysis of MAPK14 as a Potential Biomarker for Cardioembolic Stroke

BioMed Research International
Zhao LiQingxiu Wang
September 9, 2020

Swept-source optical coherence tomography angiography findings in choroidal and retinal tumors

Eye
Ahmet Kaan GündüzFunda Seher Özalp Ateş

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