| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Keval Thakkar, Fnu Raveena, Aakash Kumar, Doongro Mal, Dileep Kumar, Neha Ahuja, Rahul Mandhan, Aqsa Baig, Manjeet Singh, Heeya Shah, Taha Sajjad, Mansi Sing. Giant Retinal Astrocytoma: A Case Report of an Uncommon Presentation of Tuberous Sclerosis in a Young Female. Case reports in neurological medicine. vol 2024. 2024-05-02. PMID:38694182. |
tuberous sclerosis (ts) is a rare multisystem autosomal dominant genetic disorder with characteristic pathognomonic genetic mutations involving the tsc (tuberous sclerosis complex) group of genes. |
2024-05-02 |
2024-05-04 |
Not clear |
| Marta Banchi, Tiziana Lanzolla, Arianna Di Napoli, Arianna Bandini, Guido Bocci, Maria Christina Co. Complete Remission of a Diffuse Large B-Cell Lymphoma in a Young Patient, with Severe Tuberous Sclerosis, Treated with Metronomic Chemotherapy and Ibrutinib: A Case Report. Chemotherapy. vol 69. issue 1. 2024-02-26. PMID:37549660. |
tuberous sclerosis (ts) is a rare autosomal dominant genetic multisystem disease caused by mutations in either the tsc1 or tsc2 gene and results in the growth of non-cancerous masses in several organs. |
2024-02-26 |
2024-02-29 |
human |
| Grigory A Yanus, Ekaterina Sh Kuligina, Evgeny N Imyanito. Hereditary Renal Cancer Syndromes. Medical sciences (Basel, Switzerland). vol 12. issue 1. 2024-02-23. PMID:38390862. |
these syndromes almost always have extrarenal manifestations, for example, von hippel-lindau (vhl) disease, fumarate hydratase tumor predisposition syndrome (fhtps), birt-hogg-dubé (bhd) syndrome, tuberous sclerosis (ts), etc. |
2024-02-23 |
2024-02-25 |
Not clear |
| Paula Basso Dias, Anna Carolina Badotti Linhares, Ana Barbara Dias Lopes Urzedo, Rony Carlos Preti, Leandro Cabral Zacharias, Leonardo Provetti Cunha, Mário Luiz Ribeiro Monteiro, Kenzo Hokazon. Optical coherence tomography detection of retinal neural loss in patients with tuberous sclerosis. International journal of retina and vitreous. vol 10. issue 1. 2024-02-04. PMID:38311784. |
tuberous sclerosis (ts) is a rare, multisystem genetic disease caused by mutations in the tsc1 and tsc2 genes, leading to abnormalities in cell differentiation and proliferation. |
2024-02-04 |
2024-02-07 |
Not clear |
| Shraddha Sawhney, Keta Vagha, Shantanu Gomase, Sham Lohiya, Priyanka Hampe, Ayesha A Ansari, Jayant D Vagha, Anshul Soo. The Early Presentation of a Classic Case of Tuberous Sclerosis: A Case Report. Cureus. vol 15. issue 10. 2023-12-01. PMID:38021796. |
tuberous sclerosis (ts) is a potentially severe medical disorder that poses a life-threatening risk and can lead to drastic lifestyle changes. |
2023-12-01 |
2023-12-07 |
Not clear |
| Paula Basso Dias, Anna Carolina Badotti Linhares, Kenzo Hokazon. Retinal hamartomas at different stages in a patient with tuberous sclerosis: A OCT-SS description. Clinical case reports. vol 11. issue 11. 2023-12-01. PMID:38028108. |
retinal astrocytic hamartoma (rah) is a benign glial tumor that may be present in patients with tuberous sclerosis (ts), contributing to the diagnosis of this syndrome. |
2023-12-01 |
2023-12-10 |
Not clear |
| Shraddha Sawhney, Keta Vagha, Shantanu Gomase, Sham Lohiya, Priyanka Hampe, Ayesha A Ansari, Jayant D Vagha, Anshul Soo. The Early Presentation of a Classic Case of Tuberous Sclerosis: A Case Report. Cureus. vol 15. issue 10. 2023-12-01. PMID:38021796. |
tuberous sclerosis (ts) is a potentially severe medical disorder that poses a life-threatening risk and can lead to drastic lifestyle changes. |
2023-11-29 |
2023-12-07 |
Not clear |
| Juliette A Meyer, Andrew Graydon, Carl Muthukumaraswamy, Hannah F Jone. Brachial artery aneurysm and bilateral posterior circulation strokes in a young child with tuberous sclerosis complex. BMJ case reports. vol 16. issue 11. 2023-11-14. PMID:37963668. |
although tuberous sclerosis (ts) may affect many organs, vascular manifestations involving medium- and large-size vessels are rare. |
2023-11-14 |
2023-11-20 |
Not clear |
| Marco Fogante, Fiammetta Ventura, Nicolò Schicchi, Luana Regnicolo, Chiara Potente, Giulio Argalia, Gabriele Polonar. Cardiac rhabdomyomas and cerebral lesions in 4 pediatric patients with tuberous sclerosis. Radiology case reports. vol 18. issue 8. 2023-06-08. PMID:37287722. |
a strong association exists between cardiac rhabdomyomas and tuberous sclerosis (ts), an autosomal dominant disease, characterized by diffuse lesions in the nervous system, such as cortical-subcortical tubers and subependymal nodules. |
2023-06-08 |
2023-08-14 |
Not clear |
| Laura Duque González, David Ocampo Moreno, Alejandro Echavarria Cross, Sergio Franco Sierra, Tomas Escobar Gi. Tuberous Sclerosis Associated With Aortic Stenosis and Endocarditis: A Case Report. Cureus. vol 15. issue 5. 2023-06-05. PMID:37273293. |
tuberous sclerosis (ts) is a multisystem neurocutaneous disorder with an autosomal dominant pattern of inheritance. |
2023-06-05 |
2023-08-14 |
Not clear |
| Rupesh Raina, Francis Lomanta, Siddhartha Singh, Alisha Anand, Riti Kalra, Vignasiddh Enukonda, Oren Barat, Davinder Pandher, Sidharth K Seth. Cystic Diseases of the Kidneys: From Bench to Bedside. Indian journal of nephrology. vol 33. issue 2. 2023-05-26. PMID:37234435. |
alternatively, phakomatoses-, also known as neurocutaneous syndromes, associated cystic kidney diseases include tuberous sclerosis (ts) and von hippel-lindau (vhl) disease. |
2023-05-26 |
2023-08-14 |
mouse |
| Takahiro Suzuki, Jérémy Chéret, Fernanda Dinelli Scala, Aysun Akhundlu, Jennifer Gherardini, Dana-Lee Demetrius, James D B O'Sullivan, Gorana Kuka Epstein, Alan J Bauman, Constantinos Demetriades, Ralf Pau. mTORC1 activity negatively regulates human hair follicle growth and pigmentation. EMBO reports. 2023-05-22. PMID:37212043. |
dysregulation of the activity of the mechanistic target of rapamycin complex 1 (mtorc1) is commonly linked to aging, cancer, and genetic disorders such as tuberous sclerosis (ts), a rare neurodevelopmental multisystemic disease characterized by benign tumors, seizures, and intellectual disability. |
2023-05-22 |
2023-08-14 |
human |
| A G Melikyan, A B Kozlova, P A Vlasov, M Yu Dorofeeva, L V Shishkina, S B Agrb. [Epilepsy surgery in children with tuberous sclerosis]. Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko. vol 87. issue 2. 2023-04-03. PMID:37011323. |
most children with tuberous sclerosis (ts) present with intractable seizures. |
2023-04-03 |
2023-08-14 |
Not clear |
| Abdulrahman Al-Abdulmalek, Reem Al-Suliman, Mohammad Abu-Tineh, Mostafa Ali, Mohamed A Yassi. The effectiveness of tyrosine kinase inhibitor for chronic myeloid leukemia in tuberous sclerosis. A case report and review of literature. Clinical case reports. vol 11. issue 3. 2023-03-21. PMID:36941833. |
the relationship between chronic myelogenous leukemia (cml) and tuberous sclerosis (ts) is unusual and uncommon. |
2023-03-21 |
2023-08-14 |
Not clear |
| Alaa N Turkistani, Mahmoud Fallatah, Aliaa H Ghoneim, Fahad Alghamdi, Saleh S Baees. Subependymal Giant Cell Astrocytoma Apoplexy: A Case Report and Systematic Review. Cureus. vol 15. issue 2. 2023-03-14. PMID:36915840. |
subependymal giant cell astrocytoma (sega) is the most common intracranial tumor in tuberous sclerosis (ts) patients. |
2023-03-14 |
2023-08-14 |
Not clear |
| Suzanne Quigley, Murva Asad, Colin Doherty, Danielle Byrne, Simon Cronin, Hugh Kearne. Concurrent diagnoses of Tuberous sclerosis and multiple sclerosis. Multiple sclerosis and related disorders. vol 71. 2023-03-02. PMID:36863086. |
tuberous sclerosis (ts) is a monogenic disorder which causes disabling neurological symptoms. |
2023-03-02 |
2023-08-14 |
Not clear |
| Sajiva Aryal, Suraj Sharma, Saman Aryal, Vikash Bhattara. Late diagnosis of tuberous sclerosis complex in a 40-year-old female presenting with abdominal pain: a case report. Annals of medicine and surgery (2012). vol 85. issue 2. 2023-02-27. PMID:36845801. |
tuberous sclerosis (ts) is a rare autosomal-dominant neurocutaneous disorder that is characterized by hamartomas affecting a variety of organs, including the brain, heart, kidneys, skin, lungs, and liver. |
2023-02-27 |
2023-08-14 |
Not clear |
| Eduarda Pinto, Marcos Veiga, Amets Sagarribay, Carla Conceiçã. Periodontoid Pseudotumor in Tuberous Sclerosis Associated With Neck Diffuse Lipomatosis. Cureus. vol 14. issue 12. 2023-01-20. PMID:36660515. |
tuberous sclerosis (ts) is a genetic multisystem disorder associated with the development of benign tumors in many organs. |
2023-01-20 |
2023-08-14 |
Not clear |
| Karen Litw. Shared mechanisms of neural circuit disruption in tuberous sclerosis across lifespan: Bridging neurodevelopmental and neurodegenerative pathology. Frontiers in genetics. vol 13. 2022-12-12. PMID:36506334. |
tuberous sclerosis (ts) is a rare genetic disorder manifesting with multiple benign tumors impacting the function of vital organs. |
2022-12-12 |
2023-08-14 |
Not clear |
| J Apps, R Gagen, E Neumann, G Solanki, M Englis. A 13-year patient journey of infant giant clival chordoma: case report and literature review. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2022-11-22. PMID:36414866. |
in 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (ts) kombogiorgas (childs nerv syst 22(10):1369-1374, 2006). |
2022-11-22 |
2023-08-14 |
Not clear |