نتایج جستجو برای: tuberous sclerosis

تعداد نتایج: 65457  

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1992

2012
Mary Kay Koenig Adelaide A. Hebert Joan Roberson Joshua Samuels John Slopis Audrey Woerner Hope Northrup

BACKGROUND AND OBJECTIVES Facial angiofibromas are disfiguring facial lesions, present in up to 80% of patients with tuberous sclerosis complex. Recent elucidation of the complex cell signaling pathways that are disrupted in tuberous sclerosis indicates that rapamycin may be successful in alleviating the appearance of these lesions. The objectives of the current study were to evaluate the safet...

2014
Pietro Sciacca Valentina Giacchi Carmine Mattia Filippo Greco Pierluigi Smilari Pasqua Betta Giuseppe Distefano

BACKGROUND Rhabdomyomas are the most common type of cardiac tumors in children. Anatomically, they can be considered as hamartomas. They are usually randomly diagnosed antenatally or postnatally sometimes presenting in the neonatal period with haemodynamic compromise or severe arrhythmias although most neonatal cases remain asymptomatic. Typically rhabdomyomas are multiple lesions and usually r...

Journal: :Journal of Neuropathology and Experimental Neurology 1990

Journal: :British Journal of Psychiatry 1987

Journal: :Journal of Nihon University Medical Association 2012

Journal: :Indian Journal of Radiology and Imaging 2006

Journal: :Genes & development 2008
Jill Wildonger Lily Yeh Jan Yuh Nung Jan

Neuronal function depends on the specification of neuronal processes as axons or dendrites. In this issue of Genes & Development Choi and colleagues (2485-2495) show that without Tuberous Sclerosis Complex 1 (Tsc1) or Tsc2, molecules linked to the autosomal dominant disease tuberous sclerosis, an increase in the activity of the translational regulator Target of Rapamycin 1 (TORC1) causes neuron...

2009
Flavia Gavinho Vianna Edson Marchiori Glaucia Zanetti Claudia Mauro Mano Branca Sarcinelli-Luz Juliana Franca Carvalho Carla Assed Isabella Guedes Santos Alair Augusto Santos Alberto Domingues Vianna

The authors describe a case of a 31-year-old female with tuberous sclerosis, a genetic, rare, variably expressed disease. Clinical symptoms were chest pain, and progressive dyspnea. Computed tomography scan of the chest showed bilateral, diffuse, small thin-walled cysts scattered throughout the lungs characteristic for pulmonary lymphangioleiomyomatosis. Computed tomography scan of the abdomen ...

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